(1)J(CH) Coupling in Benzaldehyde Derivatives: Ortho Substitution Effect

Author(s)

Nepel, Angelita ^[1] ; Viesser, Renan V. ^[1] ; Tormena, Claudio F. ^[1]

Affiliation

^[1] Univ Campinas UNICAMP, Inst Chem, POB 6154, BR-13083970 Campinas, SP - Brazil

• Document type: Journal article
• Source: ACS OMEGA; v. 4, n. 1, p. 1494-1503, JAN 2019.
• Web of Science Citations: 1

Abstract

The natural J-coupling (NJC) method is applied to analyze the Fermi contact contribution of the NMR spin-spin coupling constant decomposing this contribution in terms of natural localized molecular orbitals. We investigated the influence of the basis set on the NJC analysis for the formyl group coupling constant ((1)J(CHf)) of benzaldehyde derivatives. NJC and other NBO analyses, like steric and natural Coulombic energy, were chosen to explain the influence of electron-donating and electron-withdrawing groups on (1)J(CHf) for some substituted benzaldehydes (Me, OH, OMe, F, Cl, Br, I, and NO2). For the ortho derivatives, electronegative substituents near the C-Hf bond increase the (1)J(CHf) coupling. This effect could be related to an increase in formyl carbon s character and changes in the carbon and hydrogen natural charges. This indicates that the substituents in ortho have a proximity effect on (1)J(CHf) coupling mainly of electrostatic origin instead of the expected hyperconjugative interactions. (AU)

• FAPESP's process: 15/08541-6 - Nuclear magnetic resonance spectroscopy: beyond molecular structure assignment
• Grantee: Claudio Francisco Tormena
• Support Opportunities: Research Projects - Thematic Grants
• FAPESP's process: 17/20890-1 - Evaluation of shielding and transmission mechanisms of 1H, 13C and 19F NMR
• Grantee: Renan Vidal Viesser
• Support Opportunities: Scholarships in Brazil - Post-Doctoral