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Triethinylphosphin | 687-80-9

中文名称
——
中文别名
——
英文名称
Triethinylphosphin
英文别名
Triethynylphosphane
Triethinylphosphin化学式
CAS
687-80-9
化学式
C6H3P
mdl
——
分子量
106.064
InChiKey
BAOONLPEQZTTSS-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    7
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    K[arachno-B9H14] 、 Triethinylphosphin 在 HCl 作用下, 以 乙醚 为溶剂, 以38%的产率得到[arachno-B9H13-4-P(CCH)3]
    参考文献:
    名称:
    Structural Chemistry of arachno-Nonaboranes
    摘要:
    Single-crystal conventional-tube and synchrotron X-ray diffraction studies of the anions in [NMe4]-[arachno-B9H12-4,8-Br-2] 1 and K[arachno-B9H14] 2, and also of the series of adducts [arachno-B9H13-4-L], where L is P(CCH)(3) (3), NHEt2 (4), NC5H5 (5), or NH2CH2Ph (6), are reported. Structural studies of 1-6, determined at low temperatures, located all atoms, including bridging and endo-terminal hydrogen atoms. The basic boron-hydride clusters of these, and of all the other known species with the arachno nine-vertex i-nonanborane geometry reported in the literature, are isostructural and feature three bridging and two endo-terminal hydrogen atoms on the open face. This arrangement is different from that previously reported for Cs[arachno-B9H14] 7 and for [arachno-B9H13-4-(NCMe)] 9. However, a new X-ray diffraction data set and refinement experimentally confirm the {3 x mu-H, 2 x endo} arrangement for 9 also. The experimental results for 1-6 support recently reported calculations for [B9H14](-), which predict both the structures and the B-11 NMR chemical shifts. These conclusions are also supported by calculations for 3, 4, and 9 and also for the [arachno-B9H13-4-(NCS)](-) anion in [NMe4][B9H13(NCS)] 8.
    DOI:
    10.1021/ja025700d
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文献信息

  • Unusual, Bifurcated Photoreactivity of a Rhenium(I) Carbonyl Complex of Triethynylphosphine
    作者:Sean E. Hightower、Robert C. Corcoran、B. Patrick Sullivan
    DOI:10.1021/ic050901e
    日期:2005.12.1
    Preparations of the first metal complexes of triethynylphosphine (TEP) are described. They are of the type fac-Re(bpy)(CO)(3)(TEP)(+) (1) and cis,trans-[Re(bpy)(CO)(2)(TEP)L](n)(+) (CH(3)CN, n = 1, complex 2; Cl, n = 0, complex 3), where bpy is 2,2'-bipyridine. Complex 1 displays unusual photochemical behavior compared to analogous fac-[Re(bpy)(CO)(3)(PR(3))](+) complexes in that it emits from a state
    描述了三乙炔基膦(TEP)的第一金属配合物的制备。它们的类型为fac-Re(bpy)(CO)(3)(TEP)(+)(1)和cis,trans- [Re(bpy)(CO)(2)(TEP)L](n) (+)(CH(3)CN,n = 1,络合物2; Cl,n = 0,络合物3),其中bpy是2,2'-联吡啶。与类似的fac- [Re(bpy)(CO)(3)(PR(3))](+)配合物相比,配合物1显示出不同寻常的光化学行为,因为它从具有pi-pi *特性的状态发出光,但经历竞争TEP和CO的光饱和性。密度泛函理论(DFT)/随时间变化的DFT计算预测,最低的发射状态实际上应该具有pi-pi *特征。
  • Compounds for the Inhibition of Cellular Proliferation
    申请人:Chorev Michael
    公开号:US20130178505A1
    公开(公告)日:2013-07-11
    Compositions and methods for inhibiting translation are provided. Compositions, methods and kits for treating (1) cellular proliferative disorders, (2) non-proliferative, degenerative disorders, (3) viral infections, (4) disorders associated with viral infections, and/or (5) non-proliferative metabolic disorders such as type II diabetes where inhibition of translation initiation is beneficial using the compounds disclosed herein.
    提供了抑制翻译的组合物和方法。本文披露的化合物可用于治疗以下疾病:(1)细胞增殖性疾病,(2)非增殖性退行性疾病,(3)病毒感染,(4)与病毒感染有关的疾病,以及(5)非增殖性代谢性疾病,如II型糖尿病,其中抑制翻译起始有益。本文还提供了用于治疗上述疾病的方法和试剂盒。
  • US8969573B2
    申请人:——
    公开号:US8969573B2
    公开(公告)日:2015-03-03
  • Structural Chemistry of <i>arachno</i>-Nonaboranes
    作者:Jonathan Bould、Robert Greatrex、John D. Kennedy、Daniel L. Ormsby、Michael G. S. Londesborough、Karen L. F. Callaghan、Mark Thornton-Pett、Trevor R. Spalding、Simon J. Teat、William Clegg、Hong Fang、Nigam P. Rath、Lawrence Barton
    DOI:10.1021/ja025700d
    日期:2002.6.1
    Single-crystal conventional-tube and synchrotron X-ray diffraction studies of the anions in [NMe4]-[arachno-B9H12-4,8-Br-2] 1 and K[arachno-B9H14] 2, and also of the series of adducts [arachno-B9H13-4-L], where L is P(CCH)(3) (3), NHEt2 (4), NC5H5 (5), or NH2CH2Ph (6), are reported. Structural studies of 1-6, determined at low temperatures, located all atoms, including bridging and endo-terminal hydrogen atoms. The basic boron-hydride clusters of these, and of all the other known species with the arachno nine-vertex i-nonanborane geometry reported in the literature, are isostructural and feature three bridging and two endo-terminal hydrogen atoms on the open face. This arrangement is different from that previously reported for Cs[arachno-B9H14] 7 and for [arachno-B9H13-4-(NCMe)] 9. However, a new X-ray diffraction data set and refinement experimentally confirm the 3 x mu-H, 2 x endo} arrangement for 9 also. The experimental results for 1-6 support recently reported calculations for [B9H14](-), which predict both the structures and the B-11 NMR chemical shifts. These conclusions are also supported by calculations for 3, 4, and 9 and also for the [arachno-B9H13-4-(NCS)](-) anion in [NMe4][B9H13(NCS)] 8.
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