摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

氯磷酰腈 | 1832-07-1

中文名称
氯磷酰腈
中文别名
氯二氧磷基腈
英文名称
poly(dichlorophosphazene)
英文别名
(NPCl2)n;[NPCl2]n;phosphonitrile dichloride;Phosphonitrile chloride;azanylidyne(dichloro)-λ5-phosphane
氯磷酰腈化学式
CAS
1832-07-1
化学式
Cl2NP
mdl
——
分子量
115.886
InChiKey
UXJHQBVRZUANLK-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:
    135-140 °C(Press: 17 Torr)

计算性质

  • 辛醇/水分配系数(LogP):
    2.26
  • 重原子数:
    4
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    23.8
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:fa1fbe3442b0fa2a7cd3a53cbf1a69f7
查看

反应信息

  • 作为反应物:
    描述:
    triethylamine tris(hydrogen fluoride)氯磷酰腈N,N-二异丙基乙胺 作用下, 以 四氢呋喃 为溶剂, 以90%的产率得到poly(difluorophosphazene)
    参考文献:
    名称:
    Loewe, C.; Riesel, L., Zeitschrift fur Anorganische und Allgemeine Chemie
    摘要:
    DOI:
  • 作为产物:
    描述:
    六氯环三磷腈 在 [N3P3Cl6SiEt3][HCB11H5Br6] Et3Si(CHB11H5Br6) 作用下, 以 further solvent(s) 为溶剂, 生成 氯磷酰腈
    参考文献:
    名称:
    甲硅烷基离子催化的环氯磷腈三聚体[N(3)P(3)Cl(6)]的环境温度开环聚合(ROP)。
    摘要:
    通过使用三烷基甲硅烷基碳硼烷[R(3)Si(CHB(11)X(11)]作为催化剂,可以大大降低环N(3)P(3)Cl(6)开环聚合所需的温度。
    DOI:
    10.1039/b713933k
点击查看最新优质反应信息

文献信息

  • Synthesis and spectroscopic characterization of cyclic and polymeric phosphazenes bearing phosphine complexes
    作者:Gabino A Carriedo、Francisco J Garcı́a Alonso、Pedro A González、Carlos Dı́az Valenzuela、Nicolás Yutronic Sáez
    DOI:10.1016/s0277-5387(02)01233-0
    日期:2002.12
    The reactions of the cyclic phosphazenes [N3P3Cl6] and [N3P3(O2Cl2H8)(2)Cl-2] (O2Cl2H8 = 2,2'-dioxybiphenyl) with the diphenylphosphine phenol complex Mn(CO)(2)(eta(5)-C5H4Me)[PPh2(C6H4-OH)]} (1) and Cs2CO3 in refluxing acetone gave, respectively the phosphazenc-phosphine complexes N3P3[OC6H4PPh2-Mn(CO)(2)(eta(5)-C5H4Me)](6)} (2) and N3P3(o(2)Cl(2)H(8))(2)[OC6H4PPh2-Mn(CO)(2)(eta(5)-C5H4Me)](2)} (3). in good yields. The analogous reaction of the partially substituted clorophosphazene polymer [NP(O2Cl2H8)](0.6)[NPCl2](0.4)}(n) in THF gave the polymeric complex [NP(O2Cl2H8)}(0.6)NP[OC6H4PPh2-Mn(CO)(2)(eta(5)- C5H4Me)](2)}(0.4)-0.5[OC4H8](n) (4). Different spectroscopic data are provided for the new compounds that may be useful for the characterization of other more complex polymeric materials. (C) 2002 Elsevier Science Ltd. All rights reserved.
  • Direct synthesis of cyclic and polymeric phosphazenes bearing diphenylphosphine groups and their complexes with [W(CO)5] fragments
    作者:Gabino A. Carriedo、Francisco J. Garcı́a Alonso、Pedro A. González、Paloma Gómez-Elipe
    DOI:10.1016/s0277-5387(99)00194-1
    日期:1999.9
    The reactions of the cyclotriphosphazenes [N3P3Cl6] or [N3P3(O2C12H8)(2)Cl-2] with the phenolic phosphine PPh2(C6H4-OH) in the presence of Cs2CO3 give, respectively, the cyclic phosphazene phosphines [N3P3(OC6H4PPh2)(6)] (1) and [N3P3(O2C12H8)(2)(OC6H4PPh2)(2)] (2), very pure and in high yield. The similar reaction with the linear polyphosphazene [NP(O2C12H8)](0.65) [NPCl2](0.35)}(n) in THF gives the diphenylphosphine polymer [NP(O2C12H8)](0.65)[NP(OC6H4PPh2)(2)]0.35}(n) (3). The phenolic tungsten pentacarbonyl complex W(CO)(5)[PPh2(C6H4-OH)]} reacts in the same way with those cyclic and polymeric phosphazenes to give the corresponding complexes N3P3[OC6H4PPh2-W(CO)(5)](6)} (4), [N3P3(O2C12H8)(2)(OC6H4PPh2-W(CO)(5))(2)] (5), and [NP(O2C12H8)](0.65)[NP(OC6H4PPh2-W(CO)(5))(2)](0.35)}(n) (6). (C) 1999 Elsevier Science Ltd. All rights reserved.
  • Blackstone, Vivienne; Lough, Alan J.; Murray, Martin, Journal of the American Chemical Society, 2009, vol. 131, p. 3658 - 3667
    作者:Blackstone, Vivienne、Lough, Alan J.、Murray, Martin、Manners, Ian
    DOI:——
    日期:——
  • Effect of a neighboring group in alcoholysis reactions of polydichlorophosphazene
    作者:D. R. Tur、V. V. Korshak、S. V. Vinogradova、N. P. Provotorova、P. V. Petrovskii
    DOI:10.1007/bf00962001
    日期:1987.10
  • Allcock, Harry R.; Desorcie, James L.; Steven Rutt, Organometallics, 1988, vol. 7, # 3, p. 612 - 619
    作者:Allcock, Harry R.、Desorcie, James L.、Steven Rutt
    DOI:——
    日期:——
查看更多