| Literature DB >> 25950146 |
Seung Jun Hwang1, David C Powers1, Andrew G Maher1, Bryce L Anderson1, Ryan G Hadt1, Shao-Liang Zheng1, Yu-Sheng Chen2, Daniel G Nocera1.
Abstract
Halogen photoelimination reactions constitute the oxidative half-reaction of closed HX-splitting energy storage cycles. Here, we report high-yielding, endothermic Cl2 photoelimination chemistry from mononuclear Ni(III) complexes. On the basis of time-resolved spectroscopy and steady-state photocrystallography experiments, a mechanism involving ligand-assisted halogen elimination is proposed. Employing ancillary ligands to promote elimination offers a strategy to circumvent the inherently short-lived excited states of 3d metal complexes for the activation of thermodynamically challenging bonds.Entities:
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Year: 2015 PMID: 25950146 DOI: 10.1021/jacs.5b03192
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419