| 201302-49-0

• CAS: 201302-49-0；201363-43-1
• 化学式: C₁₄H₂₀B₂Fe₂O₈P₂
• 分子量: 511.572
• InChiKey: WKMFAODRQJORJV-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

• 作为反应物：
  描述：

  2,4,6-三甲基吡啶 、 以 甲苯 为溶剂， 以86.2%的产率得到Fe(CO)4(Me2PCH2BH2(2,4,6-Me3C5H2N))
  参考文献：
  名称：

  {[Bis(dimethylamino) boryl]methyl} dimethylphosphane as ligand in transition metal complexes

  摘要：

  The new alpha,omega-[phosphanyl(organyl)]borane Me(2)PCH(2)B(NMe(2))(2) (8) was obtained in good yield by the reaction of ClB(NMe(2))(2) with LiCH(2)PMe(2). Compound 8 forms the transition metal complexes [(CO)(5)Cr{Me(2)PCH(2)B(NMe(2))(2)}] (9), [(MeC(5)H(4))Mn(CO)(2){Me(2)PCH(2)B(NMe(2))(2)}] (10), and [(CO)(4)Fe{Me(2)PCH(2)B(NMe(2))(2)}] (11), which were isolated as highly volatile liquids in high yields. Complex 11 easily underwent exchange reactions of the Me(2)N substituents which led to derivatives with threefold coordinated boron such as [(CO)(4)Fe{Me(2)PCH(2)B(OMe)(2)}] (13), and [(CO)(4)Fe{Me(2)PCH(2)B(NMe(2))Cl}] (14), or to a compound with tetrafold coordinated boron, [(CO)(4)Fe{Me(2)PCH(2)BCl(2)(NHMe(2))}] (15). Li[(CO)(4)Fe(Me(2)PCH(2)BH(3))] (16), cis,trans-[{(CO)(4)Fe(Me(2)PCH(2)BH(2))}(2)] (17), and [(CO)(4)Fe{Me(2)PCH(2)BH(2)(2,4,6-Me(3)C(5)H(2)N)}] (18) were obtained from 13 by corresponding substitution of the MeO groups. The addition of HSiPh(3) to the iron center was achieved by photolysis of 13, giving [(CO)(3)FeH(SiPh(3)){Me(2)PCH(2)B(OMe)(2)}] (19). [(CO)(5)Cr{Me(2)PCH(2)B(OMe)(2)}] (12), the chromium analogue of 13, was obtained from the reaction of [(CO)(5)Cr{Me(2)PCH(2)B(NMe(2))(2)}] (9) with MeOH. The structure of compound 19 was determined by single crystal X-ray diffraction. (C) 1997 Elsevier Science S.A.

  DOI：

  10.1016/s0022-328x(97)00339-2
• 作为产物：
  描述：

  盐酸 、 以 乙醚 为溶剂， 以83.3%的产率得到
  参考文献：
  名称：

  {[Bis(dimethylamino) boryl]methyl} dimethylphosphane as ligand in transition metal complexes

  摘要：

  The new alpha,omega-[phosphanyl(organyl)]borane Me(2)PCH(2)B(NMe(2))(2) (8) was obtained in good yield by the reaction of ClB(NMe(2))(2) with LiCH(2)PMe(2). Compound 8 forms the transition metal complexes [(CO)(5)Cr{Me(2)PCH(2)B(NMe(2))(2)}] (9), [(MeC(5)H(4))Mn(CO)(2){Me(2)PCH(2)B(NMe(2))(2)}] (10), and [(CO)(4)Fe{Me(2)PCH(2)B(NMe(2))(2)}] (11), which were isolated as highly volatile liquids in high yields. Complex 11 easily underwent exchange reactions of the Me(2)N substituents which led to derivatives with threefold coordinated boron such as [(CO)(4)Fe{Me(2)PCH(2)B(OMe)(2)}] (13), and [(CO)(4)Fe{Me(2)PCH(2)B(NMe(2))Cl}] (14), or to a compound with tetrafold coordinated boron, [(CO)(4)Fe{Me(2)PCH(2)BCl(2)(NHMe(2))}] (15). Li[(CO)(4)Fe(Me(2)PCH(2)BH(3))] (16), cis,trans-[{(CO)(4)Fe(Me(2)PCH(2)BH(2))}(2)] (17), and [(CO)(4)Fe{Me(2)PCH(2)BH(2)(2,4,6-Me(3)C(5)H(2)N)}] (18) were obtained from 13 by corresponding substitution of the MeO groups. The addition of HSiPh(3) to the iron center was achieved by photolysis of 13, giving [(CO)(3)FeH(SiPh(3)){Me(2)PCH(2)B(OMe)(2)}] (19). [(CO)(5)Cr{Me(2)PCH(2)B(OMe)(2)}] (12), the chromium analogue of 13, was obtained from the reaction of [(CO)(5)Cr{Me(2)PCH(2)B(NMe(2))(2)}] (9) with MeOH. The structure of compound 19 was determined by single crystal X-ray diffraction. (C) 1997 Elsevier Science S.A.

  DOI：

  10.1016/s0022-328x(97)00339-2