OXYGEN SENSORS BASED ON LUMINESCENCE QUENCHING - INTERACTIONS OF RIS(4,7-DIPHENYL-1,10-PHENANTHROLINE)RUTHENIUM(II) CHLORIDE AND PYRENE WITH POLYMER SUPPORTS
Ka. Kneas et al., OXYGEN SENSORS BASED ON LUMINESCENCE QUENCHING - INTERACTIONS OF RIS(4,7-DIPHENYL-1,10-PHENANTHROLINE)RUTHENIUM(II) CHLORIDE AND PYRENE WITH POLYMER SUPPORTS, Applied spectroscopy, 51(9), 1997, pp. 1346-1351
Oxygen quenching of [Ru(Ph(2)phen)(3)]Cl-2 (Ph(2)phen = 4,7-diphenyl-1
,10-phenanthroline) and pyrene has been studied in a series of polymer
networks of Gp-163 (a methacryloxy functional polydimethylsiloxane) c
o-polymerized with one of several co-monomers: styrene, trimethylsilyl
-methylmethacrylate (T3642), vinyl-tris(2-methoxy-ethoxy)silane, or vi
nyl-tris(trimethylsiloxy)silane. Sensor performance was studied as a f
unction of the polymer composition in order to delineate tile importan
t features for satisfactory O-2 sensor supports. Quenching behavior wa
s examined as a function of polymer structure, including amount and ty
pe of co-monomer. This work shows that the earlier two-domain model is
too simplistic The relative affinities of the different domains for t
he [Ru(Ph(2)phen)(3)]Cl-2 and pyrene and the efficacy of the domains f
or O-2 quenching are important; however, subtle changes in microstruct
ure within domains can also strongly affect behavior. In particular, T
3642 exhibits excellent structural and goad quenching properties with[
Ru(Ph(2)phen)(3)]Cl-2.