THE PHOTOPHYSICS OF DISULFONATED METALLOPHTHALOCYANINES UPON COMPLEXATION WITH FLUORIDE

Citation
Sm. Bishop et al., THE PHOTOPHYSICS OF DISULFONATED METALLOPHTHALOCYANINES UPON COMPLEXATION WITH FLUORIDE, Journal of the Chemical Society. Faraday transactions, 92(15), 1996, pp. 2689-2695
Citations number
47
Categorie Soggetti
Chemistry Physical","Physics, Atomic, Molecular & Chemical
ISSN journal
09565000
Volume
92
Issue
15
Year of publication
1996
Pages
2689 - 2695
Database
ISI
SICI code
0956-5000(1996)92:15<2689:TPODMU>2.0.ZU;2-I
Abstract
The photophysics of the disulfonated metallophthalocyanines (MPcS(2)) AlPcS(2), GaPcS(2), and ZnPcS(2), upon complexation with the fluoride ion are characterised. The addition of fluoride to AlPcS(2) produces a decrease in the fluorescence lifetime and yield whereas the triplet l ifetime, triplet yield and singlet-oxygen yield increased. The measure d enhancement for the triplet yield in aqueous and methanol solvents w as 47 and 37% respectively, with a concomitant increase in the singlet -oxygen yield observed in both cases. The photophysical changes are du e solely to the intersystem crossing process which is seen to increase on addition of fluoride. The fluoride ion is believed to act as an ax ial ligand to the AlPcS(2) molecule; an equilibrium constant of 4.2 x 10(3) dm(3) mol(-1) was determined for this complexation. Addition of excess fluoride to aqueous solutions of AlPcS(2) at low and high pH ga ve a common absorption spectrum. This suggests the H2O axial ligand of the aluminium complex is substituted by fluoride rather than OH-. The photophysics of methanol solutions of GaPcS(2) and ZnPcS(2) are uncha nged upon addition of fluoride, although a blue shift in the absorptio n spectrum for the gallium species is indicative of complex formation The consequences of these results for the effect of added fluoride upo n the efficacy of these agents as PDT sensitisers is discussed. Also, several properties of triplet-state AlPcS(2) in the absence of fluorid e ion have been found to be different from previously reported values. The measured lower triplet quantum yields for AlPcS(2) in buffered so lutions of H2O and D2O were 0.17 and 0.22 respectively. These differen ces are attributed to the triplet extinction coefficient (A epsilon(T) ) used to calculate literature values. Using the singlet depletion tec hnique we have shown that A epsilon(T) = 36 000 dm(3) mol(-1) cm(-1) a t the triplet absorption maximum of 490 nm, in all solvents. Similarly , the singlet-oxygen yield, determined in D2O buffered solution was fo und to be 0.17, giving an S-Delta of 0.77.