Chen Chi-Tien, Lai Zi-Ling
Department of Chemistry, National Chung Hsing University Taichung 402 Taiwan
RSC Adv. 2022 Oct 3;12(43):28052-28058. doi: 10.1039/d2ra05112e. eCollection 2022 Sep 28.
A family of aluminium complexes supported by mono-anionic indolyl-phenolate ligands are described. Reactions of indolyl-phenolate based ligand precursors, IndHPhOH, with 1.0 or 0.5 equivalents of AlMeCl in toluene afforded aluminium indolyl-phenolate complexes 1-4 and aluminium bis-indolyl-phenolate complexes 5-8 respectively. The molecular structure is reported for 5. Based on the NMR spectroscopic and X-ray crystallographic studies, a 1,3-hydrogen shift could happen from nitrogen to carbon on the five-membered ring of the indolyl group upon reacting with aluminium reagents. These novel aluminium complexes demonstrate catalytic activities toward the ring-opening polymerization of cyclic esters in the presence of alcohol.
本文描述了一类由单阴离子吲哚基酚盐配体支撑的铝配合物。基于吲哚基酚盐的配体前体IndHPhOH与1.0或0.5当量的AlMeCl在甲苯中反应,分别得到吲哚基酚铝配合物1 - 4和双吲哚基酚铝配合物5 - 8。报道了配合物5的分子结构。基于核磁共振光谱和X射线晶体学研究,吲哚基与铝试剂反应时,五元环上的氢可能从氮迁移至碳。这些新型铝配合物在醇存在下对环酯的开环聚合表现出催化活性。