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一锅法从卟啉配体合成μ-氧代四苯基双核铁卟啉(英文)

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

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【作者】 佘远斌冯连顺王爱欣李修艳

【Author】 SHE Yuanbin,FENG Lianshun,WANG Aixin and LI Xiuyan Institute of Green Chemistry and Fine Chemicals,Beijing University of Technology,Beijing 100022,China

【机构】 Institute of Green Chemistry and Fine Chemicals Beijing University of TechnologyInstitute of Green Chemistry and Fine ChemicalsBeijing University of TechnologyBeijing 100022China

【摘要】 A novel method for synthesis of substituted μ-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 ra-tio 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.

【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 ra- tio 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.

【基金】 the National Natural Science Foundation of China (20776003, 20576005);the Key Project of Natural Science Foundation of Beijing (2061001)
  • 【文献出处】 Chinese Journal of Chemical Engineering ,中国化学工程学报(英文版) , 编辑部邮箱 ,2008年03期
  • 【分类号】O626
  • 【被引频次】10
  • 【下载频次】202
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