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tris(tert-butyldimethylsilyl)tren | 157642-54-1

中文名称
——
中文别名
——
英文名称
tris(tert-butyldimethylsilyl)tren
英文别名
N(CH2CH2NHSiBu(t)Me2)3;H3NN’3;N-[tert-butyl(dimethyl)silyl]-N',N'-bis[2-[[tert-butyl(dimethyl)silyl]amino]ethyl]ethane-1,2-diamine
tris(tert-butyldimethylsilyl)tren化学式
CAS
157642-54-1
化学式
C24H60N4Si3
mdl
——
分子量
489.024
InChiKey
KSLIZHWLTDKKRF-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

物化性质

  • 沸点:
    455.6±40.0 °C(Predicted)
  • 密度:
    0.864±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.07
  • 重原子数:
    31
  • 可旋转键数:
    15
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    39.3
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Complexes of Triamidoamines with the Early Actinides. Synthetic Routes to Monomeric Compounds of Tetravalent Uranium and Thorium Containing Halide and Amide Ligands
    作者:Paul Roussel、Nathaniel W. Alcock、Rita Boaretto、Andrew J. Kingsley、Ian J. Munslow、Christopher J. Sanders、Peter Scott
    DOI:10.1021/ic990563f
    日期:1999.8.1
    [Li(3)(NN'(3))(THF)(3)] [NN'(3) = N(CH(2)CH(2)NSiMe(2)Bu(t))(3)] with AnCl(4) (An = U, Th) followed by sublimation gives monomeric [An(NN'(3))Cl]. Reaction of these complexes with SiMe(3)X (X = Br, I) gives [An(NN'(3))X]. The amido derivatives [An(NN'(3))(NEt(2))] are prepared from H(3)(NN'(3)) and [U(NEt(2))(4)] and from [Th(NN'(3))Cl] and [Li(NEt(2))]. In each case, the complexes [U(NN'(3))X] (X
    化三酰基胺[Li(3)(NN'(3))(THF)(3)] [NN'(3)= N(CH(2)CH(2)NSiMe(2)Bu(t) )(3)]与AnCl(4)(An = U,Th),然后升华,得到单体[An(NN'(3))Cl]。这些配合物与SiMe(3)X(X = Br,I)反应得到[An(NN'(3))X]。酰胺衍生物[An(NN'(3))(NEt(2))]由H(3)(NN'(3))和[U(NEt(2))(4)]和[Th (NN'(3))Cl]和[Li(NEt(2))]。在每种情况下,复合物[U(NN'(3))X](X = Cl,Br,I,NEt(2))均通过X射线晶体学显示含有三酰胺对称的三酰胺基配体属中心。由于原子从三个酰胺基氮原子的赤道平面移出了大约20个,从而使结构从三角形双锥体中变形了。0.8Å。配体主链以一种方式变形,以致使叔丁基二甲基甲硅烷基包围属原子的赤道平面,
  • Triamidoamine Chemistry of Zirconium
    作者:Colin Morton、Ian J. Munslow、Christopher J. Sanders、Nathaniel W. Alcock、Peter Scott
    DOI:10.1021/om990347e
    日期:1999.10.1
    The reactions of H3(NN‘3) (NN‘3 = N(CH2CH2NSiButMe2)3) with [Zr(CH2Ph)4] and [Zr(NMe2)4] give the azazirconatranes [Zr(NN‘3)(CH2Ph)] and [Zr(NN‘3)(NMe2)], respectively. The reaction of [Li3(NN‘3)(THF)3] with [ZrCl4(THF)2] fails to yield [Zr(NN‘3)Cl] cleanly, but this compound is accessible by reaction of [Zr(NN‘3)(CH2Ph)] with BCl3 or of [Zr(NN‘3)(NMe2)] with SiMe3Cl. The molecular structures of [Zr(NN‘3)X]
    H的反应3(NN ' 3)(N-N' 3 = N(CH 2 CH 2 NSiBu吨我2)3)与[(CH 2 PH)4 ]和[Zr的(NME 2)4 ],得到azazirconatranes [(NN ' 3)(CH 2 PH)]和[Zr的(NN' 3)(NME 2)]中。[Li的反应3(NN ' 3)(THF)3 ]与[的ZrCl 4(THF)2 ]未能得到[(NN' 3)CL]干净,但此化合物通过'[(NN的反应可访问3)(CH 2与Bcl PH)] 3或[(NN的' 3)(NME 2)]与森达3。[(NN”的分子结构3)X](X = CH 2 PH,NME 2,Cl)的结果表明,该配体triamidoamine采用通常的3倍对称布置,得到大约三角-双锥络合物。[(NN”的尝试升华3)(CH 2 PH)]或其与H处理2导致完全转化成metallacyclic复合物[Zr的N(CH
  • Novel Volatile Azatranes of Group 4 Metals
    作者:Zhibang Duan、Ahmad A. Naiini、Jong-Hwan Lee、John G. Verkade
    DOI:10.1021/ic00126a017
    日期:1995.10
    New azametallatranes of the type Me(2)NM(RNCH(2)CH(2))(3)N, where R = i-Pr, M = Ti (16), Zr (17), and Hf (18); R= SiMe(3), M = Ti (19), Zr (20), and Hf (21); and R = SiMe(2)(t-Bu), M = Zr (23) and Hf (24), were prepared by metathesis reactions in moderate to high yield. During the course of the preparation of 19, Me(3)SiOTi(Me(3)-SiNCH2CH2)(3)N, 25, was formed in trace amounts. The latter compound was also synthesized by a metathesis reaction in a quantitive yield. Compounds 21 and 25 were structurally characterized and both were shown to exhibit a distorted trigonal bipyramidal metal center. Crystal data: 21, orthorhombic, space group P2(1),2(1),2(1), a = 11.837(2) Angstrom, b = 14.284(3) Angstrom, c = 15.750(4) Angstrom, V = 2662.9(9) Angstrom(3), Z = 4, R = 0.0352; 25 orthorhombic, space group Pna2(1), a = 21.772(2) Angstrom, b = 11.481(4) Angstrom, c = 11.566(1) Angstrom, V = 2891(1) Angstrom(3), Z = 4, R = 0.0341.
  • Pinkas, Jiri; Wang, Tieli; Jacobson, Robert A., Inorganic Chemistry, 1994, vol. 33, # 19, p. 4202 - 4210
    作者:Pinkas, Jiri、Wang, Tieli、Jacobson, Robert A.、Verkade, John G.
    DOI:——
    日期:——
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