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二氧化硒催化的氮掺杂聚(苯并二呋喃二酮)(n-PBDF)及其衍生物的聚合反应

Selenium Dioxide Catalyzed Polymerization of N-doped Poly(benzodifurandione) (n-PBDF) and Its Derivatives.

作者信息

Liu Guangchao, Hsu Hsuan-Hao, Samal Sanket, Lee Won-June, Ke Zhifan, You Liyan, Savoie Brett M, Mei Jianguo

机构信息

Department of Chemistry, Purdue University West Lafayette, Indiana, 47907, United States.

Davidson School of Chemical Engineering, Purdue University West Lafayette, Indiana, 47907, United States.

出版信息

Angew Chem Int Ed Engl. 2025 Feb 3;64(6):e202418668. doi: 10.1002/anie.202418668. Epub 2024 Nov 16.

Abstract

The recent discovery of highly conductive, solution-processable, n-doped poly(benzodifurandione) (n-PBDF) marks a milestone in the development of conducting polymers. Currently, n-PBDF is prepared by either duroquinone-mediated or copper-catalyzed polymerizations, where scalability and cost-effectiveness may present challenges. Here, we report a general, scalable, and cost-effective method for n-PBDF and its derivatives, namely selenium dioxide (SeO) catalyzed polymerization. We discovered that a catalytic amount of selenium dioxide leads to high monomer conversions (>99 % by NMR). The obtained n-PBDF exhibits a consistently narrow hydrodynamic diameter distribution and its thin films show high conductivities. Furthermore, we revealed that this polymerization involves a mechanism distinct from the previously reported radical pathway. It involves successive Riley oxidation and aldol polycondensation processes. It was also found that the reduced selenium precipitates from dimethyl sulfoxide (DMSO) when the catalytic cycle is terminated, allowing for a straightforward purification process through centrifugation and filtration. This method thus eliminates the need for the costly and slow dialysis process. Finally, we demonstrated that SeO catalyzed polymerization is applicable to n-PBDF derivatives, proving the generality of this method.

摘要

最近发现的高导电性、可溶液加工的n型掺杂聚(苯并二呋喃二酮)(n-PBDF)是导电聚合物发展中的一个里程碑。目前,n-PBDF是通过对苯二酚介导或铜催化聚合制备的,其中可扩展性和成本效益可能面临挑战。在此,我们报道了一种用于n-PBDF及其衍生物的通用、可扩展且具有成本效益的方法,即二氧化硒(SeO)催化聚合。我们发现,催化量的二氧化硒可实现高单体转化率(通过核磁共振>99%)。所获得的n-PBDF表现出始终狭窄的流体动力学直径分布,其薄膜具有高导电性。此外,我们揭示了这种聚合涉及一种不同于先前报道的自由基途径的机制。它涉及连续的莱利氧化和羟醛缩聚过程。还发现,当催化循环终止时,还原态硒会从二甲基亚砜(DMSO)中沉淀出来,从而可通过离心和过滤进行直接纯化。因此,该方法无需进行昂贵且耗时的透析过程。最后,我们证明了SeO催化聚合适用于n-PBDF衍生物,证明了该方法的通用性。

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