bis(ethene)(3,1-dimethyl-3,11,17,18-tetraazatricyclo[11.3.1.1(5,9)]octadeca-1(17),5(18),6,8,13,15-hexaene-κ3N1,N2,N3)rhodium(I) hexafluorophosphate | 585533-01-3

• 英文名称: bis(ethene)(3,1-dimethyl-3,11,17,18-tetraazatricyclo[11.3.1.1(5,9)]octadeca-1(17),5(18),6,8,13,15-hexaene-κ3N1,N2,N3)rhodium(I) hexafluorophosphate
• CAS: 585533-01-3
• 化学式: C₂₀H₂₈N₄Rh*F₆P
• 分子量: 572.339
• InChiKey: LEWIAMIGUCMYIO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
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• 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：

  bis(ethene)(3,1-dimethyl-3,11,17,18-tetraazatricyclo[11.3.1.1(5,9)]octadeca-1(17),5(18),6,8,13,15-hexaene-κ3N1,N2,N3)rhodium(I) hexafluorophosphate 以 氘代丙酮 为溶剂， 以48%的产率得到ethene(3,1-dimethyl-3,11,17,18-tetraazatricyclo[11.3.1.1(5,9)]octadeca-1(17),5(18),6,8,13,15-hexaene-κ4N1,N2,N3,N4)rhodium(I) hexafluorophosphate
  参考文献：
  名称：

  3‐Metalla‐1,2‐dioxolanes and Their Reactivity

  摘要：

  AbstractThe ethene complexes [MI(CH2CH2)]+ (M = Ir, Rh) can be oxygenated by molecular oxygen or air in the solid state, to form isolable unsubstituted 3‐metalla‐1,2‐dioxolanes [MIII(CH2CH2OO‐κ2C1,O2)]+. Such selectivity could not be achieved in solution. The stereoselectivity of the oxygenation process is highly dependent on the ligand, the metal and the counterion used. Oxygenation of [(tpa)M(CH2CH2)]PF6 {tpa = tri(2‐pyridylmethyl)amine; 4PF6, 7PF6} results in the formation of two isomeric 3‐metalladioxolanes, whereas oxygenation of [(tpa)M(CH2CH2)]BPh4 (4BPh4, 7BPh4) only yields one isomer. Furthermore, oxygenation of [(Metpa)Rh(CH2CH2)]PF6 {14PF6, Metpa = [(6‐methyl‐2‐pyridyl)methyl]bis(2‐pyridylmethyl)amine} proved to be much slower than that of [(tpa)Rh(CH2CH2)]PF6 (7PF6). The solid propene complex [(tpa)Rh(CH2CHCH3)]BPh4 (23BPh4) loses propene on reaction with molecular oxygen, and selectively forms the peroxo complex [(tpa)Rh(η2‐O2)]BPh4 (24BPh4). The obtained 3‐metalla‐1,2‐dioxolanes rearrange, both in the solid state and in solution, to formylmethyl hydroxy complexes on exposure to photons or protons. The isomeric 3‐rhoda‐1,2‐dioxolanes [(tpa)Rh(CH2CH2OO‐κ2C1,O2)]+ 8a+ and 8b+ differ in reactivity. On exposure of a solution of 8aPF6/8bPF6 to glass‐filtered daylight, isomer 8b+ rearranges to form the formylmethyl hydroxy complex 9b+. This rearrangement is three times faster than the rearrangement of 8a+ to 9a+. The iridadioxolanes are much more reactive than the corresponding rhodadioxolanes, whereas the iridium formylmethyl hydroxy complexes are less reactive than the corresponding rhodium formylmethyl hydroxy complexes. The tpa formylmethyl hydroxy complexes react reversibly with carbon dioxide to form formylmethyl hydrogen carbonate complexes. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

  DOI：

  10.1002/ejic.200390139
• 作为产物：
  描述：

  乙烯 、 六氟磷酸钾 、 N,N′-dimethyl-2,11-diaza[3.3](2,6)pyridinophane 、 chlorobis(ethylene)rhodium(I) dimer 在 NaHCO₃ 作用下， 以 甲醇 为溶剂， 以83%的产率得到bis(ethene)(3,1-dimethyl-3,11,17,18-tetraazatricyclo[11.3.1.1(5,9)]octadeca-1(17),5(18),6,8,13,15-hexaene-κ3N1,N2,N3)rhodium(I) hexafluorophosphate
  参考文献：
  名称：

  3‐Metalla‐1,2‐dioxolanes and Their Reactivity

  摘要：

  AbstractThe ethene complexes [MI(CH2CH2)]+ (M = Ir, Rh) can be oxygenated by molecular oxygen or air in the solid state, to form isolable unsubstituted 3‐metalla‐1,2‐dioxolanes [MIII(CH2CH2OO‐κ2C1,O2)]+. Such selectivity could not be achieved in solution. The stereoselectivity of the oxygenation process is highly dependent on the ligand, the metal and the counterion used. Oxygenation of [(tpa)M(CH2CH2)]PF6 {tpa = tri(2‐pyridylmethyl)amine; 4PF6, 7PF6} results in the formation of two isomeric 3‐metalladioxolanes, whereas oxygenation of [(tpa)M(CH2CH2)]BPh4 (4BPh4, 7BPh4) only yields one isomer. Furthermore, oxygenation of [(Metpa)Rh(CH2CH2)]PF6 {14PF6, Metpa = [(6‐methyl‐2‐pyridyl)methyl]bis(2‐pyridylmethyl)amine} proved to be much slower than that of [(tpa)Rh(CH2CH2)]PF6 (7PF6). The solid propene complex [(tpa)Rh(CH2CHCH3)]BPh4 (23BPh4) loses propene on reaction with molecular oxygen, and selectively forms the peroxo complex [(tpa)Rh(η2‐O2)]BPh4 (24BPh4). The obtained 3‐metalla‐1,2‐dioxolanes rearrange, both in the solid state and in solution, to formylmethyl hydroxy complexes on exposure to photons or protons. The isomeric 3‐rhoda‐1,2‐dioxolanes [(tpa)Rh(CH2CH2OO‐κ2C1,O2)]+ 8a+ and 8b+ differ in reactivity. On exposure of a solution of 8aPF6/8bPF6 to glass‐filtered daylight, isomer 8b+ rearranges to form the formylmethyl hydroxy complex 9b+. This rearrangement is three times faster than the rearrangement of 8a+ to 9a+. The iridadioxolanes are much more reactive than the corresponding rhodadioxolanes, whereas the iridium formylmethyl hydroxy complexes are less reactive than the corresponding rhodium formylmethyl hydroxy complexes. The tpa formylmethyl hydroxy complexes react reversibly with carbon dioxide to form formylmethyl hydrogen carbonate complexes. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

  DOI：

  10.1002/ejic.200390139