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tris(8-quinolinolato)iron(III) | 14514-43-3

中文名称
——
中文别名
——
英文名称
tris(8-quinolinolato)iron(III)
英文别名
tris(8-hydroxyquinoline)iron;tris(8-quinolinolato)iron;Fe(8-hq)3;Fe(8-hydroxyquinoline)3;Fe(8-quinolinate)3;tris(quinoline-8-oxy)iron(III);[Fe(8-hydroxyquinolate)2];ferric 8-hydroxyquinoline;Fe(III) quinolin-8-olate;Fe(8-quinolate)3;Iron(3+);quinolin-8-olate
tris(8-quinolinolato)iron(III)化学式
CAS
14514-43-3
化学式
C27H18FeN3O3
mdl
——
分子量
488.305
InChiKey
VKAVCIOVGWLGCW-UHFFFAOYSA-K
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):
    3.92
  • 重原子数:
    34
  • 可旋转键数:
    0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    108
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    tris(8-quinolinolato)iron(III) 在 poly(ethylene glycol) 作用下, 以 neat (no solvent) 为溶剂, 生成 iron oxide
    参考文献:
    名称:
    摘要:
    A novel combustion method of employing poly(ethylene glycol) with the precursor in a fixed ratio for the synthesis of ultrafine gamma-Fe2O3 through a self-propagating combustion synthesis is reported. Four different precursors viz. ferrous hydroxide, ferrous oxalate dihydrate, ferric 8-hydroxyquitioline and ferric acetylacetonate are employed in this study for the conversion of these precursors to ultrafine gamma-Fe2O3 particles. The as synthesized gamma-Fe2O3 samples are characterized by XRD, SEM and thermal techniques. A case study for the synthesis Of gamma-Fe2O3 employing ferric acetyl acetonate as precursor is reported. The importance of employing thermal analysis techniques in understanding the combustion synthesis is envisaged.
    DOI:
    10.1023/a:1023342713483
  • 作为产物:
    描述:
    8-羟基喹啉 、 iron bis(8-hydroxyquinolinate) 在 air 作用下, 以 further solvent(s) 为溶剂, 生成 tris(8-quinolinolato)iron(III)
    参考文献:
    名称:
    Mikhailov, O. V., Journal of general chemistry of the USSR, 1991, vol. 61, p. 1759 - 1760
    摘要:
    DOI:
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文献信息

  • Kinetics and mechanism of ligand substitution in β-diketone complexes of iron(III). Solvolysis controlling the substitution process in alcohol media
    作者:Gerhard Gumbel、Horst Elias
    DOI:10.1016/s0020-1693(02)01143-x
    日期:2003.1
    Abstract Conventional and stopped-flow spectrophotometry was used to study the kinetics of ligand substitution in a number of tris β-diketone iron(III) complexes, Fe(O ∩ O) 3 , by 8-hydroxyquinoline (=HO ∩ N) in alcohol media (O ∩ O − =anion of the β-diketones pentane-2,4-dione, 2,6-dimethylheptane-3,5-dione, 2,2,6,6-tetramethylheptane-3,5-dione, 1-phenylbutane-1,3-dione, 1,3-diphenylpropane-2,3-dione
    摘要用常规分流光度法和分流光度法研究了酒精中的8-​​羟基喹啉(= HO∩N)在许多trisβ-二酮铁(III)配合物Fe(O∩O)3中的配体取代动力学。介质(O∩O-=β-二酮戊烷-2,4-二酮的阴离子,2,6-二甲基庚烷-3,5-二酮,2,2,6,6-四甲基庚烷-3,5-二酮,1 -苯基丁烷-1,3-二酮,1,3-二苯基丙烷-2,3-二酮和1-(2-噻吩基)-4,4,4-三氟丁烷-1,3-二酮)。如分光光度法所示,络合物Fe(O∩O)3在醇ROH中的溶液会发生溶剂分解,从而形成溶剂型Fe(O∩O)2 S 2和双核络合物[Fe(O∩O)2 (RO)] 2(分别为S = ROH和RO-)。Fe(O∩O)3与HO∩N在醇介质中的反应导致Fe(O∩N)3的反应是三次的。相应的一阶速率常数k 1,k 2和k 3与进入配体HO∩N的浓度无关,并且遵循k 1> k 2> k 3的顺序,其中k 1 /
  • Spectra-structure correlations from the infrared spectra of some transition metal complexes of 8-hydroxyquinoline
    作者:Carola Engelter、Graham E. Jackson、Cheryl L. Knight、David A. Thornton
    DOI:10.1016/0022-2860(89)85112-9
    日期:1989.10
    Jahn-Teller distortion on the spectra of the complexes of Cu(II) and Mn(III) are discussed. The spectra of the bis (aquo) adducts support the previously proposed trans -octahedral structure. The spectra of the anhydrous complexes are consistent with tetrahedral Mn, Ni and Zn but suggest that the Co complex has polymeric octahedral coordination rather than the previously-proposed tetrahedral structure. The six-coordinate
    摘要 讨论了 8-羟基喹啉的 21 种过渡金属配合物在 700-50 cm -1 范围内的 IR 光谱及其已知或推断的结构。配合物分为三种类型:(a) 3d 金属 (II) 离子反式 -[M(ox) 2 (H 2 O) 2 ] (M = Mn、Fe、Co、Ni) 的双 (aquo) 配合物, 铜, 锌); (b) 相应的无水配合物 [M(ox) 2 ] (M = Mn、Co、Ni、Cu、Zn);(c) 金属 (III) 离子的络合物 [M(ox) 3 ] (M = Sc, V, Cr, Mn, Fe, Co, Ga)。8-羟基喹啉-d 7 已被合成并用于辅助金属配体分配,这进一步基于双(水)锌配合物的 64,68 Zn 标记以及金属离子取代对基于预期的影响关于晶体场论。讨论了 Jahn-Teller 畸变对 Cu(II) 和 Mn(III) 配合物光谱的影响。双 (aquo) 加合物的光谱
  • Surface layer-by-layer chemical deposition reaction for thin film formation of nano-sized metal 8-hydroxyquinolate complexes
    作者:Mohamed E. Mahmoud、Sawsan S. Haggag、Tarek M. Abdel-Fattah
    DOI:10.1016/j.poly.2008.09.030
    日期:2009.1
    confirmed from the metal analysis and molar stoichiometric ratio of metal ion to 8-hydroxyquinoline. This was characterized as 1:2 for the Co(II), Ni(II), Cu(II) and Zn(II)–quinolate complexes. The Fe(III)–quinolate thin film was found to exhibit a 1:3 ratio. Electron impact-mass spectra (EI-MS) of all the synthesized thin film metal quinolate complexes were recorded and the results refer to the existence
    已经研究并报道了新颖且简单的逐层化学沉积方法用于制备纳米级8-羟基喹啉金属配合物的可行性。通过将基材交替浸入金属离子溶液中,然后再浸入配体溶液中,可以合成出均匀的纳米晶体薄膜。通过金属分析和金属离子与8的摩尔化学计量比确定了已生长的无水Fe(III),Co(II),Ni(II),Cu(II)和Zn(II)配合物晶体的化学计量。羟基喹啉。对于Co(II),Ni(II),Cu(II)和Zn(II)-喹诺酮酸酯络合物,其特征为1:2。发现Fe(III)-喹啉薄膜具有1:3的比例。m / z值。从(EI-MS)研究中也证实了这种化学计量比为1:2和1:3的比例。还通过扫描电子显微镜(SEM)对沉积的薄膜进行分析,并检测到粒径≤50nm。FT-IR和UV-Vis光谱进一步用于确认8-羟基喹啉金属配合物的结构。热重分析(TGA)还用于跟踪可能的热分解步骤并计算纳米级金属配合物的热力学参数。
  • Post-synthetically modified SBA-15 with NH<sub>2</sub>-coordinately immobilized iron-oxine: SBA-15/NH<sub>2</sub>-FeQ<sub>3</sub> as a Fenton-like hybrid catalyst for the selective oxidation of organic sulfides
    作者:Habib Golchin Hosseini、Sadegh Rostamnia
    DOI:10.1039/c7nj02742g
    日期:——

    We herein report the synthesis and catalysis of SBA-15 grafted iron-oxine. SBA-15/NH2-FeQ3 showed efficient catalytic activity in sulfide oxidation.

    我们在此报告了SBA-15接枝铁氧啶的合成和催化。SBA-15/NH2-FeQ3在硫化物氧化中表现出高效的催化活性。
  • Encapsulation of 8-HQ as a corrosion inhibitor in PF and UF shells for enhanced anticorrosive properties of renewable source based smart PU coatings
    作者:R. J. Marathe、V. V. Gite
    DOI:10.1039/c6ra21684f
    日期:——
    Encapsulation of 8-HQ into PF and UF microcapsules was carried out to enhance the anticorrosive properties of renewable source based PU coatings. Microcapsules were characterized using optical microscopy and FE-SEM for their morphological behavior as well as using a particle size analyzer to determine the mean diameter of the microcapsules. A release study of the inhibitor used to form both shell materials
    进行了将8-HQ封装到PF和UF微胶囊中,以增强可再生来源的PU涂料的防腐性能。使用光学显微镜和FE-SEM对其微胶囊的形态进行表征,并使用粒度分析仪确定微胶囊的平均直径。使用紫外可见光谱法估计了用于形成两种壳材料的抑制剂的释放研究。使用TGA对微胶囊和由该微胶囊配制的聚氨酯(PU)智能涂料进行了热研究。检查所制备的智能涂料的物理机械性能和防腐性能,并通过0.5 M HCl溶液对其进行测试。浸没法和重量法。装有PF和UF微胶囊的PU涂料显示出最佳的防腐性能。在比较壳时,负载有8-HQ封装到PF中的PU涂层比负载有UF基微胶囊的涂层具有更好的效果。
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