Araki Ikuko, Fukui Kaoru, Fujii Hiroshi
Department of Chemistry, Graduate School of Humanities and Sciences, Nara Women's University , Kitauoyanishi, Nara 630-8506, Japan.
Inorg Chem. 2018 Feb 19;57(4):1685-1688. doi: 10.1021/acs.inorgchem.7b02661. Epub 2018 Feb 5.
A bis-hypochlorite adduct of a manganese(IV) salen complex having a chiral (R,R)-cyclohexane-1,2-diamine linkage (2-Bu) is successfully prepared and characterized by various spectroscopic methods. The reactions of 2-Bu with various organic substrates show that 2-Bu is capable of sulfoxidation, epoxidation, chlorination, and hydrogen abstraction reactions. However, the enantioselectivity of the epoxidation reactions by 2-Bu is much lower than that reported for the catalytic reactions by Jacobsen's catalyst. The low enantioselectivity is consistent with a planar conformation of the salen ligand, which is suggested by circular dichroism spectroscopy. This study suggests that 2-Bu is not a reactive intermediate of Jacobsen's enantioselective epoxidation catalysis.