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Theoretical and experimental investigations of the enantioselective epoxidation of olefins catalyzed by manganese complexes
被引:9
|作者:
Lin, Jin
[1
,3
]
Wang, Fang
[1
]
Tian, Jing
[1
,3
]
Zhang, Jisheng
[1
]
Wang, Yong
[2
]
Sun, Wei
[1
,3
]
机构:
[1] Chinese Acad Sci, Ctr Excellence Mol Synth, Suzhou Res Inst LICP, Lanzhou Inst Chem Phys LICP,State Key Lab Oxo Syn, Lanzhou 730000, Peoples R China
[2] Ningbo Univ, Inst Drug Discovery Technol, Ningbo 315211, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Epoxidation of olefins;
Manganese complexes;
Metal oxo;
Enantioselective;
DFT;
NONHEME IRON-CATALYSTS;
C-H;
CIS-DIHYDROXYLATION;
HYDROGEN-PEROXIDE;
ACETIC-ACID;
H2O2;
INTERMEDIATE;
OXIDANTS;
INSIGHTS;
ALKENES;
D O I:
10.1016/j.cclet.2021.08.092
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The enantioselective epoxidation of olefin by Mn-II(R,R-PMCP)(OTf)(2), H2O2 and H2SO4 was explored by DFT calculations and experiments. Theoretical results suggest that [Mn-V(O)(R,R-PMCP)(SO4)](+) species with a triplet ground spin state serves as the active species for the olefin epoxidation. It can be generated by the H2SO4 assisted O-O heterolysis of Mn-III(OOH) species. Mn-III-persulfate is also involved in this system, but it cannot promote the olefin epoxidation directly, preferring instead to transform into Mn-V(O). Actually, the asymmetric epoxidation reactions with H2O2/H2SO4 or Oxone provide similar enantioselectivity in the presence of manganese catalyst. These observations further support the transformation of Mn-III-persulfate to Mn-V(O) species. (C) 2021 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
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页码:1515 / 1518
页数:4
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