Synthesis of fluorinated alkoxyamines and alkoxyamine-initiated nitroxide-mediated precipitation polymerizations of styrene in supercritical carbon dioxide
Polymer Chemistry, ISSN: 1759-9962, Vol: 5, Issue: 19, Page: 5725-5733
2014
- 16Citations
- 17Captures
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Article Description
TIPNO (2,2,5-trimethyl-4-phenyl-3-azahexane-3-nitroxide)-alkoxyamine was found to give reasonably controlled/living nitroxide-mediated (NMP) precipitation polymerizations of styrene in supercritical carbon dioxide (scCO). In contrast under the same conditions, the analogous SG1 (N-tert-butyl-N-(1-diethylphosphono-2,2-dimethylpropyl)nitroxide)-alkoxyamine gave higher rates of polymerization and inferior controlled/living character. The circumvention of the requirement for excess free [nitroxide] allowed the study of nitroxide partitioning effects in scCO for three newly synthesized fluorinated alkoxyamines. Two alkoxyamines dissociated into scCO-philic fluorinated TIPNO-nitroxide derivatives, while another contains a similar sized fluorinated "foot". Despite the increased steric bulk about the N-O bond for the novel fluorinated alkoxyamines, all polymerizations proceeded at a similar rate and level of control to the TIPNO system in solution (toluene). PREDICI simulations for the styrene/TIPNO system are used to support extensive partitioning effects observed in scCO for the fluorinated alkoxyamines. © 2014 the Partner Organisations.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84906684305&origin=inward; http://dx.doi.org/10.1039/c4py00757c; http://xlink.rsc.org/?DOI=C4PY00757C; http://pubs.rsc.org/en/content/articlepdf/2014/PY/C4PY00757C; https://xlink.rsc.org/?DOI=C4PY00757C; https://dx.doi.org/10.1039/c4py00757c; https://pubs.rsc.org/en/content/articlelanding/2014/PY/C4PY00757C
Royal Society of Chemistry (RSC)
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