dc.contributor.author |
Papadopoulos, K |
en |
dc.contributor.author |
Lignos, J |
en |
dc.contributor.author |
Stamatakis, M |
en |
dc.contributor.author |
Dimotikali, D |
en |
dc.contributor.author |
Nikokavouras, J |
en |
dc.date.accessioned |
2014-03-01T01:14:06Z |
|
dc.date.available |
2014-03-01T01:14:06Z |
|
dc.date.issued |
1998 |
en |
dc.identifier.issn |
1010-6030 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/12867 |
|
dc.subject |
9-Benzylacridine |
en |
dc.subject |
Acridone |
en |
dc.subject |
Chemiluminescence |
en |
dc.subject |
Radiochemiluminescence |
en |
dc.subject.classification |
Chemistry, Physical |
en |
dc.title |
Radiochemiluminescence of acridones and alkyl acridines |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1016/S1010-6030(98)00236-6 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1016/S1010-6030(98)00236-6 |
en |
heal.language |
English |
en |
heal.publicationDate |
1998 |
en |
heal.abstract |
Acridone and 9-benzylacridine in dialkylated amides are radiolyzed to novel acridan derivatives which emit light upon addition of strong bases regenerating acridone. The chemiluminescence quantum yields are as high as 2.4 x 10(-2) for acridone, while for the 9-benzylacridine 3.1 x 10(-3) einstein mol(-1). The acridone quantum yield is higher than those of most classical chemiluminescent reactions. The radiolysis and chemiluminescence mechanisms are discussed. The radiochemiluminescence reactions constitute prospective radiation dosemeters. (C) 1998 Elsevier Science S.A. All rights reserved. |
en |
heal.publisher |
ELSEVIER SCIENCE SA |
en |
heal.journalName |
Journal of Photochemistry and Photobiology A: Chemistry |
en |
dc.identifier.doi |
10.1016/S1010-6030(98)00236-6 |
en |
dc.identifier.isi |
ISI:000074332900007 |
en |
dc.identifier.volume |
115 |
en |
dc.identifier.issue |
2 |
en |
dc.identifier.spage |
137 |
en |
dc.identifier.epage |
142 |
en |