Catalytic Transformation of Aliphatic Alcohols to Corresponding Esters in O2 under Neutral Conditions Using Visible-Light Irradiation

• Published in: Journal of the American Chemical Society Vol. 137; no. 5; pp. 1956 - 1966
• Main Authors: Xiao, Qi, Liu, Zhe, Bo, Arixin, Zavahir, Sifani, Sarina, Sarina, Bottle, Steven, Riches, James D, Zhu, Huaiyong
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 11.02.2015
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja511619c

Selective oxidation of aliphatic alcohols under mild and base-free conditions is a challenging process for organic synthesis. Herein, we report a one-pot process for the direct oxidative esterification of aliphatic alcohols that is significantly enhanced by visible-light irradiation at ambient temperatures. The new methodology uses heterogenerous photocatalysts of gold–palladium alloy nanoparticles on a phosphate-modified hydrotalcite support and molecular oxygen as a benign oxidant. The alloy photocatalysts can absorb incident light, and the light-excited metal electrons on the surface of metal nanoparticles can activate the adsorbed reactant molecules. Tuning the light intensity and wavelength of the irradiation can remarkably change the reaction activity. Shorter wavelength light (<550 nm) drives the reaction more efficiently than light of longer wavelength (e.g., 620 nm), especially at low temperatures. The phosphate-exchanged hydrotalcite support provides sufficient basicity (and buffer) for the catalytic reactions; thus, the addition of base is not required. The photocatalysts are efficient and readily recyclable. The findings reveal the first example of using “green” oxidants and light energy to drive direct oxidative esterification of aliphatic alcohols under base-free, mild conditions.