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Ratcheting synthesis.
Borsley, Stefan; Gallagher, James M; Leigh, David A; Roberts, Benjamin M W.
Afiliação
  • Borsley S; Department of Chemistry, University of Manchester, Manchester, UK.
  • Gallagher JM; Department of Chemistry, University of Manchester, Manchester, UK.
  • Leigh DA; Department of Chemistry, University of Manchester, Manchester, UK. david.leigh@manchester.ac.uk.
  • Roberts BMW; Department of Chemistry, University of Manchester, Manchester, UK.
Nat Rev Chem ; 8(1): 8-29, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38102412
ABSTRACT
Synthetic chemistry has traditionally relied on reactions between reactants of high chemical potential and transformations that proceed energetically downhill to either a global or local minimum (thermodynamic or kinetic control). Catalysts can be used to manipulate kinetic control, lowering activation energies to influence reaction outcomes. However, such chemistry is still constrained by the shape of one-dimensional reaction coordinates. Coupling synthesis to an orthogonal energy input can allow ratcheting of chemical reaction outcomes, reminiscent of the ways that molecular machines ratchet random thermal motion to bias conformational dynamics. This fundamentally distinct approach to synthesis allows multi-dimensional potential energy surfaces to be navigated, enabling reaction outcomes that cannot be achieved under conventional kinetic or thermodynamic control. In this Review, we discuss how ratcheted synthesis is ubiquitous throughout biology and consider how chemists might harness ratchet mechanisms to accelerate catalysis, drive chemical reactions uphill and programme complex reaction sequences.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Rev Chem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Rev Chem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido