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Adhikari D, Raghavachari K. H2S Reactivity on Oxygen-Deficient Heterotrimetallic Cores: Cluster Fluxionality Simulates Dynamic Aspects of Surface Chemical Reactions. J Phys Chem A. 2016;120(3):466-72doi: 10.1021/acs.jpca.5b10899.
Adhikari, D., & Raghavachari, K. (2016). H2S Reactivity on Oxygen-Deficient Heterotrimetallic Cores: Cluster Fluxionality Simulates Dynamic Aspects of Surface Chemical Reactions. The journal of physical chemistry. A, 120(3), 466-72. https://doi.org/10.1021/acs.jpca.5b10899
Adhikari, Debashis, and Raghavachari, Krishnan. "H2S Reactivity on Oxygen-Deficient Heterotrimetallic Cores: Cluster Fluxionality Simulates Dynamic Aspects of Surface Chemical Reactions." The journal of physical chemistry. A vol. 120,3 (2016): 466-72. doi: https://doi.org/10.1021/acs.jpca.5b10899
Adhikari D, Raghavachari K. H2S Reactivity on Oxygen-Deficient Heterotrimetallic Cores: Cluster Fluxionality Simulates Dynamic Aspects of Surface Chemical Reactions. J Phys Chem A. 2016 Jan 28;120(3):466-72. doi: 10.1021/acs.jpca.5b10899. Epub 2016 Jan 19. PMID: 26730799.
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J Phys Chem A. 2016 Jan 28;120(3):466-72. doi: 10.1021/acs.jpca.5b10899. Epub 2016 Jan 19.

H2S Reactivity on Oxygen-Deficient Heterotrimetallic Cores: Cluster Fluxionality Simulates Dynamic Aspects of Surface Chemical Reactions.

The journal of physical chemistry. A

Debashis Adhikari, Krishnan Raghavachari

Affiliations

  1. Department of Chemistry, Indiana University , Bloomington, Indiana 47405, United States.
  2. Department of Chemistry and the Institute of Catalysis for Energy Processes, Northwestern University , Evanston, Illinois 60208, United States.

PMID: 26730799 DOI: 10.1021/acs.jpca.5b10899

Abstract

Understanding the mechanistic aspects of heterogeneous reactions on supported metal catalysts is challenging due to several disparate factors, among which the dynamic nature of the surface is a major contributor. In this study, the dynamic aspect of a surface has been probed by choosing small metal clusters as illustrative models. Two anionic hetero-trimetallic clusters, namely, W2TcO6(-) and W2OsO6(-), were reacted with H2S gas to exhibit splitting of the gas molecule and complete oxygen-sulfur exchange in the metal core. During this atom-exchange process, the core exhibits remarkable fluxionality to augment a thiol proton migration from one metal center to another, as well as a rapid interchange of the terminal and bridging oxygens. The fluxional nature of the core is further evidenced by two oppositely oriented oxo groups working in concert to accomplish the proton transfer, upon introduction of sulfur inside the core. These fluxional processes in the small hetero-trimetallic cores closely resemble the dynamic nature of the surface in a heterogeneous reaction. Throughout the fluxional processes investigated in this study, two-state reactivity and multiple instances of spin crossover are observed in our computational studies. Interestingly, the neutral hetero-trimetallic cores can also undergo complete oxygen-sulfur exchange reaction with H2S. The investigated metal clusters are promising materials, since they not only can liberate dihydrogen from water (reported in J. Phys. Chem. A, 2014, 118, 11047) but also can completely strip the sulfur from environmentally hazardous H2S gas.

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