Eosin B/amine as photoinitiator system of vinyl polymerization. A photophysical study of the dye

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-01 Epub Date: 2025-01-30 DOI:10.1016/j.jphotochem.2025.116313
M.Paula Militello , Micaela E. Grassano , Ernesto M. Arbeloa , Sonia G. Bertolotti , Carlos M. Previtali
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Abstract

The photopolymerization of acrylamide in water under visible irradiation was initiated by the system eosin B/triethanolamine in deaerated conditions. In order to understand the mechanism of photoinitiation, the photophysics of the dye in the absence and presence of the amine was studied. The absorption and fluorescence properties in ethanol–water mixtures were determined. The fluorescence quantum yields were 0.003 and 0.02 in water and ethanol, respectively. The triplet state was observed by laser flash photolysis only in the alcohol. In water, the transient signal could not be detected. The triplet quantum yield was estimated at 0.08. In the absence of the amine or in air equilibrated solutions the polymer was not formed. Since no triplet is detected by laser flash photolysis in water, the question regarding the photoinitiation mechanism arises. It is suggested that, despite the lack of transient signal with our laser photolysis system, the triplet is formed in very low yield. Since the dye is photostable under the irradiation conditions of the polymerization experiments, in the long term polymerization could take place initiated by the triplet.
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以伊红B/胺为光引发剂的乙烯基聚合体系。染料的光物理研究
在脱氧条件下,以伊红B/三乙醇胺体系引发丙烯酰胺在水中的光聚合反应。为了了解光引发的机理,研究了该染料在无胺和有胺情况下的光物理性质。测定了其在乙醇-水混合物中的吸收特性和荧光特性。在水和乙醇中的荧光量子产率分别为0.003和0.02。激光闪光光解只在醇中观察到三重态。在水中,无法检测到瞬态信号。三重态量子产率估计为0.08。在没有胺或在空气平衡溶液中,聚合物不形成。由于在水中激光闪光光解没有检测到三重态,关于光引发机制的问题就出现了。这表明,尽管我们的激光光解系统缺乏瞬态信号,但在很低的产率下形成了三重态。由于染料在聚合实验的辐照条件下具有光稳定性,因此长期聚合可能由三元态引发。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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