期刊
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
卷 2021, 期 3, 页码 243-251出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.202000790
关键词
Molybdenum; Epoxidation; 2-Pyridylimino; Turnover frequency; Homogeneous catalysis
资金
- DGAPA-UNAM [PAPIIT IA-203820]
- CONACyT [626716]
A series of pyridylimine ligands with variations of the substituent at the imine nitrogen were synthesized and coordinated to the [MoCl2O2] core. The novel complexes showed excellent catalytic activity and fine selectivity in the epoxidation reaction, with complex [MoCl2O2(L)] (L: N-(2-Pyridinylmethylene)-1-tert-butylimine) C-5 being the best catalytic precursor.
A series of pyridylimine ligands with variations of the substituent at the imine nitrogen were synthesized and coordinated to the [MoCl2O2] core. The novel molecular structures of the complexes were fully characterized by H-1 and C-13 NMR, FT-IR, ESI, EA, and X-ray crystallography, and their catalytic activity was studied for the epoxidation of alkenes using tert-butyl hydroperoxide (TBHP) as the oxidant. The new complexes showed excellent catalytic activity and fine selectivity in the epoxidation reaction compared with similar homogeneous molybdenum complexes. The results demonstrated that there is a significant change in the catalytic performance, depending on the alkyl arm on the structure of the pyridilimine ligand. The catalytic results indicated that complex [MoCl2O2(L)] (L: N-(2-Pyridinylmethylene)-1-tert-butylimine) C-5 is the best catalytic precursor in the epoxidation of cyclohexene (TON: 92920 and TOF: 30974 h(-1)).
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