Role of O–H⋯O/S conventional hydrogen bonds in considerable Csp2–H blue-shift in the binary systems of acetaldehyde and thioacetaldehyde with substituted carboxylic and thiocarboxylic acids
Author:
Affiliation:
1. Faculty of Natural Sciences, Quy Nhon University, Quy Nhon, Vietnam
2. Laboratory of Computational Chemistry and Modelling (LCCM), Quy Nhon University, Quy Nhon, Vietnam
Abstract
Funder
National Foundation for Science and Technology Development
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/RA/D2RA05391H
Reference79 articles.
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4. THE NATURE OF THE CHEMICAL BOND. APPLICATION OF RESULTS OBTAINED FROM THE QUANTUM MECHANICS AND FROM A THEORY OF PARAMAGNETIC SUSCEPTIBILITY TO THE STRUCTURE OF MOLECULES
5. Electronic Basis of Improper Hydrogen Bonding: A Subtle Balance of Hyperconjugation and Rehybridization
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1. Profound importance of the conventional O–H⋯O hydrogen bond versus a considerable blue shift of the Csp2–H bond in complexes of substituted carbonyls and carboxyls;Physical Chemistry Chemical Physics;2024
2. Characteristics of nonconventional hydrogen bonds and stability of dimers of chalcogenoaldehyde derivatives: a noticeable role of oxygen compared to other chalcogens;RSC Advances;2024
3. Comparison of the Molecular Properties of Euglobals Differing by the Mutual Positions of the Two R–C=O Groups (R = H and CH2CH(CH3)2): A Computational Study;Chemistry;2023-10-12
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