Covalence and π-electron delocalization influence on hydrogen bonds in proton transfer process of o-hydroxy aryl Schiff bases: A combined NMR and QTAIM analysis-Reference-Cited by-同舟云学术

Covalence and π-electron delocalization influence on hydrogen bonds in proton transfer process of o-hydroxy aryl Schiff bases: A combined NMR and QTAIM analysis

Published:2021-08-07 Issue:5 Volume:155 Page:054307
ISSN:0021-9606
Container-title:The Journal of Chemical Physics
language:en
Short-container-title:J. Chem. Phys.

Author:

Zarycz M. Natalia C.¹^ORCID,Schiel M. Ayelén¹^ORCID,Angelina Emilio²^ORCID,Enriz Ricardo D.¹^ORCID

Affiliation:

1. Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis; Instituto Multidisciplinario de Investigaciones Biológicas (IMIBIO-SL). CONICET, Ejército de los Andes 950, 5700 San Luis, Argentina

2. Laboratorio de Estructura Molecular y Propiedades, Facultad de Ciencias Exactas y Naturales y Agrimensura, Universidad Nacional del Nordeste; Instituto de Química Básica y Aplicada (IQUIBA-NEA). CONICET, Avda. Libertad 5460, 3400 Corrientes, Argentina

Funder

Universidad Nacional de San Luis

Publisher

AIP Publishing

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

https://aip.scitation.org/doi/pdf/10.1063/5.0058422

Reference171 articles.

1. Hydrogen Bonding in Biological Structures

2. Theoretical studies of strong hydrogen bonds

3. The Hydrogen Bond in the Solid State

4. Designer crystals: intermolecular interactions, network structures and supramolecular synthons

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A NMR hybrid J-coupling alternation (hJCA) parameter linearly correlated to properties of intermolecular H-bonded chains;Computational and Theoretical Chemistry;2022-11

2. Evaluating the conformational space of the active site of D ₂ dopamine receptor. Scope and limitations of the standard docking methods;Journal of Computational Chemistry;2022-05-31