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K[Ru(TFA)3(CO)3] | 1147124-76-2

中文名称
——
中文别名
——
英文名称
K[Ru(TFA)3(CO)3]
英文别名
potassium [Ru(trifluoroaceto)3(CO)3];K[Ru(trifluoroacetate)3(CO)3]
K[Ru(TFA)3(CO)3]化学式
CAS
1147124-76-2
化学式
C9F9O9Ru*K
mdl
——
分子量
563.248
InChiKey
IPQATNQBNGNZDA-UHFFFAOYSA-K
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

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:
    K[Ru(TFA)3(CO)3]二甲基苯基磷丙酮 为溶剂, 反应 24.0h, 以27%的产率得到
    参考文献:
    名称:
    Ru(TFA)(CO)(PPh3)2(L)(L=2-苯基吡啶、2-对甲苯基吡啶)和Ru(CO)(PPhMe2)2(L)(L的合成、结构、光物理和电化学性质') (L= TFA, H) (L'= 联吡啶, L'= 4,4'-二甲基联吡啶) 辅助配体结构与发光特性之间的关系。
    摘要:
    配合物[Ru[(CO)(TFA) (PPh 3 ) 2 (L)][(L = ppy = 2-苯基吡啶, ( 1a ); L = 2–(p–tolyl)的合成、结构和光物理性质)报道了[Ru(CO)( )吡啶] ( 1b )。配合物通过UV-VIS、IR和NMR以及单晶X射线衍射技术进行了表征。我们还报道了[Ru(CO)( L)(PPhMe 2 ) 2 (L′)] + [PF 6 ] − [L′ = 联吡啶,L = TFA,( 3a );L = H,( 3b ) 且 L = H,L′ = 4,4 '-二甲基联吡啶 ( 3c )]。这些化合物通过 UV-VIS、IR 和 NMR 技术进行了表征,在3a的情况下通过单晶 X 射线衍射进行了表征。[Ru(Me 2 PhP) 2的固态结构(CO) 2 (TFA) 2 (2)是合成3a - 3c的起始材料,也被报道用于验证体积较小的 PPhMe 2的反式关系,并与之前报道的
    DOI:
    10.1016/j.jorganchem.2017.03.026
  • 作为产物:
    描述:
    参考文献:
    名称:
    Rosenberg, Edward; Skinner, David M.; Aime, Silvio, Gazzetta Chimica Italiana, 1991, vol. 121, p. 313 - 320
    摘要:
    DOI:
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文献信息

  • Tuning photophysical properties with ancillary ligands in Ru(II) mono-diimine complexes
    作者:Ayesha Sharmin、Reuben C. Darlington、Kenneth I. Hardcastle、Mauro Ravera、Edward Rosenberg、J.B. Alexander Ross
    DOI:10.1016/j.jorganchem.2008.11.048
    日期:2009.3
    the neutral complex Ru(Ph3P)(CO)(1,10-phenanthroline)(TFA)2 is also obtained and its solid state structure is reported. Solid state structures are also reported for the cationic complexes where L–L = phenanthroline, L2 = 2PPh3 and X = Cl and for L–L = 2,2′-bipyridyl, L2 = 2PPh3 and X = H. All the complexes were characterized in solution by a combination of 1H and 31P NMR, IR, mass spectrometry and elemental
    系列配合物 [XRu(CO)(L–L)(L′) 2 ][PF 6 ] (X = H, TFA, Cl; L–L = 2,2′-联吡啶,1,10-咯啉, 5-基-1,10-咯啉和4,4'-二羧基-2,2'-联吡啶; L' 2  = 2PPh 3 , Ph 2 PC 2 H 4 PPh 2 , Ph 2 PCH CHPPh 2 ) 已由以下合成首先与膦配体反应,然后与 L–L 反应并与 NaPF 6进行阴离子交换,得到起始配合物 K[Ru(CO) 3 (TFA) 3 ] (TFA = CF 3 CO 2 ) 。在L–L = 咯啉和L′ 2  = 2PPh 3的情况下,还获得了中性配合物Ru(Ph 3 P)(CO)(1,10-咯啉)(TFA) 2并报道了其固态结构。还报告了阳离子配合物的固态结构,其中 L–L = 咯啉,L 2  = 2PPh 3和 X = Cl,对于 L–L = 2
  • Photophysical Studies of Bioconjugated Ruthenium Metal–Ligand Complexes Incorporated in Phospholipid Membrane Bilayers
    作者:Ayesha Sharmin、Luca Salassa、Edward Rosenberg、J. B. Alexander Ross、Geoffrey Abbott、Labe Black、Michelle Terwilliger、Robert Brooks
    DOI:10.1021/ic400706u
    日期:2013.10.7
    The luminescent, mono-diimine ruthenium complexes [(H)Ru(CO)(PPh3)(2)(dcbpy)][PF6] (1) (dcbpy = 4,4'-dicarboxy-2,2'-bipyridyl) and [(H)Ru(CO)(dppene)(5-amino-1,10-phen)][PF6] (2) (dppene = bis(diphenylphosphino)ethylene; phen = phenanthroline) were conjugated with 1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine (DPPE) and with cholesterol in the case of complex 2. Using standard conjugation techniques, compound 1 gives the bis-lipid derivative [(H)Ru(CO)(PPh3)(2)(dcbpy-N-DPPE2)][PF6] (3), while 2 provides the monolipid conjugate [(H)Ru(CO)(dppene)(1,10-phen-5-NHC(S)-N-DPPE)][PF6] (4) and the cholesterol derivative [(H)Ru(CO)(dppene)(1,10-phen-5-NHC(O)Ocholesteryl)][PF6] (5). These compounds were characterized by spectroscopic methods, and their photophysical properties were measured in organic solvents. The luminescence of lipid conjugates 3 and 4 is quenched in organic solvents while compound 4 shows a weak, short-lived, blue-shifted emission in aqueous solution. The cholesterol conjugate 5 shows the long-lived, microsecond-time scale emission associated with triplet metal-to-ligand charge-transfer excited states. Incorporation of conjugate 3 in lipid bilayer vesicles restores the luminescence, but with blue shifts (similar to 80 nm) accompanied by nanosecond-time scale lifetimes. In the vesicles conjugate 4 shows a short-lived and blue-shifted emission similar to that observed in solution but with increased intensity. Conjugation of the complex [(H)Ru(CO)(PhP2C2H4C(O)O-N-succinimidyl)(2)(bpy)][PF6] (6 '') (bpy = 2,2'-bipyridyl) with DPPE gives the phosphine-conjugated complex [(H)Ru(CO)(PhP2C2H4C(O)-N-DPPE)(2)(bpy)][PF6] (7). Complex 7 also exhibits a short-lived and blue-shifted emission in solution and in vesicles as observed for complexes 3 and 4. We have also conjugated the complex [Ru(bpy)(2)(5-amino-1,10-phen)][PF6](2) (8) with both cholesterol (9) and DPPE (10). Neither complex 9 nor the previously reported complex 10 exhibited the blue shifts observed for complexes 3 and 4 when incorporated into large unilamellar vesicles (LUVs). The anisotropies of the emissions of complexes 3, 4, and 7 were also measured in LUVs, and those of complex 5 were measured in both glycerol and LUVs. High fundamental anisotropies were observed for complexes 3, 4, and 7.
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