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[(scandium)N(SiMe2(2-methylfuryl))Cl2]2 | 1226953-73-6

中文名称
——
中文别名
——
英文名称
[(scandium)N(SiMe2(2-methylfuryl))Cl2]2
英文别名
——
[(scandium)N(SiMe2(2-methylfuryl))Cl2]2化学式
CAS
1226953-73-6
化学式
C28H44Cl4N2O4Sc2Si4
mdl
——
分子量
816.734
InChiKey
USEDDDHQWNIOBC-UHFFFAOYSA-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:
    Li[(1,3-bis(2-methylfuryl)-1,1,3,3-tetramethyldisilazide)] 、 氯化钪甲苯 为溶剂, 以60%的产率得到[(scandium)N(SiMe2(2-methylfuryl))Cl2]2
    参考文献:
    名称:
    Group 3 complexes incorporating (furyl)-substituted disilazide ligands
    摘要:
    A series of mono-and bis-amide scandium and yttrium compounds incorporating the furyl-substituted disilazide ligand, [N{SiMe2R}(2)] {i} (where R = 2-methylfuryl) have been synthesized. The compounds Sc{i}Cl-2 (1), Sc{i}(CH2SiMe3)(2) (2) and Sc{i}(OAr)(2) (3) were made from suitable scandium starting materials employing either a salt metathesis protocol with Li{i} or via protonolysis of Sc-C bonds by the neutral amine H{i}. The thermally unstable bis-alkyl yttrium compound, 'Y{i}(CH2SiMe3)(2)' was isolated as the bis-THF adduct (4) and the bis-aryloxide Y{i}(OAr)(2) (5) was synthesized by elimination of LiOAr from Y(OAr)(3). The bis-amide complex Y{i}(2)Cl (6) and conversion to a rare example of an yttrium benzyl compound Y{i}(2)(CH2Ph) (7) are described. The yttrium cation, [Y{i}(2)](+), was synthesized by benzyl abstraction from 7 using B(C6F5)(3). Structural characterization of representative examples show variation in the coordination modes for amide ligand {i}, differing primarily in the number of furyl groups that coordinate to the metal, with examples in which zero, one or two M-O-furyl bonds are present. Preliminary investigation in two areas of catalysis are presented. (C) 2009 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2009.09.051
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