Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/12878
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dc.contributor.authorEargle Jr., Dolan H.-
dc.date.accessioned2010-03-12T13:15:52Z-
dc.date.available2010-03-12T13:15:52Z-
dc.date.issued1971-
dc.identifier.citationJournal of the American Chemical Society. 93:16 (1971) 3859–3862en_US
dc.identifier.issn0002-7863-
dc.identifier.urihttps://hdl.handle.net/10316/12878-
dc.description.abstractThe ir aryl skeletal vibrations (1600-cm-' region) and the nmr spectrum of tetraphenylethylene dianion (TPE2-) have been recorded. Evidence points to the conclusion that the antibonding electrons of the dianion are highly delocalized and that the K-bonding electrons of TPE2- essentially retain their bonding power, requiring the dianion t o assume a nearly planar configurationen_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsopenAccessen_US
dc.titleTetraphenylethylene. Infrared and nuclear magnetic resonance evidence on the nature of the dianionen_US
dc.typearticleen_US
dc.identifier.doi10.1021/ja00745a004-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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