17850162

Source:http://linkedlifedata.com/resource/pubmed/id/17850162

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0070417, umls-concept:C0205131, umls-concept:C1880022
pubmed:issue	21
pubmed:dateCreated	2007-10-5
pubmed:abstractText	Spectroscopic data are consistent with computations that show that, in their most stable conformations, the peroxyl moiety is equatorial in cyclohexylperoxyl radicals and axial in oxa- and most polyoxacyclohexyl-2-peroxyl radicals.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Oct
pubmed:issn	0022-3263
pubmed:author	pubmed-author:DiLabioGino AGA, pubmed-author:IngoldKeith UKU, pubmed-author:WaltonJohn CJC
pubmed:issnType	Print
pubmed:day	12
pubmed:volume	72
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	8095-8
pubmed:year	2007
pubmed:articleTitle	Characterization of equatorial and axial six-membered-ring peroxyl radicals.
pubmed:affiliation	National Institute for Nanotechnology, National Research Council of Canada, 11421 Saskatchewan Drive, Edmonton, AB, Canada T6G 2M9.
pubmed:publicationType	Journal Article