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

tetracarbonyl{1,2-bis(diphenylphosphino)ethane}iodovanadium | 36643-83-1

中文名称
——
中文别名
——
英文名称
tetracarbonyl{1,2-bis(diphenylphosphino)ethane}iodovanadium
英文别名
——
tetracarbonyl{1,2-bis(diphenylphosphino)ethane}iodovanadium化学式
CAS
36643-83-1
化学式
C30H24IO4P2V
mdl
——
分子量
688.312
InChiKey
LMQQZLRZTLWZTC-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):
    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:
    tetraethylammonium hexacarbonylvanadium(-1)1,2-双(二苯基膦)乙烷 在 I2 作用下, 以 四氢呋喃 为溶剂, 以75%的产率得到tetracarbonyl{1,2-bis(diphenylphosphino)ethane}iodovanadium
    参考文献:
    名称:
    ∑-Alkenyl and halogeno complexes of vanadium (I and II). The crystal structures of (C1V(CO)2(Ph2PCH2CH2PEt2)2 · benzene, Br2V(Me2PCH2CH2PMe2)2 and I2V(Me2PCH2CH2PMe2)2 · toluene
    摘要:
    Various sigma-alkenyl complexes of the general composition (alkenyl)V(CO6-npm (where n = 2, 3 and p(m) is a potentially m-dentate phosphine coordinated through n of its donor centres, n less-than-or-equal-to m) have been prepared by photo-induced hydrovanadation of the alkynes 2-butyne, 1-hexyne, 3-hexyne and 3,3-dimethyl-1-butyne. In each case the Z isomer is formed exclusively or as the predominant product. Reaction of hexacarbonylvanadate with pyridinium bromide and p(m) leads to the bromo complexes BrV(CO)6-npm (n = 2-4). In the case of p(m) = Me2PCH2CH2PMe2 (dmpe), the complex Br2V(dmpe) is also formed. The complex I2V(dmpe)2 . toluene was obtained as a by-product from the reaction between [Et4N][V(CO)4dmpe] and perfluoro-isopropyl iodide. The face-capped, trigonal-prismatic complex ClV(CO)2(pepe)2 . benzene (pepe = Ph2PCH2CH2PEt2) was obtained from the photo-reaction between HV(CO)4pepe and [Et4N]Cl. Single-crystal X-ray diffraction studies were carried out on all three complexes. The V-50 NMR chemical shifts for the seven-coordinate complexes XV(CO)npm have been used to arrange the ligands X in a magnetochemical series of ligand strengths (alkenyl congruent-to alkyl < SiMe3 < H congruent-to Br congruent-to I < O2CR < Cl congruent-to N3 < CN).
    DOI:
    10.1016/0022-328x(94)80199-1
点击查看最新优质反应信息

文献信息

  • Electron-transfer processes with substituted group 5 metal carbonyls. Synthesis, crystal and molecular structure of Ag3M3(CO)12(Me2PCH2CH2PMe2)3, M = Nb, Ta, the first structurally characterized carbonyl derivatives of niobium(0) and tantalum(0)
    作者:Fausto Calderazzo、Guido Pampaloni、Ullrich Englert、Joachim Strähle
    DOI:10.1016/0022-328x(90)85121-e
    日期:1990.2
    Some new tetracarbonyl derivatives of tantalum(I), TaI(CO)4LL (LL = tmeda, dppm, 2,2′-dipy), have been obtained by diiodine oxidation of [Ta(CO)6]− in the presence of the bidentate ligand.
    (I)的一些新的四羰衍生物,TAI(CO)4 LL(LL = TMEDADPPM,2,2'-枇),已经通过二氧化得到[TA(CO)6 ] -在存在二齿配体
  • Synthesis of hexacarbonyl derivatives of Group 5 metals and electron-transfer processes. Crystal and molecular structure of tetracarbonyl[1,2-bis(diphenylphosphino)ethane]iodotantalum
    作者:Fausto. Calderazzo、Guido. Pampaloni、Giancarlo. Pelizzi、Francesca. Vitali
    DOI:10.1021/om00095a011
    日期:1988.5.1
查看更多