Tertiary
and quaternary phosphonium borane catalysts are employed
as catalysts for CO2/epoxide copolymerization. Catalyst
structures are strategically modified to gain insights into the intricate
structure–activity relationship. To quantitatively and rigorously
compare these catalysts, the copolymerization reactions were monitored
by in situ Raman spectroscopy, allowing the determination of polymerization
rate constants. The polymerization rates are very sensitive to perturbations
in phosphonium/borane substituents as well as the tether length. To
further evaluate catalysts, a nonisothermal kinetic technique has
been developed, enabling direct mapping of polymerization rate constant
(k
p) as a function of polymerization temperatures.
By applying this method, key intrinsic attributes governing catalyst
performance, such as activation enthalpy (ΔH
‡), entropy (ΔS
‡), and optimal polymerization temperature (T
opt), can be extracted in a single continuous temperature sweep
experiment. In-depth analyses reveal intricate trends between ΔH
‡, ΔS
‡, and Lewis acidity (as determined using the Gutmann–Beckett
method) with respect to structural variations. Collectively, these
results are more consistent with the mechanistic proposal in which
the resting state is a carbonate species, and the rate-determining
step is the ring-opening of epoxide. In agreement with the experimental
results, DFT calculations indicate the important contributions of
noncovalent stabilizations exerted by the phosphonium moieties. Excitingly,
these efforts identify tertiary phosphonium borane analogues, featuring
an acidic phosphonium proton, as leading catalysts on the basis of k
p and T
opt. Mediated
by phosphonium borane catalysts, epoxides such as butylene oxide (BO), n-butyl glycidyl ether (BGE), 4-vinyl cyclohexene oxide
(VCHO), and cyclohexene oxide (CHO) were copolymerized with CO2 to form polyalkylene carbonate with >95% chemo-selectivity.
The tertiary phosphonium catalysts maintain their high activity in
the presence of large excess of di-alcohols as chain-transferring
agents, affording well-defined telechelic polyols. The results presented
herein shed light on the cooperative catalysis between phosphonium
and borane.