SCI和EI收录∣中国化工学会会刊

›› 2008, Vol. 16 ›› Issue (3): 369-372.

• • 上一篇    下一篇

Synthesis of Substituted μ-Oxo-bis[tetra-phenyl porphyrinatoiron] Compounds from Free Base Porphyrins by a One-pot Method

佘远斌, 冯连顺, 王爱欣, 李修艳   

  1. Institute of Green Chemistry and Fine Chemicals, Beijing University of Technology, Beijing 100022, China
  • 收稿日期:2007-09-20 修回日期:2008-02-17 出版日期:2008-06-28 发布日期:2008-06-28
  • 通讯作者: SHE Yuanbin,E-mail:sheyb@bjut.edu.cn
  • 基金资助:
    Supported the National Natural Science Foundation of China (20776003,20576005);the Key Project of Natural Science Foundation of Beijing (2061001)

Synthesis of Substituted μ-Oxo-bis[tetra-phenyl porphyrinatoiron] Compounds from Free Base Porphyrins by a One-pot Method

SHE Yuanbin, FENG Lianshun, WANG Aixin, LI Xiuyan   

  1. Institute of Green Chemistry and Fine Chemicals, Beijing University of Technology, Beijing 100022, China
  • Received:2007-09-20 Revised:2008-02-17 Online:2008-06-28 Published:2008-06-28
  • Supported by:
    Supported the National Natural Science Foundation of China (20776003,20576005);the Key Project of Natural Science Foundation of Beijing (2061001)

摘要: A novel method for synthesis of substitutedμ-oxo-bis[tetraphenyl porphyrinatoiron]compounds([TRPPFe]2O) based on the reaction among free base porphyrins(TRPPH2),FeSO4·7H2O and H2O in one pot was proposed and investigated.Four kinds of[TRPPFe]2O were synthesized by this novel synthetic method,and their structures were characterized by elemental analysis,infrared spectra and UV-vis spectroscopy.The reaction conditions,including the effect of different iron salts on the formation of[TRPPFe]2O,the reaction time between FeSO4·7H2O and TRPPH2,the molar ratio of FeSO4·7H2O/TRPPH2 as well as the volume ratio of H2O/DMF,were investigated.The [TRPPFe]2O yield of 93%-98%could be obtained under the following optimal conditions:the reaction time of FeSO4·7H2O with TRPPH2 was about 10 h,the molar ratio of FeSO4·7H2O/TRPPH2 about 5:1,and the volume ratio of H2O/DMF exceeded 2:1.Further research indicated that only TRPPFeCl were formed once FeSO4·7H2O was replaced by FeCl2·4H2O,the reason of which might be that halogen ions in iron salts interfered the formation of [TRPPFe]2O,suggesting that halogen ions should be avoided in this novel synthetic method.

关键词: substituted μ-oxo-bis[tetraphenylporphyrinatoiron]compounds, one-pot method, free base porphyrins

Abstract: A novel method for synthesis of substitutedμ-oxo-bis[tetraphenyl porphyrinatoiron]compounds([TRPPFe]2O) based on the reaction among free base porphyrins(TRPPH2),FeSO4·7H2O and H2O in one pot was proposed and investigated.Four kinds of[TRPPFe]2O were synthesized by this novel synthetic method,and their structures were characterized by elemental analysis,infrared spectra and UV-vis spectroscopy.The reaction conditions,including the effect of different iron salts on the formation of[TRPPFe]2O,the reaction time between FeSO4·7H2O and TRPPH2,the molar ratio of FeSO4·7H2O/TRPPH2 as well as the volume ratio of H2O/DMF,were investigated.The [TRPPFe]2O yield of 93%-98%could be obtained under the following optimal conditions:the reaction time of FeSO4·7H2O with TRPPH2 was about 10 h,the molar ratio of FeSO4·7H2O/TRPPH2 about 5:1,and the volume ratio of H2O/DMF exceeded 2:1.Further research indicated that only TRPPFeCl were formed once FeSO4·7H2O was replaced by FeCl2·4H2O,the reason of which might be that halogen ions in iron salts interfered the formation of [TRPPFe]2O,suggesting that halogen ions should be avoided in this novel synthetic method.

Key words: substituted μ-oxo-bis[tetraphenylporphyrinatoiron]compounds, one-pot method, free base porphyrins