Publication Type Journal Article
Title Potentiometric, NMR, and fluorescence-emission studies on the binding of adenosine 5 -triphosphate (ATP) by open-chain polyamine receptors containing naphthylmethyl and/or anthrylmethyl groups
Authors MT Albelda J Aguilar Sérgio Alves R Aucejo P Diaz Carlos Lodeiro JC Lima E Garcia-Espana Fernando Pina C Soriano
Groups
Journal HELVETICA CHIMICA ACTA
Year 2003
Month
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Volume 86
Number 9
Pages 3118-3135
Abstract The interaction in aqueous solution of adenosine 5 -triphosphate (ATP) with a series of open-chain polyamines linked at one or both ends to anthrylmethyl or naphthylmethyl fragments was followed by potentiometric titration, H-1-, C-13-, and P-31-NMR spectroscopy, and by steady-state fluorescence measurements. The results revealed greater stabilities for the compounds containing one anthracene moiety than for those with one naphthalene moiety, the stabilities of the compounds with both ends N-substituted with naphthylmethyl groups being close to those containing just one anthrylmethyl unit. The H-1-NMR spectra showed that in all systems, there is involvement of pi-pi stacking interactions in the stabilization of the adduct species. The competitive effect of the anions afforded by the supporting electrolyte was checked in some of the studied systems working at two different ionic strenghts (0.15m and 1.0m NaCl). The joint analysis of the spectrofluorimetric titrations and pH-metric species-distribution curves showed that for all the ATP-receptor systems, a quenching of the fluorescence occurred upon protonation of the adenine N(1)atom. Steady-state fluorescence and time-correlated single-photon-counting analysis of a system made up of ATP and a bischromophoric polyamine receptor containing anthracene and naphthalene fluorophores established that the energy-transfer process between the naphthalene and anthracene moieties is still operative despite the presence of ATP.
DOI http://dx.doi.org/10.1002/hlca.200390253
ISBN
Publisher
Book Title
ISSN 0018-019X
EISSN
Conference Name
Bibtex ID ISI:000185730000011
Observations
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