platinum hexafluoride

• 分子结构分类: 无机化合物 - 混合金属/非金属化合物 - 过渡金属盐
• 英文名称: platinum hexafluoride
• 英文别名: platinum;hexahydrofluoride
• 化学式: F₆Pt
• 分子量: 309.07
• InChiKey: XUPHULNDUQKGOT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.91
• 重原子数：
  7.0
• 可旋转键数：
  0.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  0.0
• 氢给体数：
  0.0
• 氢受体数：
  0.0

反应信息

• 作为反应物：
  描述：

  钚 、 platinum hexafluoride 生成 六氟化钚
  参考文献：
  名称：

  Platinum hexafluoride and method of fluorinating plutonium containing mixtures therewith

  摘要：

  公开号：

  US02893826A1
• 作为产物：
  描述：

  fluorine 、 铂 以 neat (no solvent) 为溶剂， 生成 platinum hexafluoride
  参考文献：
  名称：

  Time‐of‐flight neutron powder diffraction study on the third row transition metal hexafluorides WF₆, OsF₆, and PtF₆

  摘要：

  A neutron diffraction study on the third-row transition metal hexafluorides MF6 (M≡W, Os, Pt) has been performed using the high resolution neutron powder diffractometer (HRPD) at the spallation source ISIS, England. The previously unknown structures of the low-temperature phases of OsF6 and PtF6 are reported. WF6, OsF6, and PtF6, which exhibit a (5dt2g)0, (5dt2g)2, and (5dt2g)4 electronic configuration, respectively, are found to be isostructural and crystallize in the UF6 structure, space group Pmnb, (No. 62). The geometry of the MF6 molecules is to good approximation octahedral for each compound, the mean M–F bond length increasing only slightly from 182.5 (W) to 185.0 (Pt). For WF6 deviations from ideal octahedral geometry are only marginally significant [181.8(2) to 183.2(2) pm] and may be interpreted on the basis of packing effects. Deviations for the d2 complex OsF6 are somewhat larger [181.5(2) to 184.4(3) pm] and may be assumed to be caused by packing effects essentially the same as for WF6, in addition to a first-order Jahn–Teller effect arising from the (5dt2g)2 electronic configuration. While eliminating the effects of packing by a comparison of individual M–F bond lengths for WF6 and OsF6, the OsF6 molecule shows to have D4h symmetry with two apical M–F bonds about 1.8 pm longer than the four equatorial bonds as a result of the Jahn–Teller distortion. Only small deviations from ideal octahedral geometry [184.4(3) to 185.8(3) pm] are found for the d4 complex PtF6. Within the series W to Pt a substantial shortening of the F...F van der Waals contact distances is observed. This shortening more than compensates for the increase in the M–F bond lengths and leads to unit cell volumes and cell parameters decreasing continuously from W to Pt. The variation of F...F contact distances and M–F bond lengths may be rationalized in terms of polarization of the F-ligands in the field of the highly charged nuclei of the central atoms which are only incompletely shielded by the 5d electrons.

  DOI：

  10.1063/1.471473

文献信息

• Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Np: TrU.C, 5, page 100 - 128
  作者：

  DOI：——

  日期：——
• Time‐of‐flight neutron powder diffraction study on the third row transition metal hexafluorides WF₆, OsF₆, and PtF₆
  作者：R. Marx、K. Seppelt、R. M. Ibberson

  DOI：10.1063/1.471473

  日期：1996.5.15

  A neutron diffraction study on the third-row transition metal hexafluorides MF6 (M≡W, Os, Pt) has been performed using the high resolution neutron powder diffractometer (HRPD) at the spallation source ISIS, England. The previously unknown structures of the low-temperature phases of OsF6 and PtF6 are reported. WF6, OsF6, and PtF6, which exhibit a (5dt2g)0, (5dt2g)2, and (5dt2g)4 electronic configuration, respectively, are found to be isostructural and crystallize in the UF6 structure, space group Pmnb, (No. 62). The geometry of the MF6 molecules is to good approximation octahedral for each compound, the mean M–F bond length increasing only slightly from 182.5 (W) to 185.0 (Pt). For WF6 deviations from ideal octahedral geometry are only marginally significant [181.8(2) to 183.2(2) pm] and may be interpreted on the basis of packing effects. Deviations for the d2 complex OsF6 are somewhat larger [181.5(2) to 184.4(3) pm] and may be assumed to be caused by packing effects essentially the same as for WF6, in addition to a first-order Jahn–Teller effect arising from the (5dt2g)2 electronic configuration. While eliminating the effects of packing by a comparison of individual M–F bond lengths for WF6 and OsF6, the OsF6 molecule shows to have D4h symmetry with two apical M–F bonds about 1.8 pm longer than the four equatorial bonds as a result of the Jahn–Teller distortion. Only small deviations from ideal octahedral geometry [184.4(3) to 185.8(3) pm] are found for the d4 complex PtF6. Within the series W to Pt a substantial shortening of the F...F van der Waals contact distances is observed. This shortening more than compensates for the increase in the M–F bond lengths and leads to unit cell volumes and cell parameters decreasing continuously from W to Pt. The variation of F...F contact distances and M–F bond lengths may be rationalized in terms of polarization of the F-ligands in the field of the highly charged nuclei of the central atoms which are only incompletely shielded by the 5d electrons.
• Platinum hexafluoride and method of fluorinating plutonium containing mixtures therewith
  申请人：MALM JOHN G

  公开号：US02893826A1

  公开（公告）日：1959-07-07