dc.creatorDo Canto E.L.
dc.creatorTasic L.
dc.creatorRittner R.
dc.date2000
dc.date2015-06-30T19:50:32Z
dc.date2015-11-26T14:46:59Z
dc.date2015-06-30T19:50:32Z
dc.date2015-11-26T14:46:59Z
dc.date.accessioned2018-03-28T21:57:05Z
dc.date.available2018-03-28T21:57:05Z
dc.identifier
dc.identifierCanadian Journal Of Analytical Sciences And Spectroscopy. , v. 45, n. 2, p. 1 - 35, 2000.
dc.identifier12056685
dc.identifier
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0034354283&partnerID=40&md5=513fe470630ac8b3180493b82c4a69ac
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/107224
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/107224
dc.identifier2-s2.0-0034354283
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1253078
dc.descriptionThe 13C NMR Substituent-induced Chemical Shifts (SCS) of aromatic carbons in 1,4-disubstituted benzenes were correlated with inductive and mesomeric effects, expressed in σI and σR (NMR) scales, and with charge alterations (Δ) provoked by introducing a new substituent (X) at position C-1. 105 different compounds with groups attached to C-1 (X) and C-4 (Y) in a sequence: NMe2, NH2, OMe, F, Cl, Br, Me, H, CF3, CN, C(O)OEt, C(O)Me, NO2 and CHO were studied. Correlations of σI and σR with SCS and with Δq, and of SCS with Δq, showed statistical relevance just for C-4. SCS and Δq were correlated only with σR for C-2. No correlation was found for C-1 (ipso-carbon), except between Δq and σR, while for C-3 the occurrence or not of any correlation was strongly dependent on the classes of compounds, fixed by the substituent at C-4 (Y).
dc.description45
dc.description2
dc.description1
dc.description35
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dc.languageen
dc.publisher
dc.relationCanadian Journal of Analytical Sciences and Spectroscopy
dc.rightsfechado
dc.sourceScopus
dc.titleSubstituent-induced Chemical Shifts (scs) Of 1,4-disubstituted Benzenes: Correlation Analysis
dc.typeArtículos de revistas


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