Abstract
We previously reported that a tris-(o-phenylenediamine) iron(ii) complex promotes photochemical H2 generation and C-H carboxylation of o-phenylenediamine without any additives under N2 and CO2 atmospheres, respectively, in tetrahydrofuran at room temperature. Herein, the key mechanistic process, namely, excited-state hydrogen detachment from the o-phenylendiamine moiety, is demonstrated under an N2 atmosphere.
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