Conformational and spectroscopic properties of π-extended, bipyrrole-fused rubyrin and sapphyrin derivatives
Conformational and spectroscopic properties of π-extended, bipyrrole-fused rubyrin and sapphyrin derivatives
| dc.contributor.author | Kee, Se Young | |
| dc.contributor.author | Lim, Jong Min | |
| dc.contributor.author | Kim, Soo Jin | |
| dc.contributor.author | Yoo, Jaeduk | |
| dc.contributor.author | Park, Jung Su | |
| dc.contributor.author | Sarma, Tridib | |
| dc.contributor.author | Lynch, Vincent M. | |
| dc.contributor.author | Panda, Pradeepta K. | |
| dc.contributor.author | Sessler, Jonathan L. | |
| dc.contributor.author | Kim, Dongho | |
| dc.contributor.author | Lee, Chang Hee | |
| dc.date.accessioned | 2022-03-27T08:38:33Z | |
| dc.date.available | 2022-03-27T08:38:33Z | |
| dc.date.issued | 2011-01-01 | |
| dc.description.abstract | Two new expanded porphyrins, naphthorubyrin and naphthosapphyrin, were synthesized. The π-extended rubyrin was isolated and structurally characterized in its monoprotonated form. The sapphyrin congener undergoes pyrrole inversion as a function of the protonation state. These conformational effects are reflected in the spectroscopic features, including the excited singlet state lifetimes. © 2011 The Royal Society of Chemistry. | |
| dc.identifier.citation | Chemical Communications. v.47(24) | |
| dc.identifier.issn | 13597345 | |
| dc.identifier.uri | 10.1039/c1cc11733e | |
| dc.identifier.uri | http://xlink.rsc.org/?DOI=c1cc11733e | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/11332 | |
| dc.title | Conformational and spectroscopic properties of π-extended, bipyrrole-fused rubyrin and sapphyrin derivatives | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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