[Ru(η5-C5H5)(4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazinium-6-yl)(CO)(P(i-Pr)3)]BF4 | 306968-91-2

• 英文名称: [Ru(η5-C5H5)(4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazinium-6-yl)(CO)(P(i-Pr)3)]BF4
• CAS: 306968-91-2
• 化学式: BF₄*C₃₆H₄₂N₂OPRuS
• 分子量: 769.657
• InChiKey: CFFDNTUHLCDQBS-UHFFFAOYSA-O

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：

  [Ru(η5-C5H5)(4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazinium-6-yl)(CO)(P(i-Pr)3)]BF4 在 NaOCH₃ 作用下， 以 四氢呋喃 为溶剂， 以60%的产率得到[Ru(η5-C5H5)(4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazin-6-yl)(CO)(P(i-Pr)3)]
  参考文献：
  名称：

  The Allenylidene Complex [Ru(η⁵-C₅H₅)(CCCPh₂)(CO)(PⁱPr₃)]BF₄ as a Precursor of Novel Pyrido[1,2-a]pyrimidinyl and 1,3-Thiazinyl Complexes

  摘要：

  The allenylidene complex [Ru(eta (5)-C5H5)(C=C=CPh2)(CO)((PPr3)-Pr-i)]BF4 (1) reacts with 2-aminopyridine to give a mixture of the complexes [Ru(eta (5)-C5H5){2,2-diphenyl-2H-pyridinium-[1,2-alpha ]pyrimidin-4-yl}(CO)((PPr3)-Pr-i)]BF4 (2) and [Ru(eta (5)-C5H5){C(CH=CPh2)=NHC(CH)(4)N}-(CO)((PPr3)-Pr-i)]BF4 (3). The molar ratio of the isomers in the mixture depends on the reaction temperature. At temperatures lower than -30 degreesC, isomer 2 is the main reaction product, while at 0 degreesC an inverse relationship is observed. The structure of 2 has been determined by an X-ray Investigation, revealing a Ru-C(bicycle) distance of 2.08(1) Angstrom. Treatment of 2 with sodium methoxide results in the deprotonation of the NH group of the heterocycle to give the pyrido[1,2-alpha ]pyrimidinyl derivative Ru(eta (5)-C5H5){2,2-diphenyl-2H-pyrido[1,2-alpha]- pyrimidin-4-yl}(Co)((PPr3)-Pr-i) (4), which has been also characterized by an X-ray diffraction analysis. In this case, the study reveals a Ru-C(bicycle) distance of 2.097(5) Angstrom. The deprotonation of 2 is reversible. Thus, the addition of HBF4. OEt2 to dichloromethane solutions of 4 regenerates 2, Similarly, the treatment of 4 with methyl trifluoromethanesulfonate affords [Ru(eta (5)-C5H5){1-methyl-2,2-diphenyl-2H-pyridium[1,2-alpha ]pyrimidin-4-yl}(CO)- ((PPr3)-Pr-i)1CF(3)SO(3) (5). Complex 1 also reacts with thioisonicotinamide. The reaction yields [Ru-(eta (5)-C5H5){4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazinium-6-yl}(CO)((PPR3)-P-i)BF4 (6), which in the presence of sodium methoxide affords Ru(eta (5)-C5H5){4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazin-6-yl}(CO)((PPr3)-Pr-i) (7) The structure of 7 has been determined by an X-ray investigation, revealing a Ru-C(cycle) distance of 2.067(4) Angstrom The deprotonation of 6 is also reversible. Thus, the addition of HBF4. OEt2 to dichloromethane solutions of 7 regenerates 6. Similarly, treatment of 7 with methyl trifluoromethanesulfonate gives [Ru(eta (5)-C5H5){3-methy1-4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazininium-6-yl}(CO)((PPR3)-P-i)]CF3SO3 (8). (8).

  DOI：

  10.1021/om000415t
• 作为产物：
  描述：

  [Ru(η(5)-C5H5)(=C=C=CPh2)(CO)(P(Pr(i))3)](tetrafluoroborate) 、 硫代异烟酰胺 以 二氯甲烷 为溶剂， 以86%的产率得到[Ru(η5-C5H5)(4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazinium-6-yl)(CO)(P(i-Pr)3)]BF4
  参考文献：
  名称：

  The Allenylidene Complex [Ru(η⁵-C₅H₅)(CCCPh₂)(CO)(PⁱPr₃)]BF₄ as a Precursor of Novel Pyrido[1,2-a]pyrimidinyl and 1,3-Thiazinyl Complexes

  摘要：

  The allenylidene complex [Ru(eta (5)-C5H5)(C=C=CPh2)(CO)((PPr3)-Pr-i)]BF4 (1) reacts with 2-aminopyridine to give a mixture of the complexes [Ru(eta (5)-C5H5){2,2-diphenyl-2H-pyridinium-[1,2-alpha ]pyrimidin-4-yl}(CO)((PPr3)-Pr-i)]BF4 (2) and [Ru(eta (5)-C5H5){C(CH=CPh2)=NHC(CH)(4)N}-(CO)((PPr3)-Pr-i)]BF4 (3). The molar ratio of the isomers in the mixture depends on the reaction temperature. At temperatures lower than -30 degreesC, isomer 2 is the main reaction product, while at 0 degreesC an inverse relationship is observed. The structure of 2 has been determined by an X-ray Investigation, revealing a Ru-C(bicycle) distance of 2.08(1) Angstrom. Treatment of 2 with sodium methoxide results in the deprotonation of the NH group of the heterocycle to give the pyrido[1,2-alpha ]pyrimidinyl derivative Ru(eta (5)-C5H5){2,2-diphenyl-2H-pyrido[1,2-alpha]- pyrimidin-4-yl}(Co)((PPr3)-Pr-i) (4), which has been also characterized by an X-ray diffraction analysis. In this case, the study reveals a Ru-C(bicycle) distance of 2.097(5) Angstrom. The deprotonation of 2 is reversible. Thus, the addition of HBF4. OEt2 to dichloromethane solutions of 4 regenerates 2, Similarly, the treatment of 4 with methyl trifluoromethanesulfonate affords [Ru(eta (5)-C5H5){1-methyl-2,2-diphenyl-2H-pyridium[1,2-alpha ]pyrimidin-4-yl}(CO)- ((PPr3)-Pr-i)1CF(3)SO(3) (5). Complex 1 also reacts with thioisonicotinamide. The reaction yields [Ru-(eta (5)-C5H5){4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazinium-6-yl}(CO)((PPR3)-P-i)BF4 (6), which in the presence of sodium methoxide affords Ru(eta (5)-C5H5){4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazin-6-yl}(CO)((PPr3)-Pr-i) (7) The structure of 7 has been determined by an X-ray investigation, revealing a Ru-C(cycle) distance of 2.067(4) Angstrom The deprotonation of 6 is also reversible. Thus, the addition of HBF4. OEt2 to dichloromethane solutions of 7 regenerates 6. Similarly, treatment of 7 with methyl trifluoromethanesulfonate gives [Ru(eta (5)-C5H5){3-methy1-4,4-diphenyl-2-(p-pyridinyl)-4H-1,3-thiazininium-6-yl}(CO)((PPR3)-P-i)]CF3SO3 (8). (8).

  DOI：

  10.1021/om000415t