| Year |
Citation |
Score |
| 2019 |
Yang Z, Hrovat DA, Hou GL, Borden WT, Wang XB. Negative Ion Photoelectron Spectroscopy Confirms the Prediction of a Singlet Ground State for the 1,8-Naphthoquinone Diradical. The Journal of Physical Chemistry. A. PMID 30869889 DOI: 10.1021/Acs.Jpca.8B11063 |
0.587 |
|
| 2018 |
Hrovat DA, Wang XB, Borden WT. Calculations on 1,8-naphthoquinone predict that the ground state of this diradical is a singlet. Journal of Computational Chemistry. PMID 30284300 DOI: 10.1002/Jcc.25551 |
0.583 |
|
| 2018 |
Yang Z, Hrovat DA, Hou GL, Borden WT, Wang XB. Negative Ion Photoelectron Spectroscopy Confirms the Prediction of the Relative Energies of the Low-Lying Electronic States of 2,7- Napthoquinone. The Journal of Physical Chemistry. A. PMID 29745661 DOI: 10.1021/Acs.Jpca.8B03239 |
0.612 |
|
| 2018 |
Hrovat DA, Wang X, Borden WT. Calculations of the relative energies of the low-lying electronic states of 2,7-naphthoquinodimethane and 2,7-naphthoquinone. Substitution of oxygen for CH2
is predicted to increase the singlet-triplet energy difference (ΔE
ST
) Journal of Physical Organic Chemistry. 31: e3824. DOI: 10.1002/Poc.3824 |
0.582 |
|
| 2017 |
Nandi A, Gerbig D, Schreiner PR, Borden WT, Kozuch S. Isotope-Controlled Selectivity by Quantum Tunneling: Hydrogen Migration versus Ring Expansion in Cyclopropylmethylcarbenes. Journal of the American Chemical Society. PMID 28635268 DOI: 10.1021/Jacs.7B04593 |
0.774 |
|
| 2016 |
Hou GL, Chen B, Transue WJ, Hrovat DA, Cummins CC, Borden WT, Wang XB. Negative ion photoelectron spectroscopy of PN: electron affinity and electronic structures of PN˙. Chemical Science. 7: 4667-4675. PMID 30155115 DOI: 10.1039/C5Sc04667J |
0.567 |
|
| 2016 |
Hrovat DA, Hou GL, Chen B, Wang XB, Borden WT. Negative ion photoelectron spectroscopy confirms the prediction that carbon trioxide (CO) has a singlet ground state. Chemical Science. 7: 1142-1150. PMID 29910870 DOI: 10.1039/C5Sc03542B |
0.587 |
|
| 2016 |
Hou GL, Chen B, Transue WJ, Hrovat DA, Cummins CC, Borden WT, Wang XB. A Joint Experimental and Computational Study of the Negative Ion Photoelectron Spectroscopy of the 1-Phospha-2,3,4-triazolate Anion, HCPN3(.) The Journal of Physical Chemistry. A. PMID 27434547 DOI: 10.1021/Acs.Jpca.6B06343 |
0.583 |
|
| 2016 |
Hrovat DA, Hou GL, Chen B, Wang XB, Borden WT. Negative ion photoelectron spectroscopy confirms the prediction that D3h carbon trioxide (CO3) has a singlet ground state Chemical Science. 7: 1142-1150. DOI: 10.1039/c5sc03542b |
0.492 |
|
| 2016 |
Chen B, Hrovat DA, Borden WT. Calculations of the energies of the low-lying electronic states of dioxatrimethylenemethane (H2CCO2) and prediction of the negative ion photoelectron (NIPE) spectrum of its radical anion Journal of Physical Organic Chemistry. 30: e3594. DOI: 10.1002/Poc.3594 |
0.584 |
|
| 2015 |
Liu J, Bao X, Hrovat DA, Borden WT. Theoretical Analysis of the Fragmentation of (CO)5: A Symmetry-Allowed Highly Exothermic Reaction that Follows a Stepwise Pathway. The Journal of Organic Chemistry. PMID 26375997 DOI: 10.1021/Acs.Joc.5B01546 |
0.586 |
|
| 2015 |
Hrovat DA, Hou GL, Wang XB, Borden WT. Negative Ion Photoelectron Spectroscopy Confirms the Prediction that 1,2,4,5-Tetraoxatetramethylenebenzene Has a Singlet Ground State. Journal of the American Chemical Society. PMID 26172391 DOI: 10.1021/Jacs.5B04416 |
0.603 |
|
| 2014 |
Chen B, Hrovat DA, West R, Deng SH, Wang XB, Borden WT. The negative ion photoelectron spectrum of cyclopropane-1,2,3-trione radical anion, (CO)3(•-)--a joint experimental and computational study. Journal of the American Chemical Society. 136: 12345-54. PMID 25148567 DOI: 10.1021/Ja505582K |
0.63 |
|
| 2014 |
Chen B, Scott ME, Adams BA, Hrovat DA, Borden WT, Lautens M. Computational and ¹³C investigations of the diazadienes and oxazadienes formed via the rearrangement of methylenecyclopropyl hydrazones and oximes. Organic Letters. 16: 3930-3. PMID 25047868 DOI: 10.1021/Ol501710M |
0.604 |
|
| 2014 |
Ertelt M, Hrovat DA, Borden WT, Sander W. Heavy-atom tunneling in the ring opening of a strained cyclopropene at very low temperatures. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 4713-20. PMID 24616081 DOI: 10.1002/Chem.201303792 |
0.515 |
|
| 2014 |
Chen B, Hrovat DA, Deng SH, Zhang J, Wang XB, Borden WT. The negative ion photoelectron spectrum of meta-benzoquinone radical anion (MBQ˙⁻): a joint experimental and computational study. Journal of the American Chemical Society. 136: 3589-96. PMID 24548105 DOI: 10.1021/Ja412433T |
0.641 |
|
| 2013 |
Kozuch S, Hrovat DA, Borden WT. Why is (SiO)(4) calculated to be tetrahedral, whereas (CO)(4) is square planar? A molecular orbital analysis. Journal of the American Chemical Society. 135: 19282-91. PMID 24328213 DOI: 10.1021/Ja409887H |
0.758 |
|
| 2013 |
Kozuch S, Zhang X, Hrovat DA, Borden WT. Calculations on tunneling in the reactions of noradamantyl carbenes. Journal of the American Chemical Society. 135: 17274-7. PMID 24206046 DOI: 10.1021/Ja409176U |
0.736 |
|
| 2013 |
Chen B, Rogachev AY, Hrovat DA, Hoffmann R, Borden WT. How to make the σ0π2 singlet the ground state of carbenes. Journal of the American Chemical Society. 135: 13954-64. PMID 24007553 DOI: 10.1021/Ja407116E |
0.631 |
|
| 2013 |
Zhang J, Hrovat DA, Sun Z, Bao X, Borden WT, Wang XB. The ground state of (CS)4 is different from that of (CO)4: an experimental test of a computational prediction by negative ion photoelectron spectroscopy. The Journal of Physical Chemistry. A. 117: 7841-6. PMID 23886029 DOI: 10.1021/Jp406160D |
0.635 |
|
| 2013 |
Bao X, Hrovat DA, Borden WT. Like (CO)4, Do (CS)4 and (CSe)4 have a triplet ground state? Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 5687-93. PMID 23450697 DOI: 10.1002/Chem.201204049 |
0.551 |
|
| 2013 |
Bao X, Hrovat DA, Borden WT, Wang XB. Negative ion photoelectron spectroscopy confirms the prediction that (CO)5 and (CO)6 each has a singlet ground state. Journal of the American Chemical Society. 135: 4291-8. PMID 23445075 DOI: 10.1021/Ja4005128 |
0.649 |
|
| 2013 |
Bao X, Hrovat DA, Borden WT. Cooperative and competitive effects associated with Fe(CO)3 binding to annelated benzenes Chemical Science. 4: 516-525. DOI: 10.1039/C2Sc20785K |
0.516 |
|
| 2012 |
Babinski DJ, Bao X, El Arba M, Chen B, Hrovat DA, Borden WT, Frantz DE. Synchronized aromaticity as an enthalpic driving force for the aromatic Cope rearrangement. Journal of the American Chemical Society. 134: 16139-42. PMID 22963196 DOI: 10.1021/Ja307213M |
0.58 |
|
| 2012 |
Bao X, Zhou X, Flener Lovitt C, Venkatraman A, Hrovat DA, Gleiter R, Hoffmann R, Borden WT. Molecular orbitals of the oxocarbons (CO)n, n = 2-6. Why does (CO)4 have a triplet ground state? Journal of the American Chemical Society. 134: 10259-70. PMID 22687146 DOI: 10.1021/Ja3034087 |
0.601 |
|
| 2012 |
Bao X, Hrovat DA, Borden WT. Calculations of the effects of methyl groups on the energy differences between cyclooctatetraene and bicyclo[4.2.0]octa-2,4,7-triene and between their iron tricarbonyl complexes. The Journal of Organic Chemistry. 77: 956-65. PMID 22263718 DOI: 10.1021/Jo202157N |
0.548 |
|
| 2011 |
Borden WT. With a little help from my friends: forty years of fruitful chemical collaborations. The Journal of Organic Chemistry. 76: 2943-64. PMID 21452841 DOI: 10.1021/Jo200213X |
0.351 |
|
| 2011 |
Zhang X, Hrovat DA, Datta A, Borden WT. Effects of geminal methyl groups on the tunnelling rates in the ring opening of cyclopropylcarbinyl radical at cryogenic temperature. Organic & Biomolecular Chemistry. 9: 3142-5. PMID 21431182 DOI: 10.1039/C0Ob01238F |
0.547 |
|
| 2011 |
Ichino T, Villano SM, Gianola AJ, Goebbert DJ, Velarde L, Sanov A, Blanksby SJ, Zhou X, Hrovat DA, Borden WT, Lineberger WC. Photoelectron spectroscopic study of the oxyallyl diradical. The Journal of Physical Chemistry. A. 115: 1634-49. PMID 21323385 DOI: 10.1021/Jp111311K |
0.589 |
|
| 2011 |
Bao X, Hrovat DA, Borden WT. Cooperative effects in the annelation of benzene by multiple etheno groups Collection of Czechoslovak Chemical Communications. 76: 481-501. DOI: 10.1135/Cccc2011037 |
0.59 |
|
| 2011 |
Zhang X, Kandala S, Yang L, Watson WH, Wang X, Hrovat DA, Borden WT, Richmond MG. Experimental and computational studies of the isomerization reactions of bidentate phosphine ligands in triosmium clusters: Kinetics of the rearrangements from bridged to chelated isomers and X-ray structures of the clusters Os3(CO)10(dppbz), 1,1-Os3(CO) 10(dppbzF4), HOs3(CO)9[μ-1,2- PhP(C6H4 Organometallics. 30: 1253-1268. DOI: 10.1021/Om100783F |
0.546 |
|
| 2011 |
Bao X, Hrovat DA, Borden WT. The effects of orbital interactions on the geometries of some annelated benzenes Theoretical Chemistry Accounts. 130: 261-268. DOI: 10.1007/S00214-011-0970-4 |
0.58 |
|
| 2010 |
Lovitt CF, Dong H, Hrovat DA, Gleiter R, Borden WT. Through-bond interactions in the diradical intermediates formed in the rearrangements of bicyclo[n.m.0]alkatetraenes. Journal of the American Chemical Society. 132: 14617-24. PMID 20866055 DOI: 10.1021/Ja106329T |
0.628 |
|
| 2010 |
Gonzalez-James OM, Zhang X, Datta A, Hrovat DA, Borden WT, Singleton DA. Experimental evidence for heavy-atom tunneling in the ring-opening of cyclopropylcarbinyl radical from intramolecular 12C/13C kinetic isotope effects. Journal of the American Chemical Society. 132: 12548-9. PMID 20722415 DOI: 10.1021/Ja1055593 |
0.605 |
|
| 2010 |
Zhang X, Hrovat DA, Borden WT. Calculations predict that carbon tunneling allows the degenerate cope rearrangement of semibullvalene to occur rapidly at cryogenic temperatures. Organic Letters. 12: 2798-801. PMID 20507087 DOI: 10.1021/Ol100879T |
0.558 |
|
| 2010 |
Zhou X, Hrovat DA, Borden WT. Cyclooctatetraenes tetrakis-annelated with alpha-dithio- or alpha-diselenocarbonyl groups: diradicals predicted to have ground states with 10 pi electrons in the eight-membered ring and two-center, three-electron, sigma bonds between two pairs of chalcogen atoms. The Journal of Physical Chemistry. A. 114: 3683-90. PMID 20151691 DOI: 10.1021/Jp911705Y |
0.629 |
|
| 2010 |
Zhou X, Hrovat DA, Borden WT. Calculations of the relative energies of the 2B1g and 2A2u states of cyclobutanetetraone radical cation and radical anion provide further evidence of a 3B2u ground state for the neutral molecule: a proposed experimental test of the prediction of a triplet ground state for (CO)4. The Journal of Physical Chemistry. A. 114: 1304-8. PMID 19689150 DOI: 10.1021/Jp905462B |
0.642 |
|
| 2010 |
HROVAT DA, RAUK A, SORENSEN TS, POWELL HK, BORDEN WT. ChemInform Abstract: Ring Opening of Bicyclo(n.1.0)alkanones to 2-Cycloalkanone-1,3-diyls. Why Does Oxyallyl Diradical Formation Require Less Energy from Bicyclo( 3.1.0)hexan-6-ones than from Bicyclo(1.1.0)butan-2-ones? Cheminform. 27: no-no. DOI: 10.1002/chin.199634010 |
0.528 |
|
| 2010 |
LIM D, HROVAT DA, BORDEN WT, JORGENSEN WL. ChemInform Abstract: Solvent Effects on the Ring Opening of Cyclopropanones to Oxyallyls: A Combined ab initio and Monte Carlo Study. Cheminform. 25: no-no. DOI: 10.1002/chin.199434073 |
0.634 |
|
| 2009 |
Zhang X, Datta A, Hrovat DA, Borden WT. Calculations predict a large inverse H/D kinetic isotope effect on the rate of tunneling in the ring opening of cyclopropylcarbinyl radical. Journal of the American Chemical Society. 131: 16002-3. PMID 19831346 DOI: 10.1021/Ja907406Q |
0.628 |
|
| 2009 |
Ichino T, Villano SM, Gianola AJ, Goebbert DJ, Velarde L, Sanov A, Blanksby SJ, Zhou X, Hrovat DA, Borden WT, Lineberger WC. The lowest singlet and triplet States of the oxyallyl diradical. Angewandte Chemie (International Ed. in English). 48: 8509-11. PMID 19739188 DOI: 10.1002/Anie.200904417 |
0.55 |
|
| 2009 |
Wei H, Hrovat DA, Mo Y, Hoffmann R, Borden WT. The contributions of through-bond interactions to the singlet-triplet energy difference in 1,3-dehydrobenzene. The Journal of Physical Chemistry. A. 113: 10351-8. PMID 19711935 DOI: 10.1021/Jp905222F |
0.536 |
|
| 2009 |
Wu A, Mader EA, Datta A, Hrovat DA, Borden WT, Mayer JM. Nitroxyl radical plus hydroxylamine pseudo self-exchange reactions: tunneling in hydrogen atom transfer. Journal of the American Chemical Society. 131: 11985-97. PMID 19618933 DOI: 10.1021/Ja904400D |
0.588 |
|
| 2009 |
Waidmann CR, Zhou X, Tsai EA, Kaminsky W, Hrovat DA, Borden WT, Mayer JM. Slow hydrogen atom transfer reactions of oxo- and hydroxo-vanadium compounds: the importance of intrinsic barriers. Journal of the American Chemical Society. 131: 4729-43. PMID 19292442 DOI: 10.1021/Ja808698X |
0.602 |
|
| 2009 |
Dong H, Hrovat DA, Quast H, Borden WT. Calculations of the relative energies of the low-lying electronic states of 2-methylenedihydrophenalene-1,3-diyl: effects of a 1,8-naphtho bridging group on trimethylenemethane and of a vinylidene bridging group on 1,8-naphthoquinodimethane. The Journal of Physical Chemistry. A. 113: 895-901. PMID 19140715 DOI: 10.1021/Jp809715V |
0.704 |
|
| 2009 |
Zhou X, Hrovat DA, Gleiter R, Borden WT. Reinvestigation of the ordering of the low-lying electronic states of cyclobutanetetraone with CASPT2, CCSD(T), G3B3, ccCA, and CBS-QB3 calculations Molecular Physics. 107: 863-870. DOI: 10.1080/00268970802672650 |
0.585 |
|
| 2009 |
Ichino T, Villano S, Gianola A, Goebbert D, Velarde L, Sanov A, Blanksby S, Zhou X, Hrovat D, Borden W, Lineberger W. Cover Picture: The Lowest Singlet and Triplet States of the Oxyallyl Diradical (Angew. Chem. Int. Ed. 45/2009) Angewandte Chemie International Edition. 48: 8381-8381. DOI: 10.1002/Anie.200905074 |
0.519 |
|
| 2009 |
Ichino T, Villano S, Gianola A, Goebbert D, Velarde L, Sanov A, Blanksby S, Zhou X, Hrovat D, Borden W, Lineberger W. Titelbild: The Lowest Singlet and Triplet States of the Oxyallyl Diradical (Angew. Chem. 45/2009) Angewandte Chemie. 121: 8531-8531. DOI: 10.1002/Ange.200905074 |
0.526 |
|
| 2008 |
Hrovat DA, Isborn CM, Kahr B, Borden WT. Internal dynamics and optical rotations predicted for O(h)- and O-symmetric cubanes. Organic Letters. 10: 4763-6. PMID 18834134 DOI: 10.1021/Ol801762R |
0.579 |
|
| 2008 |
Quast H, Nüdling W, Klemm G, Kirschfeld A, Neuhaus P, Sander W, Hrovat DA, Borden WT. A perimidine-derived non-Kekulé triplet diradical. The Journal of Organic Chemistry. 73: 4956-61. PMID 18547111 DOI: 10.1021/Jo800589Y |
0.667 |
|
| 2008 |
Datta A, Hrovat DA, Borden WT. Calculations predict rapid tunneling by carbon from the vibrational ground state in the ring opening of cyclopropylcarbinyl radical at cryogenic temperatures. Journal of the American Chemical Society. 130: 6684-5. PMID 18447359 DOI: 10.1021/Ja801089P |
0.646 |
|
| 2008 |
Datta A, Hrovat DA, Borden WT. Calculations find that tunneling plays a major role in the reductive elimination of methane from hydridomethylbis(trimethylphosphine)platinum: how to confirm this computational prediction experimentally. Journal of the American Chemical Society. 130: 2726-7. PMID 18266369 DOI: 10.1021/Ja710260V |
0.544 |
|
| 2008 |
Zhou X, Hrovat DA, Borden WT. Very-low-lying electronic states result from n --> pi excitations in open-shell annulenes, annelated with alpha-dicarbonyl groups. Organic Letters. 10: 893-6. PMID 18257583 DOI: 10.1021/Ol703014A |
0.616 |
|
| 2007 |
Shelton GR, Hrovat DA, Borden WT. Calculations of the effect of tunneling on the Swain-Schaad exponents (SSEs) for the 1,5-hydrogen shift in 5-methyl-1,3-cyclopentadiene. Can SSEs be used to diagnose the occurrence of tunneling? Journal of the American Chemical Society. 129: 16115-8. PMID 18052172 DOI: 10.1021/Ja076132A |
0.593 |
|
| 2007 |
Zhou X, Hrovat DA, Borden WT. Calculations of the effects of substituents on bond localization in annelated cyclopentadienyl radicals. Journal of the American Chemical Society. 129: 10785-94. PMID 17691731 DOI: 10.1021/Ja072314T |
0.653 |
|
| 2007 |
Valliant-Saunders K, Gunn E, Shelton GR, Hrovat DA, Borden WT, Mayer JM. Oxidation of tertiary silanes by osmium tetroxide. Inorganic Chemistry. 46: 5212-9. PMID 17511445 DOI: 10.1021/Ic062468U |
0.573 |
|
| 2007 |
Wei H, Hrovat DA, Dolbier WR, Smart BE, Borden WT. The "bond-stretched invertomer" of hexafluorocyclopropane--a new type of reactive intermediate. Angewandte Chemie (International Ed. in English). 46: 2666-8. PMID 17335092 DOI: 10.1002/Anie.200604574 |
0.516 |
|
| 2007 |
Shelton GR, Hrovat DA, Borden WT. Tunneling in the 1,5-hydrogen shift reactions of 1,3-cyclopentadiene and 5-methyl-1,3-cyclopentadiene. Journal of the American Chemical Society. 129: 164-8. PMID 17199295 DOI: 10.1021/Ja0664279 |
0.623 |
|
| 2006 |
Lingwood M, Hammond JR, Hrovat DA, Mayer JM, Borden WT. MPW1K Performs Much Better than B3LYP in DFT Calculations on Reactions that Proceed by Proton-Coupled Electron Transfer (PCET). Journal of Chemical Theory and Computation. 2: 740-745. PMID 18725967 DOI: 10.1021/Ct050282Z |
0.738 |
|
| 2006 |
Wei H, Hrovat DA, Borden WT. Ab initio calculations of the potential surface for rearrangement of 2,2,3,3-tetrafluoromethylenecyclopropane to 1-(difluoromethylene)-2,2-difluorocyclopropane. Journal of the American Chemical Society. 128: 16676-83. PMID 17177417 DOI: 10.1021/Ja065963Y |
0.655 |
|
| 2006 |
Shelton GR, Hrovat DA, Wei H, Borden WT. Why does perfluorination render bicyclo[2.2.0]hex-1(4)-ene stable toward dimerization? Calculations provide the answers. Journal of the American Chemical Society. 128: 12020-7. PMID 16953645 DOI: 10.1021/Ja063848H |
0.607 |
|
| 2006 |
Shelton GR, Hrovat DA, Borden WT. Cooperative and competitive effects of substituents at C1 and C4 on the barriers to ring inversion of 5,5-difluorobicyclo[2.1.0]pentanes. The Journal of Organic Chemistry. 71: 2982-6. PMID 16599591 DOI: 10.1021/Jo052538Z |
0.609 |
|
| 2006 |
Mayer JM, Mader EA, Roth JP, Bryant JR, Matsuo T, Dehestani A, Bales BC, Watson EJ, Osako T, Valliant-Saunders K, Lam WH, Hrovat DA, Borden WT, Davidson ER. Stoichiometric oxidations of σ-bonds: Radical and possible non-radical pathways Journal of Molecular Catalysis a: Chemical. 251: 24-33. DOI: 10.1016/J.Molcata.2006.02.010 |
0.659 |
|
| 2005 |
Hrovat DA, Borden WT. A Simple Mathematical Model for the Cooperative and Competitive Substituent Effects Found in the Cope Rearrangements of Phenyl-Substituted 1,5-Hexadienes. Journal of Chemical Theory and Computation. 1: 87-94. PMID 26641120 DOI: 10.1021/Ct049929Q |
0.603 |
|
| 2005 |
Hoenigman RL, Kato S, Bierbaum VM, Borden WT. Heat of hydrogenation of 1,5-dehydroquadricyclane. A computational and experimental study of a highly pyramidalized alkene. Journal of the American Chemical Society. 127: 17772-7. PMID 16351106 DOI: 10.1021/Ja054720N |
0.808 |
|
| 2005 |
Lam WH, Gaspar PP, Hrovat DA, Trieber DA, Davidson ER, Borden WT. Computational studies of the thermal fragmentation of P-arylphosphiranes: have arylphosphinidenes been generated by this method? Journal of the American Chemical Society. 127: 9886-94. PMID 15998095 DOI: 10.1021/Ja050891G |
0.7 |
|
| 2005 |
Seefelder M, Heubes M, Quast H, Edwards WD, Armantrout JR, Williams RV, Cramer CJ, Goren AC, Hrovat DA, Borden WT. Experimental and theoretical study of stabilization of delocalized forms of semibullvalenes and barbaralanes by dipolar and polarizable solvents. Observation of a delocalized structure that is lower in free energy than the localized form. The Journal of Organic Chemistry. 70: 3437-49. PMID 15844976 DOI: 10.1021/Jo0502089 |
0.694 |
|
| 2005 |
Isborn C, Hrovat DA, Borden WT, Mayer JM, Carpenter BK. Factors controlling the barriers to degenerate hydrogen atom transfers. Journal of the American Chemical Society. 127: 5794-5. PMID 15839670 DOI: 10.1021/Ja050024B |
0.611 |
|
| 2005 |
Hrovat DA, Brown EC, Williams RV, Quast H, Borden WT. How important is bishomoaromatic stabilization in determining the relative barrier heights for the degenerate Cope rearrangements of semibullvalene, barbaralane, bullvalene, and dihydrobullvalene? The Journal of Organic Chemistry. 70: 2627-32. PMID 15787553 DOI: 10.1021/Jo048268M |
0.681 |
|
| 2005 |
Dehestani A, Lam WH, Hrovat DA, Davidson ER, Borden WT, Mayer JM. Ligand-assisted reduction of osmium tetroxide with molecular hydrogen via a [3+2] mechanism. Journal of the American Chemical Society. 127: 3423-32. PMID 15755161 DOI: 10.1021/Ja043777R |
0.645 |
|
| 2005 |
Hrovat DA, Borden WT. A simple mathematical model for the cooperative and competitive substituent effects found in the Cope rearrangements of phenyl-substituted 1,5-hexadienes Journal of Chemical Theory and Computation. 1: 87-94. DOI: 10.1021/ct049929q |
0.482 |
|
| 2005 |
Hoenigman RL, Kato S, Borden WT, Bierbaum VM. An experimental and computational study of the ions formed by the reaction of cyclopentanone with O•- International Journal of Mass Spectrometry. 241: 149-163. DOI: 10.1016/J.Ijms.2004.12.009 |
0.803 |
|
| 2005 |
Borden WT. Ab initio and DFT calculations on the Cope rearrangement, a reaction with a chameleonic transition state Theory and Applications of Computational Chemistry. 859-873. DOI: 10.1016/B978-044451719-7/50073-1 |
0.307 |
|
| 2004 |
Hayase S, Hrovat DA, Borden WT. A B3LYP study of the effects of phenyl substituents on 1,5-hydrogen shifts in 3-(Z)-1,3-pentadiene provides evidence against a chameleonic transition structure. Journal of the American Chemical Society. 126: 10028-34. PMID 15303877 DOI: 10.1021/Ja048708R |
0.624 |
|
| 2004 |
Bethke S, Hrovat DA, Borden WT, Gleiter R. Reactions of sterically congested 1,5-hexadienes: Ab initio and DFT calculations on the competition between cope rearrangements and disrotatory cyclobutene ring-opening reactions of bridged syn-tricyclo[4.2.0.0(2,5)]octa-3,7-dienes. The Journal of Organic Chemistry. 69: 3294-301. PMID 15132534 DOI: 10.1021/Jo030349F |
0.643 |
|
| 2004 |
Abe M, Adam W, Borden WT, Hattori M, Hrovat DA, Nojima M, Nozaki K, Wirz J. Effects of spiroconjugation on the calculated singlet-triplet energy gap in 2,2-dialkoxycyclopentane-1,3-diyls and on the experimental electronic absorption spectra of singlet 1,3-diphenyl derivatives. Assignment of the lowest-energy electronic transition of singlet cyclopentane-1,3-diyls. Journal of the American Chemical Society. 126: 574-82. PMID 14719956 DOI: 10.1021/Ja038305B |
0.606 |
|
| 2004 |
Park B, Hrovat DA, Borden WT. A Reinvestigation of the Fragmentation of 2-Carbena-1,3-dioxolane by CASSCF and CASPT2 Calculations Bulletin of the Korean Chemical Society. 25: 260-262. DOI: 10.5012/Bkcs.2004.25.2.260 |
0.637 |
|
| 2004 |
Isborn C, Hrovat DA, Borden WT. Does Formation of Singlet Propane-1,3-diyl from Propane Deviate from Bond Enthalpy Additivity? Results of Ab Initio Calculations That Bear on the Existence of the Benson Barrier to Diradical Ring Closure Journal of Physical Chemistry A. 108: 3024-3029. DOI: 10.1021/Jp036867B |
0.651 |
|
| 2003 |
Zhang DY, Hrovat DA, Abe M, Borden WT. DFT calculations on the effects of para substituents on the energy differences between singlet and triplet states of 2,2-difluoro-1,3-diphenylcyclopentane-1,3-diyls. Journal of the American Chemical Society. 125: 12823-8. PMID 14558830 DOI: 10.1021/Ja0355067 |
0.651 |
|
| 2003 |
Tsao ML, Gritsan N, James TR, Platz MS, Hrovat DA, Borden WT. Study of the chemistry of ortho- and para-biphenylnitrenes by laser flash photolysis and time-resolved IR experiments and by B3LYP and CASPT2 calculations. Journal of the American Chemical Society. 125: 9343-58. PMID 12889963 DOI: 10.1021/Ja0351591 |
0.601 |
|
| 2003 |
Zuev PS, Sheridan RS, Albu TV, Truhlar DG, Hrovat DA, Borden WT. Carbon tunneling from a single quantum state. Science (New York, N.Y.). 299: 867-70. PMID 12574623 DOI: 10.1126/Science.1079294 |
0.586 |
|
| 2002 |
Brown EC, Henze DK, Borden WT. Are 1,5-Disubstituted semibullvalenes that have C2v equilibrium geometries necessarily bishomoaromatic? Journal of the American Chemical Society. 124: 14977-14982. PMID 12475340 DOI: 10.1021/Ja027392P |
0.384 |
|
| 2002 |
Galbraith JM, Gaspar PP, Borden WT. What accounts for the difference between singlet phenylphosphinidene and singlet phenylnitrene in reactivity toward ring expansion? Journal of the American Chemical Society. 124: 11669-11674. PMID 12296732 DOI: 10.1021/Ja0269892 |
0.655 |
|
| 2002 |
Mayer JM, Hrovat DA, Thomas JL, Borden WT. Proton-coupled electron transfer versus hydrogen atom transfer in benzyl/toluene, methoxyl/methanol, and phenoxyl/phenol self-exchange reactions. Journal of the American Chemical Society. 124: 11142-7. PMID 12224962 DOI: 10.1021/Ja012732C |
0.621 |
|
| 2002 |
Debbert SL, Carpenter BK, Hrovat DA, Borden WT. The iconoclastic dynamics of the 1,2,6-heptatriene rearrangement. Journal of the American Chemical Society. 124: 7896-7. PMID 12095322 DOI: 10.1021/Ja026232A |
0.6 |
|
| 2002 |
Zhang DY, Borden WT. Do deviations from bond enthalpy additivity define the thermodynamic stabilities of diradicals? Journal of Organic Chemistry. 67: 3989-3995. PMID 12054931 DOI: 10.1021/Jo0111513 |
0.381 |
|
| 2002 |
Goren AC, Hrovat DA, Seefelder M, Quast H, Borden WT. The search for bishomoaromatic semibullvalenes and barbaralanes: computational evidence of their identification by UV/Vis and IR spectroscopy and prediction of the existence of a blue bishomoaromatic semibullvalene. Journal of the American Chemical Society. 124: 3469-72. PMID 11916433 DOI: 10.1021/Ja0122290 |
0.686 |
|
| 2002 |
Borden WT. Symmetry breaking, diradicals, and coping with and coping without Ernest Davidson Molecular Physics. 100: 337-347. DOI: 10.1080/00268970110079893 |
0.352 |
|
| 2002 |
Albu TV, Lynch BJ, Truhlar DG, Goren AC, Hrovat DA, Borden WT, Moss RA. Dynamics of 1,2-hydrogen migration in carbenes and ring expansion in cyclopropylcarbenes Journal of Physical Chemistry A. 106: 5323-5338. DOI: 10.1021/Jp020544I |
0.647 |
|
| 2002 |
Brown EC, Borden WT. Ab initio and density functional theory calculations on heteroatom analogues of trimethylenemethane radical ions. Can a quartet be the ground state? Journal of Physical Chemistry A. 106: 2963-2969. DOI: 10.1021/Jp013905N |
0.423 |
|
| 2001 |
Wenk HH, Balster A, Sander W, Hrovat DA, Borden WT. Matrix Isolation of Perfluorinated p-Benzyne. Angewandte Chemie (International Ed. in English). 40: 2295-2298. PMID 29711814 DOI: 10.1002/1521-3773(20010618)40:12<2295::Aid-Anie2295>3.0.Co;2-W |
0.553 |
|
| 2001 |
Hrovat DA, Borden WT. CASSCF and CASPT2 calculations on the cleavage and ring inversion of bicyclo[2.2.0]hexane find that these reactions involve formation of a common twist-boat diradical intermediate. Journal of the American Chemical Society. 123: 4069-72. PMID 11457158 DOI: 10.1021/Ja004209O |
0.624 |
|
| 2001 |
Wenk HH, Balster A, Sander W, Hrovat DA, Borden WT. Matrix Isolation of Perfluorinated p-Benzyne W.S., H.H.W., and A.B. thank the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie, W.T.B. and D.A.H. the National Science Foundation for financial support. The systematic name for perfluorinated p-benzyne is 1,4-didehydro-2,3,5,6-tetrafluorobenzene. Angewandte Chemie (International Ed. in English). 40: 2295-2298. PMID 11433499 DOI: 10.1002/1521-3773(20010618)40:12<2295::AID-ANIE2295>3.0.CO;2-W |
0.463 |
|
| 2001 |
Fleming I, Hrovat DA, Borden WT. The origin of Felkin–Anh control from an electropositive substituentadjacent to the carbonyl group Journal of the Chemical Society-Perkin Transactions 1. 331-338. DOI: 10.1039/B008409N |
0.595 |
|
| 2001 |
Bartlett KL, Goldberg KI, Borden WT. Computational study of reductive elimination reactions to form C-H bonds from platinum(II) and platinum(IV) centers with strongly coordinating trimethylphosphine ligands Organometallics. 20: 2669-2678. DOI: 10.1021/Om010072E |
0.771 |
|
| 2001 |
Gritsan NP, Likhotvorik I, Tsao ML, Çelebi N, Platz MS, Karney WL, Kemnitz CR, Borden WT. Ring-expansion reaction of cyano-substituted singlet phenyl nitrenes: Theoretical predictions and kinetic results from laser flash photolysis and chemical trapping experiments Journal of the American Chemical Society. 123: 1425-1433. DOI: 10.1021/Ja002594B |
0.398 |
|
| 2001 |
Hrovat DA, Borden WT, Eaton PE, Kahr B. A computational study of the interactions among the nitro groups in octanitrocubane Journal of the American Chemical Society. 123: 1289-1293. DOI: 10.1021/Ja001636T |
0.613 |
|
| 2001 |
Hrovat DA, Williams RV, Goren AC, Borden WT. B3LYP calculations on bishomoaromaticity in substituted semibullvalenes Journal of Computational Chemistry. 22: 1565-1573. DOI: 10.1002/Jcc.1110 |
0.632 |
|
| 2001 |
Wenk HH, Balster A, Sander W, Hrovat DA, Borden WT. Matrixisolation von perfluoriertemp-Didehydrobenzol Angewandte Chemie. 113: 2356-2359. DOI: 10.1002/1521-3757(20010618)113:12<2356::Aid-Ange2356>3.0.Co;2-S |
0.486 |
|
| 2000 |
Rablen PR, Paquette LA, Borden WT. Why Doesn't all-trans-1,2,3,4,5,6-Hexaspiro(THF)cyclohexane complex metal ions? The Journal of Organic Chemistry. 65: 9180-5. PMID 11149867 DOI: 10.1021/Jo001432V |
0.386 |
|
| 2000 |
Borden WT, Gritsan NP, Hadad CM, Karney WL, Kemnitz CR, Platz MS. The interplay of theory and experiment in the study of phenylnitrene. Accounts of Chemical Research. 33: 765-71. PMID 11087313 DOI: 10.1021/Ar990030A |
0.354 |
|
| 2000 |
Bally T, Hrovat DA, Borden WT. Attempts to model neutral solitons in polyacetylene by ab initio and density functional methods. The nature of the spin distribution in polyenyl radicals Physical Chemistry Chemical Physics. 2: 3363-3371. DOI: 10.1039/B003288N |
0.564 |
|
| 2000 |
Brown EC, Borden WT. What accounts for the remarkable difference between silabenzene and phosphabenzene in stability toward dimerization? Organometallics. 19: 2208-2214. DOI: 10.1021/Om0002172 |
0.355 |
|
| 2000 |
Bartlett KL, Goldberg KI, Borden WT. A computational study of reductive elimination reactions to form C-H bonds from Pt(II) and Pt(IV) centers. Why does ligand loss precede reductive elimination from six-coordinate but not four-coordinate platinum? Journal of the American Chemical Society. 122: 1456-1465. DOI: 10.1021/Ja9915706 |
0.77 |
|
| 2000 |
Kemnitz CR, Ellison GB, Karney WL, Borden WT. CASSCF and CASPT2 Ab initio electronic structure calculations find singlet methylnitrene is an energy minimum Journal of the American Chemical Society. 122: 1098-1101. DOI: 10.1021/Ja9907257 |
0.434 |
|
| 2000 |
Hrovat DA, Chen J, Houk KN, Borden WT. Cooperative and competitive substituent effects on the Cope rearrangements of phenyl-substituted 1,5-hexadienes elucidated by Becke3LYP/6-31G* calculations Journal of the American Chemical Society. 122: 7456-7460. DOI: 10.1021/Ja000531N |
0.611 |
|
| 1999 |
Lewis SB, Hrovat DA, Getty SJ, Borden WT. Ab Initio calculations of the potential surfaces for rearrangement of methylenecyclopropane and 2,2-difluoromethylenecyclopropane. Why do the geminal fluorines have little effect on lowering the activation energy? Journal of the Chemical Society. Perkin Transactions 2. 2339-2347. DOI: 10.1039/A902739D |
0.649 |
|
| 1999 |
Rablen PR, Hoffmann RW, Hrovat DA, Borden WT. Is hyperconjugation responsible for the "gauche effect" in 1-fluoropropane and other 2-substituted-1-fluoroethanes? Journal of the Chemical Society. Perkin Transactions 2. 1719-1726. DOI: 10.1039/A901974J |
0.648 |
|
| 1999 |
Skancke PN, Hrovat DA, Borden WT. Computational study of isomerization reactions of silacyclopropene Journal of Physical Chemistry A. 103: 4043-4048. DOI: 10.1021/Jp9838745 |
0.648 |
|
| 1999 |
Johnson WTG, Hrovat DA, Borden WT. Ab initio calculations on spiropentane stereomutations lead to a reinterpretation of the experimental results Journal of the American Chemical Society. 121: 7766-7772. DOI: 10.1021/Ja9906305 |
0.644 |
|
| 1999 |
Hrovat DA, Beno BR, Lange H, Yoo HY, Houk KN, Borden WT. A Becke3LYP/6-31G* study of the cope rearrangements of substituted 1,5- hexadienes provides computational evidence for a chameleonic transition state Journal of the American Chemical Society. 121: 10529-10537. DOI: 10.1021/Ja990476M |
0.602 |
|
| 1999 |
Hrovat DA, Duncan JA, Borden WT. Ab initio and DFT calculations on the cope rearrangement of 1,2,6- heptatriene Journal of the American Chemical Society. 121: 169-175. DOI: 10.1021/Ja983032J |
0.632 |
|
| 1999 |
Johnson WTG, Hrovat DA, Skancke A, Borden WT. Ab initio calculations find 2,2-disilylcyclopentane-1,3-diyl is a singlet diradical with a high barrier to ring closure Theoretical Chemistry Accounts. 102: 207-225. |
0.595 |
|
| 1998 |
Hrovat DA, Murcko MA, Lahti PM, Borden WT. The effects of heteroatom substitution on the singlet-triplet energy differences in diradicals - Ab initio calculations of ΔEST in meta-benzoquinomethane and in 1,3-naphthoquinomethane Journal of the Chemical Society. Perkin Transactions 2. 1037-1044. DOI: 10.1039/A706409H |
0.615 |
|
| 1998 |
Stevenson CD, Brown EC, Hrovat DA, Borden WT. Isotope effects on the ring inversion of cyclooctatetraene Journal of the American Chemical Society. 120: 8864-8867. DOI: 10.1021/Ja981496B |
0.583 |
|
| 1998 |
Tian F, Lewis SB, Barberger MD, Dolbier J, Borden WT. Experimental study of the stereomutation of 1,1-difluoro-2-ethyl-3-methylcyclopropan confirms the predicted preference for disrotatory ring opening and closure Journal of the American Chemical Society. 120: 6187-6188. DOI: 10.1021/Ja980969B |
0.311 |
|
| 1998 |
Skancke A, Hrovat DA, Borden WT. Ab initio calculations of the effects of geminal silyl substituents on the stereomutation of cyclopropane and on the singlet-triplet splitting in trimethylene Journal of the American Chemical Society. 120: 7079-7084. DOI: 10.1021/Ja980720U |
0.644 |
|
| 1998 |
Kemnitz CR, Karney WL, Borden WT. Why are nitrenes more stable than carbenes? An ab initio study Journal of the American Chemical Society. 120: 3499-3503. DOI: 10.1021/Ja973935X |
0.47 |
|
| 1998 |
Adam W, Borden WT, Burda C, Foster H, Heidenfelder T, Heubes M, Hrovat DA, Kita F, Lewis SB, Scheutzow D, Wirz J. Transient spectroscopy of a derivative of 2,2-difluoro-1,3-diphenylcyclopentane-1,3-diyl - A persistent localized singlet 1,3-diradical Journal of the American Chemical Society. 120: 593-594. DOI: 10.1021/Ja972977I |
0.476 |
|
| 1997 |
Hrovat DA, Borden WT. Ab initio calculations on the interconversion of homocub-1(9)-ene and homocub-9-ylidene Molecular Physics. 91: 891-895. DOI: 10.1080/00268979709482779 |
0.64 |
|
| 1997 |
Hrovat DA, Hammons JH, Stevenson CD, Borden WT. Calculations of the equilibrium isotope effects on the reductions of benzene-d6 and cyclooctatetraene-d8 Journal of the American Chemical Society. 119: 9523-9526. DOI: 10.1021/Ja9714144 |
0.626 |
|
| 1997 |
Kemnitz CR, Squires RR, Borden WT. Ab initio calculations on 1,3,5-trimethylenebenzene and its negative ion provide predictions about the photoelectron spectrum of the ion Journal of the American Chemical Society. 119: 6564-6574. DOI: 10.1021/Ja970195J |
0.421 |
|
| 1997 |
Karney WL, Borden WT. Why does o-fluorine substitution raise the barrier to ring expansion of phenylnitrene? Journal of the American Chemical Society. 119: 3347-3350. DOI: 10.1021/Ja9644440 |
0.365 |
|
| 1997 |
Skancke PN, Hrovat DA, Borden WT. Ab initio calculations on the preferred mode of ring opening in silacyclopropane Journal of the American Chemical Society. 119: 8012-8014. DOI: 10.1021/Ja964384Y |
0.664 |
|
| 1997 |
Hrovat DA, Fang S, Borden WT, Carpenter BK. Investigation of Cyclopropane Stereomutation by Quasiclassical Trajectories on an Analytical Potential Energy Surface Journal of the American Chemical Society. 119: 5253-5254. DOI: 10.1021/Ja964238S |
0.544 |
|
| 1997 |
Johnson WTG, Borden WT. Why are methylenecyclopropane and 1-methylcylopropene more 'strained' than methylcyclopropane? Journal of the American Chemical Society. 119: 5930-5933. DOI: 10.1021/Ja9638061 |
0.339 |
|
| 1997 |
Karney WL, Borden WT. Ab initio study of the ring expansion of phenylnitrene and comparison with the ring expansion of phenylcarbene Journal of the American Chemical Society. 119: 1378-1387. DOI: 10.1021/Ja9635241 |
0.312 |
|
| 1997 |
Hrovat DA, Borden WT. Violations of Hund's rule in molecules - Where to look for them and how to identify them Journal of Molecular Structure: Theochem. 398: 211-220. DOI: 10.1016/S0166-1280(96)04930-5 |
0.635 |
|
| 1997 |
Bulliard C, Allan M, Smith JM, Hrovat DA, Borden WT, Grimme S. Singlet and triplet excited states of a pyramidalized alkene: Electron-energy-loss spectra, photoelectron spectra, and calculations of the excited states of tricyclo[3.3.3.03,7]undec-3(7)-ene Chemical Physics. 225: 153-161. |
0.566 |
|
| 1996 |
Schreiner PR, Karney WL, von Ragué Schleyer P, Borden WT, Hamilton TP, Schaefer III HF. Carbene Rearrangements Unsurpassed: Details of the C(7)H(6) Potential Energy Surface Revealed. The Journal of Organic Chemistry. 61: 7030-7039. PMID 11667604 |
0.313 |
|
| 1996 |
Wenthold PG, Hrovat DA, Borden WT, Lineberger WC. Transition-State Spectroscopy of Cyclooctatetraene Science (New York, N.Y.). 272: 1456-9. PMID 8662467 DOI: 10.1126/Science.272.5267.1456 |
0.617 |
|
| 1996 |
Cleven CD, Hoke SH, Cooks RG, Hrovat DA, Smith JM, Lee MS, Borden WT. Effect of olefin pyramidalization on the proton affinity of tricyclo[3.3.3.03,7]undec-3(7)-ene as determined by ab initio calculations and kinetic method measurements Journal of the American Chemical Society. 118: 10872-10878. DOI: 10.1021/Ja960776T |
0.621 |
|
| 1996 |
Gunion RF, Karney W, Wenthold PG, Borden WT, Lineberger WC. Ultraviolet photoelectron spectroscopy of some C7H7-isomers: Quadricyclanide, norbornadienide, cycloheptatrienide, and 1,6-heptadiynide Journal of the American Chemical Society. 118: 5074-5082. DOI: 10.1021/Ja954026F |
0.387 |
|
| 1995 |
Powell HK, Borden WT. CASSCF and CASPT2N calculations predict singlet cyclopentan-2-one-1,3-diyl is stable toward closure to bicyclo[2.1.0]pentan-5-one Journal of Organic Chemistry. 60: 2654-2655. DOI: 10.1021/Jo00114A005 |
0.379 |
|
| 1995 |
Lee MS, Hrovat DA, Borden WT. Ab initio calculations on the β-cleavage reactions of polycyclic radicals. Why does cubylcarbinyl react much faster than either homocubyl or 1-bicyclo[1.1.1]pentyl? Journal of the American Chemical Society. 117: 10353-10357. DOI: 10.1021/Ja00146A020 |
0.607 |
|
| 1995 |
Fang S, Lee MS, Hrovat DA, Borden WT. Ab Initio calculations show why m-phenylene is not always a ferromagnetic coupler Journal of the American Chemical Society. 117: 6727-6731. DOI: 10.1021/Ja00130A012 |
0.608 |
|
| 1994 |
Getty SJ, Hrovat DA, Xu JD, Barker SA, Borden WT. Potential surfaces for cyclopropane stereomutations: What a difference geminal fluorines make Journal of the Chemical Society, Faraday Transactions. 90: 1689-1701. DOI: 10.1039/Ft9949001689 |
0.609 |
|
| 1994 |
Hrovat DA, Borden WT. Ab initio calculations indicate that a polar effect causes abstraction of cubyl hydrogens from methylcubane to be favored kinetically Journal of the American Chemical Society. 116: 6459-6460. DOI: 10.1021/Ja00093A066 |
0.611 |
|
| 1994 |
Hrovat DA, Borden WT. MCSCF and CASPT2N calculations on the excited states of 1,2,4,5-tetramethylenebenzene. The UV-vis spectrum observed belongs to the singlet state of the diradical Journal of the American Chemical Society. 116: 6327-6331. DOI: 10.1021/Ja00093A036 |
0.592 |
|
| 1994 |
Xu JD, Hrovat DA, Borden WT. Ab initio calculations of the potential surfaces for the lowest singlet and triplet states of 2,2-difluorocyclopentane-1,3-diyl. The singlet diradical lies below the triplet Journal of the American Chemical Society. 116: 5425-5427. DOI: 10.1021/Ja00091A054 |
0.632 |
|
| 1994 |
Hoke SH, Yang SS, Cooks RG, Hrovat DA, Borden WT. Proton affinities of free radicals measured by the kinetic method Journal of the American Chemical Society. 116: 4888-4892. DOI: 10.1021/Ja00090A038 |
0.558 |
|
| 1994 |
Hrovat DA, Morokuma K, Borden WT. The Cope rearrangement revisited again. Results of ab initio calculations beyond the CASSCF level. [Erratum to document cited in CA120:106195] Journal of the American Chemical Society. 116: 4529-4529. DOI: 10.1021/Ja00089A074 |
0.632 |
|
| 1994 |
Lim D, Hrovat DA, Borden WT, Jorgensen WL. Solvent Effects on the Ring Opening of Cyclopropanones to Oxyallyls: A Combined ab Initio and Monte Carlo Study Journal of the American Chemical Society. 116: 3494-3499. DOI: 10.1021/Ja00087A040 |
0.66 |
|
| 1994 |
Getty SJ, Hrovat DA, Borden WT. Ab initio calculations on the stereomutation of 1,1-difluorocyclopropane. Prediction of a substantial preference for coupled disrotation of the methylene groups Journal of the American Chemical Society. 116: 1521-1527. DOI: 10.1021/Ja00083A041 |
0.623 |
|
| 1994 |
Hrovat DA, Morokuma K, Borden WT. The cope rearrangement revisited again. Results of ab initio calculations beyond the CASSCF level Journal of the American Chemical Society. 116: 1072-1076. DOI: 10.1021/Ja00082A032 |
0.688 |
|
| 1994 |
Hrovat DA, Borden WT. Ab initio calculations of the relative resonance stabilization energies of allyl and benzyl radicals Journal of Physical Chemistry. 98: 10460-10464. DOI: 10.1021/J100092A014 |
0.631 |
|
| 1994 |
Lim D, Hrovat DA, Borden WT, Jorgensen WL. Solvent effects on the ring opening of cyclopropanones to oxyallyls: A combined ab initio and Monte Carlo study Journal of the American Chemical Society. 116: 3494-3499. |
0.546 |
|
| 1993 |
Borden WT. Qualitative Methods for Predicting the Ground States of Non-Kekule Hydrocarbons and the Effects of Heteroatom Substitution on the Ordering of the Electronic States Molecular Crystals and Liquid Crystals Science and Technology. Section a. Molecular Crystals and Liquid Crystals. 232: 195-218. DOI: 10.1080/10587259308035713 |
0.364 |
|
| 1993 |
Fort RC, Hrovat DA, Borden WT. Ab initio calculations of the stabilization energy of pentadienyl radical from rotational barriers and from lowering of bond dissociation energies Journal of Organic Chemistry. 58: 211-216. DOI: 10.1021/Jo00053A038 |
0.639 |
|
| 1993 |
Nicolaides A, Borden WT. CI calculations on didehydrobenzenes predict heats of formation for the Meta and Para isomers that are substantially higher than previous experimental values Journal of the American Chemical Society. 115: 11951-11957. DOI: 10.1021/Ja00078A037 |
0.409 |
|
| 1993 |
Smith JM, Hrovat DA, Borden WT, Allan M, Asmis KR, Bulliard C, Haselbach E, Meier UC. Synthesis and spectroscopy of tricyclo[3.3.3.03,7]undec-3(7)-ene: Confirmation of computational predictions regarding the effects of pyramidalization on alkene ionization energies and electron affinities Journal of the American Chemical Society. 115: 3816-3817. DOI: 10.1021/Ja00062A074 |
0.591 |
|
| 1993 |
Radziszewski JG, Yin TK, Renzoni GE, Hrovat DA, Borden WT, Michl J. Matrix isolation of tricyclo[3.3.1.03,7]non-3(7)-ene, a doubly pyramidalized alkene predicted to have a nearly tetrahedral geometry at the olefinic carbons Journal of the American Chemical Society. 115: 1454-1456. DOI: 10.1021/Ja00057A032 |
0.6 |
|
| 1993 |
Smith JM, Hrovat DA, Borden WT. NMR and molecular mechanics studies of the conformational dynamics of tricyclo[3.3.3.03,7]undecane derivatives Tetrahedron Letters. 34: 5991-5994. DOI: 10.1016/S0040-4039(00)61709-4 |
0.58 |
|
| 1992 |
Hrovat DA, Borden WT. Ab initio investigation of substituent effects in 4-substituted bicyclo[2.2.2]oct-1-yl cations. Computational support for through-bond stabilization via double hyperconjugation Journal of Organic Chemistry. 57: 2519-2521. DOI: 10.1021/Jo00035A002 |
0.612 |
|
| 1992 |
Hrovat DA, Waali EE, Borden WT. Ab initio calculations of the singlet-triplet energy difference in phenylnitrene Journal of the American Chemical Society. 114: 8698-8699. DOI: 10.1021/Ja00048A052 |
0.633 |
|
| 1992 |
Fort RC, Getty SJ, Hrovat DA, Lahti PM, Borden WT. Ab initio calculations on m-quinone. The ground state is a triplet Journal of the American Chemical Society. 114: 7549-7552. DOI: 10.1021/Ja00045A031 |
0.629 |
|
| 1992 |
Hrovat DA, Borden WT. CASSCF calculations find that a D8h geometry is the transition state for double-bond shifting in cyclooctatetraene Journal of the American Chemical Society. 114: 5879-5881. DOI: 10.1021/Ja00040A071 |
0.639 |
|
| 1992 |
Du P, Borden W. Correction. Ab Initio Calculations Predict a Singlet Ground State for Tetramethyleneethane Journal of the American Chemical Society. 114: 4949-4949. DOI: 10.1021/Ja00038A600 |
0.409 |
|
| 1992 |
Hrovat DA, Borden WT. Ab initio calculations of the relative energies of homocub-1(9)-ene and homocub-9-ylidene. How strong is the twisted ".pi." bond in the olefin? What is the ground state of the carbene? Journal of the American Chemical Society. 114: 2719-2720. DOI: 10.1021/Ja00033A056 |
0.665 |
|
| 1992 |
Coolidge MB, Hrovat DA, Borden WT. Ab Initio calculations on silicon analogues of the allyl radical Journal of the American Chemical Society. 114: 2354-2359. DOI: 10.1021/Ja00033A009 |
0.59 |
|
| 1992 |
Getty SJ, Davidson ER, Borden WT. Stereomutation of cyclopropane revisited. An ab initio investigation of the potential surface and calculation of secondary isotope effects Journal of the American Chemical Society. 114: 2085-2093. DOI: 10.1021/Ja00032A023 |
0.567 |
|
| 1992 |
Branan BM, Paquette LA, Hrovat DA, Borden WT. Generation and chemical trapping of a bis(ethano) derivative of tricyclo3.3.0.03,7]oct-1(5)-ene: The consummate member of a series of pyramidalized alkenes Journal of the American Chemical Society. 114: 774-776. DOI: 10.1021/Ja00028A062 |
0.535 |
|
| 1991 |
Nicolaides A, Borden WT. Ab initio calculations of the relative strengths of the .pi. bonds in acetylene and ethylene and of their effect on the relative energies of .pi.-bond addition reactions Journal of the American Chemical Society. 113: 6750-6755. DOI: 10.1021/Ja00018A005 |
0.427 |
|
| 1991 |
Hammons JH, Hrovat DA, Borden WT. Bond Alternation and Unpaired Spin Distributions in the Radical Anions of Cyclooctatetraene and Monosubstituted Derivatives. An ab Initio Study Journal of the American Chemical Society. 113: 4500-4505. DOI: 10.1021/Ja00012A019 |
0.652 |
|
| 1991 |
Getty SJ, Borden WT. Why does tetrafluoroethylene not undergo Diels-Alder reaction with 1,3-butadiene? An ab initio investigation Journal of the American Chemical Society. 113: 4334-4335. DOI: 10.1021/Ja00011A048 |
0.331 |
|
| 1991 |
Morokuma K, Borden WT. Ab Initio Calculations on (H3P)2Pt(C2H4). The Effect of Alkene Pyramidalization on Internal Rotation and Alkene Binding Energies Journal of the American Chemical Society. 113: 1912-1914. DOI: 10.1021/Ja00006A007 |
0.499 |
|
| 1990 |
Hrovat DA, Borden WT. Ab initio calculations find that formation of cubyl cation requires less energy than formation of 1-norbornyl cation Journal of the American Chemical Society. 112: 3227-3228. DOI: 10.1021/Ja00164A062 |
0.633 |
|
| 1990 |
Hrovat DA, Borden WT, Vance RL, Rondan NG, Houk KN, Morokuma K. Ab initio calculations of the effects of cyano substituents on the cope rearrangement Journal of the American Chemical Society. 112: 2018-2019. DOI: 10.1021/Ja00161A067 |
0.692 |
|
| 1990 |
Hrovat DA, Borden WT, Vance RL, Rondan NG, Houk KN, Morokuma K. Ab initio calculation of the effects of cyano substituents on the Cope rearrangement Journal of the American Chemical Society. 112: 2018-2019. DOI: 10.1021/ja00161a067 |
0.663 |
|
| 1990 |
Coolidge MB, Yamashita K, Morokuma K, Borden WT. Ab initio MCSCF and CI calculations of the singlet-triplet energy differences in oxyallyl and in dimethyloxyallyl Journal of the American Chemical Society. 112: 1751-1754. DOI: 10.1021/Ja00161A015 |
0.523 |
|
| 1990 |
Coolidge MB, Borden WT. Ab initio calculations on borylphosphines: Prediction of a synergistic subsituent effect in diborylphosphine Journal of the American Chemical Society. 112: 1704-1706. DOI: 10.1021/Ja00161A008 |
0.388 |
|
| 1990 |
Hrovat DA, Borden WT. Ab initio calculations of the relative energies of 1,2-, 1,3- and 1,4-dehydrocubane: Prediction of dominant through-bond interaction in 1,4-dehydrocubane Journal of the American Chemical Society. 112: 875-876. DOI: 10.1021/Ja00158A062 |
0.635 |
|
| 1990 |
Hammons JH, Coolidge MB, Borden WT. Ab initio calculations of the barrier to CF2 rotation in 1,1,3,3-tetrafluoropropenyl radical Journal of Physical Chemistry. 94: 5468-5470. DOI: 10.1021/J100377A009 |
0.411 |
|
| 1990 |
Hammons JH, Hrovat DA, Borden WT. Effects of CF2 group pyramidalization in the 1,1,3,3-tetrafluoropropenyl anion Journal of Physical Organic Chemistry. 3: 635-638. DOI: 10.1002/Poc.610031003 |
0.595 |
|
| 1989 |
Wang SY, Borden WT. Why is the .pi. bond in tetrafluoroethylene weaker than that in ethylene? An ab initio investigation Journal of the American Chemical Society. 111: 7282-7283. DOI: 10.1021/Ja00200A070 |
0.378 |
|
| 1989 |
Du P, Hrovat DA, Borden WT. Ab initio calculations of the singlet-triplet energy differences in planar 2,4-dimethylenecyclobutane-1,3-diyl and in mono- and dioxo derivatives Journal of the American Chemical Society. 111: 3773-3778. DOI: 10.1021/Ja00193A001 |
0.64 |
|
| 1988 |
Hrovat DA, Borden WT. Synthesis of homocub-4(5)-ene: Confirmation of a computational prediction Journal of the American Chemical Society. 110: 7229-7230. DOI: 10.1021/Ja00229A056 |
0.535 |
|
| 1988 |
Hrovat DA, Borden WT. Ab initio calculations of the olefin strain energies of some pyramidalized alkenes Journal of the American Chemical Society. 110: 4710-4718. DOI: 10.1021/Ja00222A032 |
0.564 |
|
| 1988 |
Morokuma K, Borden WT, Hrovat DA. Chair and boat transition states for the Cope rearrangement. A CASSCF study Journal of the American Chemical Society. 110: 4474-4475. DOI: 10.1021/Ja00221A092 |
0.624 |
|
| 1988 |
Du P, Hrovat DA, Borden WT. Ab initio calculations on the ring opening of cyclopropane radical cation. Trimethylene radical cation is not a stable intermediate Journal of the American Chemical Society. 110: 3405-3412. DOI: 10.1021/Ja00219A011 |
0.634 |
|
| 1988 |
Coolidge MB, Borden WT. Ab initio calculations of the effects of substituents on the stabilization of silyl radicals versus methyl radicals Journal of the American Chemical Society. 110: 2298-2299. DOI: 10.1021/Ja00215A049 |
0.386 |
|
| 1988 |
Morokuma K, Borden WT, Hrovat DA. Chair and boat transition states for the cope rearrangement. A CASSCF study [42] Journal of the Chemical Society. 110: 4474-4475. |
0.589 |
|
| 1987 |
Hrovat DA, Miyake F, Trammell G, Gilbert KE, Mitchell J, Clardy J, Borden WT. Synthesis of 10-selenatricyclo[3.3.3.03,7]undec-3(7)-ene. X-ray structure of an alkene containing a pyramidalized double bond [4] Journal of the American Chemical Society. 109: 5524-5526. DOI: 10.1021/Ja00252A038 |
0.468 |
|
| 1987 |
Du P, Borden WT. Ab initio calculations of the ring opening of methylenecyclopropane radical cation to trimethylenemethane radical cation Journal of the American Chemical Society. 109: 5330-5336. DOI: 10.1021/Ja00252A005 |
0.411 |
|
| 1987 |
Sun H, Hrovat DA, Borden WT. Why are .pi. bonds to phosphorus more stable toward addition reactions than .pi. bonds to silicon? Journal of the American Chemical Society. 109: 5275-5276. DOI: 10.1021/Ja00251A041 |
0.576 |
|
| 1987 |
Du P, Borden WT. Ab initio calculations predict a singlet ground state for tetramethyleneethane Journal of the American Chemical Society. 109: 930-931. DOI: 10.1021/Ja00237A066 |
0.411 |
|
| 1987 |
HROVAT DA, MIYAKE F, TRAMMELL G, GILBERT KE, MITCHELL J, CLARDY J, BORDEN WT. ChemInform Abstract: Synthesis of 10-Selenatricyclo(3.3.3.03,7)undec-3(7)-ene. X-Ray Structure of an Alkene Containing a Pyramidalized Double Bond. Cheminform. 18. DOI: 10.1002/chin.198751264 |
0.497 |
|
| 1987 |
Sun H, Hrovat DA, Borden WT. Why are π bonds to phosphorus more stable toward addition reactions than π bonds to silicon? Journal of the American Chemical Society. 109: 5275-5276. |
0.539 |
|
| 1986 |
Du P, Hrovat DA, Borden WT. Ab initio calculations of the singlet-triplet energy separation in 3,4-dimethylenefuran and related diradicals Journal of the American Chemical Society. 108: 8086-8087. DOI: 10.1021/Ja00285A034 |
0.625 |
|
| 1986 |
Hrovat DA, Du P, Borden WT. Has the trimethylene radical cation been observed?. An Ab initio molecular orbital study Chemical Physics Letters. 123: 337-340. DOI: 10.1016/0009-2614(86)80083-5 |
0.631 |
|
| 1986 |
Borden WT. When is H3 stable to asymmetric distortion? Theoretica Chimica Acta. 69: 171-174. DOI: 10.1007/Bf00527688 |
0.374 |
|
| 1986 |
Du P, Hrovat DA, Borden WT, Lahti PM, Rossi AR, Berson JA. Ab initio calculations on 1,2,4,5-tetramethylenebenzene at geometries optimized by π-CI calculations. Prediction of a singlet ground state for a disjoint diradical Journal of the American Chemical Society. 108: 5072-5074. DOI: 10.1002/Chin.198651050 |
0.633 |
|
| 1985 |
Hrovat DA, Borden WT. Ab initio calculations on the lowest .pi. state of difluorocarbene radical cation Journal of the American Chemical Society. 107: 8034-8035. DOI: 10.1021/Ja00312A039 |
0.65 |
|
| 1985 |
Quenemoen K, Borden WT, Davidson ER, Feller D. Some aspects of the triplet di-π-methane rearrangement: Comparison of the ring opening of cyclopropyldicarbinyl and cyclopropylcarbinyl Journal of the American Chemical Society. 107: 5054-5059. DOI: 10.1021/Ja00304A006 |
0.511 |
|
| 1985 |
Feller D, Davidson ER, Borden WT. Ab initio calculations on the diphosphine radical cation (P2H4+.cntdot.) Journal of the American Chemical Society. 107: 2596-2597. DOI: 10.1021/Ja00295A004 |
0.492 |
|
| 1985 |
FELLER D, DAVIDSON ER, BORDEN WT. ChemInform Abstract: AB INITIO CALCULATIONS ON THE DIPHOSPHINE RADICAL CATION (P2H4+.CNTDOT.) Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198535003 |
0.48 |
|
| 1985 |
Hrovat DA, Borden WT. Ab initio calculations on the lowest π state of difluorocarbene radical cation Journal of the American Chemical Society. 107: 8034-8035. |
0.619 |
|
| 1984 |
Osamura Y, Borden WT, Morokuma K. Structure and stability of oxyallyl. An MCSCF study Journal of the American Chemical Society. 106: 5112-5115. DOI: 10.1021/Ja00330A013 |
0.463 |
|
| 1984 |
Osamura Y, Kato S, Morokuma K, Feller D, Davidson ER, Borden WT. Ab initio calculation of the transition state for the Cope rearrangement Journal of the American Chemical Society. 106: 3362-3363. DOI: 10.1021/Ja00323A055 |
0.611 |
|
| 1984 |
Feller D, Davidson ER, Borden WT. Allylic resonance - when is it unimportant? Journal of the American Chemical Society. 106: 2513-2519. DOI: 10.1021/Ja00321A004 |
0.456 |
|
| 1984 |
Osamura Y, Kato S, Morokuma K, Feller D, Davidson ER, Borden WT. Ab Initio Calculation Of The Transition State For The Cope Rearrangement Cheminform. 15. DOI: 10.1002/Chin.198436075 |
0.635 |
|
| 1984 |
Feller D, Davidson ER, Borden WT. Allylic resonance - When is it unimportant? Journal of the American Chemical Society. 106: 2513-2519. |
0.335 |
|
| 1984 |
Osamura Y, Kato S, Morokuma K, Feller D, Davidson ER, Borden WT. Ab initio calculation of the transition state for the Cope rearrangement Journal of the American Chemical Society. 106: 3362-3363. |
0.464 |
|
| 1983 |
Feller D, Davidson ER, Borden WT. When is allylic resonance unimportant? Journal of the American Chemical Society. 105: 3347-3348. DOI: 10.1021/Ja00348A071 |
0.415 |
|
| 1983 |
Kato S, Morokuma K, Feller D, Davidson ER, Borden WT. Ab initio study of m-benzoquinodimethane Journal of the American Chemical Society. 105: 1791-1795. DOI: 10.1021/Ja00345A018 |
0.55 |
|
| 1983 |
Feller D, Huyser ES, Borden WT, Davidson ER. MCSCF/CI investigation of the low-lying potential energy surfaces of the formyloxyl radical, HCO2.cntdot. Journal of the American Chemical Society. 105: 1459-1466. DOI: 10.1021/Ja00344A007 |
0.506 |
|
| 1983 |
Feller D, Borden WT, Davidson ER. Ab initio calculation of the zero-field splitting parameters of vinylmethylene The Journal of Physical Chemistry. 87: 4833-4839. DOI: 10.1021/J150642A014 |
0.491 |
|
| 1983 |
Davidson ER, Borden WT. Symmetry breaking in polyatomic molecules: real and artifactual The Journal of Physical Chemistry. 87: 4783-4790. DOI: 10.1021/J150642A005 |
0.439 |
|
| 1983 |
Feller D, Davidson ER, Borden WT. Ab InitioCI Calculations of the Energy Difference between Trimethylenemethane and Butadiene Israel Journal of Chemistry. 23: 105-108. DOI: 10.1002/Ijch.198300014 |
0.562 |
|
| 1983 |
FELLER D, HUYSER ES, BORDEN WT, DAVIDSON ER. ChemInform Abstract: MCSCF/CI INVESTIGATION OF THE LOW-LYING POTENTIAL ENERGY SURFACES OF THE FORMYLOXYL RADICAL, HCO2.CNTDOT. Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198339140 |
0.512 |
|
| 1983 |
FELLER D, MCMURCHIE LE, BORDEN WT, DAVIDSON ER. ChemInform Abstract: A THEORETICAL DETERMINATION OF THE ELECTRON AFFINITY OF METHYLENE Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198310063 |
0.422 |
|
| 1983 |
Kato S, Morokuma K, Feller D, Davidson ER, Borden WT. Ab initio study of m-benzoquinodimethane Journal of the American Chemical Society. 105: 1791-1795. |
0.337 |
|
| 1982 |
Huyser ES, Feller D, Borden WT, Davidson ER. A theoretical study of the acetaldehyde-derived radical Journal of the American Chemical Society. 104: 2956-2959. DOI: 10.1021/Ja00375A002 |
0.504 |
|
| 1982 |
Feller D, Davidson ER, Borden WT. Ab initio calculations of the relative energies of triplet 2,4-dimethylenecyclobutane-1,3-diyl and singlet 2,4-dimethylenebicyclo[1.1.0]butane Journal of the American Chemical Society. 104: 1216-1218. DOI: 10.1021/Ja00369A011 |
0.58 |
|
| 1982 |
Feller D, Tanaka K, Davidson ER, Borden WT. Potential surface for the methylenecyclopropane rearrangement Journal of the American Chemical Society. 104: 967-972. DOI: 10.1021/Ja00368A007 |
0.573 |
|
| 1982 |
Borden WT, Davidson ER, Feller D. RHF and two-configuration SCF calculations are inappropriate for conjugated diradicals Tetrahedron. 38: 737-739. DOI: 10.1016/0040-4020(82)80153-1 |
0.583 |
|
| 1982 |
Feller D, McMurchie LE, Borden WT, Davidson ER. A theoretical determination of the electron affinity of methylene The Journal of Chemical Physics. 77: 6134-6143. DOI: 10.1002/Chin.198310063 |
0.481 |
|
| 1982 |
HUYSER ES, FELLER D, BORDEN WT, DAVIDSON ER. ChemInform Abstract: A THEORETICAL STUDY OF THE ACETALDEHYDE-DERIVED RADICAL Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198237125 |
0.447 |
|
| 1982 |
FELLER D, DAVIDSON ER, BORDEN WT. ChemInform Abstract: AB INITIO CALCULATIONS OF THE RELATIVE ENERGIES OF TRIPLET 2,4-DIMETHYLENECYCLOBUTANE-1,3-DIYL AND SINGLET 2,4-DIMETHYLENEBICYCLO(1.1.0)BUTANE Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198225059 |
0.321 |
|
| 1982 |
FELLER D, TANAKA K, DAVIDSON ER, BORDEN WT. ChemInform Abstract: POTENTIAL SURFACE FOR THE METHYLENECYCLOPROPANE REARRANGEMENT Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198223134 |
0.372 |
|
| 1981 |
Feller D, Borden WT, Davidson ER. Calculation of zero field splitting parameters for trimethylenemethane The Journal of Chemical Physics. 74: 2256-2259. DOI: 10.1063/1.441387 |
0.526 |
|
| 1981 |
Borden WT, Davidson ER, Feller D. The potential surface for the cyclobutadiene radical cation Journal of the American Chemical Society. 103: 5725-5729. DOI: 10.1021/Ja00409A018 |
0.482 |
|
| 1981 |
Feller D, Davidson ER, Borden WT. Theoretical study of concerted vs. stepwise fragmentation of 2-carbena-1,3-dioxolane Journal of the American Chemical Society. 103: 2558-2560. DOI: 10.1021/Ja00400A012 |
0.467 |
|
| 1981 |
Borden WT, Davidson ER. Theoretical studies of diradicals containing four .pi. electrons Accounts of Chemical Research. 14: 69-76. DOI: 10.1021/Ar00063A002 |
0.481 |
|
| 1981 |
FELLER D, DAVIDSON ER, BORDEN WT. ChemInform Abstract: THEORETICAL STUDY OF CONCERTED VS. STEPWISE FRAGMENTATION OF 2-CARBENA-1,3-DIOXOLANE Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198134139 |
0.478 |
|
| 1981 |
FELLER D, BORDEN WT, DAVIDSON ER. ChemInform Abstract: CALCULATION OF ZERO FIELD SPLITTING PARAMETERS FOR TRIMETHYLENEMETHANE Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198125063 |
0.481 |
|
| 1981 |
BORDEN WT, DAVIDSON ER. ChemInform Abstract: WHY IS TETRA-TERT-BUTYLCYCLOBUTADIENE ALMOST SQUARE? Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198114058 |
0.453 |
|
| 1980 |
Borden WT, Davidson ER. Why is tetra-tert-butylcyclobutadiene almost square? Journal of the American Chemical Society. 102: 7958-7960. DOI: 10.1021/Ja00547A035 |
0.432 |
|
| 1980 |
Borden WT, Davidson ER. Effect of through-bond interaction on terminal methylene rotation in the tetramethylene diradical Journal of the American Chemical Society. 102: 5409-5410. DOI: 10.1021/Ja00536A057 |
0.478 |
|
| 1980 |
Borden WT, Davidson ER, Feller D. Potential surfaces for (NH)32+ [triaziridenyl dication] Journal of the American Chemical Society. 102: 5302-5311. DOI: 10.1021/Ja00536A031 |
0.44 |
|
| 1980 |
Feller D, Borden WT, Davidson ER. A theoretical study of paths for decomposition and rearrangement of dihydroxycarbene Journal of Computational Chemistry. 1: 158-166. DOI: 10.1002/Jcc.540010208 |
0.565 |
|
| 1980 |
BORDEN WT, DAVIDSON ER. ChemInform Abstract: EFFECT OF THROUGH-BOND INTERACTION ON TERMINAL METHYLENE ROTATION IN THE TETRAMETHYLENE DIRADICAL Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198044081 |
0.417 |
|
| 1980 |
FELLER D, BORDEN WT, DAVIDSON ER. ChemInform Abstract: THE SINGLET AND TRIPLET STATE ROTATIONAL POTENTIAL SURFACES FOR DIHYDROXYCARBENE Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198014072 |
0.422 |
|
| 1979 |
Borden WT, Davidson ER. Singlet-Triplet Energy Separations in Some Hydrocarbon Diradicals Annual Review of Physical Chemistry. 30: 125-153. DOI: 10.1146/Annurev.Pc.30.100179.001013 |
0.515 |
|
| 1979 |
Borden WT, Young SD, Frost DC, Westwood NPC, Jorgensen WL. Photoelectron spectra of the 1,2,5,6-tetramethyl-3,4,7,8-tetramethylene derivatives of tricyclo[3.3.0.02,6]octane and tricyclo[4.2.0.02,5]octane The Journal of Organic Chemistry. 44: 737-740. DOI: 10.1021/Jo01319A016 |
0.452 |
|
| 1979 |
Borden WT, Davidson ER. Potential surfaces for the planar cyclopentadienyl radical and cation Journal of the American Chemical Society. 101: 3771-3775. DOI: 10.1021/Ja00508A012 |
0.487 |
|
| 1979 |
Volland WV, Davidson ER, Borden WT. Effect of carbon atom pyramidalization on the bonding in ethylene Journal of the American Chemical Society. 101: 533-537. DOI: 10.1021/Ja00497A005 |
0.484 |
|
| 1979 |
Feller D, Borden WT, Davidson ER. The singlet and triplet state rotational potential surfaces for dihydroxycarbene The Journal of Chemical Physics. 71: 4987. DOI: 10.1002/Chin.198014072 |
0.485 |
|
| 1979 |
BORDEN WT, DAVIDSON ER. ChemInform Abstract: POTENTIAL SURFACES FOR THE PLANAR CYCLOPENTADIENYL RADICAL AND CATION Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197943059 |
0.426 |
|
| 1978 |
Borden WT, Gold A, Jorgensen WL. Cycloaddition reactions of 1,2,5,6-tetramethyl-3,4,7,8-tetramethylenetricyclo[3.3.0.02,6]octane. Evidence for chemical consequences of orbital interactions in molecules containing unsaturatively 1,3-bridged cyclobutane rings The Journal of Organic Chemistry. 43: 491-497. DOI: 10.1021/Jo00397A024 |
0.49 |
|
| 1978 |
Davidson ER, Borden WT, Smith J. The potential surface for 1,3-dimethylenecyclobutadiene Journal of the American Chemical Society. 100: 3299-3302. DOI: 10.1021/Ja00479A007 |
0.426 |
|
| 1978 |
Borden WT, Davidson ER, Andersen NH, Denniston AD, Epiotis ND. Regarding the mechanism of carbon-hydrogen bond acidification by sulfur Journal of the American Chemical Society. 100: 1604-1605. DOI: 10.1021/Ja00473A048 |
0.59 |
|
| 1978 |
Borden WT, Davidson ER, Hart P. The potential surfaces for the lowest singlet and triplet states of cyclobutadiene Journal of the American Chemical Society. 100: 388-392. DOI: 10.1021/Ja00470A006 |
0.491 |
|
| 1978 |
Davidson ER, Borden WT, Smith J. The Potential Surface For 1,3-Dimethylenecyclobutadiene Cheminform. 9. DOI: 10.1002/Chin.197835085 |
0.426 |
|
| 1978 |
BORDEN WT, DAVIDSON ER, ANDERSEN NH, DENNISTON AD, EPIOTIS ND. ChemInform Abstract: REGARDING THE MECHANISM OF CARBON-HYDROGEN BOND ACIDIFICATION BY SULFUR Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197826121 |
0.554 |
|
| 1978 |
BORDEN WT, DAVIDSON ER, HART P. ChemInform Abstract: THE POTENTIAL SURFACES FOR THE LOWEST SINGLET AND TRIPLET STATES OF CYCLOBUTADIENE Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197818043 |
0.43 |
|
| 1977 |
Davidson ER, Borden WT. The potential surface for planar cyclopropenyl radical and anion The Journal of Chemical Physics. 67: 2191. DOI: 10.1063/1.435106 |
0.541 |
|
| 1977 |
Borden WT, Davidson ER. Effects of electron repulsion in conjugated hydrocarbon diradicals Journal of the American Chemical Society. 99: 4587-4594. DOI: 10.1021/Ja00456A010 |
0.466 |
|
| 1977 |
Davidson ER, Borden WT. Some aspects of the potential surface for singlet trimethylenemethane Journal of the American Chemical Society. 99: 2053-2060. DOI: 10.1021/Ja00449A007 |
0.439 |
|
| 1977 |
BORDEN WT, DAVIDSON ER. ChemInform Abstract: EFFECTS OF ELECTRON REPULSION IN CONJUGATED HYDROCARBON DIRADICALS Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/chin.197741140 |
0.406 |
|
| 1976 |
Davidson ER, Borden WT. Configuration interaction calculations for 1E′ trimethylenemethane The Journal of Chemical Physics. 64: 663-666. DOI: 10.1063/1.432258 |
0.576 |
|
| 1975 |
Borden WT. Can a square or effectively square singlet be the ground state of cyclobutadiene Journal of the American Chemical Society. 97: 5968-5970. DOI: 10.1021/Ja00854A002 |
0.302 |
|
| 1975 |
Borden WT. Lowest singlet state of planar trimethylenemethane Journal of the American Chemical Society. 97: 2906-2907. DOI: 10.1021/Ja00843A052 |
0.312 |
|
| 1975 |
Jorgensen WL, Borden WT. Orbital interactions in molecules containing unsaturatively bridged cyclobutane and bicyclobutane rings Tetrahedron Letters. 16: 223-226. DOI: 10.1016/S0040-4039(00)71828-4 |
0.471 |
|
| 1975 |
BORDEN WT. ChemInform Abstract: THE LOWEST SINGLE STATE OF PLANAR TRIMETHYLENEMETHANE Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197530089 |
0.301 |
|
| 1973 |
Jorgensen WL, Borden WT. Chemical consequences of orbital interactions in hydrocarbons containing unsaturativety bridged small rings Journal of the American Chemical Society. 95: 6649-6654. DOI: 10.1021/Ja00801A021 |
0.468 |
|
| 1973 |
Borden WT, Salem L. Electron repulsion pericyclic transition states Journal of the American Chemical Society. 95: 932-933. DOI: 10.1021/Ja00784A056 |
0.311 |
|
| 1970 |
BORDEN WT. ChemInform Abstract: MECHANISMUS DES HYDRID-ANGRIFFS BEI DER RED. VON TRANS-1-TERT.-BUTYL-3-PHENYL-ALLYL- UND 1-TERT.-BUTYL-3-PHENYL-PROPARGYLALKOHOL Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197044141 |
0.322 |
|
| 1966 |
Borden WT. Electronic Structure and Isomerism in Allene The Journal of Chemical Physics. 45: 2512-2513. DOI: 10.1063/1.1727969 |
0.425 |
|
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