| 138234-26-1

• CAS: 138234-26-1
• 化学式: C₂₀H₄₂P₂Pd
• 分子量: 452.905
• InChiKey: UIVYOZMCPIECGT-FGULQQBVSA-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

• 作为反应物：
  描述：

  (d(t)bpe)Pd(ethene) 、 以 乙醚 为溶剂， 生成
  参考文献：
  名称：

  (R2PC2H4PR2)Pd0 alkene and ethyne complexes

  摘要：

  The palladium eta(3)-allyl complex Pd(eta(3)-C3H5)2 reacts with bidentate phosphanes iPr2PC2H4PiPr2 and tBu2PC2H4PtBu2 below -30-degrees-C to yield the light yellow, microcrystalline palladium(II) eta(1)-allyl compounds (R2PC2H4PR2)Pd(eta(1)-C3H5)2 (R = (i)Pr (1), (t)Bu (2)), which are stable to about -30-degrees-C. Above -30-degrees-C, the allyl substituents of 1 and 2 couple with reduction of palladium to form a mixture of (R2PC2H4PR2)Pd0 1,5-hexadiene complexes. When this reaction is carried out in 1,5-hexadiene, the complexes (R2PC2H4PR2)Pd(eta(2)-C6H10) (R = (i)Pr (3), (t)Bu (4)) are obtained in pure form. According to IR and NMR spectral data, the palladium atoms in 3 and 4 are coordinated at low temperature by the chelating diphosphane and (statically) by one of the two diene double bonds in a trigonal-planar geometry. At higher temperatures, a rapid exchange of the coordinated and uncoordinated double bonds occurs, passing through an intermediate with C2 symmetry. When suspensions of 1 in pentane and 2 in THF are warmed to 20-degrees-C, dinuclear diastereomers rac-/meso-{(R2PC2H4PR2)Pd}2(mu-eta(2):eta(2)-C6H10) (R = (i)Pr (5a,b), (t)Bu (6a,b)) are obtained, which upon treatment with 1,5-hexadiene furnish mononuclear derivatives 3 and 4. Similarly, when 1 is reacted with 1,5-cyclooctadiene at 20-degrees-C, the mono- and dinuclear interconvertible complexes ((i)Pr2PC2H4P(i)Pr2)Pd(eta(2)-C8H12) (7) and {((i)Pr2PC2H4P(i)Pr2)Pd}2(mu-eta(2):eta(2)-C8H12) (8) are produced. From the reaction of 1 and 2 with ethene, stable complexes (R2PC2H4PR2)Pd(C2H4) (R = (i)Pr (9), colorless; R = (t)Bu (10), tan) result. The colorless mononuclear palladium(0) ethyne complexes (R2PC2H4PR2)Pd(C2H2) (R = (i)Pr (11), (t)Bu (12)) may be prepared (a) by a displacement reaction of one of the isolated alkene complexes with ethyne, (b) by a reductive elimination and concomitant displacement reaction of the eta(1)-allyl complexes 1 and 2 with ethyne, or (c) in a one-pot synthesis from either Pd(eta(3)-C3H5)2 or Pd(eta(3)-2-MeC3H4)2 with (i)Pr2PC2H4P(i)Pr2 or (t)Bu2PC2H4P(t)Bu2, respectively, and ethyne in excess. When the mononuclear ethyne complexes 11 and 12 are combined with an equimolar amount of the corresponding eta(1)-allyl complex 1 or 2, or the alkene complexes (especially the mononuclear 1,5-hexadiene (3, 4) or ethene (9, 10) derivatives), yellow dinuclear palladium(0) complexes {(R2PC2H4PR2)Pd}2(mu-C2H2) (R = (i)Pr (13), (t)Bu (14)) are produced, in which the ethyne ligand bridges two palladium atoms. All the (diphosphane)palladium(0) alkene (3-10) and ethyne complexes (11-14) exhibit a trigonal-planar coordination geometry about the palladium atom. Most of the compounds have been isolated in high yield.

  DOI：

  10.1021/om00039a023
• 作为产物：
  描述：

  乙炔-1,2-D2 、 以 乙醚 为溶剂， 生成
  参考文献：
  名称：

  (R2PC2H4PR2)Pd0 alkene and ethyne complexes

  摘要：

  The palladium eta(3)-allyl complex Pd(eta(3)-C3H5)2 reacts with bidentate phosphanes iPr2PC2H4PiPr2 and tBu2PC2H4PtBu2 below -30-degrees-C to yield the light yellow, microcrystalline palladium(II) eta(1)-allyl compounds (R2PC2H4PR2)Pd(eta(1)-C3H5)2 (R = (i)Pr (1), (t)Bu (2)), which are stable to about -30-degrees-C. Above -30-degrees-C, the allyl substituents of 1 and 2 couple with reduction of palladium to form a mixture of (R2PC2H4PR2)Pd0 1,5-hexadiene complexes. When this reaction is carried out in 1,5-hexadiene, the complexes (R2PC2H4PR2)Pd(eta(2)-C6H10) (R = (i)Pr (3), (t)Bu (4)) are obtained in pure form. According to IR and NMR spectral data, the palladium atoms in 3 and 4 are coordinated at low temperature by the chelating diphosphane and (statically) by one of the two diene double bonds in a trigonal-planar geometry. At higher temperatures, a rapid exchange of the coordinated and uncoordinated double bonds occurs, passing through an intermediate with C2 symmetry. When suspensions of 1 in pentane and 2 in THF are warmed to 20-degrees-C, dinuclear diastereomers rac-/meso-{(R2PC2H4PR2)Pd}2(mu-eta(2):eta(2)-C6H10) (R = (i)Pr (5a,b), (t)Bu (6a,b)) are obtained, which upon treatment with 1,5-hexadiene furnish mononuclear derivatives 3 and 4. Similarly, when 1 is reacted with 1,5-cyclooctadiene at 20-degrees-C, the mono- and dinuclear interconvertible complexes ((i)Pr2PC2H4P(i)Pr2)Pd(eta(2)-C8H12) (7) and {((i)Pr2PC2H4P(i)Pr2)Pd}2(mu-eta(2):eta(2)-C8H12) (8) are produced. From the reaction of 1 and 2 with ethene, stable complexes (R2PC2H4PR2)Pd(C2H4) (R = (i)Pr (9), colorless; R = (t)Bu (10), tan) result. The colorless mononuclear palladium(0) ethyne complexes (R2PC2H4PR2)Pd(C2H2) (R = (i)Pr (11), (t)Bu (12)) may be prepared (a) by a displacement reaction of one of the isolated alkene complexes with ethyne, (b) by a reductive elimination and concomitant displacement reaction of the eta(1)-allyl complexes 1 and 2 with ethyne, or (c) in a one-pot synthesis from either Pd(eta(3)-C3H5)2 or Pd(eta(3)-2-MeC3H4)2 with (i)Pr2PC2H4P(i)Pr2 or (t)Bu2PC2H4P(t)Bu2, respectively, and ethyne in excess. When the mononuclear ethyne complexes 11 and 12 are combined with an equimolar amount of the corresponding eta(1)-allyl complex 1 or 2, or the alkene complexes (especially the mononuclear 1,5-hexadiene (3, 4) or ethene (9, 10) derivatives), yellow dinuclear palladium(0) complexes {(R2PC2H4PR2)Pd}2(mu-C2H2) (R = (i)Pr (13), (t)Bu (14)) are produced, in which the ethyne ligand bridges two palladium atoms. All the (diphosphane)palladium(0) alkene (3-10) and ethyne complexes (11-14) exhibit a trigonal-planar coordination geometry about the palladium atom. Most of the compounds have been isolated in high yield.

  DOI：

  10.1021/om00039a023