The
catalytic conversion of greenhouse gas CO2 into
valuable chemicals is a vital goal toward carbon balance and sustainability.
In recent decades, the chemical fixation of CO2 into cyclic
carbonates has gained much attention. In this work, a series of zinc
complexes bearing tetradentate aminopyridine (N4) ligands have been
synthesized and characterized. These zinc complexes were applied to
the coupling of CO2 with epoxides in excellent yields and
with a broad substrate scope under cocatalyst- and solvent-free conditions.
Moreover, the zinc catalysts could be readily recovered and reused
five times without an obvious loss in catalytic activity. Based on
spectroscopic characterizations and experimental results, catalyst Zn-3 (DAP-ZnBr2, DAP = 1,4-bis(2-pyridymethyl)-1,4-diazepane)
has been found to be a multifunctional catalyst because of the presence
of a Lewis acidic zinc center and a nuclephilic halide anion, and
one pyridine is released for the activation of CO2 during
the reaction