Premium
Ionic Polymer Microspheres Bearing a Co III –Salen Moiety as a Bifunctional Heterogeneous Catalyst for the Efficient Cycloaddition of CO 2 and Epoxides
Author(s) -
Leng Yan,
Lu Dan,
Zhang Chenjun,
Jiang Pingping,
Zhang Weijie,
Wang Jun
Publication year - 2016
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201600755
Subject(s) - bifunctional , catalysis , chemistry , cycloaddition , moiety , cobalt , polymer chemistry , bipyridine , ionic bonding , schiff base , medicinal chemistry , organic chemistry , ion , crystal structure
We report a unique strategy to obtain the bifunctional heterogeneous catalyst TBB‐Bpy@Salen‐Co (TBB=1,2,4,5‐tetrakis(bromomethyl)benzene, Bpy=4,4’‐bipyridine, Salen‐Co= N , N ’‐bis({4‐dimethylamino}salicylidene)ethylenediamino cobalt(III) acetate) by combining a cross‐linked ionic polymer with a Co III –salen Schiff base. The catalyst showed extra high activity for CO 2 fixation under mild, solvent‐free reaction conditions with no requirement for a co‐catalyst. The synthesized catalyst possessed distinctive spherical structural features, abundant halogen Br − anions with good leaving group ability, and accessible Lewis acidic Co metal centers. These unique features, together with the synergistic role of the Co and Br − functional sites, allowed TBB‐Bpy@Salen‐Co to exhibit enhanced catalytic conversion of CO 2 into cyclic carbonates relative to the corresponding monofunctional analogues. This catalyst can be easily recovered and recycled five times without significant leaching of Co or loss of activity. Moreover, based on our experimental results and previous work, a synergistic cycloaddition reaction mechanism was proposed.