Defect-engineered indium-organic framework displays the higher CO2 adsorption and more excellent catalytic performance on the cycloaddition of CO2 with epoxides under mild conditions

被引:0
|
作者
Ren, Meiyu [1 ]
Zhao, Bo [1 ]
Li, Chong [1 ]
Fei, Yang [1 ]
Wang, Xiaotong [1 ]
Fan, Liming [1 ]
Hu, Tuoping [1 ]
Zhang, Xiutang [1 ]
机构
[1] North Univ China, Sch Chem & Chem Engn, Taiyuan 030051, Peoples R China
基金
中国国家自然科学基金;
关键词
In-MOF; Coexisted Lewis acid-base sites; Chemical fixation of CO2; Heterogeneous catalysis; Knoevenagel condensation; CHEMICAL FIXATION; HETEROGENEOUS CATALYST; COORDINATION POLYMERS; KNOEVENAGEL; EFFICIENT;
D O I
10.1007/s11030-024-10956-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In order to achieve the high adsorption and catalytic performance of CO2, the direct self-assembly of robust defect-engineered MOFs is a scarcely reported and challenging proposition. Herein, a highly robust nanoporous indium(III)-organic framework of {[In-2(CPPDA)(H2O)(3)](NO3)<middle dot>2DMF<middle dot>3H(2)O}(n) (NUC-107) consisting of two kinds of inorganic units of chain-shaped [In(COO)(2)(H2O)](n) and watery binuclear [In-2(COO)(4)(H2O)(8)] was generated by regulating the growth environment. It is worth mentioning that [In-2(COO)(4)(H2O)(8)] is very rare in terms of its richer associated water molecules, implying that defect-enriched metal ions in the activated host framework can serve as strong Lewis acid. Compared to reported skeleton of [In-4(CPPDA)(2)(mu(3)-OH)(2)(DMF)(H2O)(2)](n) (NUC-66) with tetranuclear clusters of [In-4(mu(3)-OH)(2)(COO)(10)(DMF)(H2O)(2)] as nodes, the void volume of NUC-107 (50.7%) is slightly lower than the one of NUC-66 (52.8%). However, each In3+ ion in NUC-107 has an average of 1.5 coordinated small molecules (H2O), which far exceeds the average of 0.75 in NUC-66 (H2O and DMF). After thermal activation, NUC-107a characterizes the merits of unsaturated In3+ sites, free pyridine moieties, solvent-free nanochannels (10.2 x 15.7 & Aring;(2)). Adsorption tests prove that the host framework of NUC-107a has a higher CO2 adsorption (113.2 cm(3)/g at 273 K and 64.8 cm(3)/g at 298 K) than NUC-66 (91.2 cm(3)/g at 273 K and 53.0 cm(3)/g at 298 K). Catalytic experiments confirmed that activated NUC-107a with the aid of n-Bu4NBr was capable of efficiently catalyzing the cycloaddition of CO2 with epoxides into corresponding cyclic carbonates under the mild conditions. Under the similar conditions of 0.10 mol% MOFs, 0.5 mol% n-Bu4NBr, 0.5 MP CO2, 60 degrees C and 3 h, compared with NUC-66a, the conversion of SO to SC catalyzed by NUC-107a increased by 21%. Hence, this work offers a valuable perspective that the in situ creation of robust defect-engineered MOFs can be realized by regulating the growth environment. [GRAPHICS] .
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页数:15
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