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(((CH3)2CH)3C6H2C5H3NNC6H2(CH3)3)Y(2,6-diisopropylaniline(-1H))2(bipy) | 1388888-69-4

中文名称
——
中文别名
——
英文名称
(((CH3)2CH)3C6H2C5H3NNC6H2(CH3)3)Y(2,6-diisopropylaniline(-1H))2(bipy)
英文别名
(((CH3)2CH)3C6H2C5H3NNC6H2(CH3)3)Y(2,6-diisopropylaniline(-1H))2(2,2'-bipyridine)
(((CH<sub>3</sub>)<sub>2</sub>CH)<sub>3</sub>C<sub>6</sub>H<sub>2</sub>C<sub>5</sub>H<sub>3</sub>NNC<sub>6</sub>H<sub>2</sub>(CH<sub>3</sub>)<sub>3</sub>)Y(2,6-diisopropylaniline(-1H))<sub>2</sub>(bipy)化学式
CAS
1388888-69-4
化学式
C63H81N6Y
mdl
——
分子量
1011.28
InChiKey
VOCWVUJRHAFGLV-UHFFFAOYSA-N
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

反应信息

  • 作为产物:
    描述:
    2,2'-联吡啶 、 (((CH3)2CH)3C6H2C5H3NNC6H2(CH3)3)Y(C≡CPh)(2,6-diisopropylaniline(-1H))(DME) 以 甲苯 为溶剂, 反应 1.0h, 以43%的产率得到(((CH3)2CH)3C6H2C5H3NNC6H2(CH3)3)Y(2,6-diisopropylaniline(-1H))2(bipy)
    参考文献:
    名称:
    Reactions of Bis(alkyl)yttrium Complexes Supported by Bulky N,N Ligands with 2,6-Diisopropylaniline and Phenylacetylene
    摘要:
    The reactions of bis(trimethylsilylmethyl)yttrium complexes supported by bulky amidopyridinate (Ap) and amidinate (Amd) ligands (LY(CH2SiMe3)(2)(THF)(n): L = Ap, n = 1 (1); L = Amd, n = 1 (2)) with 2,6-diisopropylaniline and phenylacetylene were performed. The reaction of 1 with an equimolar amount of 2,6-diisopropylaniline occurs with TMS elimination and affords an yttrium alkyl anilido species which was isolated as a DME adduct, ApY(CH2SiMe3)(NH-2,6-(Pr2C6H3)-Pr-i)-(DME) (3). The protonolysis of 3 with phenylacetylene results in the alkynyl anilido derivative ApY(C CPh)(NH-2,6-(Pr2C6H3)-Pr-i)-(DME) (6). The treatment of complexes 3 and 6 with 2,2'-bipy leads to the formation of the bis(anilido) derivative ApY(NH-2,6-iPr(2)C(6)H(3))(2)(bipy) (5). The formation of a dimeric complex containing two ApY fragments linked by two mu(2)-alkynyl groups and a mu-eta(2):eta(2)-butatrienediyl fragment, [{AmdY(mu(2)-C CPh)}2(mu(2)-eta(2):eta(2)-PhCCCCPh)] (7), was observed in the reaction of 2 with 2 equiv of phenylacetylene.
    DOI:
    10.1021/om300377h
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