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{[PhC(NC6H4iPr2-2,6)2]Y(μ-η12-O2CCH2C6H4NMe2-o)(μ-η11-O2CCH2C6H4NMe2-o)}2 | 1512828-77-1

中文名称
——
中文别名
——
英文名称
{[PhC(NC6H4iPr2-2,6)2]Y(μ-η12-O2CCH2C6H4NMe2-o)(μ-η11-O2CCH2C6H4NMe2-o)}2
英文别名
——
{[PhC(NC<sub>6</sub>H<sub>4</sub><sup>i</sup>Pr<sub>2</sub>-2,6)<sub>2</sub>]Y(μ-η<sup>1</sup>:η<sup>2</sup>-O<sub>2</sub>CCH<sub>2</sub>C<sub>6</sub>H<sub>4</sub>NMe<sub>2</sub>-o)(μ-η<sup>1</sup>:η<sup>1</sup>-O<sub>2</sub>CCH<sub>2</sub>C<sub>6</sub>H<sub>4</sub>NMe<sub>2</sub>-o)}<sub>2</sub>化学式
CAS
1512828-77-1
化学式
C102H126N8O8Y2
mdl
——
分子量
1769.98
InChiKey
KTFQCSFGYJDXAT-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:
    二氧化碳[(NCNdipp)Y(CH2C6H4NMe2-o)2]甲苯 为溶剂, 反应 0.08h, 以78%的产率得到{[PhC(NC6H4iPr2-2,6)2]Y(μ-η12-O2CCH2C6H4NMe2-o)(μ-η11-O2CCH2C6H4NMe2-o)}2
    参考文献:
    名称:
    Synthesis, Structural Characterization, and Reactivity of Mono(amidinate) Rare-Earth-Metal Bis(aminobenzyl) Complexes
    摘要:
    Three kinds of solvated lithium amidinates with different coordination models were obtained via recrystallization of [PhC((NC6H4Pr2)-Pr-i-2,6)(2)]Li(THF) (1a) in different solvents. Treatment of o-Me2NC6H4CH2Li with LLnCl(2)(THF)(n) (2; L = [PhC((NC6H4Pr2)-Pr-i-2,6)(2)](-) (NCNdipp), [o-Me2NC6H4CH2C-((NC6H4Pr2)-Pr-i-2,6)(2)](-) (NCNdipp)) formed in situ from reaction of LnCl(3)(THF)(x) with LLi(THF) gave the rare-earth-metal bis(aminobenzyl) complexes LLn-(CH2C6H4NMe2-o)(2) (L = NCNdipp, Ln = Sc (3a), Y (3b), Lu (3c); L = NCNdipp, Ln = Sc (3d), Lu (3e)) in high yields. Reactions of complexes 3 with CO2, PhNCO, 2,6-diisopropylaniline, and S have been explored. CO2 inserted into each Ln-C bond of complexes 3a-c to form the dual-core complexes [(NCNdipp)Sc(mu-eta(1):eta(1)-O2C CH2C6H4NMe2-o)(2)](2) (4a) and [(NCNdipp)Ln(mu-eta(1):eta(2-)/O2CCH2C6H4NMe2-o)(mu-eta(1):eta(O2CCH2C6H4NMe2)-O-2-o)](2) (Ln = Y (4b), Lu (4c)). The reaction of 3b,c,e with PhNCO produced LLu[OC(CH2C6H4NMe2-o)NPh](2)(thf) (L = NCN&PP, Ln = Y (5b), Lu (5c);.L = NCNdipp, Ln = Lu (Se)). Protonolysis of 3a,b by 2,6-diisopropylaniline formed straightforwardly the mu(2)-imido complexes [(NCNdipp)Ln(mu-(NC6H4Pr2)-Pr-i-2,6)](2) (Ln = Sc (6a), Lu (6c)). Reaction of 3e with S-8 afforded the sulfur insertion products (NCNdipp')(CH2C6H4NMe2-o)(SCH2C6H4NMe2-o)(thf) (7e) and (NCNdipp)Lu(SCH2C6H4NMe2-o)2(thf)(2) (7f) in high yields, respectively, depending on the stoichiometric ratio. All of these complexes were fully characterized by elemental analysis, NMR spectroscopy, and X-ray structural determinations.
    DOI:
    10.1021/om400787j
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