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用于引发传统自由基和基于原子转移自由基聚合(ATRP)的光聚合过程的生物质衍生碳点。

Biomass-derived carbon dots for the initiation of conventional radical and ATRP-based photopolymerization processes.

作者信息

Luo Xiongfei, Liu Xue, Guo Hongda, Li Ruiping, Wang Min, Li Xiaotong, Li Shujun, Liu Shouxin, Li Jian, Strehmel Veronika, Wang Qunying, Yilmaz Gorkem, Matyjaszewski Krzysztof, Strehmel Bernd, Chen Zhijun

机构信息

College of Chemistry, Chemical Engineering and Resource Utilization, Northeast Forestry University, Harbin, China.

Key Laboratory of Bio-based Material Science and Technology Northeast Forestry University, Ministry of Education, Harbin, China.

出版信息

Nat Protoc. 2025 Aug 4. doi: 10.1038/s41596-025-01210-3.

Abstract

In recent years, there has been increasing interest in using carbon nanodots (CDs) as a component photoinitiator to initiate photopolymerization. These systems support conventional radical photopolymerization and light-mediated atom transfer radical polymerization (photo-ATRP), emphasizing single-component (Type I initiators) and multicomponent systems, which involve at least two reaction partners, specifically, the Type II CD initiator. The latter can function in both photoinduced conventional radical polymerization and photo-ATRP. CDs provide an important advantage by reducing toxicological concerns, as they are nontoxic to cells, and minimizing migration issues typically associated with molecular systems. Here we present two novel photopolymerization methods utilizing biomass-derived CDs as light-sensitive components. The first approach uses biobased furfural to create a Type I CD initiator for photoinduced uncontrolled radical polymerization, which initiates polymerization via homolytic bond cleavage of oxime ester groups attached to the CD surface. The second method employs sodium alginate to generate CDs capable of initiating photoinduced radical polymerization or activating alkyl halides in photo-ATRP processes. Key topics covered in these methods include (1) preparation and characterization of biomass-derived CDs; (2) experimental procedures for CD-assisted photo-induced conventional radical polymerization and photo-ATRP and (3) analysis of the resulting polymers. Preparing and characterizing the CDs takes ~4 d, while photochemical reactions can be conducted within 1 h, depending on requirements. Product separation and analysis take an additional 0.5 h. This protocol is designed for users with experience in polymer chemistry and CD handling.

摘要

近年来,人们越来越关注使用碳纳米点(CDs)作为组分光引发剂来引发光聚合反应。这些体系支持传统的自由基光聚合和光介导的原子转移自由基聚合(光引发原子转移自由基聚合,photo-ATRP),重点是单组分(I型引发剂)和多组分体系,后者涉及至少两个反应伙伴,特别是II型CD引发剂。II型CD引发剂可在光诱导的传统自由基聚合和光引发原子转移自由基聚合中发挥作用。CDs具有减少毒理学问题的重要优势,因为它们对细胞无毒,并且可将通常与分子体系相关的迁移问题降至最低。在此,我们展示了两种利用生物质衍生的CDs作为光敏组分的新型光聚合方法。第一种方法使用生物基糠醛来制备用于光诱导的无控自由基聚合的I型CD引发剂,该引发剂通过CD表面连接的肟酯基团的均裂来引发聚合反应。第二种方法采用海藻酸钠来制备能够引发光诱导自由基聚合或在光引发原子转移自由基聚合过程中活化卤代烃的CDs。这些方法涵盖的关键主题包括:(1)生物质衍生的CDs的制备和表征;(2)CD辅助的光诱导传统自由基聚合和光引发原子转移自由基聚合的实验步骤;(3)所得聚合物的分析。制备和表征CDs大约需要4天,而光化学反应根据要求可在1小时内完成。产物分离和分析还需要额外0.5小时。本方案是为有聚合物化学和CD处理经验的用户设计的。

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