1-(diphenylphosphino)cyclopropane carbonitrile | 413570-90-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1-(diphenylphosphino)cyclopropane carbonitrile
• 英文别名: (1-diphenylphosphino)cyclopropanecarbonitrile；1-diphenylphosphanylcyclopropane-1-carbonitrile
• CAS: 413570-90-8
• 化学式: C₁₆H₁₄NP
• 分子量: 251.268
• InChiKey: ARLSGFFPOZTIBM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  23.8
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer 、 1-(diphenylphosphino)cyclopropane carbonitrile 以 二氯甲烷 为溶剂， 以76%的产率得到[[1-(diphenylphosphino)cyclopropane carbonitrile]pentamethylcyclopentadienyl] rhodium dichloride
  参考文献：
  名称：

  Novel functionalised P-ligands: advances and application

  摘要：

  Novel endo- and exocyclic phosphine ligands possessing different functionalities obtained by reduction of the P=O precursors with desired stereochemistry are discussed. The diastereoselective deoxygenation including the catalytic reduction processes, the factors defining the reactivity and the role of the substituents on the stability of phosphorus atom configuration in a series of 3-aryl-3-phosphabicyclo[3.1.0]hexanes are reported. The complexation features of the ligands with Rh(III) and Pd(II) were examined and Rh(III) complexes were tested in styrene hydroformylation showing the structure-activity dependence. (c) 2004 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jorganchem.2004.09.030
• 作为产物：
  描述：

  (二苯基磷酰)乙腈 在 phase-transfer catalysts 三氯硅烷 作用下， 以 苯 为溶剂， 反应 15.0h， 生成 1-(diphenylphosphino)cyclopropane carbonitrile
  参考文献：
  名称：

  Vinogradova, Natalya M.; Odinets, Irene L.; Lyssenko, Konstantin A., Mendeleev Communications, 2001, # 6, p. 219 - 221

  摘要：

  DOI：

文献信息

• Novel functionalised P-ligands: advances and application
  作者：Irina L. Odinets、Natalya M. Vinogradova、Ekaterina V. Matveeva、Denis D. Golovanov、Konstantin A. Lyssenko、György Keglevich、László Kollár、Gerd-Volker Roëschenthaler、Tatyana A. Mastryukova

  DOI：10.1016/j.jorganchem.2004.09.030

  日期：2005.5

  Novel endo- and exocyclic phosphine ligands possessing different functionalities obtained by reduction of the P=O precursors with desired stereochemistry are discussed. The diastereoselective deoxygenation including the catalytic reduction processes, the factors defining the reactivity and the role of the substituents on the stability of phosphorus atom configuration in a series of 3-aryl-3-phosphabicyclo[3.1.0]hexanes are reported. The complexation features of the ligands with Rh(III) and Pd(II) were examined and Rh(III) complexes were tested in styrene hydroformylation showing the structure-activity dependence. (c) 2004 Elsevier B.V. All rights reserved.
• Vinogradova, Natalya M.; Odinets, Irene L.; Lyssenko, Konstantin A., Mendeleev Communications, 2001, # 6, p. 219 - 221
  作者：Vinogradova, Natalya M.、Odinets, Irene L.、Lyssenko, Konstantin A.、Pasechnik, Margarita P.、Petrovskii, Pavel V.、Mastryukova, Tatyana A.

  DOI：——

  日期：——