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An Acrylonitrile-Based Copolymer Gel as an NMR Alignment Medium for Extraction of Residual Dipolar Couplings of Small Molecules in Aqueous Solution.
Carvalho, Daiane S; da Silva, Danilo G B; Hallwass, Fernando; Navarro-Vázquez, Armando.
Afiliación
  • Carvalho DS; Departamento de Química Fundamental, Universidade Federal de Pernambuco Cidade Universitria, CEP, 50.740-540, Recife, PE, Brazil.
  • da Silva DGB; Departamento de Química Fundamental, Universidade Federal de Pernambuco Cidade Universitria, CEP, 50.740-540, Recife, PE, Brazil.
  • Hallwass F; Departamento de Química Fundamental, Universidade Federal de Pernambuco Cidade Universitria, CEP, 50.740-540, Recife, PE, Brazil.
  • Navarro-Vázquez A; Departamento de Química Fundamental, Universidade Federal de Pernambuco Cidade Universitria, CEP, 50.740-540, Recife, PE, Brazil.
Chempluschem ; 88(2): e202200446, 2023 Feb.
Article en En | MEDLINE | ID: mdl-36782376
ABSTRACT
An NMR weakly-aligning polymer gel has been prepared by copolymerization of acrylonitrile and 2-acrylamide-2-methyl-1-propanesulfonic acid in the presence of 1,4-butanediol diacrylate as a cross-linker. The polymer readily swells in water in a large range of temperatures, although the swelling ratio is decreased in saline solutions. The swollen gel can be mechanically compressed, in a reversible way, generating anisotropy, as easily shown in 2 H NMR experiments, and allowing measurement of 1 DCH residual dipolar couplings (RDCs) through F1-coupled HSQC experiments. The performance of this gel as a NMR alignment medium was evaluated in several water-soluble organic molecules and, while it provided RDCs of proper size for sucrose and even such as small molecule as 5-norbornen-2-ol, in the case of azidothymidine and cefuroxime sodium salt the strong interaction of these molecules with the gel prevented successful extraction of the RDCs.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chempluschem Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chempluschem Año: 2023 Tipo del documento: Article