Oxygen sensors based on luminescence quenching: Interactions of tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) chloride and pyrene with polymer supports
Oxygen sensors based on luminescence quenching: Interactions of tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) chloride and pyrene with polymer supports
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DOI:
10.1366/0003702971942024
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发表时间:
1997-09-01
影响因子:
3.5
通讯作者:
DeGraff, BA
中科院分区:
文献类型:
--
作者:
Kneas, KA;Xu, WY;DeGraff, BA
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) co-polymerized with one of several co-monomers: styrene, trimethylsilyl-methylmethacrylate (T3642), vinyl-tris(2-methoxy-ethoxy)silane, or vinyl-tris(trimethylsiloxy)silane. Sensor performance was studied as a function of the polymer composition in order to delineate the important features for satisfactory O-2 sensor supports. Quenching behavior was examined as a function of polymer structure, including amount and type of co-monomer. This work shows that the earlier two-domain model is too simplistic The relative affinities of the different domains for the [Ru(Ph(2)phen)(3)]Cl-2 and pyrene and the efficacy of the domains for O-2 quenching are important; however, subtle changes in microstructure within domains can also strongly affect behavior. In particular, T3642 exhibits excellent structural and goad quenching properties with[Ru(Ph(2)phen)(3)]Cl-2.