Cluster-based MOFs with accelerated chemical conversion of CO2 through C-C bond formation

Cluster-based MOFs with accelerated chemical conversion of CO2 through C-C bond formation
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基于簇的 MOF 通过 C-C 键形成加速 CO2 的化学转化

DOI:
10.1039/c7cc01136a
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发表时间:
2017
影响因子:
4.9
通讯作者:
He Liang-Nian
He Liang-Nian
中科院分区:
化学2区
文献类型:
--
作者:
Xiong Gang;Yu Bing;Dong Jie;Shi Ying;Zhao Bin;He Liang-Nian

文献摘要

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Investigations on metal–organic frameworks (MOFs) as direct catalysts have been well documented, but direct catalysis of the chemical conversion of terminal alkynes and CO2 as chemical feedstock by MOFs into valuable chemical products has never been reported. We report here two cluster-based MOFs I and II assembled from a multinuclear Gd-cluster and Cu-cluster, displaying high thermal and solvent stabilities. I and II as heterogeneous catalysts possess active catalytic centers [Cu12I12] and [Cu3I2], respectively, exhibiting excellent catalytic performance in the carboxylation reactions of CO2 with 14 kinds of terminal alkynes under 1 atm and mild conditions. For the first time catalysis of the carboxylation reaction of terminal alkynes with CO2 by MOF materials without any cocatalyst/additive is reported. This work not only reduces greenhouse gas emission but also provides highly valuable materials, opening a wide space in seeking recoverable catalysts to accelerate the chemical conversion of CO2.