异构化
化学
氢化物
反应性(心理学)
催化作用
过渡金属
无机化学
乙腈
键裂
化学计量学
光化学
计算化学
物理化学
金属
有机化学
医学
替代医学
病理
作者
Eric S. Wiedner,Matthew B. Chambers,Catherine L. Pitman,R. Morris Bullock,Alexander J. M. Miller,Aaron M. Appel
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2016-08-02
卷期号:116 (15): 8655-8692
被引量:467
标识
DOI:10.1021/acs.chemrev.6b00168
摘要
Transition metal hydrides play a critical role in stoichiometric and catalytic transformations. Knowledge of free energies for cleaving metal hydride bonds enables the prediction of chemical reactivity, such as for the bond-forming and bond-breaking events that occur in a catalytic reaction. Thermodynamic hydricity is the free energy required to cleave an M-H bond to generate a hydride ion (H(-)). Three primary methods have been developed for hydricity determination: the hydride transfer method establishes hydride transfer equilibrium with a hydride donor/acceptor pair of known hydricity, the H2 heterolysis method involves measuring the equilibrium of heterolytic cleavage of H2 in the presence of a base, and the potential-pKa method considers stepwise transfer of a proton and two electrons to give a net hydride transfer. Using these methods, over 100 thermodynamic hydricity values for transition metal hydrides have been determined in acetonitrile or water. In acetonitrile, the hydricity of metal hydrides spans a range of more than 50 kcal/mol. Methods for using hydricity values to predict chemical reactivity are also discussed, including organic transformations, the reduction of CO2, and the production and oxidation of hydrogen.
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