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1-(2-azidophenyl)-3-methyl-1H-imidazol-3-ium iodide | 1196117-40-4

中文名称
——
中文别名
——
英文名称
1-(2-azidophenyl)-3-methyl-1H-imidazol-3-ium iodide
英文别名
——
1-(2-azidophenyl)-3-methyl-1H-imidazol-3-ium iodide化学式
CAS
1196117-40-4
化学式
C10H10N5*I
mdl
——
分子量
327.127
InChiKey
DLJWOHSMAQBAKO-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):
    -0.75
  • 重原子数:
    16.0
  • 可旋转键数:
    2.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    57.57
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis and characterization of zinc complexes supported by NHC-based CNN- and CNP-tridentate ligands and their catalysis in the ring-opening polymerization of rac-lactide and ε-caprolactone
    摘要:
    A series of zinc complexes bearing NHC-based C,N,N- or C,N,P-tridentate ligands were synthesized and characterized and the catalysis of the complexes toward the ring-opening polymerization of rac-lactide was evaluated. The ligand precursors [2-(CHN(R)(CH)(2)N)C6H4N=P(Pb)(2)CH2(Ph)(2)CH2Py](+) I- (2a, R = Me; 2b, R = iPr) prepared from [2-N3C6H4(N(CH)(2)N(R)CH)](+) I- (R = Me or iPr) and Ph2PCH2Py were successively treated with nBuLi and ZnEt2 to afford corresponding zinc complexes [Zn(Et){2-(CN(R)(CH)(2)N)(C6H4NP(Ph)(2)=CHpy}] (3a, R = Me; 3b, R = iPr). Similar treatment of [2-(CHN(Me)(CH)(2)N)C6H4N P(Ph)(2)CH2PPh2]I-+(-) (4a) (prepared from [2-N3C6H4(N(CH)(2)N(Me)CH)(+) I- and Ph2PCH2PPh2) with nBuLi and then ZnEt2 gave [Zn(Et){2-(CN(Me)(CH)(2)N)C6H4NP(Ph)(2)=CHPPh2)] (5). Treatment of [2-(CHN(R)(CH2N)C6H4N-P(Ph)(2)CH2PPh2]X-+(-) (4a, R = Me, X = l; 4h, R = Bn, X = Br; 4c, R = iPr, X = l) with p-MeC6H4N3 resulted in [2-(CHN(R)(CH)(2)N)C6H4N P(Ph)(2)CH2F(Ph)(2)=N(p-MeC6H4)(+) X-(6a, R = Me, X = l; 6b, R = Bn, X = Br; 6c, R = iPr, X = l). The reaction of 6a with nBuLi and ZnEt2 in sequence produced IZn(Et){2-(CN(Me)(CH)(2)N)C6H4NP(Ph)(2)=C1IP(Ph)(2)=N(p-McC(6)H(4))}1 (7). Whereas the reaction of 6a c with an equimolar amount of ZnEt2 gave [Zn(X){2-(ON(R)(CH)(2))C6H4NP(Ph)(2)=CHP(Ph)(2)=N(p-MeC6H4)}1(8a, R = Me, X = l; 8b, R = Bn, X = Br; 8c, R = iPr, X = l). All new compounds were characterized by H-1, C-13 and P-31 NMR spectroscopy and elemental analyses. The structures of complexes 3a, 5 and 8b were additionally characterized by single crystal X-ray diffraction. In the presence of BnOH complexes 3a, 3b, 5 and 7 catalyze the ring-opening polymerization of rac-lactide at room temperature and 3a, 3b, and 5 exhibited high activity. Complexes 8a c are inactive under the same conditions. Complexes 3a and 5 were also tested for the catalysis in the ROP of epsilon-caprolactone and both showed good catalytic activity. (C) 2015 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2015.02.013
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文献信息

  • Cross-Coupling of ArX with ArMgBr Catalyzed by N-Heterocyclic Carbene-Based Nickel Complexes
    作者:Wang-Jun Guo、Zhong-Xia Wang
    DOI:10.1021/jo302425x
    日期:2013.2.1
    N-Heterocyclic carbene-based pincer nickel complexes were synthesized and characterized. These complexes efficiently catalyze cross-coupling of aryl Grignard reagents with aryl chlorides or fluorides under mild conditions.
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