@article {6736,
	title = {COMPARISON OF MUONATED FREE-RADICALS FORMED IN PURE LIQUIDS WITH THOSE IN DILUTE-SOLUTIONS - ORIGINS OF RADICALS},
	journal = {Hyperfine Interactions},
	volume = {65},
	number = {1-4},
	year = {1990},
	note = {ISI Document Delivery No.: EZ856Times Cited: 1Cited Reference Count: 95TH INTERNATIONAL CONF ON MUON SPIN ROTATION RELAXATION AND RESONANCEAPR 09-12, 1990OXFORD, ENGLAND},
	pages = {945-951},
	type = {Proceedings Paper},
	abstract = {LCR spectroscopy was used to explore the mechanism by which muonated free radicals form in unsaturated organic liquids. This was achieved by comparing the relative yields of the different radicals formed from the compound as a pure liquid with those found when it was studied as a solute in dilute aqueous micelle solutions. In the latter medium, thermalized muonium atoms are the only precursors. Two types of examples were evaluated: first, styrene and allylbenzene since they give a full range of side-chain and ring addition products; and second, methyl acrylate and acrylonitrile since the former alone shows conformational s-cis-trans isomerism. Both types of process were expected to be particularly sensitive to the nature and charge of the reactive species involved. The results suggest that neutral muonium is the dominant precursor in all these liquids, with {\textquoteright}hot{\textquoteright} muonium perhaps contributing about 30\% of the radicals.},
	keywords = {LEVEL-CROSSING-RESONANCE, muonium},
	isbn = {0304-3843},
	url = {<Go to ISI>://A1990EZ85600024},
	author = {Barnabas, M. V. and Venkateswaran, K. and Stadlbauer, J. M. and Ng, B. W. and Wu, Z. and Gonzalez, A. and Walker, D. C.}
}
