Nitrogen-Rich Tetrazole-Amide-Functionalised Zn Metal-Organic Framework as Catalyst for Efficient Catalytic CO2 Cycloaddition with Epoxides

被引:3
作者
Paul, Anup [1 ]
Garazade, Ismayil M. [1 ,2 ]
Karmakar, Anirban [1 ]
Khan, Rais Ahmad [3 ]
da Silva, Maria Fatima C. Guedes [1 ,4 ]
Nunes, Ana V. M. [5 ]
Pombeiro, Armando J. L. [1 ]
机构
[1] Univ Lisbon, Inst Mol Sci, Ctr Quim Estrutura, Inst Super Tecn, Av Rovisco Pais, P-1049001 Lisbon, Portugal
[2] Baku State Univ, Dept Chem, Z Khalilov Str 23, Baku 1148, Azerbaijan
[3] King Saud Univ, Dept Chem, Riyadh 11451, Saudi Arabia
[4] Univ Lisbon, Dept Engn Quim, Inst Super Tecn, Av Rovisco Pais, P-1049001 Lisbon, Portugal
[5] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Quim, LAQV REQUIMTE, P-2829516 Caparica, Portugal
关键词
tetrazole; amide functionalised; MOF; CO2; epoxides; COORDINATION POLYMERS; HIGH-PERFORMANCE; CARBON-DIOXIDE; LIGANDS; TRANSFORMATIONS; ADSORPTION; REDUCTION; COMPLEXES; FIXATION; CO(II);
D O I
10.3390/catal14010006
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, we report the design, synthesis, and catalytic application of the novel nitrogen-rich Zn(II) MOF [Zn-2(mu(3)-1 kappa N,2 kappa N ',3 kappa O-HL)(2)(DMF)(2)](n)<middle dot>nH(2)O (HL2- = 4-((4-(1H-tetrazol-5-yl)phenyl)carbamoyl)benzoate), denoted as ZnMOF, for the efficient conversion of carbon dioxide (CO2) to cyclic carbonates via cycloaddition with epoxides. It was synthesised from a tetrazole appended amide-functionalised pro-ligand (H3L) and Zn(NO3)(2)<middle dot>6H(2)O under hydrothermal conditions. The synthesised material was characterised namely by elemental analysis, infrared spectroscopy, powder X-ray diffraction (PXRD), and single-crystal X-ray diffraction analyses. The catalytic potential of ZnMOF was investigated in the CO2 cycloaddition reaction with various epoxides, with conversions ranging from 17% to 99%. The catalyst retained its activity across multiple reaction cycles, demonstrating its stability and reusability. The influence of co-catalysts on the reaction was explored, with tetrabutylammonium bromide (TBABr) emerging as the most effective one. A plausible reaction mechanism is proposed.
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页数:14
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