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[NBu4][Ni(C6F5)2(S(O)P(C5H4FeC5H5)(O(i)Pr))] | 691873-68-4

中文名称
——
中文别名
——
英文名称
[NBu4][Ni(C6F5)2(S(O)P(C5H4FeC5H5)(O(i)Pr))]
英文别名
——
[NBu4][Ni(C6F5)2(S(O)P(C5H4FeC5H5)(O(i)Pr))]化学式
CAS
691873-68-4
化学式
C16H36N*C25H16F10FeNiO2PS
mdl
——
分子量
958.43
InChiKey
BGJUEOJAGVKSEE-XMWANKNGSA-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    描述:
    (NBu4)2{(C6F5)2Ni(μ-OH)2Ni(C6F5)2} 、 2,4-diferrocenyl-1,3-dithiadiphosphetane-2,4-disulfide异丙醇二氯甲烷异丙醇 为溶剂, 以68%的产率得到[NBu4][Ni(C6F5)2(S(O)P(C5H4FeC5H5)(O(i)Pr))]
    参考文献:
    名称:
    Organometallic nickel(II) complexes with dithiophosphate, dithiophosphonate and monothiophosphonate ligands
    摘要:
    The hydroxo complex [NBu4](2)[Ni-2(C6F5)(4)(mu-OH)(2)] reacts with ammonium O, O'-dialkyldithiophosphates, O-alkyl-p-methoxyphenyldithiophosphonate acids and ammonium O-alkylferrocenyldithiophosphonates in dichloromethane under mild conditions to give, respectively, [NBu4][Ni(C6F5)(2){S(S)P(OR)(2)}] (R=Me (1), Et (2), Pr-i (3)) and [NBu4][Ni(C6F5)(2){S(S)P(OR)Ar}] (Ar=p-MeOC6H4, R = Me (4), Et (5), Pr-i (6); Ar = ferrocenyl; R = Me (7), Et (8), Pr-i (9)). The monothiophosphonate nickel complexes [NBu4][Ni(C6F5)(2) {S(S)P(OR)(ferrocenyl))] (R=Et (10), Pr-i (11)) are obtained by reaction of the hydroxo complex with O-alkylferrocenyldithiophosphonate acids. Analytical (C, H, N, S), conductivity, and spectroscopic (IR, H-1, F-19 and P-31 NMR, and FAB-MS) data were used for structural assignments. A single-crystal X-ray diffraction study of [NBu4][Ni(C6F5)(2){S(S)P(OMe)(p-MeOC6H4)}] (4) and [NBu4][Ni(C6F5)(2){S(O)P(OEt)(ferrocenyl)}] (10) shows that in both cases the coordination around the nickel atom es essentially square planar with NiC2S2 and NiC2SO central cores, respectively. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2003.06.013
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