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di-μ-benzoato-di-μ-hydrido-bis[(pentamethyl-η5-cyclopentadienyl)ruthenium] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134148-49-5

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134148-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134148-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,1,4 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134148-49:
(8*1)+(7*3)+(6*4)+(5*1)+(4*4)+(3*8)+(2*4)+(1*9)=115
115 % 10 = 5
So 134148-49-5 is a valid CAS Registry Number.

134148-49-5Upstream product

134148-49-5Downstream Products

134148-49-5Relevant academic research and scientific papers

Synthesis, structures, and reactions of coordinatively unsaturated trinuclear ruthenium polyhydrido complexes, [{Ru(C(5)Me (5))}(3)(μ-H)(6)](Y) (Y = BF(4), CF (3)SO(3), 1/2(SO(4)), C(6)H (5)CO(2), CH(3)CO(2), B(C(6)H (5))(4), PF(6)) and [{Ru(C(5)M (5))}(3)(μ-H)(3)(μ(3)-H)(2)]

Suzuki, Hiroharu,Kakigano, Takeaki,Tada, Ken-Ichi,Igarashi, Minoru,Matsubara, Kouki,Inagaki, Akiko,Oshima, Masato,Takao, Toshiro

, p. 67 - 87 (2005)

Cationic triruthenium hexahydrido complexes, [{Ru(C5Me 5)}3(μ-H)6](Y) (Y = BF4, CF 3SO3, 1/2(SO4), C6H 5CO2, CH3CO2), have been synthesized by the reaction of diruthenium tetrahydride [{Ru(C5Me 5)}2(μ-H)4] with the corresponding acid, HBF4, CF3CO2H, H2SO4, C6H5CO2H, and CH3CO2H. The trimeric structure of these complexes has been confirmed by a crystallographic study of [{Ru(C5Me5)}3(μ-H) 6](PF6). The treatment of [{Ru(C5Me 5)}3(μ-H)6](Y) with CH3ONa in methanol selectively afforded a neutral trinuclear pentahydrido complex, [{Ru(C5Me5)}3(μ-H)3(μ 3-H)2], which underwent an intermolecular H/D exchange reaction with benzene-d6, toluene-d8, or o-xylene-d 10 to give [{Ru(C5Me5)}3(μ-D) 3(μ3-D)2] as the result of arene C-H bond activation via an η2-arene intermediate complex. A cationic hydrido complex, [{Ru(C5Me5)}3(μ-H) 6](Y), having a carboxylate as a counter anion was equilibrated with [{Ru(C5Me5)}3(μ-H)3(μ 3-H)2] in solution, and the equilibrium constant depended on the counter anion. An X-ray diffraction study showed that [{Ru(C 5Me5)}3(μ-H)3(μ3-H) 2] has a triangular reaction field surrounded by three C 5Me5 ligands. The reaction of [{Ru(C5Me 5)}3(μ-H)3(μ3-H)2] with 1 equiv of O2 proceeded with the retention of the Ru3 framework to yield an 80/20 mixture of a mono-μ3-oxo complex [{Ru(C5Me5)}3(μ-H)3(μ 3-O)] and a di-μ3-oxo complex [{Ru(C5Me 5)}3(μ-H)3(μ3-O)2]. A novel trinuclear μ3-iodo-tetra-μ-hydrido complex, [{Ru(C5Me5)}3(μ3-H)(μ-H) 3(μ3-I)] was formed upon the treatment of [{Ru(C 5Me5)}3(μ-H)3(μ3-H) 2] with 1 equiv of CH3I in tetrahydrofuran. The treatment of [{Ru(C5Me5)}3(μ-H) 3(μ3-H)2] with carbon monoxide generated a paramagnetic trinuclear tetracarbonyl complex, [{Ru(C5Me 5)}3(μ-CO)3(μ3-CO)].

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