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Titolo:
COMPETING PATHWAYS IN THE PHOTOLYTIC CYCLOADDITION REACTIONS OF N-ETHOXYCARBONYLAZEPINE TO [60]FULLERENE - FORMATION OF [2+4] AND [2+6] PHOTOADDUCTS
Autore:
BANKS MR; CADOGAN JIG; GOSNEY I; HODGSON PKG; LANGRIDGESMITH PRR; MILLAR JRA; PARKINSON JA; SADLER IH; TAYLOR AT;
Indirizzi:
UNIV EDINBURGH,DEPT CHEM,W MAINS RD EDINBURGH EH9 3JJ MIDLOTHIAN SCOTLAND UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED,DEPT CHEM LONDON SW7 2AY ENGLAND BP INT LTD,CTR RES & ENGN SUNBURY TW16 7LN MIDDX ENGLAND
Titolo Testata:
Journal of the Chemical Society, Chemical Communications
fascicolo: 11, , anno: 1995,
pagine: 1171 - 1172
SICI:
0022-4936(1995):11<1171:CPITPC>2.0.ZU;2-H
Fonte:
ISI
Lingua:
ENG
Soggetto:
C-60; C60;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Citazioni:
17
Recensione:
Indirizzi per estratti:
Citazione:
M.R. Banks et al., "COMPETING PATHWAYS IN THE PHOTOLYTIC CYCLOADDITION REACTIONS OF N-ETHOXYCARBONYLAZEPINE TO [60]FULLERENE - FORMATION OF [2+4] AND [2+6] PHOTOADDUCTS", Journal of the Chemical Society, Chemical Communications, (11), 1995, pp. 1171-1172

Abstract

The photochemical reaction between [60]fullerene and N-ethoxycarbonylazepine, formed in situ by light-induced decomposition of ethyl azidoformate in benzene, produces two photoadducts in the ratio of 4:1 by formal [2 + 4] and [2 + 6] cycloaddition reactions as established by a series of high-field (600 MHz) NMR experiments.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 03/07/20 alle ore 23:03:15