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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20055
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dc.contributor.authorBullock, Anthony T-
dc.date.accessioned2025-11-17T04:50:30Z-
dc.date.available2025-11-17T04:50:30Z-
dc.date.issued1978-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20055-
dc.descriptionA high molecular weight sample of anionically prepared polystyrene has been labelled specifically at the chain ends with nitroxide radicals. Line width analysis of the e.s.r. spectra of dilute solutions of the polymer gave rotational correlation times of the chain ends. The solvents used were toluene, α-chloronaphthalene and cyclohexane. After making allowance for the viscous drag of the solvent energy barriers to rotation were obtained and compared with those found previously for the random segmentally labelled polymer. Differences have been shown to arise through the internal barrier to rotation rather than through the pre-exponential term. It was found possible to show that the rotational mobility of the nitroxide was strictly governed by the mobility of the polymer chain end since the correlation time for rotation about the polymer—label bond was never less than 4τc, where τc is the observed correlation time for rotational diffusion of the nitroxide.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (3)en_US
dc.subjectChemistryen_US
dc.subjectElectron spin resonanceen_US
dc.subjectSpin-labelled polymersen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleElectron Spin Resonance Studies of Spin-Labelled Polymers: Part 14.—End-group Mobility of Polystyrene as a Function of Temperature and Solventen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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