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Synthesis of Asymmetrical Monobenzo‐Substituted Cobalt Thioporphyrazines and Their Biomimetic Catalytic Property
Author(s) -
Zhou Peng,
Jin Juanjuan,
Zhang Bingguang,
Yang Changjun,
Zhang Zehui,
Li Zhe,
Deng Kejian
Publication year - 2016
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.201600467
Subject(s) - chemistry , benzil , cobalt , catalysis , benzoin , photochemistry , benzene , porphyrazine , olefin fiber , yield (engineering) , polymer chemistry , organic chemistry , materials science , metallurgy
Two novel monobenzo porphyrazines bearing nitro and methoxyl respectively on fused benzene ring were successfully synthesized. Also, an asymmetrical porphyrazine with one butylthio branch at the pyrrolic β ‐position substituted by hydrogen atom was successfully isolated in the course of synthesis of symmetric octakis(butylthio) porphyrazine. Their corresponding cobalt complexes were subsequently obtained and characterized. Their catalytic ability was assessed by aerobic oxidation of benzoin, showing the highest benzil yield of 95.2% for 60 min. A possible mechanism was also presented from the in‐situ UV‐Vis spectra, in which a novel and characteristic absorption peak of metal‐oxo was observed. At the same time, similar results of the extended oxidation of benzyl alcohol also confirmed the reactive mechanism.