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trichloro(4-methyl-2,6-bis(1-(2-pyrrolidinoethyl)iminomethyl)-phenolato)zinc(II) | 1163155-68-7

中文名称
——
中文别名
——
英文名称
trichloro(4-methyl-2,6-bis(1-(2-pyrrolidinoethyl)iminomethyl)-phenolato)zinc(II)
英文别名
——
trichloro(4-methyl-2,6-bis(1-(2-pyrrolidinoethyl)iminomethyl)-phenolato)zinc(II)化学式
CAS
1163155-68-7
化学式
C21H31Cl3N4OZn2
mdl
——
分子量
592.642
InChiKey
RKPPBXLGKOQFIJ-MXXJQBQISA-J
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    参考文献:
    名称:
    Radical Pathway in Catecholase Activity with Zinc-Based Model Complexes of Compartmental Ligands
    摘要:
    Four dinuclear and three mononuclear Zn-II complexes of phenol-based compartmental ligands (HL1-HL7) have been synthesized with the aim to investigate the viability of a radical pathway in catecholase activity. The complexes have been characterized by routine physicochemical studies as well as X-ray single-crystal structure analysis: [Zn-2(H2L1)(OH)(H2O)(NO3)](NO3)(3) (1), [Zn2L2Cl3] (2), [Zn2L3Cl3] (3), [Zn-2(L-4)(2)(CH3COO)(2)] (4), [Zn(HL5)Cl-2] (5), [Zn(HL6)Cl-2] (6), and [Zn(HL7)Cl-2] (7) [L-1-L-3 and L-5-L-7 = 2,6-bis(R-iminomethyl)-4-methylphenolato, where R= N-ethylpiperazine for L-1, R = 2-(N-ethyl)pyridine for L-2, R = N-ethylpyrrolidine for L-3, R = N-methylbenzene for 1,5, R = 2-(N-methyl)thiophene for L-6, R = 2-(N-ethyl)thiophene for L-7, and L-4 = 2-formyl-4-methyl-6-N-methylbenzene-iminomethyl-phenolato]. Catecholase-like activity of the complexes has been investigated in methanol medium by UV-vis spectrophotometric study using 3,5-di-tert-butylcatechol as model substrate. All complexes are highly active in catalyzing the aerobic oxidation of 3,5-di-tert-butylcatechol (3,5-DTBC) to 3,5-di-tert-butylbenzoquinone (3,5-DTBQ). Conversion of 3,5-DTBC to 3,5-DTBQ catalyzed by mononuclear complexes (5-7) is observed to proceed via formation of two enzyme-substrate adducts, ES1 and ES2, detected spectroscopically, a finding reported for the first time in any ZnII complex catalyzed oxidation of catechol. On the other hand, no such enzyme-substrate adduct has been identified, and 3,5-DTBC to 3,5-DTBQ conversion is observed to be catalyzed by the dinuclear complexes (14) very smoothly. EPR experiment suggests generation of radicals in the presence of 3,5-DTBC, and that finding has been strengthened by cyclic voltammetric study. Thus, it may be proposed that the radical pathway is probably responsible for conversion of 3,5-DTBC to 3,5-DTBQ promoted by complexes of redox-innocent Zn-II ion. The ligand-centered radical generation has further been verified by density functional theory calculation.
    DOI:
    10.1021/ic300400v
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文献信息

  • Synthesis, characterization and selective fluorescent zinc(II) sensing property of three Schiff-base compounds
    作者:Partha Roy、Koushik Dhara、Mario Manassero、Pradyot Banerjee
    DOI:10.1016/j.ica.2009.01.023
    日期:2009.6
    Three Schiff-base compounds, 4-methyl-2,6-bis(1-(2-piperidinoethyl)iminomethyl)-phenol (HL1), 4-methyl-2,6-bis( 1-(2-pyrrolidinoethyl)-iminomethyl)-phenol (HL2) and (4-methyl-2,6-bis(1-(2- morpholinoethyl) iminomethyl)-phenol) (HL3), have been synthesized and characterized by elemental analysis, FT-IR, H-1 NMR, UV-Vis, electrospray ionisation mass and fluorescence spectroscopy. The emission quantum yield of the compounds increases by ca. 10-17 times by the addition of Zn2+ ion. Introduction of other metal ions of biological and environmental relevance either keeps unaltered or quenches the emission intensity of the ligands. This happens because of large binding constant (similar to 10(4) M-1) of the ligand with Zn2+ ion in acetonitrile. Each of the three ligands forms 1: 2 (ligand: metal) complexes which are characterized by single crystal X-ray diffraction analyses. This imposes rigidity to the ligand due to the complexation and, as a result, the radiative decay constant increases and the corresponding nonradiative decay parameter decreases. All of the ligands react with zinc chloride in acetonitrile to form dinuclear complexes which have been characterized by the elemental analysis, FT-IR, UV-Vis, electrospray ionisation mass spectroscopies and single crystal X-ray structural determinations. (C) 2009 Elsevier B.V. All rights reserved.
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