Influence of stereoelectronic interactions on the 13C NMR chemical shift in iodine-containing molecules

Autor(es)

Viesser, Renan V. ; Tormena, Claudio F.

• Tipo de documento: Artigo Científico
• Fonte: JOURNAL OF MAGNETIC RESONANCE OPEN; v. 12-13, p. 9-pg., 2022-12-01.

Resumo

Methyl substitution in ortho position causes a deshielding of 6-7 ppm on the 13C NMR chemical shift of the own methyl group and the carbon nucleus bonded to iodine atom (ipso) in iodobenzene-like molecules. In contrast, the carbon ipso is 3-4 ppm shielded when methyl is in para. To understand how the position of methyl substitution perturbs nuclear magnetic responses in iodobenzene and diacetoxyiodobenzene derivatives, shielding mechanisms are theoretically investigated via density functional theory calculations. We show the relative ortho position between iodine and methyl allows through-space and through-bond interactions to take place, generating additional paramagnetic currents and affecting the spin-orbit coupling propagation. Relevant paramagnetic couplings that explain the para methyl substitution behavior are also presented. Shielding mechanisms discussed here for monomethylated compounds can be summed to predict the 13C NMR chemical shift in multi methyl substituted iodine-containing compounds. (AU)

• Processo FAPESP: 20/10246-0 - Ressonância magnética nuclear: das sequências de pulso a determinação estrutural
• Beneficiário: Claudio Francisco Tormena
• Modalidade de apoio: Auxílio à Pesquisa - Temático
• Processo FAPESP: 17/20890-1 - Avaliação dos mecanismos de blindagem e de transmissão dos acoplamentos em RMN de 1H, 13C e 19F
• Beneficiário: Renan Vidal Viesser
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
• Processo FAPESP: 15/08541-6 - Ressonância magnética nuclear: além da determinação estrutural
• Beneficiário: Claudio Francisco Tormena
• Modalidade de apoio: Auxílio à Pesquisa - Temático