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Solvent Effects on the Intramolecular Charge Transfer Character of N,N-Diaryl Dihydrophenazine Catalysts for Organocatalyzed Atom Transfer Radical Polymerization.


ABSTRACT: The nature of intramolecular charge transfer of N,N-diaryl dihydrophenazine photocatalysts (PCs) in different solvents is explored in context of their performance in organocatalyzed atom transfer radical polymerization (O-ATRP). PCs having a computationally predicted lowest energy excited state exhibiting charge transfer (CT) character can operate a highly controlled O-ATRP in a wide range of solvent polarities, from non-polar hexanes to highly polar N,N-dimethylacetamide. For PCs having a computationally predicted lowest energy excited state not possessing CT character, their ability to operate a controlled O-ATRP is decreased. This study confirms the importance of CT character in the excited state for N,N-diaryl dihydrophenazine PCs, and a deeper understanding of the activity of CT PCs has enabled the synthesis of polymers of low dispersity ( < 1.10) in a controlled fashion.

SUBMITTER: Ryan MD 

PROVIDER: S-EPMC5614505 | biostudies-literature | 2017 Sep

REPOSITORIES: biostudies-literature

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Solvent Effects on the Intramolecular Charge Transfer Character of <i>N</i>,<i>N</i>-Diaryl Dihydrophenazine Catalysts for Organocatalyzed Atom Transfer Radical Polymerization.

Ryan Matthew D MD   Theriot Jordan C JC   Lim Chern-Hooi CH   Yang Haishen H   Lockwood Andrew A   Garrison Nathaniel G NG   Lincoln Sarah R SR   Musgrave Charles B CB   Miyake Garret M GM  

Journal of polymer science. Part A, Polymer chemistry 20170316 18


The nature of intramolecular charge transfer of <i>N</i>,<i>N</i>-diaryl dihydrophenazine photocatalysts (PCs) in different solvents is explored in context of their performance in organocatalyzed atom transfer radical polymerization (O-ATRP). PCs having a computationally predicted lowest energy excited state exhibiting charge transfer (CT) character can operate a highly controlled O-ATRP in a wide range of solvent polarities, from non-polar hexanes to highly polar <i>N</i>,<i>N</i>-dimethylaceta  ...[more]

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