Please use this identifier to cite or link to this item: https://doi.org/10.1039/c2cc33728b
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dc.titleTetrakis(4-tert-butylphenyl) substituted and fused quinoidal porphyrins
dc.contributor.authorZeng, W.
dc.contributor.authorLee, B.S.
dc.contributor.authorSung, Y.M.
dc.contributor.authorHuang, K.-W.
dc.contributor.authorLi, Y.
dc.contributor.authorKim, D.
dc.contributor.authorWu, J.
dc.date.accessioned2014-06-23T05:52:19Z
dc.date.available2014-06-23T05:52:19Z
dc.date.issued2012-08-11
dc.identifier.citationZeng, 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.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/77218
dc.description.abstract4-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.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2cc33728b
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c2cc33728b
dc.description.sourcetitleChemical Communications
dc.description.volume48
dc.description.issue62
dc.description.page7684-7686
dc.description.codenCHCOF
dc.identifier.isiut000306176300006
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