Thermodynamic properties of the Ni-H bond in complexes of the type [HNi(P2RN2R')2](BF4) and evaluation of factors that control catalytic activity for hydrogen oxidation/production

被引:138
作者
Fraze, Kendra
Wilson, Aaron D.
Appel, Aaron M.
DuBois, M. Rakowski
DuBois, Daniel L.
机构
[1] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
[2] Pacific NW Natl Lab, Richland, WA 99352 USA
关键词
D O I
10.1021/om070143v
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Thermodynamic data for hydride complexes of the general formula [HNi((P2N2R')-N-R)(2)](BF4), 3, which have been reported previously to function as effective catalysts for the electrochemical oxidation or production of hydrogen, have been determined. Values of Delta G degrees(H+), Delta G degrees(H center dot), and Delta G degrees(H-) have been determined for 3a where R = Cy, R' = Bz, for 3b where R = R' = Ph, and for the new complex 3c, R = Ph, R' = Bz. In addition, the Delta G values for the heterolytic addition of hydrogen to the Ni(II) precursor complexes [Ni((P2N2R')-N-R)(2)](BF4)(2), 1a-c, have been determined experimentally or calculated. The data are useful for understanding the factors that control the catalytic activities observed for these complexes and for the design of additional catalysts.
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页码:3918 / 3924
页数:7
相关论文
共 49 条
[1]  
[Anonymous], 1990, IUPAC CHEM DATA SERI
[2]   Molybdenum-sulfur dimers as electrocatalysts for the production of hydrogen at low overpotentials [J].
Appel, AM ;
DuBois, DL ;
DuBois, MR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (36) :12717-12726
[3]   Free-energy relationships between the proton and hydride donor abilities of [HNi(diphosphine)2]+ complexes and the half-wave potentials of their conjugate bases [J].
Berning, DE ;
Miedaner, A ;
Curtis, CJ ;
Noll, BC ;
DuBois, MCR ;
Dubois, DL .
ORGANOMETALLICS, 2001, 20 (09) :1832-1839
[4]   Relative hydride, proton, and hydrogen atom transfer abilities of [HM(diphosphine)2]PF6 complexes (M = Pt, Ni) [J].
Berning, DE ;
Noll, BC ;
DuBois, DL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (49) :11432-11447
[5]   Electron transfer at a dithiolate-bridged diiron assembly: Electrocatalytic hydrogen evolution [J].
Borg, SJ ;
Behrsing, T ;
Best, SP ;
Razavet, M ;
Liu, XM ;
Pickett, CJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (51) :16988-16999
[6]   Comprehensive thermodynamic characterization of the metal-hydrogen bond in a series of cobalt-hydride complexes [J].
Ciancanelli, R ;
Noll, BC ;
DuBois, DL ;
DuBois, MR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (12) :2984-2992
[7]   Periodic trends in metal hydride donor thermodynamics:: Measurement and comparison of the hydride donor abilities of the series HM(PNP)2+ (M = Ni, Pd, Pt; PNP = Et2PCH2N(Me)CH2PEt2) [J].
Curtis, CJ ;
Miedaner, A ;
Raebiger, JW ;
DuBois, DL .
ORGANOMETALLICS, 2004, 23 (03) :511-516
[8]   [Ni(Et2PCH2NMeCH2PEt2)2]2+ as a functional model for hydrogenases [J].
Curtis, CJ ;
Miedaner, A ;
Ciancanelli, R ;
Ellis, WW ;
Noll, BC ;
DuBois, MR ;
DuBois, DL .
INORGANIC CHEMISTRY, 2003, 42 (01) :216-227
[9]   Measurement of the hydride donor abilities of [HM(diphosphine)2]+ complexes (M = Ni, Pt) by heterolytic activation of hydrogen [J].
Curtis, CJ ;
Miedaner, A ;
Ellis, WW ;
DuBois, DL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (09) :1918-1925
[10]   Di-iron aza diphosphido complexes:: Mimics for the active site of Fe-only hydrogenase, and effects of changing the coordinating atoms of the bridging ligand in [Fe2{μ-(ECH2)2NR}(CO)6] [J].
Das, P ;
Capon, JF ;
Gloaguen, F ;
Pétillon, FY ;
Schollhammer, P ;
Talarmin, J ;
Muir, KW .
INORGANIC CHEMISTRY, 2004, 43 (26) :8203-8205