Abstract

A series of thiol-ene (1.1:1 equiv) polymer microbeads (PMBs) were prepared via a high-shear suspension photopolymerization method to explore the physical properties of the networks as a function of composition. 1,3,5-triallyl-1,3,5-triazine-2,4,6(1H, 3H, 5H)-trione (TTT) and pentaerythritol tetrakis (3-mercaptopropionate) (PETMP) PMBs were selected for the synthesis of a heterogeneous photocatalyst. Particle size was characterized using DLS and OM, and thermal stability and Tg were assessed using TGA and DSC. PMBs produced from higher functionality monomers produce smaller particles, and Tg increased with monomer rigidity. TTT-PETMP PMBs were derivatized with C60 to demonstrate the accessibility and reactivity of the residual thiols, successful inclusion of C60 as the reactive ene moiety, and overall PMB utility as a scaffold material. Upon capping with C60, the Tg of the composite particles increased significantly. Most importantly, the C60-capped PMBs produced singlet oxygen in direct and indirect chemical assays, and the efficiency did not decrease after recycling.

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