| Year |
Citation |
Score |
| 2014 |
Payton JL, Morton SM, Moore JE, Jensen L. A hybrid atomistic electrodynamics-quantum mechanical approach for simulating surface-enhanced Raman scattering. Accounts of Chemical Research. 47: 88-99. PMID 23965411 DOI: 10.1021/Ar400075R |
0.647 |
|
| 2012 |
Pathem BK, Zheng YB, Payton JL, Song TB, Yu BC, Tour JM, Yang Y, Jensen L, Weiss PS. Effect of Tether Conductivity on the Efficiency of Photoisomerization of Azobenzene-Functionalized Molecules on Au{111}. The Journal of Physical Chemistry Letters. 3: 2388-94. PMID 26292120 DOI: 10.1021/Jz300968M |
0.449 |
|
| 2012 |
Peng HL, Payton JL, Protasiewicz JD, Simpson MC. P=P bond photophysics in an Ar-P=P-Ar diphosphene. Dalton Transactions (Cambridge, England : 2003). 41: 13204-9. PMID 23014850 DOI: 10.1039/C2Dt30568B |
0.688 |
|
| 2012 |
Zheng YB, Payton JL, Song TB, Pathem BK, Zhao Y, Ma H, Yang Y, Jensen L, Jen AK, Weiss PS. Surface-enhanced Raman spectroscopy to probe photoreaction pathways and kinetics of isolated reactants on surfaces: flat versus curved substrates. Nano Letters. 12: 5362-8. PMID 22978482 DOI: 10.1021/Nl302750D |
0.437 |
|
| 2012 |
Payton JL, Morton SM, Moore JE, Jensen L. A discrete interaction model/quantum mechanical method for simulating surface-enhanced Raman spectroscopy. The Journal of Chemical Physics. 136: 214103. PMID 22697526 DOI: 10.1063/1.4722755 |
0.649 |
|
| 2012 |
Peng HL, Payton JL, Protasiewicz JD, Simpson MC. PP bond photophysics in an Ar-PP-Ar diphosphene Dalton Transactions. 41: 13204-13209. DOI: 10.1039/c2dt30568b |
0.663 |
|
| 2012 |
Pathem BK, Zheng YB, Payton JL, Song TB, Yu BC, Tour JM, Yang Y, Jensen L, Weiss PS. Effect of tether conductivity on the efficiency of photoisomerization of azobenzene-functionalized molecules on Au{111} Journal of Physical Chemistry Letters. 3: 2388-2394. DOI: 10.1021/jz300968m |
0.41 |
|
| 2011 |
Zheng YB, Payton JL, Chung CH, Liu R, Cheunkar S, Pathem BK, Yang Y, Jensen L, Weiss PS. Surface-enhanced Raman spectroscopy to probe reversibly photoswitchable azobenzene in controlled nanoscale environments. Nano Letters. 11: 3447-52. PMID 21749070 DOI: 10.1021/Nl2019195 |
0.478 |
|
| 2011 |
Washington MP, Payton JL, Simpson MC, Protasiewicz JD. Redox behavior of 2-substituted 1,3-benzoxaphospholes and 2,6-substituted benzo[1,2- d:4,5- d]bisoxaphospholes Organometallics. 30: 1975-1983. DOI: 10.1021/Om200014F |
0.567 |
|
| 2010 |
Washington MP, Gudimetla VB, Laughlin FL, Deligonul N, He S, Payton JL, Simpson MC, Protasiewicz JD. Phosphorus can also be a "photocopy". Journal of the American Chemical Society. 132: 4566-7. PMID 20235546 DOI: 10.1021/Ja1009426 |
0.607 |
|
| 2010 |
Protasiewicz JD, Washington MP, Gudimetla VB, Payton JL, Cather Simpson M. A closer look at the phosphorus-phosphorus double bond lengths in meta-terphenyl substituted diphosphenes Inorganica Chimica Acta. 364: 39-45. DOI: 10.1016/J.Ica.2010.07.018 |
0.363 |
|
| 2010 |
Gudimetla VB, Ma L, Washington MP, Payton JL, Cather Simpson M, Protasiewicz JD. Meta-terphenyl phosphaalkenes bearing electron-donating and -accepting groups European Journal of Inorganic Chemistry. 854-865. DOI: 10.1002/Ejic.200900870 |
0.328 |
|
| 2009 |
Peng HL, Payton JL, Protasiewicz JD, Simpson MC. Twisting the phenyls in aryl diphosphenes (Ar-P=P-Ar). Significant impact upon lowest energy excited states Journal of Physical Chemistry A. 113: 7054-7063. PMID 19496568 DOI: 10.1021/Jp810119K |
0.695 |
|
| 2006 |
Gudimetla VB, Rheingold AL, Payton JL, Peng HL, Simpson MC, Protasiewicz JD. Photochemical E-Z isomerization of meta-terphenyl-protected phosphaalkenes and structural characterizations Inorganic Chemistry. 45: 4895-4901. PMID 16780309 DOI: 10.1021/Ic0520521 |
0.685 |
|
| 2004 |
Zeller M, Hunter AD, Perrine CL, Payton J. Tricarbonyl(η6-trifluoromethylbenzene)-chromium(0) Acta Crystallographica Section E: Structure Reports Online. 60. DOI: 10.1107/S1600536804009584 |
0.441 |
|
| 2004 |
Zeller M, Hunter AD, Perrine CL, Payton J. Tricarbonyl(η6-fluorobenzene)chromium Acta Crystallographica Section E: Structure Reports Online. 60. DOI: 10.1107/S1600536804009250 |
0.448 |
|
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