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一种大环化合物的晶体结构及其双核铜配合物的酪氨酸酶活性研究
引用本文:周红,潘志权,罗勤慧,梅光全,龙德良,陈久桐. 一种大环化合物的晶体结构及其双核铜配合物的酪氨酸酶活性研究[J]. 中国化学, 2005, 23(7): 835-842. DOI: 10.1002/cjoc.200590835
作者姓名:周红  潘志权  罗勤慧  梅光全  龙德良  陈久桐
作者单位:[1]HubeiKeyLaboratoryofNovelChemicalReactorandGreenChemicalTechnology,WuhanInstituteofChemicalTechnology,Wuhan,Hubei430073,China [2]HubeiKeyLaboratoryofNovelChemicalReactorandGreenChemicalTechnology,WuhanInstituteofChemicalTechnology//StateKeyLaboratoryofCoordinationChemistry,NanjingUniversity [3]CoordinationChemistryInstitute,StateKeyLaboratoryofCoordinationChemistry,NanjingUniversity,Nanjing,Jiangsu210093,China [4]FuzhouStateKeyLaboratoryofStructureChemistry,Fuzhou,Fujian350002,China
摘    要:
A ring-contracted form macrocycle, 29,30-dioxo-3,6,9,17,20,23,29,30-octaazapentacyclo[23,3,1,1^11,15,0^2,6,0^16,20]-triacontaneocta- 1 (28),9,11 (12), 13,15(30),23,25(29),26-ene (L) was synthesized by condensation of diethyltriamine with pyridine-1-oxide-2,6-dicarboxaldehyde. A porous three-dimensional layer structure in its crystal was formed by self-assembly through hydrogen bonds and π-π interaction. Its dinuclear copper(I) complex [Cu2L(MeOH)2]-(BF4)2*2H2O and dinuclear-copper(II) complex [Cu2L(MeOH)2](ClO4)4*2H2O were obtained and could oxidize catalytically four phenolic substrates hydroquinone, 2-methyl-hydroquinone, 2,6-di-tert-butylphenol and 2,6-dimethylphenol, in a mixture of methanol and acetonitrile (V : V, 4 : 1). The copper(I) complex reacted with dioxygen to form an oxygenated species as an initial active intermediate for oxidation of the phenols. Oxidation of the substrates by the copper(II) complex produced a copper(I) complex and the oxidation products of the substrates.

关 键 词:晶体结构 酪氨酸酶 酶活性 铜配合物 双核配合物 合成 氧分子 催化氧化 大环化合物
收稿时间:2004-10-25
修稿时间:2005-03-28

Study on the Crystal Structure of a Macrocycle and Tyrosinase Activity of Its Dinuclear Copper Complexes
Zhou Hong,Pan Zhi‐Quan,Luo Qin‐Hui,Mei Guang‐Quan,Long De‐Liang,Chen Jiu‐Tong. Study on the Crystal Structure of a Macrocycle and Tyrosinase Activity of Its Dinuclear Copper Complexes[J]. Chinese Journal of Chemistry, 2005, 23(7): 835-842. DOI: 10.1002/cjoc.200590835
Authors:Zhou Hong  Pan Zhi‐Quan  Luo Qin‐Hui  Mei Guang‐Quan  Long De‐Liang  Chen Jiu‐Tong
Abstract:
A ring‐contracted form macrocycle, 29,30‐dioxo‐3,6,9,17,20,23,29,30‐octaazapentacyclo[23,3,1,111,15,02,6,016,20]‐triacontaneocta‐1(28),9,11(12),13,15(30),23,25(29),26‐ene (L) was synthesized by condensation of diethyltriamine with pyridine‐1‐oxide‐2,6‐dicarboxaldehyde. A porous three‐dimensional layer structure in its crystal was formed by self‐assembly through hydrogen bonds and π‐π interaction. Its dinuclear copper(I) complex [Cu2L(MeOH)2](BF4)2·2H2O and dinuclear‐copper(II) complex [Cu2L(MeOH)2](ClO4)4·2H2O were obtained and could oxidize catalytically four phenolic substrates hydroquinone, 2‐methyl‐hydroquinone, 2,6‐di‐tert‐butylphenol and 2,6‐dimethylphenol, in a mixture of methanol and acetonitrile (V:V, 4:1). The copper(I) complex reacted with dioxygen to form an oxygenated species as an initial active intermediate for oxidation of the phenols. Oxidation of the substrates by the copper(II) complex produced a copper(I) complex and the oxidation products of the substrates.
Keywords:dinuclear copper complex  ring‐contracted macrocycle  crystal structure  dioxygen complex  catalytic oxidation
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