Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/70300
Type: Artigo de periódico
Title: Principal component analysis of carbon-13 substituent-induced chemical shifts of some unsaturated compounds
Author: Tasic, L
Rittner, R
Abstract: Principal component analysis (PCA) is applied to 32 disubstituted unsaturated compounds (Y-CH(2)-X): Cyanides, oximes and propenes; bearing 12 alpha-substituents: F, Cl, Br, I, OMe, OEt, SMe, SEt, NMe(2), NEt(2), Me, and Et. The experimental (13)C chemical shifts for the alpha-carbon and functional carbon atoms are correlated with theoretically derived molecular properties, i.e. partial charges, electronegativity, hardness, dipole moments and the nuclear repulsion energies. In the first PCA, the clustering of these three classes of organic compounds occurred mostly because of the chemical shifts and partial charges, and also of the dipole moments, hardness and electronegativity parameters as confirmed by loading graph. A strong grouping is observed in the second PCA, showing the chemical shift dependence on the type of heteroatom substituents. Therefore, sulfur, nitrogen, oxygen and neutral groups exhibit four types of C-13 SCS influences, indicating that the heteroatom (Y) properties play a significant role on the effects on chemical shifts. The alpha-halogenated compounds represent a very heterogeneous group due to possible orbital interactions between the functional group and the substituent. The third PCA shows the grouping of F, Cl, Br and I derivatives, confirming the second PCA results that same halogen presents the same or very similar effects on the chemical shifts. (C) 2002 Elsevier Science B.V. All rights reserved.
Subject: (13)C NMR
principal component analysis
unsaturated compounds
theoretical parameters
Country: Holanda
Editor: Elsevier Science Bv
Rights: fechado
Identifier DOI: 10.1016/S0022-2860(02)00272-7
Date Issue: 2002
Appears in Collections:Unicamp - Artigos e Outros Documentos

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