β-octamethoxyporphycenes

dc.contributor.author Rana, Anup
dc.contributor.author Panda, Pradeepta K.
dc.date.accessioned 2022-03-27T08:38:12Z
dc.date.available 2022-03-27T08:38:12Z
dc.date.issued 2014-01-03
dc.description.abstract Porphycene with eight methoxy substituents at its β-positions was synthesized for the first time in three steps from 3,4-dimethoxypyrrole. The presence of methoxy groups increases its hydrophilicity as evident from their increased solubility in methanol. Among its metallo-derivatives, the Pd(II)-complex displays efficient singlet oxygen quantum yield (73%) and hence can be a potentially good photosensitizer for photo-oxidation, DNA cleavage, and photodynamic therapy (PDT). © 2013 American Chemical Society.
dc.identifier.citation Organic Letters. v.16(1)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/ol403068j
dc.identifier.uri https://pubs.acs.org/doi/10.1021/ol403068j
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11309
dc.title β-octamethoxyporphycenes
dc.type Journal. Article
dspace.entity.type
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