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

Pentakis[(pentafluoro-lambda6-tellanyl)oxy]-lambda5-arsane | 87197-53-3

中文名称
——
中文别名
——
英文名称
Pentakis[(pentafluoro-lambda6-tellanyl)oxy]-lambda5-arsane
英文别名
pentakis[(pentafluoro-λ6-tellanyl)oxy]-λ5-arsane
Pentakis[(pentafluoro-lambda6-tellanyl)oxy]-lambda5-arsane化学式
CAS
87197-53-3
化学式
AsF25O5Te5
mdl
——
分子量
1267.88
InChiKey
NYXUDIGAOKYTBR-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):
    7.88
  • 重原子数:
    36
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    46.2
  • 氢给体数:
    0
  • 氢受体数:
    30

反应信息

  • 作为反应物:
    描述:
    Pentakis[(pentafluoro-lambda6-tellanyl)oxy]-lambda5-arsane 以 further solvent(s) 为溶剂, 以60%的产率得到tetramethylammonium hexakis((pentafluoro-l6-tellaneyl)oxy)arsenate(V)
    参考文献:
    名称:
    Hexakis(pentafluorooxotellurato)pnictate(V) Anions, M(OTeF5)6- (M = As, Sb, Bi): A Series of Very Weakly Coordinating Anions
    摘要:
    The weakly coordinating pnicogen anion series, M(OTeF5)(6-) (M = As, Sb, Bi), has been synthesized as their tetraalkylammonium salts and have been structurally characterized by X-ray crystallography, F-19, As-75, Sb-121,Sb-123, Te-125, Bi-209 NMR spectroscopy, and Raman spectroscopy. The following crystal structures are reported: N(CH3)(4)As-+(OTeF5)(6-), trigonal system, space group , a = 10.109(2) Angstrom, c = 55.443(18) Angstrom, V = 4907 Angstrom(3), D-calc = 3.209 g cm(-3), Z = 6, R = 0.0644; N(CH3)(4)Sb-+(OTeF5)(6-), monoclinic system, space group: C2/c, a = 17.875(3) Angstrom, b = 10.448(2) Angstrom, c = 19.752(2) Angstrom, beta = 110.83(1)degrees, V = 3447.8 Angstrom(3), D-calc = 3.135 g cm(-3), Z = 4, R = 0.0710; N(CH2CH3)(4)Sb-+(OTeF5)(6-), monoclinic system,space group C2/c, a = 10.506(3) Angstrom, b = 18.370(6) Angstrom, c = 20.352(7) Angstrom, beta = 91.23(2)degrees, V = 3926.9 Angstrom(3), D-calc = 2.848 g cm(-3), Z = 4, R = 0.0548; N(CH3)(4)Bi-+(OTeF5)(6-), triclinic system, space group , a = 8.945(2) Angstrom, b = 9.217(2) Angstrom, c = 10.029(2) Angstrom, alpha = 100.03(3)degrees, beta = 99.95(3)degrees, gamma = 98.06(3)degrees, V = 789.5 Angstrom(3), D-calc = 3.606 g cm(-3), Z = 1, R = 0.0456. The central pnicogen atoms of the anions are bonded octahedrally to the six oxygen atoms and each of the six tellurium atoms is octahedrally bonded to an oxygen and five fluorines. Each anion structure can be described as composed of an octahedron of octahedra. Average M-O bond distances (corrected for libration) and M-O-Te bond angles are As-O = 1.807 Angstrom, Sb-O = 1.96/1.91 Angstrom, Bi-O = 2.065 Angstrom and As-O-Te = 140(2)degrees, Sb-O-Te = 150.9(8)/162.8(9)degrees, Bi-O-Te = 136.2(3)degrees. Low electric field gradients at the pnicogen nuclei result in spin-lattice relaxation times which are sufficiently long to allow for the observation of the NMR spectra of the four quadrupolar pnicogen nuclei and their couplings to Te-125. The anions are nonlabile on the NMR time scale in both SO2ClF and CH3CN solvents. Key frequencies,in the Raman spectra of the three anions have been assigned. The M(OTeF5)(6-) anions are likely to be weaker OTeF5- donors and less basic than,current examples of weakly coordinating anion derivatives of the OTeF5 group, i.e., B(OTeF5)(4-), Pd(OTeF5)(4)(2-), Nd(OTeF5)(6-) and Ti(OTeF5)(6)(2-).
    DOI:
    10.1021/ja00086a025
  • 作为产物:
    描述:
    xenon bis(pentafluorotellurate)Tris(pentafluoro-lambda6-tellanyl) arsorite 以 further solvent(s) 为溶剂, 以12%的产率得到Pentakis[(pentafluoro-lambda6-tellanyl)oxy]-lambda5-arsane
    参考文献:
    名称:
    Lentz, D.; Seppelt, K., Zeitschrift fur Anorganische und Allgemeine Chemie
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Tetrachloro- and Tetrabromoarsonium(V) Cations:  Raman and <sup>75</sup>As, <sup>19</sup>F NMR Spectroscopic Characterization and X-ray Crystal Structures of [AsCl<sub>4</sub>][As(OTeF<sub>5</sub>)<sub>6</sub>] and [AsBr<sub>4</sub>][AsF(OTeF<sub>5</sub>)<sub>5</sub>]
    作者:Michael Gerken、Peter Kolb、Andreas Wegner、Hélène P. A. Mercier、Horst Borrmann、David A. Dixon、Gary J. Schrobilgen
    DOI:10.1021/ic000118g
    日期:2000.6.1
    The salts [AsX4][As(OTeF5)6] and [AsBr4][AsF(OTeF5)5] (X = Cl, Br) have been prepared by oxidation of AsX3 with XOTeF5 in the presence of the OTeF5 acceptors As(OTeF5)5 and AsF(OTeF5)4. The mixed salts [AsCl4][Sb(OTeF5)6-nCl(n-2)] and [AsCl4][Sb(OTeF5)6-nCl(n)] (n > or = 2) have also been prepared. The AsBr4+ cation has been fully structurally characterized for the first time in SO2ClF solution by
    盐[AsX4] [As(OTeF5)6]和[AsBr4] [AsF(OTeF5)5](X = Cl,Br)是通过在OTeF5受体As(OTeF5)存在下用XOTeF5氧化AsX3制备的。 5和AsF(OTeF5)4。还制备了混合盐[AsCl4] [Sb(OTeF5)6-nCl(n-2)]和[AsCl4] [Sb(OTeF5)6-nCl(n)](n>或= 2)。通过[AsAsBr4] [AsF(OTeFs)5]的单晶X射线衍射研究,首次在SO2ClF溶液中通过75As NMR光谱对AsBr4 +阳离子进行了全面结构表征,并在固态下对AsBr4 +阳离子进行了结构表征。 9.778(4)A,b = 17.731(7)A,c = 18.870(8)A,alpha = 103.53(4)度,beta = 103.53(4)度,γ= 105.10(4)度,V = 2915( 2)在-183℃下,A3,Z
  • Collins, Michael J.; Schrobilgen, Gary J., Inorganic Chemistry, 1985, vol. 24, # 17, p. 2608 - 2614
    作者:Collins, Michael J.、Schrobilgen, Gary J.
    DOI:——
    日期:——
查看更多