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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Heavy Halogen Atom Effect on C-13 NMR Chemical Shifts in Monohalo Derivatives of Cyclohexane and Pyran. Experimental and Theoretical Study

Texto completo
Autor(es):
Cunha Neto, Alvaro [1] ; Ducati, Lucas C. [1] ; Rittner, Roberto [1] ; Tormena, Claudio F. [1] ; Contreras, Ruben H. [2, 3] ; Frenking, Gernot [4]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] Univ Estadual Campinas, Inst Chem, BR-13084971 Campinas, SP - Brazil
[2] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF - Argentina
[3] Univ Buenos Aires, Dept Phys, FCEyN, Buenos Aires, DF - Argentina
[4] Univ Marburg, D-35032 Marburg - Germany
Número total de Afiliações: 4
Tipo de documento: Artigo Científico
Fonte: JOURNAL OF CHEMICAL THEORY AND COMPUTATION; v. 5, n. 9, p. 2222-2228, SEP 2009.
Citações Web of Science: 25
Resumo

As a first step, a qualitative analysis of the spin-orbit operator was performed to predict the kind of organic compounds, where it could be expected that the SO/FC (spin-orbit/Fermi contact) and SO/SD (spin-orbit/spin dipolar) yield unusually small contributions to the ``heavy atom effect{''} on (13)C SCSs (substituent chemical shifts). This analysis led to the conclusion that compounds presenting strong hyperconjugative interactions involving the sigma(star)(c-x) orbital (X = halogen) are good examples where such effects can be expected to take place. On the basis of such results, the following set of model compounds was chosen: 2-eq-halocyclohexane (2-eq), 2-ax-halocyclohexane (2-ax), and 2-ax-halopyran (3), to measure (13)C SCSs. Such experimental values, as well as those of methane and halomethanes taken from the literature, were compared to calculated values at a nonrelativistic approach using B3LYP, and at a relativistic approach with BP86 using scalar ZORA, spin-orbit ZORA, scalar PAULI, and spin-orbit PAULI. Results from relativistic calculations are in agreement with the trends predicted by the qualitative model discussed in this work. (AU)

Processo FAPESP: 06/02783-9 - Desenvolvimento de funções de base para cálculo teórico de acoplamentos J(P,P), J(P,C) e J(P,H)
Beneficiário:Lucas Colucci Ducati
Modalidade de apoio: Bolsas no Brasil - Doutorado