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Mono- and dinuclear organotin(IV) complexes for solvent free cycloaddition of CO2 to epoxides at ambient pressure

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成果类型:
期刊论文
作者:
Khattak, Zafar A. K.;Younus, Hussein A.;Ahmad, Nazir;Yu, Baoyi;Ullah, Habib;...
通讯作者:
Verpoort, Francis
作者机构:
[Moosavi, Bibimaryam; Khattak, Zafar A. K.; Ahmad, Nazir; Somboon, Chaemchuen; Suleman, Suleman; Ullah, Habib; Verpoort, Francis; Younus, Hussein A.] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan, Hubei, Peoples R China.
[Khattak, Zafar A. K.; Suleman, Suleman; Ullah, Habib; Verpoort, Francis] Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan, Hubei, Peoples R China.
[Younus, Hussein A.] Fayoum Univ, Dept Chem, Fac Sci, Al Fayyum 63514, Egypt.
[Yu, Baoyi] Beijing Agr Univ, Coll Biol Sci Engn, Key Lab Urban Agr North China, Minist Agr, Beijing 102206, Peoples R China.
[Chughtai, Adeel H.] Bahauddin Zakariya Univ, Inst Chem Sci, Multan 60800, Pakistan.
通讯机构:
[Verpoort, Francis] W
Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan, Hubei, Peoples R China.
语种:
英文
关键词:
Homogeneous catalysis;Organotin complexes;Solvent-free;Ambient pressure;CO(2)cycloaddition
期刊:
Journal of CO2 Utilization
ISSN:
2212-9820
年:
2018
卷:
28
页码:
313-318
基金类别:
Acknowledgments The authors gratefully acknowledge “State Key Lab of Advanced Technology for Materials Synthesis and Processing” for financial support. F.V. and M.S.Y. acknowledge the support from the Russian Foundation for Basic Research (No 18-29-04047) and Tomsk Polytechnic University Competitiveness Enhancement Program grant (VIU-195/2018). Z.A.K.K. acknowledges funding (2014GXZ330) from the Chinese Scholarship Council (CSC) for pH.D. studies.
机构署名:
本校为第一且通讯机构
院系归属:
材料科学与工程学院
材料复合新技术国家重点实验室
摘要:
Novel mono- and dinuclear dimethyltin(IV) complexes were synthesized using tridentate Schiff base ligands, derived from 2-amino-2-hydroxymethyl-propane-1,3-diol and various aldehydes. These diorganotin(IV) compounds displayed good catalytic activity for solvent-free cycloaddition of CO2 to epoxides at ambient pressure. These catalysts efficiently completed the insertion of CO2 to various epoxides at low catalyst loadings (0.1-1.0 mol%) in 1-6 hours giving high values of TONs around 1000. The catalyst further usability for three continuous reaction runs in the reaction mixture gives the same ac...

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