Consecutive ligand-based PCET processes affording a doubly reduced nickel pyrazinedithiolate which transforms into a metal hydride required to evolve H 2
Our DFT results demonstrate that hydrogen evolution from water catalyzed by a nickel pyradinedithiolate (dcpdt) molecular hydrogen evolution catalyst [NiII(dcpdt)2]2- proceeds via the formation of a square-planar nickel(ii) hydride intermediate which is given by unprecedented structural transformati...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2019-01, Vol.48 (2), p.635-640 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Our DFT results demonstrate that hydrogen evolution from water catalyzed by a nickel pyradinedithiolate (dcpdt) molecular hydrogen evolution catalyst [NiII(dcpdt)2]2- proceeds via the formation of a square-planar nickel(ii) hydride intermediate which is given by unprecedented structural transformation of a doubly reduced triply protonated species [NiII(dcpdtH2)(dcpdtH)]-, afforded as a result of two consecutive ligand-based reductions of [NiII(dcpdt)(dcpdtH)]- through proton-coupled electron transfer (PCET) pathways. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c8dt04497j |