Institut für Technische und Makromolekulare Chemie, RWTH Aachen University, Worringerweg 1, 52074 Aachen (Germany) www.itmc.rwth-aachen.de.
Angew Chem Int Ed Engl. 2015 May 11;54(20):5859-63. doi: 10.1002/anie.201410620. Epub 2015 Mar 25.
Ruthenium-triphos complexes exhibited unprecedented catalytic activity and selectivity in the redox-neutral C-C bond cleavage of the β-O-4 lignin linkage of 1,3-dilignol model compounds. A mechanistic pathway involving a dehydrogenation-initiated retro-aldol reaction for the C-C bond cleavage was proposed in line with experimental data and DFT calculations.
钌-三膦配合物在 1,3-二木质素模型化合物β-O-4 木质素键的氧化还原中性 C-C 键断裂中表现出前所未有的催化活性和选择性。根据实验数据和 DFT 计算,提出了一种涉及脱氢引发反羟醛反应的 C-C 键断裂的机理途径。