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1.
Molecules ; 26(4)2021 Feb 12.
Article in English | MEDLINE | ID: mdl-33673146

ABSTRACT

9H-Xanthenes, 9H-thioxanthenes and 9,10-dihydroacridines can be easily oxidized to the corresponding xanthones, thioxanthones and acridones, respectively, by a simple photo-oxidation procedure carried out using molecular oxygen as oxidant under the irradiation of visible blue light and in the presence of riboflavin tetraacetate as a metal-free photocatalyst. The obtained yields are high or quantitative.


Subject(s)
Acridones/chemical synthesis , Oxygen/chemistry , Thioxanthenes/chemical synthesis , Xanthones/chemical synthesis , Acridones/chemistry , Acridones/radiation effects , Light , Metals/chemistry , Oxidants, Photochemical/chemistry , Oxidants, Photochemical/pharmacology , Oxidation-Reduction/radiation effects , Thioxanthenes/chemistry , Thioxanthenes/radiation effects , Xanthones/chemistry , Xanthones/radiation effects
2.
Dent Mater ; 28(12): 1199-206, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23083514

ABSTRACT

OBJECTIVES: The purpose of this study was to evaluate the reactivity and polymerization kinetics behavior of a model dental adhesive resin with water-soluble initiator systems. METHODS: A monomer blend based on Bis-GMA, TEGDMA and HEMA was used as a model dental adhesive resin, which was polymerized using a thioxanthone type (QTX) as a photoinitiator. Binary and ternary photoinitiator systems were formulated using 1mol% of each initiator. The co-initiators used in this study were ethyl 4-dimethylaminobenzoate (EDAB), diphenyliodonium hexafluorophosphate (DPIHFP), 1,3-diethyl-2-thiobarbituric acid (BARB), p-toluenesulfinic acid and sodium salt hydrate (SULF). Absorption spectra of the initiators were measured using a UV-Vis spectrophotometer, and the photon absorption energy (PAE) was calculated. The binary system camphorquinone (CQ)/amine was used as a reference group (control). Twelve groups were tested in triplicate. Fourier-transform infrared spectroscopy (FTIR) was used to investigate the polymerization reaction during the photoactivation period to obtain the degree of conversion (DC) and maximum polymerization rate (R(p)(max)) profile of the model resin. RESULTS: In the analyzed absorption profiles, the absorption spectrum of QTX is almost entirely localized in the UV region, whereas that of CQ is in the visible range. With respect to binary systems, CQ+EDAB exhibited higher DC and R(p)(max) values. In formulations that contained ternary initiator systems, the group CQ+QTX+EDAB was the only one of the investigated experimental groups that exhibited an R(p)(max) value greater than that of CQ+EDAB. The groups QTX+EDAB+DPIHFP and QTX+DPIHFP+SULF exhibited values similar to those of CQ+EDAB with respect to the final DC; however, they also exhibited lower reactivity. SIGNIFICANCE: Water-soluble initiator systems should be considered as alternatives to the widely used CQ/amine system in dentin adhesive formulations.


Subject(s)
Composite Resins/chemistry , Dental Materials/chemistry , Photoinitiators, Dental/chemistry , Absorptiometry, Photon , Biphenyl Compounds/chemistry , Biphenyl Compounds/radiation effects , Bisphenol A-Glycidyl Methacrylate/chemistry , Bisphenol A-Glycidyl Methacrylate/radiation effects , Camphor/analogs & derivatives , Camphor/chemistry , Camphor/radiation effects , Composite Resins/radiation effects , Dental Materials/radiation effects , Humans , Light-Curing of Dental Adhesives , Methacrylates/chemistry , Methacrylates/radiation effects , Onium Compounds/chemistry , Onium Compounds/radiation effects , Photoinitiators, Dental/radiation effects , Polyethylene Glycols/chemistry , Polyethylene Glycols/radiation effects , Polymerization , Polymethacrylic Acids/chemistry , Polymethacrylic Acids/radiation effects , Solubility , Spectrophotometry, Ultraviolet , Spectroscopy, Fourier Transform Infrared , Thiobarbiturates/chemistry , Thiobarbiturates/radiation effects , Thioxanthenes/chemistry , Thioxanthenes/radiation effects , Toluene/analogs & derivatives , Toluene/chemistry , Toluene/radiation effects , Water/chemistry , Xanthones/chemistry , Xanthones/radiation effects , para-Aminobenzoates/chemistry , para-Aminobenzoates/radiation effects
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