20373818

Source:http://linkedlifedata.com/resource/pubmed/id/20373818

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0205360, umls-concept:C0220781, umls-concept:C1749467, umls-concept:C1883254
pubmed:issue	9
pubmed:dateCreated	2010-4-30
pubmed:abstractText	The synthesis of new silylethyne-substituted hexacene derivatives to investigate their solubility, stability, and pi-stacking is reported. It was found that "butterfly" dimerization, rather than photooxidation, is the dominant decomposition pathway for these molecules and that stability can be enhanced by functionalization to prevent close contact between specific regions of the aromatic core. Dimerization regioselectivity can be altered by suitable engineering of the solid-state arrangement of the chromophores.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	May
pubmed:issn	1523-7052
pubmed:author	pubmed-author:AnthonyJohn EJE, pubmed-author:ParkinSean RSR, pubmed-author:PurushothamanBalajiB
pubmed:issnType	Electronic
pubmed:day	7
pubmed:volume	12
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2060-3
pubmed:year	2010
pubmed:articleTitle	Synthesis and stability of soluble hexacenes.
pubmed:affiliation	Department of Chemistry, University of Kentucky, Lexington, Kentucky 40506-0055, USA.
pubmed:publicationType	Journal Article