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dc.creatorRezende, Fátima M. P. de-
dc.creatorFreitas, Matheus P.-
dc.creatorRamalho, Teodorico C.-
dc.date.accessioned2020-05-12T18:28:37Z-
dc.date.available2020-05-12T18:28:37Z-
dc.date.issued2019-03-15-
dc.identifier.citationREZENDE, F. M. P. de; FREITAS, M. P.; RAMALHO, T. C. The Perlin effect in 2-halocyclohexanones and 2-halocyclohexanethiones. Computational and Theoretical Chemistry, Amsterdam, v. 1152, p. 28-31, 15 Mar. 2019.pt_BR
dc.identifier.urihttps://www.sciencedirect.com/science/article/abs/pii/S2210271X19300507#!pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/40850-
dc.description.abstractThe Perlin effect is an NMR phenomenon observed in six-membered rings and it is referred to as 1JC−Hax < 1JC−Heq. In the present work, the influence of halogens (F, Cl and Br) at position 2 in cyclohexanones and cyclohexanethiones is theoretically evaluated on the one-bond C2H2 coupling constants, i.e. on the Perlin effect. An important hyperconjugative interaction (πC=Y → σ*C-H, Y = O and S) operating in the studied systems seems to play a significant role for the observed 1JC−Hax < 1JC−Heq behavior. In addition, the Lewis contribution (JLewis) dominates the Fermi Contact term (JFC), which plays the major role for the overall one-bond CH coupling constant. Compared to the gas phase, this behavior was found to be insensitive to implicit solvents (DMSO and water).pt_BR
dc.languageen_USpt_BR
dc.publisherElsevierpt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceComputational and Theoretical Chemistrypt_BR
dc.subjectPerlin effectpt_BR
dc.subjectOne-bond coupling constantpt_BR
dc.subjectFermi contactpt_BR
dc.subjectLewis-type interactionspt_BR
dc.subjectEfeito perlinpt_BR
dc.subjectConstante de acoplamento de uma ligaçãopt_BR
dc.subjectContato Fermipt_BR
dc.subjectInterações do tipo Lewispt_BR
dc.titleThe Perlin effect in 2-halocyclohexanones and 2-halocyclohexanethionespt_BR
dc.typeArtigopt_BR
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