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Eberson, L 삭제
1980 삭제
Royal Society of Chemistry 삭제
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1 저널기사 Generation of tricyanomethyl spin adducts of �phenyl-N-tert-butylnitrone (PBN) via non-conventional mechanisms 미리보기
Eberson, L Royal Society of Chemistry 1980
2 저널기사 Radical cation mechanism of aromatic halogenation by halogens or iodine chloride in 1,1,1,3,3,3-hexafluoropropan-2-ol 미리보기
Eberson, L Royal Society of Chemistry 1980
3 저널기사 1,3-Dipolar cycloaddition of �phenyl-N-tert-butylnitrone (PBN) to dichloro- and dibromomalononitrile, chlorotricyanomethane and tetracyanomethane. Structure of products and kinetics of their formation 미리보기
Eberson, L Royal Society of Chemistry 1980
4 저널기사 Radical cations of non-alternant systems as probes of the Shaik-Pross VBconfiguration mixing model 미리보기
Eberson, L Royal Society of Chemistry 1980
5 저널기사 Fluoro spin adducts and their modes of formation 미리보기
Eberson, L Royal Society of Chemistry 1980
6 저널기사 Formation and EPR spectra of radical species derived from the oxidation of the spin trap, �phenyl-N-tert-butylnitrone (PBN), and some of its derivatives in 1,1,1,3,3,3-hexafluoropropan-2-ol. Formation of isoxazolidineradical cartons 미리보기
Eberson, L Royal Society of Chemistry 1980
7 저널기사 Spin adduct formation from the spontaneous reaction between spin traps and weak electron acceptors, as exemplified by trichloroacetonitrile. An acid promoted version of the Forrester-Hepburn addition-oxidation mechanism 미리보기
Eberson, L Royal Society of Chemistry 1980
8 저널기사 On the existence of quinone radical cations. A study in 1,1,1,3,3,3-hexafluoropropan-2-ol 미리보기
Eberson, L Royal Society of Chemistry 1980
9 저널기사 Generation of acyloxyl spin adducts from N-tert-butyl-�phenylnitrone (PBN) and 4,5dihydro-5,5-dimethylpyrrole 1-oxide (DMPO) via nonconventionalmechanisms 미리보기
Eberson, L Royal Society of Chemistry 1980
10 저널기사 EPR spectra and redox properties of radical cations of dibenzofuran, methylated dibenzofurans and bidibenzofurans: relation to the chemistry of dibenzofuran radical cation 미리보기
Eberson, L Royal Society of Chemistry 1980
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