4.7 Article

Threefold reactivity of a COF-embedded rhenium catalyst: reductive etherification, oxidative esterification or transfer hydrogenation

期刊

CHEMICAL COMMUNICATIONS
卷 58, 期 86, 页码 12074-12077

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cc03173f

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资金

  1. COF for H2 project through the Portuguese Foundation for Science and Technology -FCT funds under UT Austin Portugal [UTA-EXPL/NPN/0055/2019]
  2. FCT (Fundacao para a Ciencia e Technologia) [2020.04021.CEECIND]
  3. Welch Foundation [F-1822]
  4. National Science Foundation [CHE-1808311]
  5. Spanish Ministry of Science through the Ramon y Cajal grant [RYC2020-030414-1]

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The reactivity of a novel Re(i) catalyst is controlled by its interactions with a covalent organic framework (COF), allowing for different catalytic reactions depending on the local environment. The study highlights the potential of COFs in modulating the reactivity of homogeneous catalysts.
The reactivity of the novel Re(i) catalyst [Re((C12)Anth-py(2))(CO)(3)Br] is modulated by its interactions with the covalent organic framework (COF) TFB-BD. The complex catalyzes either reductive etherification, oxidative esterification, or transfer hydrogenation depending on its local environment (embedded in TFB-BD, in homogeneous solution or co-incubated with TFB-BD, respectively). The results highlight that COFs can drastically modulate the reactivity of homogeneous catalysts.

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