Chemiluminescent 10‐methyl‐acridinium‐9‐(N‐sulphonylcarboxamide) salts. Synthesis and kinetics of light emission
- 1 April 1991
- journal article
- research article
- Published by Wiley in Journal of Bioluminescence and Chemiluminescence
- Vol. 6 (2) , 107-114
- https://doi.org/10.1002/bio.1170060208
Abstract
10-Methyl-acridinium-9-(N-sulphonylcarboxamide) salts are prepared via acylation of sulphonamides with acridine-9-carboxylic acid chloride and subsequent N-alkylation with methyl triflate. Substituents on the sulphonamide component were varied to show the effect of steric and electronic factors on the kinetics of light output. The lifetime of the chemiluminescence light output ranged from 1 to 50 seconds for the 15 compounds reported. The long-term stability of the new compounds was superior to the phenyl ester counterparts.Keywords
This publication has 12 references indexed in Scilit:
- Chemiluminogenic labels, old and newAnalytica Chimica Acta, 1989
- Novel poly‐substituted aryl acridinium esters and their use in immunoassayJournal of Bioluminescence and Chemiluminescence, 1989
- Synthesis and properties of new luminescent acridinium‐9‐carboxylic acid derivatives and their application in luminescence immunoasays (LIA)Journal of Bioluminescence and Chemiluminescence, 1989
- Chemiluminescence AnalysisAnalytical Chemistry, 1987
- The use of acridinium ester-labelled streptavidin in immunoassaysJournal of Immunological Methods, 1987
- Enhanced chemiluminescence enzyme immunoassayPublished by Walter de Gruyter GmbH ,1987
- Chemiluminescence as an Analytical Tool in Cell Biology and MedicinePublished by Wiley ,1985
- Synthesis of .beta.-lactams from substituted hydroxamic acidsJournal of the American Chemical Society, 1980
- Chemiluminescence yields and detection limits of some isoluminol derivatives in various oxidation systemsAnalytical Chemistry, 1978
- Chemiluminescence from the Reaction of 9-Chlorocarbonyl-10-methylacridinium Chloride with Aqueous Hydrogen Peroxide1The Journal of Organic Chemistry, 1965