The
synthesis of metal-free heterogeneous catalyst in environmental
catalysis has become a hot area of research. To achieve the goal of
sustainable recycling of biological resources and mitigation of greenhouse
gases, a novel metal-free cellulose-based Schiff-base heterogeneous
catalyst (Cell-2L) is reported in the ring-opening addition
reaction of CO2 with epoxides to synthesize cyclic carbonates
for the first time. The as-prepared samples were characterized by
Fourier-transform infrared, X-ray photoelectron spectroscopy, scanning
electron microscope, Brunauer–Emmett–Teller/Barrett–Joyner–Halenda,
solid-state NMR, and thermogravimetric analysis analyses. The successful
anchoring of nonmetal Schiff-base complex on chlorinated cellulose
is evident from the structural composition studies. The catalytic
activity results showed that the samples exhibited excellent catalytic
performance in the solvent-free condition. The yield of resultant
propylene carbonate was measured to be 98.7% with ∼100% selectivity.
The enhanced role of the present catalyst for the ring-opening addition
could be attributed to the synergy of its structural hydroxyl, phenolic
−OH, and Lewis basic (imine) groups in the catalyst, which
are capable of activating the epoxide and CO2, which efficiently
participate in the reaction together with the substantial role of
nucleophilic ionic (Br–) group from the co-catalyst.
The catalyst was effectively reused for five consequent runs without
a significant loss in the catalytic activity and showed high effectiveness
for a series of other epoxides.