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- W3099856823 abstract "ConspectusResearch interest in the isocyanide-based reaction can be traced back to 1921 when the Passerini reaction was first reported. However, most of these research efforts did not lead to important progress in the synthesis of isocyanide-based polymers (IBPs). The major challenge resides in the lack of highly efficient polymerization methods, which limits large-scale preparation and applications. Modern organic chemistry provides efficient access to develop functional IBPs on the basis of isocyanide chemistry. However, it is still challenging to prepare the IBPs with small molecular isocyanide reaction. Our investigations into catalyst exploration and polymerization methodology have prompted the synthesis of a series of IBPs. Two classes of isocyanide monomers can be used for the construction of IBPs. The first class includes monomers with a single isocyanide. Novel catalysts for the synthetic chemistry of isocyanide allow the introduction of functional pendants into the linear polymer chains. This molecular functionalization endows the polymers with an array of new functional properties. For example, the incorporation of a chromophore on the polymeric side chain provides novel functional properties, such as aggregation-induced emission and optical activity. Diisocyanide monomers can be also utilized for the construction of heterocyclic, spiro-heterocyclic, and bispiro-heterocyclic polymers in the polymeric backbones. A new concept of “multi-component spiropolymerization” has been developed for the preparation of spiropolymers using the catalysis-free one-pot reaction. Proper structural design allows for the preparation of a heterocyclic polymeric chain with natural bioactivity and biological compatibility, generating new IBPs with biofunctionalities.In this Account, we discuss progress mainly made in our lab and related fields for the design of isocyanide monomers, exploration of new catalysts, and optimization of reaction conditions. The subsequent section discusses the characteristic properties and applications of selected examples of these functional polymers, mainly focusing on their optical applications. We have investigated the UV-sensitive IBPs that could potentially be used for lithography applications. One-pot highly efficient polymerization of diisocyanides and CO2 under mild conditions can provide a new method for realizing the reuse of CO2 and reducing the greenhouse effect. Through a combination of structural modifications, IBPs bearing dimethylbenzene moieties exhibit characteristics of black materials that can be potentially utilized as pyroelectric sensors, thermal detectors, and optical instruments. Most recently, our group synthesized a spiro-heterocyclic IBP with clusterization-triggered emission properties that can be used to discriminate cancer cells from normal cells and provides a new method for the treatment of cancer. The studies reviewed in this Account suggest that polymerization with isocyanide chemistry can be implemented in diverse functional macromolecules and materials." @default.
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- W3099856823 date "2020-11-20" @default.
- W3099856823 modified "2023-10-17" @default.
- W3099856823 title "Functional Isocyanide-Based Polymers" @default.
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- W3099856823 cites W1990944927 @default.
- W3099856823 cites W1992167318 @default.
- W3099856823 cites W2001838359 @default.
- W3099856823 cites W2004097711 @default.
- W3099856823 cites W2011308025 @default.
- W3099856823 cites W2024193909 @default.
- W3099856823 cites W2027931033 @default.
- W3099856823 cites W2050172055 @default.
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- W3099856823 cites W2111369411 @default.
- W3099856823 cites W2111677437 @default.
- W3099856823 cites W2127378043 @default.
- W3099856823 cites W2163275184 @default.
- W3099856823 cites W2179947938 @default.
- W3099856823 cites W2312242265 @default.
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- W3099856823 cites W2626741012 @default.
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- W3099856823 doi "https://doi.org/10.1021/acs.accounts.0c00514" @default.
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