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Selective Formation of Small and Large Coordination Cages and Their Catalytic Differences.
Kim, Daeun; Back, Hyo Jeong; An, Seonghyeon; Han, Jihun; Jung, Ok-Sang.
Afiliação
  • Kim D; Department of Chemistry, Pusan National University, Busan 46241, Korea.
  • Back HJ; Department of Chemistry, Pusan National University, Busan 46241, Korea.
  • An S; Department of Chemistry, Pusan National University, Busan 46241, Korea.
  • Han J; Department of Chemistry, Pusan National University, Busan 46241, Korea.
  • Jung OS; Department of Chemistry, Pusan National University, Busan 46241, Korea.
Inorg Chem ; 2024 Jul 20.
Article em En | MEDLINE | ID: mdl-39031787
ABSTRACT
Self-assembly of CuX2 (X- = BF4-, ClO4-, and CF3SO3-) with a new tridentate 5,5',5″-(((2,4,6-trimethylbenzene-1,3,5-triyl)tris(methylene))tris(oxy))triisoquinoline (L) gives rise to single-crystal pairs consisting of small and large cages, [X@Cu2X2L4]X and [Cu6X12L8], respectively, via selection of solvents. In particular, the large cage is transformed into a small cage in acetonitrile above 50 °C. A significant difference in heterogeneous catechol oxidation catalysis between the small and large cages is observed. Such notable catechol-oxidation-catalytic effects can be explained by maintenance of the Cu···Cu distance at the catalytic center. This research is a direct systematic example of both cage-size control via solvent selection and the significance of the Cu···Cu distance in catechol oxidation catalysis with copper (Cu).

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article