liu.seSearch for publications in DiVA
Change search
ReferencesLink to record
Permanent link

Direct link
Allyl type radical formation in X-irradiated glutarimide crystals studied by ENDOR and ENDOR-induced EPR
Linköping University, The Institute of Technology. Linköping University, Department of Physics, Chemistry and Biology, Chemical Physics .
Department of Physics, University of Oslo, PO Box 1048, Blindern, N-0316, Oslo, Norway.
2004 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, Vol. 6, no 13, 3604-3610 p.Article in journal (Refereed) Published
Abstract [en]

Glutarimide single crystals X-irradiated at room temperature were reinvestigated at 150 K with the purpose to obtain information about possible ring opening and other fragmentation processes involving free radicals in this compound, previously only observed to take place in aqueous solutions. In previous work, using EPR,ENDOR and EIE spectroscopy, two H-abstraction radicals present in a 3:1 relative ratio in the irradiated crystals were identified. In the present work the detection of a third radical species, III, is reported. The g- and hyperfine coupling tensors for all three radicals at 150 K were obtained. Based on simulations of the EPR spectra the relative abundance of the three radicals was estimated to be 60, 25 and 15% for radicals I, II and III, respectively. Radical III is proposed to be of the allyl radical type -CH=CH-1CH- formed formally by a concerted H2 elimination from C2 and C3 of radical I and/or from C3 and C4 of radical II. This proposal and structure is at variance with observations from aqueous solution studies of succinimide, where the CO-CH2 bond was susceptible for rupture. However, the assignment is consistent with density functional theory (DFT) calculations, predicting equivalent hyperfine interactions to the two a-type protons at C2 and C4 in excellent. agreement with the experimentally determined hyperfine coupling tensors. EIE results confirmed that both couplings originate from the same radical species. Possible mechanisms for the formation of radical III are discussed.

Place, publisher, year, edition, pages
2004. Vol. 6, no 13, 3604-3610 p.
National Category
Engineering and Technology
URN: urn:nbn:se:liu:diva-45690DOI: 10.1039/b400730aOAI: diva2:266586
Available from: 2009-10-11 Created: 2009-10-11 Last updated: 2011-01-12

Open Access in DiVA

No full text

Other links

Publisher's full text

Search in DiVA

By author/editor
Lund, Anders
By organisation
The Institute of TechnologyChemical Physics
In the same journal
Physical Chemistry, Chemical Physics - PCCP
Engineering and Technology

Search outside of DiVA

GoogleGoogle Scholar
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Altmetric score

Total: 6 hits
ReferencesLink to record
Permanent link

Direct link