Autor según el artículo: Dieguez, Montserrat; Pamies, Oscar; Moberg, Christina;

Departamento: Química Física i Inorgànica

Autor/es de la URV: Diéguez Fernández, Montserrat / Pamies Ollé, Oscar

Palabras clave: Phosphite-oxazoline ligands Inversion Hydrogenation Enantioselectivity Design Conjugate addition Conformational preferences Complexes Chirality control Allylic substitutions

Resumen: Biological systems have often served as inspiration for the design of synthetic catalysts. The lock and key analogy put forward by Emil Fischer in 1894 to explain the high substrate specificity of enzymes has been used as a general guiding principle aimed at enhancing the selectivity of chemical processes by optimizing attractive and repulsive interactions in molecular recognition events. However, although a perfect fit of a substrate to a catalytic site may enhance the selectivity of a specific catalytic reaction, it inevitably leads to a narrow substrate scope, exduding substrates with different sizes and shapes from efficient binding. An ideal catalyst should instead be able to accommodate a wide range of substrates-it has indeed been recognized that enzymes also are often highly promiscuous as a result of their ability to change their conformation and shape in response to a substrate-and preferentially be useful in various types of processes. In biological adaptation, the process by which species become fitted to new environments is crucial for their ability to cope with changing environmental conditions. With this in mind, we have been exploring catalytic systems that can adapt their size and shape to the environment with the goal of developing synthetic catalysts with wide scope.In this Account, we describe our studies aimed at elucidating how metal catalysts with flexible structural units adapt their binding pockets to the reacting substrate. Throughout our studies, ligands equipped with tropos biaryl units have been explored, and the palladium-catalyzed allylic alkylation reaction has been used as a suitable probe to study the adaptability of the catalytic systems. The conformations of catalytically active metal complexes under different conditions have been studied by both experimental and theoretical methods. By the design of ligands incorporating two flexible units, the symmetry properties of metal complexes could be used to facilitate conformational analysis and thereby provide valuable insight into the structures of complexes involved in the catalytic cycle. The importance of flexibility was convincingly demonstrated when a phosphine group in a privileged ligand that is well-known for its versatility in a number of processes was exchanged for a tropos biaryl phosphite unit: the result was a truly self-adaptive ligand with dramatically increased scope.

Áreas temáticas: Química Medicine (miscellaneous) Interdisciplinar General medicine General chemistry Farmacia Ciências biológicas iii Ciências biológicas ii Ciências biológicas i Ciências ambientais Chemistry, multidisciplinary Chemistry (miscellaneous) Chemistry (all) Chemistry Astronomia / física

Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/

Direcció de correo del autor: montserrat.dieguez@urv.cat oscar.pamies@urv.cat

Identificador del autor: 0000-0002-8450-0656 0000-0002-2352-8508

Página final: 3263

Fecha de alta del registro: 2023-02-19

Volumen de revista: 54

Versión del articulo depositado: info:eu-repo/semantics/publishedVersion

Enlace a la fuente original: https://pubs.acs.org/doi/10.1021/acs.accounts.1c00326

URL Documento de licencia: http://repositori.urv.cat/ca/proteccio-de-dades/

Referencia al articulo segun fuente origial: Accounts Of Chemical Research. 54 (16): 3252-3263

Referencia de l'ítem segons les normes APA: Dieguez, Montserrat; Pamies, Oscar; Moberg, Christina; (2021). Self-Adaptable Tropos Catalysts. Accounts Of Chemical Research, 54(16), 3252-3263. DOI: 10.1021/acs.accounts.1c00326

DOI del artículo: 10.1021/acs.accounts.1c00326

Entidad: Universitat Rovira i Virgili

Año de publicación de la revista: 2021

Página inicial: 3252

Tipo de publicación: Journal Publications