| 123320-90-1

• CAS: 123320-90-1
• 化学式: C₅O₅W
• 分子量: 323.902
• InChiKey: CMSMPIUUMUBBFW-UHFFFAOYSA-N

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：

  {bis(triphenylphosphine)nitrogen}{HW(CO)5} 以 neat (no solvent, solid phase) 为溶剂， 生成
  参考文献：
  名称：

  Hynes, Rosemary C.; Preston, Keith F.; Springs, Jerry J., Organometallics, 1990, vol. 9, # 8, p. 2298 - 2304

  摘要：

  DOI：

文献信息

• Electrochemistry of phosphaferrocenes
  作者：Paul Lemoine、Maurice Gross、Pierre Braunstein、François Mathey、Bernard Deschamps、John H. Nelson

  DOI：10.1016/0022-328x(85)80271-0

  日期：1985.11

  The redox behaviour of a series of heterometallic phosphaferrocenes (hereafter refered to as I, II and III) has been studied in propylene carbonate containing 0.1 M (C2H5)4N+ ClO4− both mercury and platinum electrodes.

  一系列异金属phosphaferrocenes（以下refered为I，II和III）的氧化还原行为已经在含有0.1碳酸丙烯酯被研究中号（C 2 H ^ 5）4 Ñ + CLO 4 -既汞和铂电极。
• Dissociative electron attachment reactions of transition metal carbonyls and their apparent influence on the thermalization of electrons by CO₂
  作者：Patricia M. George、J. L. Beauchamp

  DOI：10.1063/1.443389

  日期：1982.3.15

  Dissociative electron attachment rates are measured for the transition metal carbonyls V(CO)6, Cr(CO)6, Fe(CO)5, Ni(CO)4, Mo(CO)6, and W(CO)6. Rates are measured as a function of the pressure of CO2 added to relax epithermal electrons. Derived thermal rate constants for the formation of M(CO)−n−1 from M(CO)n are 0.6, 3.0, 2.0, 2.0, 1.3, and 1.2×10−7 cm3 molecule−1 s−1, respectively. The differences in these rate constants may be attributed to the different stabilities of the molecular anion with regard to dissociation versus autodetachment. The measured rate of thermalization of electrons by CO2 varies with the metal carbonyl used and depends on the variation of the dissociative electron capture cross section with electron energy. Each system is thus tightly coupled in that the electron energy distribution is determined not only by collisional processes involving CO2 but varies as well with the energy dependent depletion of the distribution by reactant species.