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用于高效光氧化的均相供体-受体共轭聚合物的异质化:一种实现可持续和可回收光催化的方法。

Heterogenization of Homogeneous Donor-Acceptor Conjugated Polymers for Efficient Photooxidation: An Approach Toward Sustainable and Recyclable Photocatalysis.

作者信息

Maity Krishnendu, Sau Soumitra, Banerjee Flora, Samanta Suman Kalyan

机构信息

Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302, India.

出版信息

ACS Appl Mater Interfaces. 2024 Sep 25;16(38):50834-50845. doi: 10.1021/acsami.4c11131. Epub 2024 Sep 16.

DOI:10.1021/acsami.4c11131
PMID:39284797
Abstract

Recovery of homogeneous photocatalysts from reaction mixture is challenging, affecting the cost-effectiveness, and masks their advantages, including 4-8 fold higher catalytic activity than corresponding heterogeneous counterparts. Incorporation of long alkyl chains within the rigid π-conjugated backbone of conjugated polymers can augment their solubility in particular organic solvents; accordingly, they can function as homogeneous photocatalysts. Consequently, these polymers facilitate the recovery of catalysts through the reverse dissolution process, thus creating a well-suited platform to meet certain advantages of both homo- and heterogeneous photocatalysts. This work exemplifies the unprecedented perks of donor-acceptor conjugated polymers from benzodithiophene and substituted dibenzothiophene sulfone moieties for their homogeneous phase photoredox activities along with their heterogeneous recovery and reuse up to five runs. The potential intermediate singlet oxygen (O) and superoxide (O•) as reactive oxygen species generated by these photostable conjugated polymers efficiently catalyze the visible-light-driven oxidation of aryl sulfides (up to 92% yield) and oxidative hydroxylation of phenylboronic acids (up to 93% yield), respectively. Therefore, to actualize the heightened catalytic performance and formulate a design strategy for polymeric photoredox catalyst, our work introduces an alternative approach to the advancement of photocatalysis with diverse catalytic activities.

摘要

从反应混合物中回收均相光催化剂具有挑战性,这影响了成本效益,并掩盖了它们的优势,包括其催化活性比相应的非均相光催化剂高4至8倍。在共轭聚合物的刚性π共轭主链中引入长烷基链可以提高它们在特定有机溶剂中的溶解度;因此,它们可以作为均相光催化剂发挥作用。因此,这些聚合物通过反向溶解过程促进了催化剂的回收,从而创建了一个适合的平台,兼具均相和非均相光催化剂的某些优势。这项工作例证了由苯并二噻吩和取代二苯并噻吩砜部分组成的供体-受体共轭聚合物在均相光氧化还原活性以及非均相回收和重复使用高达五次方面前所未有的优势。这些光稳定的共轭聚合物产生的潜在活性氧物种——单线态氧(O)和超氧阴离子(O•),分别有效地催化了芳基硫化物的可见光驱动氧化反应(产率高达92%)和苯基硼酸的氧化羟基化反应(产率高达93%)。因此,为了实现更高的催化性能并制定聚合物光氧化还原催化剂的设计策略,我们的工作为具有不同催化活性的光催化研究引入了一种替代方法。

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