Photo-controlled RAFT polymerization mediated by organic/inorganic hybrid photoredox catalysts: enhanced catalytic efficiency
Literature Information
Wulong Wang, Sheng Zhong, Guicheng Wang, Hongliang Cao, Yun Gao, Weian Zhang
Metalloporphyrins (MTPPs) play an important role in the conversion of light energy to initiate photoinduced electron transfer–reversible addition–fragmentation chain transfer (PET-RAFT) polymerization, in which zinc tetraphenylporphyrin (ZnTPP) has attracted a high degree of attention. However, the self-aggregation effect of porphyrins in some organic solvents such as dimethyl sulphoxide (DMSO) leads to quenching of the excited state of the MTPPs and reduces their photocatalytic capacity in a concentration-dependent manner. In this study, a ZnTPP–POSS organic/inorganic complex was fabricated by linking a polyhedral oligomeric silsesquioxane (POSS) to ZnTPP. The aggregation of the photocatalyst was efficiently depressed in a PET-RAFT polymerization which was catalyzed by ZnTPP–POSS under green light (λmax = 515 nm, 3 mW cm−2). Compared to ZnTPP, the reactions using ZnTPP–POSS as the photocatalyst were well controlled for different monomers with accelerated reaction rates. Well-defined block copolymers were successfully achieved by the chain-extension reaction which demonstrates the high-end fidelities of this polymerization approach.
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