Literature DB >> 27483171

Thermodynamic Hydricity of Transition Metal Hydrides.

Eric S Wiedner1, Matthew B Chambers2, Catherine L Pitman2, R Morris Bullock1, Alexander J M Miller2, Aaron M Appel1.   

Abstract

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.

Entities:  

Year:  2016        PMID: 27483171     DOI: 10.1021/acs.chemrev.6b00168

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  23 in total

Review 1.  Frustration across the periodic table: heterolytic cleavage of dihydrogen by metal complexes.

Authors:  R Morris Bullock; Geoffrey M Chambers
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2017-08-28       Impact factor: 4.226

Review 2.  Reactivity, Mechanism, and Assembly of the Alternative Nitrogenases.

Authors:  Andrew J Jasniewski; Chi Chung Lee; Markus W Ribbe; Yilin Hu
Journal:  Chem Rev       Date:  2020-03-04       Impact factor: 60.622

3.  Directing the reactivity of metal hydrides for selective CO2 reduction.

Authors:  Bianca M Ceballos; Jenny Y Yang
Journal:  Proc Natl Acad Sci U S A       Date:  2018-11-21       Impact factor: 11.205

4.  Remote Oxidative Activation of a [Cp*Rh] Monohydride.

Authors:  Emily A Boyd; Julie A Hopkins Leseberg; Emma L Cosner; Davide Lionetti; Wade C Henke; Victor W Day; James D Blakemore
Journal:  Chemistry       Date:  2022-02-03       Impact factor: 5.236

5.  Iridium-Catalyzed Enantioselective and Diastereoselective Hydrogenation of 1,3-Disubstituted Isoquinolines.

Authors:  Alexia N Kim; Aurapat Ngamnithiporn; Eric R Welin; Martin T Daiger; Christian U Grünanger; Michael D Bartberger; Scott C Virgil; Brian M Stoltz
Journal:  ACS Catal       Date:  2020-02-10       Impact factor: 13.084

6.  Toward Combined Carbon Capture and Recycling: Addition of an Amine Alters Product Selectivity from CO to Formic Acid in Manganese Catalyzed Reduction of CO2.

Authors:  Moumita Bhattacharya; Sepehr Sebghati; Ryan T VanderLinden; Caroline T Saouma
Journal:  J Am Chem Soc       Date:  2020-10-01       Impact factor: 15.419

7.  Computational studies on the hydride transfer barrier for the catalytic hydrogenation of CO2 by different Ni(II) complexes.

Authors:  Santu Biswas; Animesh Chowdhury; Prodyut Roy; Anup Pramanik; Pranab Sarkar
Journal:  J Mol Model       Date:  2018-08-07       Impact factor: 1.810

8.  Preparation of Neutral trans - cis [Ru(O2CR)2P2(NN)], Cationic [Ru(O2CR)P2(NN)](O2CR) and Pincer [Ru(O2CR)(CNN)P2] (P = PPh3, P2 = diphosphine) Carboxylate Complexes and their Application in the Catalytic Carbonyl Compounds Reduction.

Authors:  Salvatore Baldino; Steven Giboulot; Denise Lovison; Hans Günter Nedden; Alexander Pöthig; Antonio Zanotti-Gerosa; Daniele Zuccaccia; Maurizio Ballico; Walter Baratta
Journal:  Organometallics       Date:  2021-04-14       Impact factor: 3.876

9.  Diazaphosphinanes as hydride, hydrogen atom, proton or electron donors under transition-metal-free conditions: thermodynamics, kinetics, and synthetic applications.

Authors:  Jingjing Zhang; Jin-Dong Yang; Jin-Pei Cheng
Journal:  Chem Sci       Date:  2020-03-05       Impact factor: 9.825

10.  Panchromatic dirhodium photocatalysts for dihydrogen generation with red light.

Authors:  Jie Huang; Judith C Gallucci; Claudia Turro
Journal:  Chem Sci       Date:  2020-08-05       Impact factor: 9.825

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