Thermodynamic and kinetic studies of hydride transfer for a series of molybdenum and tungsten hydrides

被引:47
作者
Sarker, N [1 ]
Bruno, JW [1 ]
机构
[1] Wesleyan Univ, Dept Chem, Middletown, CT 06459 USA
关键词
D O I
10.1021/ja982017b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The free energies for hydride donation (Delta G(M)(+)) have been determined in acetonitrile solution for a series of seven molybdenum and tungsten compounds (1-7) of general formula (C5R5)M(CO)(2)(L)H, which yield the salts [(C5R5)M(CO)(2)(L)(NCMe)][BF4] in these reactions. These data constitute the first thermodynamic data for hydride transfer by transition metal hydrides, and were gathered from equilibrium studies with carbenium ion salts of known hydride ion affinities in acetonitrile. The metal hydride Delta G(M)(double dagger) values range from ca. 79 to 89 kcal/mol, and these values may be compared with pK(a)s for related compounds to demonstrate that proton-transfer processes are somewhat more sensitive to changes in co-ligands than are hydride transfer processes. Additionally, kinetic studies of hydride transfer reactions with hydride acceptor [(p-MeOPh)(2)CPh][BF4] exhibit second-order rate constants ranging from ca. 200 to 7500 M-1 s(-1). These rates Show a correlation with thermodynamic driving force, and a Bronsted plot yields a slope of 0.20. The thermodynamic data may be used in conjuction with the appropriate thermodynamic cycles to calculate energies for various processes in which compounds such as 1-7 are known to function as hydride donors.
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页码:2174 / 2180
页数:7
相关论文
共 75 条
[1]   THERMODYNAMIC PROPERTIES OF ORGANIC OXYGEN COMPOUNDS .11. THERMODYNAMIC PROPERTIES FROM 10 TO 330 DEGREES K OF ISOPROPYL ALCOHOL [J].
ANDON, RJL ;
COUNSELL, JF ;
MARTIN, JF .
TRANSACTIONS OF THE FARADAY SOCIETY, 1963, 59 (487) :1555-&
[2]  
[Anonymous], PRINCIPLES APPL ORGA
[3]   BRONSTED COEFFICIENTS AND THE THEORY OF ACID-BASE CATALYSIS OF PROTON TRANSFERS FROM CARBON ACIDS [J].
ARNAUT, LG ;
FORMOSINHO, SJ .
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 1990, 3 (02) :95-109
[4]  
Arnett EM, 1997, J PHYS ORG CHEM, V10, P499, DOI 10.1002/(SICI)1099-1395(199707)10:7<499::AID-POC896>3.3.CO
[5]  
2-U
[6]  
ATWOOD JD, 1985, INORGANIC ORGANOMETA, P108
[7]   STRONG ORGANOMETALLIC LEWIS-ACIDS - TRICARBONYL-PI-CYCLOPENTADIENYL CATIONS OF MOLYBDENUM AND TUNGSTEN [(PI-C5H5)(OC)3M]+ (M=MO,W) [J].
BECK, W ;
SCHLOTER, K .
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES, 1978, 33 (11) :1214-1222
[8]   SOLVATION THERMODYNAMICS OF NONIONIC SOLUTES [J].
BENNAIM, A ;
MARCUS, Y .
JOURNAL OF CHEMICAL PHYSICS, 1984, 81 (04) :2016-2027
[9]   INTRINSIC BARRIERS OF REACTIONS AND THE PRINCIPLE OF NONPERFECT SYNCHRONIZATION [J].
BERNASCONI, CF .
ACCOUNTS OF CHEMICAL RESEARCH, 1987, 20 (08) :301-308
[10]   Kinetics of proton transfer from 2-nitro-4-X-phenylacetonitriles to piperidine and morpholine in aqueous Me(2)SO. Solvent and substituent effects on intrinsic rate constants. Transition state imbalances [J].
Bernasconi, CF ;
Wenzel, PJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (46) :11446-11453