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Tetracosanuclear nickel complexes as effective catalysts for cycloaddition of carbon dioxide with epoxides.
Liu, Guan-Lin; Wu, En-Hsu; Hung, Yu-Ching; Chou, Wei-Chi; Hung, Chia-Hsin; Lin, Chu-Chieh; Ko, Bao-Tsan.
Affiliation
  • Liu GL; Department of Chemistry, National Chung Hsing University, Taichung 402, Taiwan. cchlin@mail.nchu.edu.tw.
  • Wu EH; Department of Chemistry, National Chung Hsing University, Taichung 402, Taiwan. cchlin@mail.nchu.edu.tw.
  • Hung YC; Department of Chemistry, National Chung Hsing University, Taichung 402, Taiwan. cchlin@mail.nchu.edu.tw.
  • Chou WC; Department of Chemistry, National Chung Hsing University, Taichung 402, Taiwan. cchlin@mail.nchu.edu.tw.
  • Hung CH; Department of Chemistry, National Chung Hsing University, Taichung 402, Taiwan. cchlin@mail.nchu.edu.tw.
  • Lin CC; Department of Chemistry, National Chung Hsing University, Taichung 402, Taiwan. cchlin@mail.nchu.edu.tw.
  • Ko BT; Department of Chemistry, National Chung Hsing University, Taichung 402, Taiwan. cchlin@mail.nchu.edu.tw.
Dalton Trans ; 53(4): 1425-1429, 2024 Jan 23.
Article in En | MEDLINE | ID: mdl-38179831
ABSTRACT
A series of well-defined tetracosanuclear nickel complexes 3-7 facilely produced by one-pot synthesis were active catalysts for cycloaddition of CO2 and cyclohexene oxide (CHO). These nickel complexes were doughnut-like supramolecular coordination complexes involving eight repeating units, and each of them contains one Schiff base ligand and three nickel(II) ions. Notably, the 24-nuclear nickel cluster complex 3 in combination with nucleophilic additives was the most efficient catalyst to mediate CO2 coupling with CHO to generate CO2-based cis-cyclohexene carbonates. In addition to CO2/CHO cycloaddition, complex 3 was also found to effectively couple CO2 with other alicyclic epoxides, generating the corresponding cyclic carbonates. Additionally, kinetic investigations for CO2 cycloaddition of CHO using 3 were reported.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2024 Document type: Article Affiliation country: Country of publication: