Trapping polystyrene radicals using nitrones: Synthesis of polymers with mid-chain alkoxyamine functionality
Polystyrene radicals were formed in the presence of NtBPN under a variety of reaction conditions and reactant ratios, forming polymer dimers of twice the molecular weight of the monobrominated polystyrene (PStBr) precursors. The polystyrene radicals were generated by the activation of the monohaloge...
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Published in | Polymer (Guilford) Vol. 52; no. 26; pp. 6003 - 6010 |
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Main Authors | , |
Format | Journal Article |
Language | English |
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13.12.2011
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Abstract | Polystyrene radicals were formed in the presence of NtBPN under a variety of reaction conditions and reactant ratios, forming polymer dimers of twice the molecular weight of the monobrominated polystyrene (PStBr) precursors. The polystyrene radicals were generated by the activation of the monohalogentated polystyrene precursors, prepared by atom transfer radical polymerization (ATRP). The extent of radicals trapped by the nitrone, and therefore containing mid-chain alkoxyamine functionality, was determined by thermolysis of the polymer dimers, with the C–O bond in this functionality being cleaved and reverting the chains back to the approximate size of the precursors. Polymer dimers could also be formed simply by radical–radical combination of the chain-ends, which is conventional atom transfer radical coupling (ATRC) and thus contains a head-to-head C–C bond, rendering them inert to thermolysis under conditions that cleave the C–O bond. It was found that near quantitative alkoxyamine mid-chain functionality could be achieved by activating the PStBr in the presence of 10 equivalents of nitrone, 5 equivalents of copper bromide, and 2 equivalents of copper metal. Further reducing the amount of copper metal led to incomplete coupling, while increasing the equivalents beyond 2 generated polymer dimers with less than quantitative mid-chain functionality. Monochlorinated polystyrene (PStCl) precursors gave much poorer coupling results compared to reactions with PStBr, which is consistent with the stronger C–Cl bond resisting activation and the formation of the polystyryl radicals.
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AbstractList | Polystyrene radicals were formed in the presence of NtBPN under a variety of reaction conditions and reactant ratios, forming polymer dimers of twice the molecular weight of the monobrominated polystyrene (PStBr) precursors. The polystyrene radicals were generated by the activation of the monohalogentated polystyrene precursors, prepared by atom transfer radical polymerization (ATRP). The extent of radicals trapped by the nitrone, and therefore containing mid-chain alkoxyamine functionality, was determined by thermolysis of the polymer dimers, with the C–O bond in this functionality being cleaved and reverting the chains back to the approximate size of the precursors. Polymer dimers could also be formed simply by radical–radical combination of the chain-ends, which is conventional atom transfer radical coupling (ATRC) and thus contains a head-to-head C–C bond, rendering them inert to thermolysis under conditions that cleave the C–O bond. It was found that near quantitative alkoxyamine mid-chain functionality could be achieved by activating the PStBr in the presence of 10 equivalents of nitrone, 5 equivalents of copper bromide, and 2 equivalents of copper metal. Further reducing the amount of copper metal led to incomplete coupling, while increasing the equivalents beyond 2 generated polymer dimers with less than quantitative mid-chain functionality. Monochlorinated polystyrene (PStCl) precursors gave much poorer coupling results compared to reactions with PStBr, which is consistent with the stronger C–Cl bond resisting activation and the formation of the polystyryl radicals. Polystyrene radicals were formed in the presence of NtBPN under a variety of reaction conditions and reactant ratios, forming polymer dimers of twice the molecular weight of the monobrominated polystyrene (PStBr) precursors. The polystyrene radicals were generated by the activation of the monohalogentated polystyrene precursors, prepared by atom transfer radical polymerization (ATRP). The extent of radicals trapped by the nitrone, and therefore containing mid-chain alkoxyamine functionality, was determined by thermolysis of the polymer dimers, with the C–O bond in this functionality being cleaved and reverting the chains back to the approximate size of the precursors. Polymer dimers could also be formed simply by radical–radical combination of the chain-ends, which is conventional atom transfer radical coupling (ATRC) and thus contains a head-to-head C–C bond, rendering them inert to thermolysis under conditions that cleave the C–O bond. It was found that near quantitative alkoxyamine mid-chain functionality could be achieved by activating the PStBr in the presence of 10 equivalents of nitrone, 5 equivalents of copper bromide, and 2 equivalents of copper metal. Further reducing the amount of copper metal led to incomplete coupling, while increasing the equivalents beyond 2 generated polymer dimers with less than quantitative mid-chain functionality. Monochlorinated polystyrene (PStCl) precursors gave much poorer coupling results compared to reactions with PStBr, which is consistent with the stronger C–Cl bond resisting activation and the formation of the polystyryl radicals. [Display omitted] |
Author | Radzinski, Scott C. Tillman, Eric S. |
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Keywords | Atom transfer radical polymerization Polystyrene Nitroxide mediated polymerization Copper bromide End group Nitrone Atom transfer polymerization Activation Experimental study Free radical reaction Optimization Operating conditions Chemical coupling Monodispersed polymer Macroradical Styrene polymer Dimerization Functional group |
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Snippet | Polystyrene radicals were formed in the presence of NtBPN under a variety of reaction conditions and reactant ratios, forming polymer dimers of twice the... |
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SubjectTerms | Activation Applied sciences Atom transfer radical polymerization Bonding Dimers Equivalence Exact sciences and technology free radicals Joining molecular weight Nitroxide mediated polymerization Organic polymers Physicochemistry of polymers Polymerization Polystyrene Polystyrene resins polystyrenes Precursors Preparation, kinetics, thermodynamics, mechanism and catalysts Radicals thermal degradation |
Title | Trapping polystyrene radicals using nitrones: Synthesis of polymers with mid-chain alkoxyamine functionality |
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