Year |
Citation |
Score |
2014 |
Hutchins KM, Sumrak JC, MacGillivray LR. Resorcinol-templated head-to-head photodimerization of a thiophene in the solid state and unusual edge-to-face stacking in a discrete hydrogen-bonded assembly. Organic Letters. 16: 1052-5. PMID 24499324 DOI: 10.1021/Ol4035403 |
0.695 |
|
2014 |
Hutchins KM, Sumrak JC, Swenson DC, Macgillivray LR. Head-to-tail photodimerization of a thiophene in a co-crystal and a rare adipic acid dimer in the presence of a heterosynthon Crystengcomm. 16: 5762-5764. DOI: 10.1039/C4Ce00481G |
0.682 |
|
2014 |
Hutchins KM, Sumrak JC, Macgillivray LR. Resorcinol-templated head-to-head photodimerization of a thiophene in the solid state and unusual edge-to-face stacking in a discrete hydrogen-bonded assembly Organic Letters. 16: 1052-1055. DOI: 10.1021/ol4035403 |
0.704 |
|
2013 |
Ghorai S, Sumrak JC, Hutchins KM, Bu?ar DK, Tivanski AV, Macgillivray LR. From co-crystals to functional thin films: Photolithography using [2+2] photodimerization Chemical Science. 4: 4304-4308. DOI: 10.1039/C3Sc51073E |
0.663 |
|
2012 |
Elacqua E, Kaushik P, Groeneman RH, Sumrak JC, Bučar DK, MacGillivray LR. A supramolecular protecting group strategy introduced to the organic solid state: enhanced reactivity through molecular pedal motion. Angewandte Chemie (International Ed. in English). 51: 1037-41. PMID 22162410 DOI: 10.1002/Anie.201106842 |
0.656 |
|
2012 |
Elacqua E, Kaushik P, Groeneman RH, Sumrak JC, Bu?ar DK, MacGillivray LR. A supramolecular protecting group strategy introduced to the organic solid state: Enhanced reactivity through molecular pedal motion Angewandte Chemie - International Edition. 51: 1037-1041. DOI: 10.1002/anie.201106842 |
0.704 |
|
2011 |
Sumrak JC, Sokolov AN, Macgillivray LR. Crystal Engineering Organic Semiconductors Self-Organized Organic Semiconductors. 1-19. DOI: 10.1002/9780470949122.ch1 |
0.61 |
|
2010 |
Sokolov AN, Sumrak JC, MacGillivray LR. Conformational polymorphism facilitates assignment of trans and cis-conformers of an alpha-substituted oligothiophene via IR spectroscopy. Chemical Communications (Cambridge, England). 46: 82-4. PMID 20024300 DOI: 10.1039/B915609G |
0.625 |
|
2010 |
Sokolov AN, Sumrak JC, MacGillivray LR. Conformational polymorphism facilitates assignment of trans and cis-conformers of an α-substituted oligothiophene via IR spectroscopy Chemical Communications. 46: 82-84. DOI: 10.1039/b915609g |
0.595 |
|
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