(1-phenyl-3,4-dimethylphosphole)2PdBr2 | 72402-88-1

• 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-phenyl-3,4-dimethylphosphole)2PdBr2
• 英文别名: dibromopalladium;3,4-dimethyl-1-phenylphosphole
• CAS: 72402-88-1；122170-82-5；72442-19-4
• 化学式: C₂₄H₂₆Br₂P₂Pd
• 分子量: 642.646
• InChiKey: JAWJBZGAWCOAOG-UHFFFAOYSA-L

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：

  (1-phenyl-3,4-dimethylphosphole)2PdBr2 以 丙酮 为溶剂， 生成 cis-dibromobis(1-phenyl-3,4-trimethylphosphole)palladium(II)
  参考文献：
  名称：

  Thermal Coupling Reactions of 1-Phenyl-3,4-dimethylphosphole within the Coordination Sphere of Palladium(II)

  摘要：

  The thermolyses of dihalobis(1-phenyl-3,4-dimethylphosphole)palladium(II) complexes [(DMPP)(2)PdX(2), X = Cl, Br, I] were investigated in 1,1,2,2-tetrachloroethane solutions at 145 degrees C and in the crystalline state at 140 OC. For cis-(DMPP)(2) PdCl2 and cis- or trans-(DMPP)(2) PdBr2 four types of products were formed: (1) [4 + 2] cycloaddition products, (2) [2 + 2] cycloaddition products, (3) compounds that result from 1,5-hydrogen migration from a methyl group on one phosphole to the beta-carbon of an adjacent phosphole (exo-methylene), and (4) products that result from an intermolecular [4 + 2] coupling of two phospholes followed sequentially by phosphinidene elimination and intramolecular [4 + 2] cycloaddition to another phosphole to give diphosphatetracyclotetradecatrienes (DPTCT). trans-(DMPP)(2)PdBr2 undergoes thermal isomerization to cis-(DMPP)(2)PdBr2 in the solid state, and cis- and trans-(DMPP)2PdBr2 give the same products in both their solid- and solution-slate thermolyses. In contrast, trans-(DMPP)(2) PdI2 neither isomerizes to the cis-isomer nor undergoes any of the phosphole coupling reactions in either the solution or solid state. The crystal structures of trans-(DMPP)(2)PdX(2) (X = Br, I), {(DMPP)(2)[2 + 2]}PdBr2, {(DMPP)(2)(exo-methylene)}PdBr2, and (DPTCT)PdCL(2) were determined. They crystallize in the monoclinic P2(1)/c, triclinic P (1) over bar, monoclinic P2(1)/c, monoclinic P2(1)/n, and orthorhombic P2(1)2(1)2(1) space groups in units cells of the following dimensions: a 10.158 (3) Angstrom, b = 14.876 (4) Angstrom, 16.829 (5) Angstrom, beta = 104.25 (2)degrees, rho(calc) 1.732 g/cm(3), Z = 4; a = 9.025(1) Angstrom, b = 11.023 (1) Angstrom, c 13.833 (1) Angstrom, alpha = 101.15 (1)degrees, beta = 98.82 (1)degrees, gamma = 105.30 (1)degrees, rho(calc) = 1,886 g/cm(3), Z = 2; a = 13.090 (2) Angstrom, b = 17.637 (2) Angstrom, c = 21.834 (2) Angstrom, beta = 100.51 (1)degrees, rho(calc) = 1.738 g/cm(3), Z = 4, a = 10.721 (1) Angstrom, b = 16.929 (1) Angstrom, c = 14.675(1) Angstrom, beta = 97.86 (1)degrees, rho(calc) = 1.663 g/cm(3), Z = 4; and a = 15.532 (3) Angstrom, b = 19.401 (4) Angstrom, c = 9.910 (2) Angstrom, rho(calc) = 1.490 g/cm(3), Z = 2, respectively. Least-squares refinements converged at final values of R(F) of 0.041, 0.0354, 0.0624, 0.0533, and 0.035 for 2770, 2672, 2729, 2159, and 2525 independent observed reflections, respectively. Kinetic studies suggest that the reaction mechanisms are the same in both the solid and solution states and that the reaction mechanisms are substantially different from those previously reported for the thermolyses of the analogous cis-(DMPP)(2)PtX(2) complexes.

  DOI：

  10.1021/ic951307f
• 作为产物：
  描述：

  potassium bromide 、 palladium dichloride 、 1-苯基-3,4-二甲基膦杂环戊二烯) 以 二氯甲烷 、 水 为溶剂， 以83.9%的产率得到(1-phenyl-3,4-dimethylphosphole)2PdBr2
  参考文献：
  名称：

  Thermal Coupling Reactions of 1-Phenyl-3,4-dimethylphosphole within the Coordination Sphere of Palladium(II)

  摘要：

  The thermolyses of dihalobis(1-phenyl-3,4-dimethylphosphole)palladium(II) complexes [(DMPP)(2)PdX(2), X = Cl, Br, I] were investigated in 1,1,2,2-tetrachloroethane solutions at 145 degrees C and in the crystalline state at 140 OC. For cis-(DMPP)(2) PdCl2 and cis- or trans-(DMPP)(2) PdBr2 four types of products were formed: (1) [4 + 2] cycloaddition products, (2) [2 + 2] cycloaddition products, (3) compounds that result from 1,5-hydrogen migration from a methyl group on one phosphole to the beta-carbon of an adjacent phosphole (exo-methylene), and (4) products that result from an intermolecular [4 + 2] coupling of two phospholes followed sequentially by phosphinidene elimination and intramolecular [4 + 2] cycloaddition to another phosphole to give diphosphatetracyclotetradecatrienes (DPTCT). trans-(DMPP)(2)PdBr2 undergoes thermal isomerization to cis-(DMPP)(2)PdBr2 in the solid state, and cis- and trans-(DMPP)2PdBr2 give the same products in both their solid- and solution-slate thermolyses. In contrast, trans-(DMPP)(2) PdI2 neither isomerizes to the cis-isomer nor undergoes any of the phosphole coupling reactions in either the solution or solid state. The crystal structures of trans-(DMPP)(2)PdX(2) (X = Br, I), {(DMPP)(2)[2 + 2]}PdBr2, {(DMPP)(2)(exo-methylene)}PdBr2, and (DPTCT)PdCL(2) were determined. They crystallize in the monoclinic P2(1)/c, triclinic P (1) over bar, monoclinic P2(1)/c, monoclinic P2(1)/n, and orthorhombic P2(1)2(1)2(1) space groups in units cells of the following dimensions: a 10.158 (3) Angstrom, b = 14.876 (4) Angstrom, 16.829 (5) Angstrom, beta = 104.25 (2)degrees, rho(calc) 1.732 g/cm(3), Z = 4; a = 9.025(1) Angstrom, b = 11.023 (1) Angstrom, c 13.833 (1) Angstrom, alpha = 101.15 (1)degrees, beta = 98.82 (1)degrees, gamma = 105.30 (1)degrees, rho(calc) = 1,886 g/cm(3), Z = 2; a = 13.090 (2) Angstrom, b = 17.637 (2) Angstrom, c = 21.834 (2) Angstrom, beta = 100.51 (1)degrees, rho(calc) = 1.738 g/cm(3), Z = 4, a = 10.721 (1) Angstrom, b = 16.929 (1) Angstrom, c = 14.675(1) Angstrom, beta = 97.86 (1)degrees, rho(calc) = 1.663 g/cm(3), Z = 4; and a = 15.532 (3) Angstrom, b = 19.401 (4) Angstrom, c = 9.910 (2) Angstrom, rho(calc) = 1.490 g/cm(3), Z = 2, respectively. Least-squares refinements converged at final values of R(F) of 0.041, 0.0354, 0.0624, 0.0533, and 0.035 for 2770, 2672, 2729, 2159, and 2525 independent observed reflections, respectively. Kinetic studies suggest that the reaction mechanisms are the same in both the solid and solution states and that the reaction mechanisms are substantially different from those previously reported for the thermolyses of the analogous cis-(DMPP)(2)PtX(2) complexes.

  DOI：

  10.1021/ic951307f

文献信息

• Redistribution reactions of platinum(II) and palladium(II) phosphine complexes
  作者：Jeffrey A. Rahn、Mark S. Holt、John H. Nelson

  DOI：10.1016/s0277-5387(00)86441-4

  日期：1989.1

  Abstract Anion redistribution equilibria of the type (R 3 P) 2 MX 2 + (R 3 P) 2 MY 2 ⇆ 2(R 3 P) 2 MXY (X, Y = Cl, Br, I, CN, N 3 ; R 3 P = Me 2 PhP, MePh 2 P, (Bzl) 3 P, (CH 2 CH) 2 PhP, (CH 2 CH)Ph 2 P and 1-phenyl-3,4-dimethylphosphole; M = Pd, Pt) have been studied by 31 P 1 H} and in some cases 195 Pt 1 H} NMR spectroscopy. It was found that except for the two cases when R 3 P = MePh 2 P, M

  摘要（R 3 P）2 MX 2 +（R 3 P）2 MY 2⇆2（R 3 P）2 MXY（X，Y = Cl，Br，I，CN，N 3; R 3 P = Me 2 PhP，MePh 2 P，（Bzl）3 P，（CH 2 = CH）2 PhP，（CH 2 = CH）Ph 2 P和1-苯基-3,4-二甲基磷脂; M = Pd， Pt）已通过31 P 1 H}和某些情况下的195 Pt 1 H} NMR光谱进行了研究。发现除了两种情况，当R 3 P = MePh 2 P，M = Pd，X = Cl，Y = Br和R 3 P = Me 2 PhP，M = Pd，X = Cl，Y = Br时，重新分配通常是瞬时的。（R 3 P）2 PdCl 2 +（R 3 P）2 Pd（CN）2反应较慢，但已完成。相反，当一个阴离子为CN-时，即使一个月后，铂络合物也未观察到阴离子再分布。混合阴离子物质相对于对称物
• Rahn, Jeffrey A.; Holt, Mark S.; Gray, George A., Inorganic Chemistry, 1989, vol. 28, # 2, p. 217 - 226
  作者：Rahn, Jeffrey A.、Holt, Mark S.、Gray, George A.、Alcock, Nathaniel W.、Nelson, John H.

  DOI：——

  日期：——
• Phospholes as ligands: palladium(II) complexes of 1-substituted 3,4-dimethylphospholes. Structure and properties
  作者：J. Jeffrey MacDougall、John H. Nelson、Francois Mathey、James J. Mayerle

  DOI：10.1021/ic50205a026

  日期：1980.3