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pubmed-article:17590004rdf:typepubmed:Citationlld:pubmed
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pubmed-article:17590004pubmed:issue15lld:pubmed
pubmed-article:17590004pubmed:dateCreated2007-7-12lld:pubmed
pubmed-article:17590004pubmed:abstractTextA methodology for the synthesis of monodisperse homoconjugated oligomers (dimer, trimer, and tetramer) derived from cofacial 7,7-diphenylnorbornane (DPN) is described. Extended aromatic homoconjugation is observed in these oligomers as revealed by the electronic spectra. The effective homoconjugation length (EHL) is in the range of 4-5 DPN subunits.lld:pubmed
pubmed-article:17590004pubmed:languageenglld:pubmed
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pubmed-article:17590004pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:17590004pubmed:monthJullld:pubmed
pubmed-article:17590004pubmed:issn1523-7060lld:pubmed
pubmed-article:17590004pubmed:authorpubmed-author:MartínezAnton...lld:pubmed
pubmed-article:17590004pubmed:authorpubmed-author:BarcinaJosé...lld:pubmed
pubmed-article:17590004pubmed:authorpubmed-author:Caraballo-Mar...lld:pubmed
pubmed-article:17590004pubmed:authorpubmed-author:HerasMaría...lld:pubmed
pubmed-article:17590004pubmed:authorpubmed-author:BlazquezMyria...lld:pubmed
pubmed-article:17590004pubmed:authorpubmed-author:SalvadorMaría...lld:pubmed
pubmed-article:17590004pubmed:issnTypePrintlld:pubmed
pubmed-article:17590004pubmed:day19lld:pubmed
pubmed-article:17590004pubmed:volume9lld:pubmed
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pubmed-article:17590004pubmed:pagination2943-6lld:pubmed
pubmed-article:17590004pubmed:year2007lld:pubmed
pubmed-article:17590004pubmed:articleTitleSynthesis of homoconjugated oligomers derived from 7,7-diphenylnorbornane.lld:pubmed
pubmed-article:17590004pubmed:affiliationDepartamento de Química OrgAnica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n, 28040 Madrid, Spain.lld:pubmed
pubmed-article:17590004pubmed:publicationTypeJournal Articlelld:pubmed