17590004

Source:http://linkedlifedata.com/resource/pubmed/id/17590004

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0599219, umls-concept:C1441547, umls-concept:C1883254
pubmed:issue	15
pubmed:dateCreated	2007-7-12
pubmed:abstractText	A 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.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jul
pubmed:issn	1523-7060
pubmed:author	pubmed-author:BarcinaJosé OsíoJO, pubmed-author:BlazquezMyriam MbaMM, pubmed-author:Caraballo-MartínezNoeliaN, pubmed-author:HerasMaría Del Rosario ColoradoMdel R, pubmed-author:MartínezAntonio GarcíaAG, pubmed-author:SalvadorMaría Del Rosario TorresMdel R
pubmed:issnType	Print
pubmed:day	19
pubmed:volume	9
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2943-6
pubmed:year	2007
pubmed:articleTitle	Synthesis of homoconjugated oligomers derived from 7,7-diphenylnorbornane.
pubmed:affiliation	Departamento de Química OrgAnica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n, 28040 Madrid, Spain.
pubmed:publicationType	Journal Article