A Calix[4]resorcinarene-Based [Co] Coordination Cage for Highly Efficient Cycloaddition of CO to Epoxides.

Clicks: 257
ID: 76701
2019
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Steady

Ranked #48 of 86 articles by views in Inorganic chemistry

Most read Least read

Bar heights use a square-root scale.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
The design and synthesis of polynuclear metal cluster-based coordination cages is of considerable interest due to their appealing structural characteristics and potential applications. Herein, we report a calix[4]resorcinarene-based [Co] coordination cage, [Co(TPC4R-I)(1,3-BDC)(μ-OH)(HO)(DMF)]·7DMF·23HO (), assembled with 2 bowl-shaped calix[4]resorcinarenes (TPC4R-I), 10 angular 1,3-benzenedicarboxylates (1,3-BDC), and 12 Co(II) cations. Remarkably, it is shown to be a highly efficient recyclable heterogeneous catalyst for CO conversion due to its exposed Co(II) Lewis acid sites.
Reference Key
guo2019ainorganic Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Guo, Ting-Ting;Su, Xiao-Fang;Xu, Xianxiu;Yang, Jin;Yan, Li-Kai;Ma, Jian-Fang;
Journal Inorganic chemistry
Year 2019
DOI
10.1021/acs.inorgchem.9b02473
URL
Keywords

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.