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Flexible Tethered Binuclear Porphyrin Aluminum for the Copolymerization of CO2 and Epoxide
- Acta Polymerica Sinica Vol. 56, Issue 1, Pages: 47-57(2025)
- 作者机构：
1.中国科学院长春应用化学研究所 生态环境高分子材料重点实验室 长春 130022
2.中国科学技术大学应用化学与工程学院 合肥 230026
- 作者简介：
Shun-jie Liu, E-mail: sjliu@ciac.ac.cn
Xian-hong Wang, E-mail: xhwang@ciac.ac.cn
- 基金信息：
DOI：10.11777/j.issn1000-3304.2024.24182
CLC：- CSTR：32057.14.GFZXB.2024.7286
Published：20 January 2025，
Published Online：14 November 2024，
Received：25 June 2024，
Accepted：2024-07-19
- 稿件说明：
移动端阅览
范培鑫, 刘顺杰, 张若禹, 杨列航, 高凤翔, 陈学思, 王献红. 柔性桥联双核卟啉铝催化二氧化碳/环氧化物交替共聚反应. 高分子学报, 2025, 56(1), 47-57
Fan, P. X.; Liu, S. J.; Zhang, R. Y.; Yang, L. H.; Gao, F. X.; Chen, X. S.; Wang, X. H. Flexible tethered binuclear porphyrin aluminum for the copolymerization of CO2 and epoxide. Acta Polymerica Sinica, 2025, 56(1), 47-57
范培鑫, 刘顺杰, 张若禹, 杨列航, 高凤翔, 陈学思, 王献红. 柔性桥联双核卟啉铝催化二氧化碳/环氧化物交替共聚反应. 高分子学报, 2025, 56(1), 47-57 DOI： 10.11777/j.issn1000-3304.2024.24182. CSTR： 32057.14.GFZXB.2024.7286.
Fan, P. X.; Liu, S. J.; Zhang, R. Y.; Yang, L. H.; Gao, F. X.; Chen, X. S.; Wang, X. H. Flexible tethered binuclear porphyrin aluminum for the copolymerization of CO2 and epoxide. Acta Polymerica Sinica, 2025, 56(1), 47-57 DOI： 10.11777/j.issn1000-3304.2024.24182. CSTR： 32057.14.GFZXB.2024.7286.
摘要
受天然酶启发，协同作用被广泛应用于小分子的识别及其催化转化，但在聚合物合成领域的研究仍然有限. 本文报道了一种柔性桥联双核卟啉铝催化剂(FTBC)，成功实现了CO
2
与环氧丙烷(PO)的高效交替共聚. 该策略的关键在于通过调控柔性链的长度使得活性位点相互靠近，从而促进分子内协同作用. 受益于活性位点的协同效应，以―CH
2
―为柔性链的C
1
-Al
2
表现出优异的催化活性(380 h
-1
)及较高的聚合物选择性(96%)，优于相同条件下的单分子卟啉铝(活性为300 h
-1
，聚合物选择性为78%). 即使在低催化剂浓度下，C
1
-Al
2
也能保持较好催化活性(250 h
-1
). 动力学实验表明C
1
-Al
2
反应级数为一级，证实催化剂的分子内协同催化主导共聚过程. 本文报道了一种柔性桥联双核催化剂的构筑策略，为模块化设计高性能催化剂提供了新方向.
Abstract
Inspired by natural enzymes
the synergistic effect has been widely applied in small molecule recognition and catalysis
but the exploration of synergy in the field of polymer synthesis is limited. We reported a flexible tethered binuclear porphyrin aluminum catalyst (FTBC)
aiming to boost the alternating copolymerization of CO
2
and propylene oxide (PO). The key design of FTBC is to promote intramolecular synergy by spatial proximity of active sites through shortening the flexible chains. By shortening the flexible chain length of the FTBC
the catalytic activity of the catalys
t gradually increased. The optimal catalyst C
1
-Al
2
featured with ―CH
2
― grafting two adjacent aluminum porphyrins exhibits outstanding catalytic activity (380 h
-1
) and polymer selectivity (96%)
outperforming the monomeric catalyst m-Al (300 h
-1
polymer selectivity% = 78%). Benefiting from the intramolecular synergy of C
1
-Al
2
the catalytic activity can be maintained at a low catalyst concentration of [PO
]
/[Al
]
= 20000/1
and the molecular weight of the obtained polymer can reach 48.3 kg/mol. Kinetic studies indicated a first-order dependence on C
1
-Al
2
in the copolymerization of CO
2
/PO
confirming that the intramolecular synergistic catalysis of the catalyst dominates the copolymerization process. Here
we reported a construction strategy for a flexible tethered binuclear catalyst
which opens up a new direction for the modular design of high-performance catalysts.
关键词
双核催化剂铝卟啉协同催化二氧化碳环氧化物
Keywords
Binuclear catalystsAluminum porphyrinSynergistic catalysisCarbon dioxideEpoxide
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