Please use this identifier to cite or link to this item:
https://doi.org/10.1039/c2cc33728b
DC Field | Value | |
---|---|---|
dc.title | Tetrakis(4-tert-butylphenyl) substituted and fused quinoidal porphyrins | |
dc.contributor.author | Zeng, W. | |
dc.contributor.author | Lee, B.S. | |
dc.contributor.author | Sung, Y.M. | |
dc.contributor.author | Huang, K.-W. | |
dc.contributor.author | Li, Y. | |
dc.contributor.author | Kim, D. | |
dc.contributor.author | Wu, J. | |
dc.date.accessioned | 2014-06-23T05:52:19Z | |
dc.date.available | 2014-06-23T05:52:19Z | |
dc.date.issued | 2012-08-11 | |
dc.identifier.citation | Zeng, W., Lee, B.S., Sung, Y.M., Huang, K.-W., Li, Y., Kim, D., Wu, J. (2012-08-11). Tetrakis(4-tert-butylphenyl) substituted and fused quinoidal porphyrins. Chemical Communications 48 (62) : 7684-7686. ScholarBank@NUS Repository. https://doi.org/10.1039/c2cc33728b | |
dc.identifier.issn | 13597345 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/77218 | |
dc.description.abstract | 4-tert-Butylphenyl-substituted and fused quinoidal porphyrins 1 and 2 are prepared for the first time. They show (1) intense one-photon absorption in the far-red/near-infrared region, (2) enhanced two-photon absorption compared with aromatic porphyrin monomers, and (3) amphoteric redox behavior. Their geometry and electronic structure are studied by DFT calculations. This journal is © 2012 The Royal Society of Chemistry. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2cc33728b | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1039/c2cc33728b | |
dc.description.sourcetitle | Chemical Communications | |
dc.description.volume | 48 | |
dc.description.issue | 62 | |
dc.description.page | 7684-7686 | |
dc.description.coden | CHCOF | |
dc.identifier.isiut | 000306176300006 | |
Appears in Collections: | Staff Publications |
Show simple item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.