Conjugated Carbon-Centered and Nitrogen Radicals by H. Fischer (auth.), H. Fischer (eds.)
By H. Fischer (auth.), H. Fischer (eds.)
Volume II/17 c is the 3rd a part of a complement to the pre- vious compilations II/1 and II/9 a-d2 on magnetic houses of unfastened radicals released in 1965 and 1977-1980, which lined the literature as much as 1975. because of the nonetheless very quick improvement of the sphere and the inclusion of latest sub- jects, the complement overlaying the interval 1975-85 needed to be break up into subvolumes, as a way to seem in quick succession. Togetherwith the ealier volumes, II/17 bargains an updated and accomplished surveyand a set of information on impor- tant chemical intermediates.
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Additional info for Conjugated Carbon-Centered and Nitrogen Radicals
30 y-irr. 696 9 H (3, C (CH,),): reduction/ g-Factor TKI I-s. / add. Ref. 13 Isocyclic ally1 radicals (cyclobutenyl, cyclopentenyl, . . 2\3 o- CH, 4 &H,I ’ 1 2 \ 0 5 3 4 Phot. 42 81Davl Phot. 26 84Davl/ 83Tabl 51) ‘*) Restricted rotation deduced from line broadening at 104 K. ‘9) Determination of lower limit of the barrier to valence bond tautomerization. “) Radical absorbed on synthetic H-mordenite at 308 K. 51) Radical generated by y-k. of cyclopentene in CF,CCl, and photobleacbing. Substance GJ%I ’ CH, A W CH, [C,,H,oOl ’- 02 (CH,),C’ Method/ Phot.
Of ethylene oxide at 77 K/ CFCl, ESR/ 132 110 y-irr. 14 85Nonl A :GHGl ’ H3yyHcH3 C,H,O] y-irr. 25 k &H,D,O] HCD=&HD ’+ ‘9b) Obtained from studies on 1,2-‘T, (99%) labelled ethylene oxide. lgc) INDO calculation of spin densities. ~;ICH, 3 Generation/ Matrix or Solvent Method/ y-irr. / add. Ref. 11 Semicyclic ally1 radicals W&I - 4bcc (=d H (enrlo) W-b1 * 5 . ,H (em) 4 + /ZF\ 3 H L7H3001’ - H, H,C ‘=, (endo) . ,WW, C: H,C WH,), +- /,’ Phot. 900 80Lunl Phot. 864*) 80Boll Phot. 0031 O- GH91- 6 5 .
25 86Ciol/ 80Mak1, 82Sutl 46) 84Chi14’) Phot. 325 82Sutl 45) UHF calculation of spin densities. 46) Data assigned to this radical by [74Cirl] (see vol. 11/9b) belong to the I-chloroallyl radical. 4’) Ah initio calculations of isotropic and anisotropic ‘H and ‘T coupling constants. Substance GJ%I ’ CH, A W CH, [C,,H,oOl ’- 02 (CH,),C’ Method/ Phot. 30 y-irr. 696 9 H (3, C (CH,),): reduction/ g-Factor TKI I-s. / add. Ref. 13 Isocyclic ally1 radicals (cyclobutenyl, cyclopentenyl, . . 2\3 o- CH, 4 &H,I ’ 1 2 \ 0 5 3 4 Phot.