Structural and spectroscopic study and intermolecular chalcogen bonding interactions in 1,3-dicarbonyl compounds-Reference-Cited by-同舟云学术

Structural and spectroscopic study and intermolecular chalcogen bonding interactions in 1,3-dicarbonyl compounds

Published:2024 Issue:32 Volume:48 Page:14420-14434
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Salvador Vallejo L. E.¹,Jios J. L.²³^ORCID,Ulic S. E.¹⁴^ORCID,Echeverría G. A.⁵,Piro O. E.⁵^ORCID,Pis Diez R.¹,Vázquez C.⁶,Merlo C.⁶⁷

Affiliation:

1. CEQUINOR (CONICET-UNLP), Facultad de Ciencias Exactas, Universidad Nacional de La Plata, 47 esq, 115, (1900) La Plata, Republica Argentina

2. Laboratorio UPL (UNLP-CIC), Campus Tecnológico Gonnet (CIC-BA), Cno. Centenario e/505 y 508, (1897) Gonnet, Argentina

3. Departamento de Química, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, 47 esq, 115, (1900) La Plata, Republica Argentina

4. Departamento de Ciencias Básicas, Universidad Nacional de Luján, Rutas 5 y 7, (6700) Luján, Buenos Aires, Republica Argentina

5. Departamento de Física, Facultad de Ciencias Exactas, Universidad Nacional de La Plata e IFLP (CONICET, CCT-La Plata), C, C, 67, 1900 La Plata, Argentina

6. Departamento de Recursos Naturales, Facultad de Ciencias Agropecuarias, Universidad Nacional de Córdoba, Av. Félix Aldo Marrone No 746, Ciudad Universitaria, Córdoba, Argentina

7. Instituto Multidisciplinario de Biología Vegetal (IMBIV-CONICET), Av. Vélez Sarsfield, Córdoba, 1611, Argentina

Abstract

Intra- and intermolecular contacts in 1,3-dicarbonyl compounds are dominated by O–H⋯O bonds. When molecules face each other, the unusual intermolecular O⋯O bonds can reinforce adjacent O–H⋯O bonds and form centrosymmetric dimers.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/NJ/D4NJ02508C

Reference32 articles.

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Relationship Between Structure And Antimicrobial Activity Of Zinc Oxide Nanoparticles: An Overview

5. Solvent effect on keto–enol tautomerism in a new β-diketone: a comparison between experimental data and different theoretical approaches