NH2-MIL-125(Ti)-derived porous cages of titanium oxides to support Pt-Co alloys for chemoselective hydrogenation reactions

被引:42
作者
Gu, Zhizhi [1 ]
Chen, Liyong [1 ]
Li, Xuezhao [1 ]
Chen, Lin [1 ]
Zhang, Yingyue [1 ]
Duan, Chunying [1 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; SELECTIVE HYDROGENATION; ALPHA; BETA-UNSATURATED ALDEHYDES; C=C BONDS; CATALYSTS; EFFICIENT; NANOCRYSTALS; ELECTROCATALYSTS; NANOPARTICLES; PERFORMANCE;
D O I
10.1039/c8sc05450a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The change of atom density induced structural collapse in the transformation process from metal-organic frameworks (MOFs) to their inorganic counterparts is a major challenge to the achievement of porous hollow structures. Herein, we develop an amino acid-mediated strategy for transformation of NH2-MIL-125(Ti) to successfully synthesize well-defined porous cages of titanium oxides (PCT) due to sheets serving as structural scaffolds. On this basis, PCT supported Pt-based nanoparticles are generated via a similar synthetic route, and are utilized to study the selective hydrogenation of carbonyl groups in alpha,beta-unsaturated aldehydes, benefiting from the specific structures of PCT and tunable electronic structures of Pt mainly affected by doping with metal species such as Co. In this case, Pt-Co/PCT composites give 96% selectivity for cinnamyl alcohol at 100% conversion of cinnamaldehyde under 0.2 MPa H-2 and 80 degrees C for 3 h. This research would offer a promising strategy for important organic transformations in academic and industrial research to selectively synthesize high-value-added products.
引用
收藏
页码:2111 / 2117
页数:7
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