Trityl-based alkoxyamines as NMP controllers and spin-labels Full article
Journal |
Polymer Chemistry
ISSN: 1759-9954 , E-ISSN: 1759-9962 |
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Output data | Year: 2016, Volume: 7, Number: 42, Pages: 6490-6499 Pages count : 10 DOI: 10.1039/c6py01303a | ||||||
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Abstract:
Recently, new applications of trityl-nitroxide biradicals were proposed. In the present study, attachment of a trityl radical to alkoxyamines was performed for the first time. The rate constants k(d) of C-ON bond homolysis in these alkoxyamines were measured and found to be similar to those for alkoxyamines without a trityl moiety. The electron paramagnetic resonance (EPR) spectra of the products of alkoxyamine homolysis (trityl-TEMPO and trityl-SG1 biradicals) were recorded, and the corresponding exchange interactions were estimated. The decomposition of trityl-alkoxyamines showed more than an 80% yield of biradicals, meaning that the C-ON bond homolysis is the main reaction. The suitability of these labelled initiators/controllers for polymerisation was exemplified by means of a successful nitroxide-mediated polymerisation (NMP) of styrene. Thus, this is the first report of a spin-labelled alkoxyamine suitable for NMP.
Cite:
Audran G.
, Bagryanskaya E.G.
, Bremond P.
, Edeleva M.V.
, Marque S.R.A.
, Parkhomenko D.A.
, Rogozhnikova O.Y.
, Tormyshev V.M.
, Tretyakov E.V.
, Trukhin D.V.
, Zhivetyeva S.I.
Trityl-based alkoxyamines as NMP controllers and spin-labels
Polymer Chemistry. 2016. V.7. N42. P.6490-6499. DOI: 10.1039/c6py01303a WOS Scopus РИНЦ
Trityl-based alkoxyamines as NMP controllers and spin-labels
Polymer Chemistry. 2016. V.7. N42. P.6490-6499. DOI: 10.1039/c6py01303a WOS Scopus РИНЦ
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Identifiers:
Web of science | WOS:000387071800008 |
Scopus | 2-s2.0-84992708439 |
Elibrary | 27583413 |
OpenAlex | W2530646635 |