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Peer-reviewedCC BY-NCScience Advances

Heterogeneous hydroformylation of propene over surface rhodium coordinated by immobilized multi-N ligands

  1. 1Key Lab of Mesoscopic Chemistry, School of Chemistry, School of Chemical Engineering, Nanjing University, Nanjing 210023, China.

Abstract

Olefin hydroformylation is an extremely important reaction for producing bulk oxygen-containing organic functional molecules and homogeneous rhodium catalysts with organic phosphorous ligands are most commonly used. We report here a highly active heterogeneous catalyst for propene hydroformylation with Rh immobilized by alumina bonded 3-trimethoxysilylpropyl-diethyle-netriamine, of which ligand is more readily available, inexpensive, low toxic and no loss in reaction. The catalyst Rh-NQ62/Al 2 O 3 shows a TOF value as high as 710 h −1 for propene conversion to C 4 oxygenates in selectivity higher than 99% in a fixed-bed reactor and sustains stable for at least 1000 h without any deactivation. Characterization and theoretical calculation reveal that the atomically dispersed Rh species in surface-bound configurations by the multi-N ligand effectively promotes the heterolytic cleavage of H 2 at the Rh-N site and enhances the overall propene hydroformylation. We envisage the work establishes a blueprint for development of better catalysts using multi-N ligands for heterogeneous hydroformylations.

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BibTeX
@article{he2026heterogeneous,
  title = {{Heterogeneous hydroformylation of propene over surface rhodium coordinated by immobilized multi-N ligands}},
  author = {Qiang He and Bingqing Ge and Yu Shao and Chenyang Shen and Yu Jiang and Xiangke Guo and Nianhua Xue and Xuefeng Guo and Luming Peng and Yan Zhu and Shuhua Li and Weiping Ding},
  journal = {Science Advances},
  year = {2026},
  month = oct,
  doi = {10.1126/sciadv.aej1532},
  url = {https://www.science.org/doi/10.1126/sciadv.aej1532},
  note = {CC BY-NC},
}
RIS
TY  - JOUR
TI  - Heterogeneous hydroformylation of propene over surface rhodium coordinated by immobilized multi-N ligands
AU  - Qiang He
AU  - Bingqing Ge
AU  - Yu Shao
AU  - Chenyang Shen
AU  - Yu Jiang
AU  - Xiangke Guo
AU  - Nianhua Xue
AU  - Xuefeng Guo
AU  - Luming Peng
AU  - Yan Zhu
AU  - Shuhua Li
AU  - Weiping Ding
PY  - 2026
DA  - 2026/10/02
JO  - Science Advances
DO  - 10.1126/sciadv.aej1532
UR  - https://www.science.org/doi/10.1126/sciadv.aej1532
AB  - Olefin hydroformylation is an extremely important reaction for producing bulk oxygen-containing organic functional molecules and homogeneous rhodium catalysts with organic phosphorous ligands are most commonly used. We report here a highly active heterogeneous catalyst for propene hydroformylation with Rh immobilized by alumina bonded 3-trimethoxysilylpropyl-diethyle-netriamine, of which ligand is more readily available, inexpensive, low toxic and no loss in reaction. The catalyst Rh-NQ62/Al 2 O 3 shows a TOF value as high as 710 h −1 for propene conversion to C 4 oxygenates in selectivity higher than 99% in a fixed-bed reactor and sustains stable for at least 1000 h without any deactivation. Characterization and theoretical calculation reveal that the atomically dispersed Rh species in surface-bound configurations by the multi-N ligand effectively promotes the heterolytic cleavage of H 2 at the Rh-N site and enhances the overall propene hydroformylation. We envisage the work establishes a blueprint for development of better catalysts using multi-N ligands for heterogeneous hydroformylations.
SN  - 2375-2548
ER  -