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pubmed-article:20809649rdf:typepubmed:Citationlld:pubmed
pubmed-article:20809649pubmed:issue19lld:pubmed
pubmed-article:20809649pubmed:dateCreated2010-9-24lld:pubmed
pubmed-article:20809649pubmed:abstractTextNaphthobipyrrole is a potentially useful building block for porphyrin and porphyrin analogue synthesis. Reported here is a simple, generalizable synthetic route to ?-formylated, ?-substituted naphthobipyrroles and their use in the preparation of binaphthoporphycenes. The resulting binaphthoporphycenes possess a planar geometry as determined via a single-crystal X-ray diffraction analysis; they also display absorption maxima that are bathochromically shifted compared to simple porphycenes.lld:pubmed
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pubmed-article:20809649pubmed:statusMEDLINElld:pubmed
pubmed-article:20809649pubmed:monthOctlld:pubmed
pubmed-article:20809649pubmed:issn1523-7052lld:pubmed
pubmed-article:20809649pubmed:authorpubmed-author:SesslerJonath...lld:pubmed
pubmed-article:20809649pubmed:authorpubmed-author:LynchVincentVlld:pubmed
pubmed-article:20809649pubmed:authorpubmed-author:Roznyatovskiy...lld:pubmed
pubmed-article:20809649pubmed:issnTypeElectroniclld:pubmed
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pubmed-article:20809649pubmed:volume12lld:pubmed
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pubmed-article:20809649pubmed:pagination4424-7lld:pubmed
pubmed-article:20809649pubmed:dateRevised2011-10-3lld:pubmed
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pubmed-article:20809649pubmed:year2010lld:pubmed
pubmed-article:20809649pubmed:articleTitleDinaphthoporphycenes.lld:pubmed
pubmed-article:20809649pubmed:affiliationDepartment of Chemistry and Biochemistry, The University of Texas at Austin, 1 University Station A5300, Austin, Texas 78712, USA.lld:pubmed
pubmed-article:20809649pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20809649pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
pubmed-article:20809649pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
pubmed-article:20809649pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed