Interactions and reactivity in crystalline intermediates of mechanochemical cyclorhodation reactions-Reference-Cited by-同舟云学术

Interactions and reactivity in crystalline intermediates of mechanochemical cyclorhodation reactions

Published:2024 Issue: Volume: Page:
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Gómez Sara¹^ORCID,Gómez Santiago²^ORCID,Rojas-Valencia Natalia²^ORCID,Hernández José G.²^ORCID,Ardila-Fierro Karen J.²^ORCID,Gómez Tatiana³^ORCID,Cárdenas Carlos⁴⁵,Hadad Cacier²^ORCID,Cappelli Chiara¹^ORCID,Restrepo Albeiro²^ORCID

Affiliation:

1. Scuola Normale Superiore, Classe di Scienze, Piazza dei Cavalieri 7, 56126, Pisa, Italy

2. Instituto de Química, Universidad de Antioquia UdeA, Calle 70 No. 52–21, Medellín, Colombia

3. Theoretical and Computational Chemistry Center, Institute of Applied Chemical Sciences, Faculty of Engineering, Universidad Autonoma de Chile, Avenida Pedro de Valdivia 425, Santiago, Chile

4. Departamento de Física, Facultad de Ciencias, Universidad de Chile, Casilla 653, Santiago, Chile

5. Centro para el desarrollo de las Nanociencias y Nanotecnología, CEDENNA, Av. Ecuador 3493, Santiago, Chile

Abstract

State of the art computations help explain the differences in reactivity between transient cocrystals that precede the mechanochemical activation of C–H bonds during the formation of rhodacyles.

Funder

Fondo Nacional de Desarrollo Científico y Tecnológico

Universidad de Antioquia

Centro para el Desarrollo de la Nanociencia y la Nanotecnología

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CP/D3CP04201D

Reference87 articles.

1. The many flavours of mechanochemistry and its plausible conceptual underpinnings