Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol902241u
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dc.titleA soluble and stable quinoidal bisanthene with nir absorption and amphoteric redox behavior
dc.contributor.authorZhang, K.
dc.contributor.authorHuang, K.-W.
dc.contributor.authorLi, J.
dc.contributor.authorLuo, J.
dc.contributor.authorChi, C.
dc.contributor.authorWu, J.
dc.date.accessioned2014-06-23T05:30:59Z
dc.date.available2014-06-23T05:30:59Z
dc.date.issued2009-11-05
dc.identifier.citationZhang, 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.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75489
dc.description.abstractA 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.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol902241u
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol902241u
dc.description.sourcetitleOrganic Letters
dc.description.volume11
dc.description.issue21
dc.description.page4854-4857
dc.identifier.isiut000271097100023
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