Sobrino Sonia, Navarro Marta, Fernández-Baeza Juan, Sánchez-Barba Luis F, Garcés Andrés, Lara-Sánchez Agustín, Castro-Osma José A
Universidad de Castilla-La Mancha, Departamento de Química Inorgánica, Orgánica y Bioquímica, Centro de Innovación en Química Avanzada (ORFEO-CINQA) Campus Universitario, 13071-Ciudad Real, Spain.
Universidad Rey Juan Carlos, Departamento de Biología y Geología, Física y Química Inorgánica, Móstoles-28933-Madrid, Spain.
Dalton Trans. 2019 Jul 16;48(28):10733-10742. doi: 10.1039/c9dt01844a.
A series of new chiral zwitterionic NNO-scorpionate mononuclear zinc alkyls [Zn(R)(κ3-NNO)]Br was developed in very high yields via suitable quaternization in the scorpionate ligand. These zwitterionic complexes performed as bifunctional catalysts and exhibited improved catalytic activity for the fixation of CO2 into cyclic carbonates compared to the neutral analog mononuclear [Zn(R)(κ3-NNO)] and binuclear [Zn(R)(κ2-NNμ-O)Zn(R)2] compounds. The catalyst system showed a broad substrate scope and functional group tolerance under mild and solvent-free conditions.
通过在蝎形配体中进行合适的季铵化反应,以非常高的产率制备了一系列新型手性两性离子NNO-蝎形单核锌烷基化合物[Zn(R)(κ3-NNO)]Br。与中性类似物单核[Zn(R)(κ3-NNO)]和双核[Zn(R)(κ2-NNμ-O)Zn(R)2]化合物相比,这些两性离子配合物作为双功能催化剂,在将CO2固定为环状碳酸酯方面表现出更高的催化活性。该催化体系在温和且无溶剂的条件下显示出广泛的底物范围和官能团耐受性。