Qiu, H.; Zhang, P. F.; Zhao, J. P. Amine-actuated catalyst switch for one-pot synthesis of ether-ester type block copolymers. Chinese J. Polym. Sci. 2024, 42, 1925–1932
Hong Qiu, Peng-Fei Zhang, Jun-Peng Zhao. Amine-Actuated Catalyst Switch for One-Pot Synthesis of Ether-Ester Type Block Copolymers[J]. Chinese Journal of Polymer Science, 2024, 42(12): 1925-1932.
Qiu, H.; Zhang, P. F.; Zhao, J. P. Amine-actuated catalyst switch for one-pot synthesis of ether-ester type block copolymers. Chinese J. Polym. Sci. 2024, 42, 1925–1932DOI: 10.1007/s10118-024-3193-6.
Hong Qiu, Peng-Fei Zhang, Jun-Peng Zhao. Amine-Actuated Catalyst Switch for One-Pot Synthesis of Ether-Ester Type Block Copolymers[J]. Chinese Journal of Polymer Science, 2024, 42(12): 1925-1932.DOI: 10.1007/s10118-024-3193-6.
Amine-Actuated Catalyst Switch for One-Pot Synthesis of Ether-Ester Type Block Copolymers
Amine has been used as a selectivity-switching agent in the two-component catalytic system consisting of triethylborane and a phosphazene base. The addition of an amine promptly switches Lewis pair-catalyzed ring-opening polymerization of epoxide to organobase-catalyzed ROP of δ-valerolactone
thus facilitating one-pot block copolymerization.
Abstract
Organocatalysis has shown special potency for simplifying the construction of complex polymer structures. We are reporting here a one-pot synthetic pathway using amine as a selectivity-switching agent in the two-component catalytic system consisting of triethylborane (Et
3
B) and a phosphazene base. We first modelled the interactions of a variety of amines with Et
3
B by density functional theory calculations. The results indicate that the aliphatic diamines comprising both primary and tertiary amino groups
capable of forming stable intramolecular hydrogen bonds
undergo the strongest complexation with Et
3
B. Accordingly
experimental results demonstrate that the addition of such amines promptly actuates the
in situ
selectivity switch from Lewis pair-catalyzed ring-opening polymerization (ROP) of epoxide (propylene oxide
n
-butylglycidyl ether
or glycidyl phenyl ether) to organobase-catalyzed ROP of
δ
-valerolactone
allowing one-pot continuous synthesis of ether-ester type block copolymers. We thus exploited the noncovalent interaction between amine and Et
3
B to refine the catalyst switch strategy by exempting it from loading of extra catalyst.
关键词
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references
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