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Thomas H. Kinstle - Publications

Affiliations: 
Photochemical Sciences Bowling Green State University, Bowling Green, OH, United States 
Area:
Organic Chemistry
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6 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
2011 Onicha AC, Panthi K, Kinstle TH, Castellano FN. Carbazole donor and carbazole or bithiophene bridged sensitizers for dye-sensitized solar cells Journal of Photochemistry and Photobiology a: Chemistry. 223: 57-64. DOI: 10.1016/J.Jphotochem.2011.08.001  0.635
2010 Panthi K, Adhikari RM, Kinstle TH. Aromatic fumaronitrile core-based donor-linker-acceptor-linker-donor (D-pi-A-pi-D) compounds: synthesis and photophysical properties. The Journal of Physical Chemistry. A. 114: 4542-9. PMID 20235549 DOI: 10.1021/Jp9115589  0.712
2010 Panthi K, Adhikari RM, Kinstle TH. Carbazole donor-carbazole linker-based compounds: preparation, photophysical properties, and formation of fluorescent nanoparticles. The Journal of Physical Chemistry. A. 114: 4550-7. PMID 20232882 DOI: 10.1021/Jp912286U  0.716
2010 Panthi K, El-Khoury PZ, Tarnovsky AN, Kinstle TH. Synthesis and computational studies of diphenylamine donor-carbazole linker-based donor–acceptor compounds Tetrahedron. 66: 9641-9649. DOI: 10.1016/J.Tet.2010.10.050  0.697
2010 Panthi K, Adhikari RM, Kinstle TH. Visible and near IR emitting organic nanoparticles of aromatic fumaronitrile core-based donor―acceptor compounds Journal of Photochemistry and Photobiology a-Chemistry. 215: 179-184. DOI: 10.1016/J.Jphotochem.2010.08.014  0.698
2006 Bombuwala K, Kinstle T, Popik V, Uppal SO, Olesen JB, Viña J, Heckman CA. Colchitaxel, a coupled compound made from microtubule inhibitors colchicine and paclitaxel. Beilstein Journal of Organic Chemistry. 2: 13. PMID 16813651 DOI: 10.1186/1860-5397-2-13  0.337
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