Direct Observation of Chain Lengths and Conformations in Oligofluorene Distributions from Controlled Polymerization by Double Electron-Electron Resonance
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Synthetic polymers are mixtures of chains with different lengths, and their chain length and chain conformation are often experimentally characterized by ensemble averages. We demonstrate that double electron-electron resonance (DEER) spectroscopy can reveal the chain length distribution and the chain conformation and flexibility of the individual n-mers in oligo-(9,9-dioctylfluorene) from controlled Suzuki-Miyaura coupling polymerization. The required spin-labeled chain ends were introduced efficiently via a TEMPO-substituted initiator and chain-terminating agent, respectively, with an in situ catalyst system. Individual precise chain length oligomers as reference materials were obtained by a stepwise approach. Chain length distribution, chain conformation, and flexibility can also be accessed within poly(fluorene) nanoparticles.
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BÜCKER, Dennis, Annika SICKINGER, Julian Dominik RUIZ PEREZ, Manuel OESTRINGER, Stefan MECKING, Malte DRESCHER, 2020. Direct Observation of Chain Lengths and Conformations in Oligofluorene Distributions from Controlled Polymerization by Double Electron-Electron Resonance. In: Journal of the American Chemical Society. American Chemical Society (ACS). 2020, 142(4), pp. 1952-1956. ISSN 0002-7863. eISSN 1520-5126. Available under: doi: 10.1021/jacs.9b11404BibTex
@article{Bucker2020-01-29Direc-48198, year={2020}, doi={10.1021/jacs.9b11404}, title={Direct Observation of Chain Lengths and Conformations in Oligofluorene Distributions from Controlled Polymerization by Double Electron-Electron Resonance}, number={4}, volume={142}, issn={0002-7863}, journal={Journal of the American Chemical Society}, pages={1952--1956}, author={Bücker, Dennis and Sickinger, Annika and Ruiz Perez, Julian Dominik and Oestringer, Manuel and Mecking, Stefan and Drescher, Malte} }
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