Mechanism of the photoreduction of carbon dioxide catalyzed by the benchmarking rhenium dimethylbipyridine complexes; operando measurements by XAFS and FT-IR
Yoki Kou, Yu Nabetani, Ryosuke Nakazato, Nair V. Pratheesh, Tokushi Sato, Shunsuke Nozawa, Shin‐ichi Adachi, Hiroshi Tachibana, Haruo Inoue
Abstract
The photoreduction of CO2 catalyzed by [fac-Re(dmbpy)(CO)3Cl] was precisely investigated through operando measurements of X-ray absorption fine structure spectroscopy (XAFS) and laser-flash FT-IR transient spectroscopy. In the early stage of the photoreaction, Re0-species assigned as penta-coordinated complex, [Re0(dmbpy)(CO)3], appeared and a delayed rise of ReII-species, [ReII(dmbpy)(CO)3CO2] (3)/[ReII(dmbpy)(CO)3COOH]+ (3′), were observed in XAFS measurements. The valence state of Re-center in the catalytic cycle changed as ReI → Re0 → ReII to be a clear evidence of an oxidative addition of CO2 to the Re0 center. In the laser-flash induced FT-IR measurements, a rise and decay of 3 followed by a delayed rise and decay of 3′ was observed. The second electron transfer from the carbon radical of triethylamine (TEA•) to 3′ induced the formation of [ReI(dmbpy)(CO)4]+ through [ReI(dmbpy)COOH]. The rate determining step of the catalytic cycle was revealed to be the protonation process of forming 3′ from 3.