Castillo-Lora Janelle, Delley Murielle F, Laga Stephanie M, Mayer James M
Department of Chemistry, Yale University, 255 Prospect Street, New Haven, Connecticut 06520-8107, United States.
J Phys Chem Lett. 2020 Sep 17;11(18):7687-7691. doi: 10.1021/acs.jpclett.0c02359. Epub 2020 Aug 31.
Transfers of multiple electrons and protons are challenging yet central to many energy-conversion processes and other chemical and biochemical reactions. Semiconducting oxides can hold multiple redox equivalents. This study describes the 2e/2H transfer reactivity of photoreduced ZnO and TiO nanoparticle (NP) colloids with molecular 2e/2H acceptors, to form new O-H, N-H, and C-H bonds. The reaction stoichiometries were monitored by NMR and optical spectroscopies. Faster 2e/2H transfer rates were observed for substrates forming O-H or N-H bonds, presumably due to initial hydrogen bonding at the oxide surface. Chemically reduced ZnO NPs stabilized by Na or Ca also engage in 2e/2H transfer reactivity, showing that protons transferred in these processes are inherent to the oxide nanoparticles and do not exclusively stem from photoreduction. These results highlight the potential of ZnO and TiO for multiple proton-coupled electron transfer (PCET) reactions.
多个电子和质子的转移具有挑战性,但却是许多能量转换过程以及其他化学和生化反应的核心。半导体氧化物可以容纳多个氧化还原当量。本研究描述了光还原的ZnO和TiO纳米颗粒(NP)胶体与分子2e/2H受体的2e/2H转移反应性,以形成新的O-H、N-H和C-H键。通过核磁共振(NMR)和光谱学监测反应化学计量。对于形成O-H或N-H键的底物,观察到更快的2e/2H转移速率,这可能是由于在氧化物表面最初形成了氢键。由Na或Ca稳定的化学还原ZnO纳米颗粒也参与2e/2H转移反应,表明在这些过程中转移的质子是氧化物纳米颗粒所固有的,并非完全源于光还原。这些结果突出了ZnO和TiO在多质子耦合电子转移(PCET)反应中的潜力。