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Tris(3-diethylphosphanylpropyl)phosphane | 93254-31-0

中文名称
——
中文别名
——
英文名称
Tris(3-diethylphosphanylpropyl)phosphane
英文别名
——
Tris(3-diethylphosphanylpropyl)phosphane化学式
CAS
93254-31-0
化学式
C21H48P4
mdl
——
分子量
424.507
InChiKey
YEMSPHOMKPUVDN-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:
    499.7±40.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    25
  • 可旋转键数:
    18
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

点击查看最新优质反应信息

文献信息

  • Carbonylvanadates, hydrido- and alkyl-carbonylvanadium complexes containing alkylated oligophosphines as ancillary ligands
    作者:Frank Süssmilch、Wolfgang Glöckner、Dieter Rehder
    DOI:10.1016/0022-328x(90)85351-x
    日期:1990.5
    ionic complexes cis-[Et4N][V(CO)4pm] (pm = m-dentate phosphine: Cy2PCH2CH2PCy2; RP(CH2CH2CH2PR2′)2 with R/R′ = Me/Me, Me/Et, Et/Et; P(CH2CH2CH2PEt2)3] have been prepared. Isomers with 6- and 10-membered chelate rings are present in the case of p3 (51V NMR evidence). Ion exchange on silica gel yields HV(CO)4p2, HV(CO)3pm (m = 3, 4), which, for m = 4, can be converted photochemically into cis-[HV(CO)2p4]
    离子络合物顺式-[Et 4 N] [V(CO)4 p m ](p m = m-齿状膦:Cy 2 PCH 2 CH 2 PCy 2; RP(CH 2 CH 2 CH 2 PR 2 ')2(R / R'= Me / Me,Me / Et,Et / Et; P(CH 2 CH 2 CH 2 PEt 2)3 ]的制备。在这种情况下,存在具有6-和10-元螯合环的异构体之p 3(511 H NMR证据)。在硅胶上进行离子交换可得到HV(CO)4 p 2,HV(CO)3 p m(m = 3,4),对于m = 4,可以将其光化学转化为顺式-[HV(CO)2 p 4 ]。在1个中所述氢化物区域H NMR图案指示的面部封端的八面体与所述封盖H的行动不便- 。[Et 4 N] [V(CO)4 dppe]与RI(R = Me,i-Pr,t-Bu,SiMe 3)之间的反应导致RV(CO)4 dppe(δ(51 V)-1032至相对于VOCl
  • ∑-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
    作者:Frank Süßmilch、Falk Olbrich、Hartmut Gailus、Dieter Rodewald、Dieter Rehder
    DOI:10.1016/0022-328x(94)80199-1
    日期:1994.6
    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).
  • Aspects of carbonyltantalum chemistry
    作者:Michael Fornalczyk、Frank Süssmilch、Wolfgang Priebsch、Dieter Rehder
    DOI:10.1016/0022-328x(92)83042-g
    日期:1992.3
    UV irradiation of [Et4N][Ta(CO)6] in the presence of 2- to 4-dentate phosphines, p(n), yields [Et4N][Ta(CO)4pn]. Ion exchange chromatography on silica gel affords the hydrido complexes HTa(CO)4p2 or HTa(CO)3pn (n = 3, 4), which can be photochemically converted into HTa(CO)2pn. The structure in solution as judged from spectroscopic data is probably an octahedron capped by the hydride. In the solid state, an X-ray diffraction study of trans-[HTa(CO)2(dppe)2] indicates the presence of a pentagonal bipyramid with H-, Ta and the four P in the pentagonal plane. 2-methyl-2-butene is "hydrotantalated", mainly in the anti-Markovnikov manner, to yield the sigma-alkyl complex Me2CH-H(Me)CTa(CO)4p2 (p2 = Ph2PCH2CH2PEt2). The complexes HTa(CO)4/3pn react with pentafulvenes to form eta-5-(C5H4CHR2)Ta(CO)2pn (R2 = Me2, Ph2, NMe2 + H; p(n) = PhP(CH2CH2 PPh2)2). The hepta-coordinated chloride complexes ClTa(CO)6-npn have been prepared photochemically from [Et4N]Cl and HTa(CO)4pn (n = 4, p(n) = 2 dppe), or by reductive carbonylation of TaCl4 in the presence of p(n) (n = 3, p(n) = MeP(CH2CH2CH2PMe2)2).
  • COMPOSITION AND POLYMER
    申请人:Asahi Kasei Kabushiki Kaisha
    公开号:EP2735581B1
    公开(公告)日:2021-07-14
  • Composition and Polymer
    申请人:Nakamura Akitake
    公开号:US20140121293A1
    公开(公告)日:2014-05-01
    Disclosed is a composition comprising (A) at least one compound selected from the group consisting of an ether compound having two or more ether groups, a trivalent phosphorus compound, and a ketone compound, (B) a boron trihalide, and (C) an episulfide compound.
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