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The reductive demetalation of manganese corroles was investigated in CH_2Cl_2/HCl(aqueous)solvent by using SnCl_2 as reducing agent.It was found that the demetalation yields depend on the substituents of corrole macrocycle significantly.Electron- rich manganese corrole undergoes reductive demetalation more easily than electron-deficient ones.The isolated reductive demetalation yield of manganese 5,10,15-tris(phenyl)corrole in present system is moderate(46%).As for electron-deficient Mn(Ⅲ)5,10,15-tds(pentafluorophenyl)corrole,the acid-induced demetalation in HOAc-H_2SO_4(V/V=3:1)is preferable with an isolated yield of 67%.
The reductive demetalation of manganese corroles was investigated in CH 2 Cl 2 / HCl (aqueous) solvent by using SnCl 2 as reducing agent. It was found that the degeneration of depend on the substituents of corrole macrocycle significantly. Electron-rich manganese corrole undergoes reductive demetalation more easily than electron-deficient ones. The isolated reductive demetalation yield of manganese 5,10,15-tris (phenyl) corrole in present system is moderate (46%). As for electron-deficient Mn (III) 5,10,15-tds pentafluorophenyl) corrole, the acid-induced demetalation in HOAc-H 2 SO 4 (V / V = 3: 1) is preferably with an isolated yield of 67%.