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双核金属卟啉的合成及其催化羟基化环己烷的研究
引用本文:唐渝,张渊明,桂明德,朱申杰.双核金属卟啉的合成及其催化羟基化环己烷的研究[J].化学研究与应用,2001,13(3):265-269.
作者姓名:唐渝  张渊明  桂明德  朱申杰
作者单位:1. 暨南大学化学系,
2. 南开大学化学系,
摘    要:合成了以乙基、丙基、丁基在卟啉5,5′-苯基邻位通过醚键联结的不同链长的双核金属铁(Ⅲ)、锰(Ⅲ)卟啉,并用NMR、元素分析和UV-Vis光谱进行了验证。以它们为催化剂,亚碘酰苯为氧化剂获得氧化环己烷的最好产率,环己醇为35.83%,环己酮为23.41%。通过产率比较,初步定性地获得了双核金属卟啉的活性和稳定性的规律,即双铁亚乙基卟啉>双铁亚丙基卟啉>双铁亚丁基卟啉>单铁卟啉和单锰卟啉>双锰亚丁基卟啉>双锰双丙基卟啉>双锰亚乙基卟啉,由于相同的条件下铁和锰的规律相反,推测在以双卟啉模型中存在着金属之间的相互作用,铁的作用和锰的作用对双卟啉的催化性能影响相反。

关 键 词:催化  氧化  合成  环己烷  羟基化  催化性能      双核金属卟啉
文章编号:1004-1656(2001)03-0265-05
修稿时间:2001年1月3日

SYNTHESIS OF METALLIC COMPLEXES OF BISPORPHYRINS AND THEIR CATALYTIC REACTIONS OF CYCLOHEXANE
TANG Yu,ZHANG Yuan-ming,GUI Ming-De,ZHU Sheng-jie.SYNTHESIS OF METALLIC COMPLEXES OF BISPORPHYRINS AND THEIR CATALYTIC REACTIONS OF CYCLOHEXANE[J].Chemical Research and Application,2001,13(3):265-269.
Authors:TANG Yu  ZHANG Yuan-ming  GUI Ming-De  ZHU Sheng-jie
Abstract:Several new metallic iron(Ⅲ) and manganese(Ⅲ) bisporphyrins bonded with chain of different length at ortho position of phenyl of 5,5′ of porphrin were was synthetized and tested by spectrum of NMR,elemental analysis and UV-Vis spectra.With these model compounds as catalyses and iodosobenzene as oxidant,iniatial and equilium yields of oxidative reactions of cyclohexane were conducted.The best yields of cyclohexanol and cyclohexanone were 35.83% and 23.41% respectively.From the data of yields,the sequence of activity and stability of these metallic bisporphyrins complexes were explored qualitatively as BFEP(13)>BFPP(15)>BFBP(17)>MFP(11) and MMP(12)>BMBP(18)>BMPP(16)>BMEP(14).It was found at the same situation iron manganese had adverse sequence.Thus there was metal-metal interaction in the matallic irons and manganeses in matallic bisporp hyrins.Furthmore the effet was adverse to iron and manganese.
Keywords:bisporphyrin  catalysis  oxidation  synthesis
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