Please use this identifier to cite or link to this item:
https://doi.org/10.1021/ol902241u
DC Field | Value | |
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dc.title | A soluble and stable quinoidal bisanthene with nir absorption and amphoteric redox behavior | |
dc.contributor.author | Zhang, K. | |
dc.contributor.author | Huang, K.-W. | |
dc.contributor.author | Li, J. | |
dc.contributor.author | Luo, J. | |
dc.contributor.author | Chi, C. | |
dc.contributor.author | Wu, J. | |
dc.date.accessioned | 2014-06-23T05:30:59Z | |
dc.date.available | 2014-06-23T05:30:59Z | |
dc.date.issued | 2009-11-05 | |
dc.identifier.citation | Zhang, K., Huang, K.-W., Li, J., Luo, J., Chi, C., Wu, J. (2009-11-05). A soluble and stable quinoidal bisanthene with nir absorption and amphoteric redox behavior. Organic Letters 11 (21) : 4854-4857. ScholarBank@NUS Repository. https://doi.org/10.1021/ol902241u | |
dc.identifier.issn | 15237060 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/75489 | |
dc.description.abstract | A soluble and stable quinoidal bisanthene (3) was synthesized, and it exhibited high molar absorptivity in the near-IR spectral region. In addition, compound 3 also showed good electrochemical amphotericity with four reversible one-electron transfer steps. Compound 3 represents a rare example of soluble and stable-conjugated polycyclic hydrocarbons with quinoidal character. © 2009 American Chemical Society. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol902241u | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1021/ol902241u | |
dc.description.sourcetitle | Organic Letters | |
dc.description.volume | 11 | |
dc.description.issue | 21 | |
dc.description.page | 4854-4857 | |
dc.identifier.isiut | 000271097100023 | |
Appears in Collections: | Staff Publications |
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