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bis(salicylaldehyde-2-hyroxyanilato(2-))titanium(IV) | 16923-37-8

中文名称
——
中文别名
——
英文名称
bis(salicylaldehyde-2-hyroxyanilato(2-))titanium(IV)
英文别名
bis[N-(2-oxophenyl)salicylideneiminato]titanium(IV);Ti(Sap)2
bis(salicylaldehyde-2-hyroxyanilato(2-))titanium(IV)化学式
CAS
16923-37-8
化学式
C26H18N2O4Ti
mdl
——
分子量
470.32
InChiKey
HEJYLSMHRFXUEG-ZNVPEIAMSA-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:
    描述:
    titanium(IV) isopropylate2-羟基缩苯胺 以90.5%的产率得到bis(salicylaldehyde-2-hyroxyanilato(2-))titanium(IV)
    参考文献:
    名称:
    Abe, Yoshimoto; Sawamura, Katsuhiko; Nagao, Yukinori, Nippon Kagaku Kaishi/Journal of the Chemical Society of Japan
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Binuclear Metal Complexes. XLII. Manganese(IV) Complexes Synthesized by Oxidation of Binuclear Manganese(II) Complexes of 2-(Salicylideneamino)phenols with Tetrachloro-<i>o</i>-benzoquinone
    作者:Hisashi Okawa、Masaaki Nakamura、Sigeo Kida
    DOI:10.1246/bcsj.55.466
    日期:1982.2
    Manganese(IV) complexes Mn(R-R′-sap)2, where H2(R-R′-sap) denotes 2-(salicylideneamino)phenols with the substituent R on the salicylaldehyde ring and the R′ on the o-aminophenol ring, were prepared by the oxidation of binuclear manganese(II) complexes Mn2(R-R′-sap)2 with tetrachloro-o-benzoquinone (TCOQ). The complexes showed magnetic moments corresponding to three unpaired electrons and strong absorptions
    制备(IV)配合物Mn(RR'-sap)2,其中H2(RR'-sap)表示水杨醛环上有取代基R和邻氨基苯酚环上有R'的2-(杨基基)苯酚通过用四-邻苯醌 (TCOQ) 氧化双核 (II) 络合物 Mn2(RR'-sap)2。复合物显示出对应于三个不成对电子的磁矩和由 CT 跃迁引起的 15-20×103 cm-1 区域的强吸收。Mn(RR'-sap)2 的循环伏安图显示出两个氧化还原波,可以用两步反应来解释,Mn(IV)\ightleftharpoonsMn(III)\ightleftharpoonsMn(II)。第一个和第二个过程的氧化还原电位都取决于取代基 R 和 R',氧化还原电位与 R 和 R' 的哈米特 σ 值与氧之间存在良好的相关性。Mn2(RR'-sap)2 与 TCOQ 反应生成双核 (III) 络合物 Mn2(RR'-sap)2(tcoq),其在存在下分解形成
  • Preparations and structures of titanium(IV) complexes containing 8-hydroxyquinolinate and a Schiff-base N-(2-oxyphenyl)salicylideneiminate
    作者:Weng Feng Zeng、Yen Hsien Chen、Michael Y. Chiang、Cheu Pyeng Cheng
    DOI:10.1016/j.poly.2006.10.048
    日期:2007.4
    In methanol, the reaction of Ti((OPr)-Pr-i)(4), N-(2-hydroxyphenyl)salicylideneimine (H(2)Sap) and 8-hydroxyquinoline (HQ) in stoichiometric ratio 1:1:x yielded Ti(Sap)(2) precipitate as initial product even when x was as high as 10. However, when the reaction mixture with x = 2 was left standing for 12 h or more, a small amount of red crystalline Ti(Sap)Q(OMe) was isolated. Addition of wet acetonitrile to the reaction mixture with x = 10, small amount of another red crystalline [Ti(Sap)Q](2)(mu-O) was obtained after standing for 2 days. The reaction between TiQ(2)((OPr)-Pr-i)(2) and H(2)Sap in methanol with stoichiometric ratio of y: 1 also yielded Ti(Sap)(2) as initial product even for y as large as 10. H-1 NMR investigation of the reaction of TiQ(2)(OMe)(2) with H(2)Sap revealed that Ti(Sap)Q(OMe) was not detected initially. These experimental results can be explained based on a mechanism that includes: (i) rapid reaction of H(2)Sap with Ti(IV) centers to form Ti(Sap)(2); (ii) equilibrium between TiQ(2)(OMe)(2) and Ti(Sap)Q(OMe); (iii) equilibrium between Ti(Sap)Q(OR) and Ti(Sap)(2); and (iv) limited solubilities of Ti(Sap)Q(OR) and Ti(Sap)(2). The equilibrium constants and solubilities in the mechanism were determined by the H-1 NMR spectral method. The structures of Ti(Sap)Q(OMe) and [Ti(Sap)Q](2)(mu-O), consisting octahedrally coordinated Ti(IV), were determined by X-ray diffraction method. (C) 2006 Elsevier Ltd. All rights reserved.
  • Hefele, H.; Ludwig, E.; Uhlemann, E., Zeitschrift fur Anorganische und Allgemeine Chemie
    作者:Hefele, H.、Ludwig, E.、Uhlemann, E.
    DOI:——
    日期:——
  • Blas, A. de; Bastida, R.; Fuentes, M. J., Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry, 1991, vol. 21 - 8, p. 1273 - 1298
    作者:Blas, A. de、Bastida, R.、Fuentes, M. J.
    DOI:——
    日期:——
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