Tuning the coordination microenvironment of Co sites embedded in porous organic polymer for the hydroformylation of diisobutylene

By regulating the coordination microenvironment of Co species, Co@POPsPPh 3 &DVB promoted the formation of HCo(CO) 3 (P-frame) active species, which was the dominant active species for the hydroformylation of diisobutylene.

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Publication Details

Journal
Journal of Materials Chemistry A
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ta04135j
Citations
1
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.70

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article

Tuning the coordination microenvironment of Co sites embedded in porous organic polymer for the hydroformylation of diisobutylene

Wei Hong, Benhan Fan, Yunjie Ding, Cunyao Li et al.
1 citations
Journal of Materials Chemistry A
Carbon dioxide utilization in catalysis
0.70
article

Tuning the coordination microenvironment of Co sites embedded in porous organic polymer for the hydroformylation of diisobutylene

Wei Hong, Benhan Fan, Yunjie Ding, Cunyao Li, Yan Li, Xinyuan Liu, Miao Jiang, Lei Ma, Sen Feng, Guangjun Ji
article en
1 citations

Abstract

By regulating the coordination microenvironment of Co species, Co@POPsPPh 3 &DVB promoted the formation of HCo(CO) 3 (P-frame) active species, which was the dominant active species for the hydroformylation of diisobutylene.

Journal of Materials Chemistry AVol. 13(36)
University of Science and Technology of China (CN), Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), Dalian National Laboratory for Clean Energy (CN), University of Chinese Academy of Sciences (CN)
Salt Science Research Foundation, National Natural Science Foundation of China, Chinese Academy of Sciences, Youth Innovation Promotion Association of the Chinese Academy of Sciences, Natural Science Foundation of Liaoning Province, Dalian Institute of Chemical Physics, Youth Innovation Promotion Association, Dalian National Laboratory for Clean Energy
Openalex Percentile: Top 34%
Carbon dioxide utilization in catalysis
0.70
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