☰

Steven M. Bischof, PhD - Publications

Affiliations: 
Chevron Phillips Chemical Co. LP 
Area:
Organometallic Catalysis
Website:
http://www.cpchem.com
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78/273 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Maley SM, Lief GR, Buck RM, Sydora OL, Yang Q, Bischof SM, Ess DH. Density functional theory and CCSD(T) evaluation of ionization potentials, redox potentials, and bond energies related to zirconocene polymerization catalysts. Journal of Computational Chemistry. PMID 35662063 DOI: 10.1002/jcc.26890  0.453
2020 Maley SM, Kwon DH, Rollins N, Stanley JC, Sydora OL, Bischof SM, Ess DH. Quantum-mechanical transition-state model combined with machine learning provides catalyst design features for selective Cr olefin oligomerization. Chemical Science. 11: 9665-9674. PMID 34094231 DOI: 10.1039/d0sc03552a  0.454
2020 Maley S, Kwon D, Rollins N, Stanley JC, Sydora OL, Bischof SM, Ess DH. Quantum-mechanical transition-state model combined with machine learning provides catalyst design features for selective Cr olefin oligomerization Chemical Science. 11: 9665-9674. DOI: 10.1039/D0Sc03552A  0.496
2020 Kwon D, Maley SM, Stanley JC, Sydora OL, Bischof SM, Ess DH. Why Less Coordination Provides Higher Reactivity Chromium Phosphinoamidine Ethylene Trimerization Catalysts Acs Catalysis. 10: 9674-9683. DOI: 10.1021/Acscatal.0C02595  0.564
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/Acs.Jpcc.9B00129  0.496
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.37
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/Acscatal.8B01972  0.657
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/Acscatal.7B04026  0.724
2017 Gunsalus NJ, Koppaka A, Park SH, Bischof SM, Hashiguchi BG, Periana RA. Homogeneous Functionalization of Methane. Chemical Reviews. PMID 28459540 DOI: 10.1021/Acs.Chemrev.6B00739  0.77
2017 Kelly CM, Fuller JT, Macaulay CM, McDonald R, Ferguson MJ, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Dehydrogenative B-H/C(sp(3) )-H Benzylic Borylation within the Coordination Sphere of Platinum(II). Angewandte Chemie (International Ed. in English). PMID 28370808 DOI: 10.1002/Anie.201700857  0.518
2015 Kelly CM, Kwon DH, Ferguson MJ, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Synthesis and Reactivity of a Neutral, Three-Coordinate Platinum(II) Complex Featuring Terminal Amido Ligation. Angewandte Chemie (International Ed. in English). PMID 26448263 DOI: 10.1002/Anie.201506871  0.519
2014 Konnick MM, Bischof SM, Yousufuddin M, Hashiguchi BG, Ess DH, Periana RA. A mechanistic change results in 100 times faster CH functionalization for ethane versus methane by a homogeneous Pt catalyst. Journal of the American Chemical Society. 136: 10085-94. PMID 24925375 DOI: 10.1021/Ja504368R  0.803
2014 Hashiguchi BG, Konnick MM, Bischof SM, Gustafson SJ, Devarajan D, Gunsalus N, Ess DH, Periana RA. Main-group compounds selectively oxidize mixtures of methane, ethane, and propane to alcohol esters. Science (New York, N.Y.). 343: 1232-7. PMID 24626925 DOI: 10.1126/Science.1249357  0.784
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4Ra90009J  0.485
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.731
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Correction: Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Adv.. 4: 43335-43335. DOI: 10.1039/C4RA90009J  0.323
2014 Bischof SM, Hashiguchi BG, Lokare KS, Gunsalus N, Yousufuddin M, Periana RA. Iridium(iii) catalyzed trifluoroacetoxylation of aromatic hydrocarbons Rsc Advances. 4: 35639-35648. DOI: 10.1039/C4Ra06251E  0.773
2014 Stowe RL, Bischof SM, Konnick MM, Hövelmann CH, Leach-Scampavia D, Periana RA, Hashiguchi BG. Making water the exciting way: A classroom demonstration of catalysis Journal of Chemical Education. 91: 550-553. DOI: 10.1021/Ed4006024  0.763
2014 Konnick MM, Bischof SM, Ess DH, Periana RA, Hashiguchi BG. Base accelerated generation of N2 and NH3 from an osmium nitride Journal of Molecular Catalysis a: Chemical. 382: 1-7. DOI: 10.1016/J.Molcata.2013.10.019  0.755
2013 Mironov OA, Bischof SM, Konnick MM, Hashiguchi BG, Ziatdinov VR, Goddard WA, Ahlquist M, Periana RA. Using reduced catalysts for oxidation reactions: mechanistic studies of the "Periana-Catalytica" system for CH4 oxidation. Journal of the American Chemical Society. 135: 14644-58. PMID 23927450 DOI: 10.1021/Ja404895Z  0.757
2013 Bischof SM, Hashiguchi BG, Konnick MM, Periana RA. Designing molecular catalysts for selective CH functionalization Topics in Organometallic Chemistry. 44: 195-231. DOI: 10.1007/3418-2012-46  0.786
2013 Konnick MM, Bischof SM, Periana RA, Hashiguchi BG. The hydroxide-promoted catalytic hydrodefluorination of fluorocarbons by ruthenium in aqueous media Advanced Synthesis and Catalysis. 355: 632-636. DOI: 10.1002/Adsc.201200870  0.796
2012 Hashiguchi BG, Bischof SM, Konnick MM, Periana RA. Designing catalysts for functionalization of unactivated C-H bonds based on the CH activation reaction. Accounts of Chemical Research. 45: 885-98. PMID 22482496 DOI: 10.1021/Ar200250R  0.817
2012 Cheng MJ, Bischof SM, Nielsen RJ, Goddard WA, Gunnoe TB, Periana RA. The para-substituent effect and pH-dependence of the organometallic Baeyer-Villiger oxidation of rhenium-carbon bonds. Dalton Transactions (Cambridge, England : 2003). 41: 3758-63. PMID 22327118 DOI: 10.1039/C2Dt11984F  0.601
2011 Bhalla G, Bischof SM, Ganesh SK, Liu XY, Jones CJ, Borzenko A, Tenn WJ, Ess DH, Hashiguchi BG, Lokare KS, Leung CH, Oxgaard J, Goddard WA, Periana RA. Mechanism of efficient anti-markovnikov olefin hydroarylation catalyzed by homogeneous Ir(iii) complexes Green Chemistry. 13: 69-81. DOI: 10.1039/C0Gc00330A  0.76
2011 Bischof SM, Cheng MJ, Nielsen RJ, Gunnoe TB, Goddard WA, Periana RA. Functionalization of rhenium aryl bonds by O-atom transfer Organometallics. 30: 2079-2082. DOI: 10.1021/Om2002365  0.599
2011 Tenn WJ, Conley BL, Bischof SM, Periana RA. Synthesis, characterization, and C-H activation reactions of novel organometallic O-donor ligated Rh(III) complexes Journal of Organometallic Chemistry. 696: 551-558. DOI: 10.1016/J.Jorganchem.2010.09.021  0.768
2010 Bischof SM, Ess DH, Meier SK, Oxgaard J, Nielsen RJ, Bhalla G, Goddard WA, Periana RA. Benzene C-H bond activation in carboxylic acids catalyzed by O-donor iridium(III) complexes: An experimental and density functional study Organometallics. 29: 742-756. DOI: 10.1021/Om900036J  0.783
2010 Bischof SM, Periana RA, Ringenberg MR, Rauchfuss TB. Iridium Complexes: Oxygen and Carbon Bound Acetylacetonato Iridium(III) Complexes Inorganic Syntheses. 35: 173-178. DOI: 10.1002/9780470651568.ch9  0.409
2009 Tenn WJ, Conley BL, Hövelmann CH, Ahlquist M, Nielsen RJ, Ess DH, Oxgaard J, Bischof SM, Goddard WA, Periana RA. Oxy-functionalization of nucleophilic rhenium(I) metal carbon bonds catalyzed by selenium(IV). Journal of the American Chemical Society. 131: 2466-8. PMID 19161305 DOI: 10.1021/Ja806814C  0.755
2008 Ess DH, Bischof SM, Oxgaard J, Periana RA, Goddard WA. Transition state energy decomposition study of Acetate-Assisted and internal electrophilic substitution C-H Bond activation by (acac-O,O) 2Ir(X) complexes (X = CH 3COO, OH) Organometallics. 27: 6440-6445. DOI: 10.1021/Om8006568  0.656
Low-probability matches (unlikely to be authored by this person)
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Macaulay CM, Gustafson SJ, Fuller JT, Kwon D, Ogawa T, Ferguson MJ, McDonald R, Lumsden MD, Bischof SM, Sydora OL, Ess DH, Stradiotto M, Turculet L. Alkene Isomerization–Hydroboration Catalyzed by First-Row Transition-Metal (Mn, Fe, Co, and Ni) N-Phosphinoamidinate Complexes: Origin of Reactivity and Selectivity Acs Catalysis. 8: 9907-9925. DOI: 10.1021/acscatal.8b01972  0.22
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2018 Kwon D, Fuller JT, Kilgore UJ, Sydora OL, Bischof SM, Ess DH. Computational Transition-State Design Provides Experimentally Verified Cr(P,N) Catalysts for Control of Ethylene Trimerization and Tetramerization Acs Catalysis. 8: 1138-1142. DOI: 10.1021/acscatal.7b04026  0.219
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2019 Kwon D, Small BL, Sydora OL, Bischof SM, Ess DH. Challenge of Using Practical DFT to Model Fe Pendant Donor Diimine Catalyzed Ethylene Oligomerization The Journal of Physical Chemistry C. 123: 3727-3739. DOI: 10.1021/acs.jpcc.9b00129  0.145
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
2016 Lewellen R, Bischof S, Plum T. EBL ebook use compared to the use of equivalent print books and other eresources Performance Measurement and Metrics. 17: 150-164. DOI: 10.1108/PMM-04-2016-0013  0.021
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