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The incorporation of strained alkynes into polymers is generally achieved by employing step-growth polymerization methods or post-polymerization reactions. Here, we demonstrate that cyclopropenone-masked strained alkynes are tolerant to chain-growth ring-opening metathesis polymerization, and that, upon post-polymerization photochemical demasking with loss of CO, the strained alkyne group appended to each repeating unit can be used to prepare functional (e.g., fluorescent or redox-active) polymers from a common polymer backbone. We support our claims about polymer transformations throughout the manuscript through the inclusion of a complete set of model reactions and characterization data for analogous molecular species. The findings of this study are transferable to other polymeric systems, opening the door to the creation of libraries of multifunctional chain-growth polymers with identical polymer backbones.

The bottom-up synthesis of self-assembled micro-compartmentalised systems that mimic basic characteristics of living cells is rapidly evolving. These types of systems are termed “protocells” and can be chemically programmed to grow and divide, to send and receive chemical signals, to transcript and translate chemical information, to adhere to surfaces or to other protocells, and to perform rudimental enzyme-mediated metabolic processes. An emerging protocell model that is attracting great attention is the colloidosome. Colloidosomes are microcapsules with a chemically crosslinked, semipermeable membrane composed of amphiphilic nanoparticles. Colloidosomes display important advantages over other protocell models (e. g., vesicles and coacervate micro-droplets) due to their physical-chemical properties that can be easily tuned through the careful engineering of their synthetic building blocks. In this review, we deliver an overview of the different types of colloidosomes that have been developed thus far and discuss how organic chemistry contributes to the design and bottom-up synthesis of novel types of colloidosomes endowed with advanced chemically programmed bio-inspired functions.