Protonation equilibrium and hydrogen production by a dinuclear cobalt-hydride complex reduced by cobaltocene with trifluoroacetic acid.

نویسندگان

  • Sukanta Mandal
  • Shinya Shikano
  • Yusuke Yamada
  • Yong-Min Lee
  • Wonwoo Nam
  • Antoni Llobet
  • Shunichi Fukuzumi
چکیده

A dinuclear Co complex with bis(pyridyl)pyrazolato (bpp(-)) and terpyridine (trpy) ligands, [Co(III)2(trpy)2(μ-bpp)(OH)(OH2)](4+) (1(4+)), undergoes three-electron reduction by cobaltocene in acetonitrile to produce 1(+), which is in the protonation equilibrium with the Co(II)Co(III)-hydride complex, and the further protonation of the hydride by trifluoroacetic acid yields hydrogen quantitatively. The kinetic study together with the detection of the Co(II)Co(III)-hydride complex revealed the mechanism of the hydrogen production by the reaction of 1(+) with trifluoroacetic acid.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Singly versus Doubly Reduced Nickel Porphyrins for Proton Reduction: Experimental and Theoretical Evidence for a Homolytic Hydrogen‐Evolution Reaction

A nickel(II) porphyrin Ni-P (P=porphyrin) bearing four meso-C6 F5 groups to improve solubility and activity was used to explore different hydrogen-evolution-reaction (HER) mechanisms. Doubly reduced Ni-P ([Ni-P](2-) ) was involved in H2 production from acetic acid, whereas a singly reduced species ([Ni-P](-) ) initiated HER with stronger trifluoroacetic acid (TFA). High activity and stability o...

متن کامل

Structural characterization and proton reduction electrocatalysis of thiolate-bridged bimetallic (CoCo and CoFe) complexes.

Using an assembly method, dinuclear CoCo and CoFe complexes supported by a bdt ligand, [Cp*Co(μ-η2:η2-bdt)(μ-I)CoCp*][PF6] (1[PF6], Cp* = η5-C5Me5, bdt = benzene-1,2-dithiolate), and [Cp*Co(μ-η2:η4-bdt)FeCp'][PF6] (3[PF6], Cp' = η5-C5Me4H) were synthesized in high yields. Upon chemical reduction with CoCp2, complexes 1[PF6] and 3[PF6] were converted to [Cp*Co(μ-η2:η2-bdt)CoCp*] (2) and [Cp*Co(μ...

متن کامل

Synthesis and Reactivity of New Ruthenium Alkyls and Hydrides. Protonation of Cp*Ru(Me2PCH2PMe2)Me and X-ray Crystal Structure of Cp*2Ru2(μ-Ph2PCH2PPh2)(AlH5)

Treatment of the pentamethylcyclopentadienylruthenium chloride tetramer [Cp*RuCl]4 with bis(dimethylphosphino)methane (dmpm) in tetrahydrofuran affords three ruthenium(II) phosphine complexes, Cp*Ru(dmpm)Cl, [Cp*Ru(dmpm)(η1-dmpm)]Cl, and Cp*2Ru2(μ-dmpm)2Cl2. Similar treatment of [Cp*RuCl]4 with bis(diphenylphosphino)methane (dppm) in tetrahydrofuran or diethyl ether affords the dinuclear specie...

متن کامل

Dissymmetric dinuclear transition metal complexes as dual site catalysts for the polymerization of ethylene

A series of dissymmetric dinuclear complexes were synthesized, as dual site catalysts in ethylene polymerization, by coupling the allylated a-diimine complexes of the metals Ti, Zr, V, Ni and Pd with the ansa-zirconocene complex [C5H4-SiH(Me)-C5H4]ZrCl2 possessing a hydride silane moiety. The different stages of syntheses included the formation of bis(cyclopentadienide)methyl silane which was u...

متن کامل

Hydrogen Desorption Properties of Nanocrystalline MgH2-10 wt.% ZrB2 Composite Prepared by Mechanical Alloying

Storage of hydrogen is one of the key challenges in developing hydrogen economy. Magnesium hydride (MgH2) is an attractive candidate for solid-state hydrogen storage for on-board applications. In this study, 10 wt.% ZrB2 was co-milled with magnesium hydride at different milling times to produce nanocrystalline composite powder. The effect of milling time and additive on the hydrogen desorption...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Journal of the American Chemical Society

دوره 135 41  شماره 

صفحات  -

تاریخ انتشار 2013