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Na(3,5-(t-Bu)2-2-(O)-C6H2CH=N-2,6-(i-Pr)2-C6H3) | 210882-25-0

中文名称
——
中文别名
——
英文名称
Na(3,5-(t-Bu)2-2-(O)-C6H2CH=N-2,6-(i-Pr)2-C6H3)
英文别名
——
Na(3,5-(t-Bu)2-2-(O)-C6H2CH=N-2,6-(i-Pr)2-C6H3)化学式
CAS
210882-25-0
化学式
C27H38NO*Na
mdl
——
分子量
415.595
InChiKey
UGNMPNSHQVEWOV-UHFFFAOYSA-M
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):
    4.36
  • 重原子数:
    30.0
  • 可旋转键数:
    4.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    35.42
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    chloromethyl(1,5-cyclooctadiene)palladium(II) 、 Na(3,5-(t-Bu)2-2-(O)-C6H2CH=N-2,6-(i-Pr)2-C6H3)三苯基膦 为溶剂, 以74%的产率得到Pd(P(C6H5)3)CH3(C6H2(C4H9)2OCHNC6H3(C3H7)2)
    参考文献:
    名称:
    Synthesis, structure and norbornene polymerization behavior of neutral palladium complexes
    摘要:
    A series of neutral palladium(II) complexes bearing non-symmetric bidentate pyrrole-iminato or salicylaldiminato chelate ligands have been synthesized, and the structure of representative complexes (3a, 4a, and 5a) have been confirmed by X-ray crystallographic analysis. These palladium complexes have been investigated as catalysts for the polymerization of norbornene. Using modified methylaluminoxane (MMAO) as a cocatalyst, these complexes display high activities and produce vinyl-addition polynorborenes. Catalytic activity of up to 8.52 x 10(3) kg/mol(Pd) h has been observed. Wide-angle X-ray diffraction (WAXD) has been used to investigate the polymer microstructure and it has been found that they are non-crystalline. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2004.03.017
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文献信息

  • Influence of Schiff Base and Lanthanide Metals on the Synthesis, Stability, and Reactivity of Monoamido Lanthanide Complexes Bearing Two Schiff Bases
    作者:Fubin Han、Qiaoqiao Teng、Yong Zhang、Yaorong Wang、Qi Shen
    DOI:10.1021/ic102529d
    日期:2011.3.21
    elimination of Ln[N(TMS)2]3 with the bulky bidentate Schiff base HL′ (L′ = 3,5-But2-2-(O)-C6H2CH═N-2,6-Pri2-C6H3) afforded the monoamido lanthanide complexes L′2LnN(TMS)2 (Ln = Yb (9), Y (10), Nd (11), and La (12)). While the amine elimination with the less bulky Schiff base HL′′ (L′′ = 3,5-But2-2-(O)-C6H2CH═N-2,6-Me2-C6H3) yielded the desired monoamido complexes with the small metals of Y and Yb, L′′2LnN(TMS)2
    通过席夫碱稳定单酰胺系络合物的配体L 2 LNN(TMS)2(L = 3,5-卜吨2 -2-(O)-C 6 H ^ 2 CH = N-8-C 9 H ^ 6 N,LN通过Ln [N(TMS)2 ] 3与1.8当量的HL的反应以高收率合成了Yb(1),Y(2),Eu(3),Nd(4)和La(5))。在室温下于己烷中。结果发现,稳定性1 - 5Yb≈Y
  • Metal and Ligand-Substituent Effects in the Immortal Polymerization of<i>rac</i>-Lactide with Li, Na, and K Phenoxo-imine Complexes
    作者:Francisco M. García-Valle、Robert Estivill、Carlos Gallegos、Tomás Cuenca、Marta E. G. Mosquera、Vanessa Tabernero、Jesús Cano
    DOI:10.1021/om501000b
    日期:2015.1.26
    A series of lithium, sodium, and potassium complexes with phenoxo-imine ligands M[(O-2-(RN=CH)-C6H4] [R = C6H5; 2-(BuC6H5)-Bu-t; 2,6-(Pr2C6H3)-Pr-i] and [O-2-(RN=CH)-4,6-(Bu2C6H4)-Bu-t] [R = C6H5; 2-(BuC6H5)-Bu-t; 2,6-(Pr2C6H3)-Pr-i] 1-3(a-f) have been synthesized. The molecular structures in the solid state of some of these complexes have been determined by X-ray diffraction. These compounds show different nuclearities and geometries around the metal center depending on the nature and the pocket of the ligand substituents. Of particular interest is the structure of compound 3e, being the first example of a potassium cubane complex obtained with this kind of ligand. The structural behavior in solution has also been studied by diffusion-ordered NMR spectroscopy (DOSY), showing a direct correlation between aggregation behavior and polymerization activity. Compounds 1-3(a-f) are extremely active catalysts in the ring-opening polymerization (ROP) of rac-lactide, achieving conversions of 100% in less than 1 min and heterorich-PLA that is modified by the metal atom and the ligand substituents. BnOH was used as co-initiator, and the presence of large amounts of the alcohol produces the immortal polymerization of rac-lactide in a more controlled process. Stoichiometric reactions involving the catalysts, BnOH, and lactide demonstrated an activated monomer mechanism for the polymerization of rac-lactide.
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