Halogen bonding, parallel to hydrogen bonding, was introduced into the catalytic cycloaddition of carbon dioxide into epoxide (CCE) reactions. A series of halogen‐bond donor (XBD) catalysts of N‐iodopyridinium halide featured with N−I bond were synthesized and evaluated in CCE reactions. The optimal XBD catalyst, 4‐(dimethylamino)‐N‐iodopyridinium bromide ([DMAPI]Br), under screened conditions at 100 °C, ambient pressure, and 1 mol % catalyst loading, realized 93 % conversion of styrene oxide into cyclic carbonate in 6 h. The substrate scope was successfully extended with excellent yields (mostly ≥93 %) and quantitative selectivity (more than 99 %). 1H NMR spectroscopy of the catalyst [DMAPI]Br on substrate epoxide certified that the N−I bond directly coordinated with the epoxide oxygen. A plausible mechanism of halogen‐bonding catalysis was proposed, in which the DMAPI cation functioned as halogen‐bond donor to activate the epoxide, and the counter anion bromide attacked the methylene carbon to initiate the ring‐opening of the epoxide. CCE reactions promoted by N‐iodopyridinium halide, exemplify a first case of halogen‐bonding catalysis in epoxide activation and CO2 transformation.

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(Thio)hydantoin (HHyd) and organic superbase binary cocatalyst was illustrated tunable catalytic tool that enabled efficient ring-opening polymerization (ROP) of various cyclic ester monomers. Series of designed HHyds of diversified substitutions...

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