Applicability of quinolizino-coumarins for monitoring free radical photopolymerization by fluorescence spectroscopy

Kamińska, Iwona; Ortyl, Joanna; Popielarz, Roman

doi:10.1016/j.polymertesting.2014.12.013

Cited by 32 publications

(15 citation statements)

References 19 publications

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“…The UV LED was powered by a 20-mA direct current from a stabilised current source. The main advantage of this measuring chamber was the high intensity of the excitation light from the same type of UV-LEDs and the small scattering of the excitation light compared to previous measuring systems [22]. This was due to the elimination of one of the fibre-optic cables and the incorporation of the UV-LED directly into the chamber head.…”

Section: Monitoring Fluorescence Changes During Photopolymerizationmentioning

confidence: 99%

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Double Role of Diphenylpyridine Derivatives as Fluorescent Sensors for Monitoring Photopolymerization and the Determination of the Efficiencies of the Generation of Superacids by Cationic Photoinitiators

Topa

Petko²,

Galek³

et al. 2020

Sensors

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Novel fluorescent sensors with electron-donating or electron-withdrawing substituents incorporated into a chromophore group based on 2,6-diphenylpyridine were designed and synthesised. The spectroscopic properties of these compounds were studied. Moreover, the positive solvatochromism of 2,6-bis-(4-methylsulphanylphenyl)pyridine (PT-SCH3) in selected solvents was studied by measurement of the absorption and emission spectra and analysed using the Dimroth–Reichardt solvent parameter set. After that, the performance of a series of 2,6-diphenylpyridine derivatives as fluorescent molecular sensors for monitoring free-radical and cationic photopolymerization processes by the Fluorescence Probe Technique (FPT) was studied. As a consequence of this stage of research, the effect of substituents on the sensitivity of the 2,6-diphenylpyridine derivatives as sensors during photopolymerization has been evaluated and discussed. It has been found that compounds containing strong electron-donating substituent (PT-SCH3) slightly shift their fluorescence spectrum during the free-radical polymerization of monomer, which enables the monitoring of the polymerization progress using the fluorescence intensity ratio measured at two different wavelengths as the progress indicator. The position of the fluorescence spectrum of 2,6-diphenylpyridine derivatives with electron-withdrawing substituents is practically insensitive to changes occurring in their environment. Hence, it is recommended to use these compounds with different indicators of the progress of the photopolymerization process based on normalised intensity of fluorescence (Imax/I0). Among the compounds studied, 2,6-bis(4-methylsulphanylphenyl)pyridine (PT-SCH3) turned out to be the best fluorescent sensor for the purpose of monitoring free-radical polymerization by FPT. Consequently, the dual application of the selected 2,6-diphenylpyridine derivatives is proposed: (a) as fluorescent sensors for monitoring the free-radical photopolymerization progress, and (b) as spectroscopic sensors for the determination of efficiencies of the generation of superacids by cationic photoinitiators during the cationic photopolymerization process. Finally, a new method for determining the relative efficiency of the photogeneration of superacids during the photo cleavage of onium salt has been devised and applied for the evaluation of the performance of 2,6-diphenylpyridine derivatives.

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Section: Monitoring Fluorescence Changes During Photopolymerizationmentioning

confidence: 99%

“…Despite the progress made in this area, there are still several problems and challenges [21,22]. In order for these probes to be used in the above-mentioned fields of science, they should meet a number of requirements and respond appropriately to changes in the environment, i.e., changes in viscosity, polarity or pH [23,24].…”

Section: Introductionmentioning

confidence: 99%

Double Role of Diphenylpyridine Derivatives as Fluorescent Sensors for Monitoring Photopolymerization and the Determination of the Efficiencies of the Generation of Superacids by Cationic Photoinitiators

Topa

Petko²,

Galek³

et al. 2020

Sensors

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“…All this means that not only has recently been an astonishingly rapid growth in the applications of technologies based on photopolymerization processes, but also the development of new materials determining the pace of this development [ 35 ]. Dynamic progress in the field of chemistry and technology of photoinitiated processes leads to the emergence of more and more sophisticated solutions in this field, an example of which may be successively developed new generation monomers [ 36 , 37 ], new, more effective photoinitiation systems [ 38 , 39 , 40 ] or new light sources [ 1 , 29 ] and methods of monitoring the online polymerization processes [ 41 , 42 , 43 , 44 ].…”

Section: Introductionmentioning

confidence: 99%

Moving Towards a Finer Way of Light-Cured Resin-Based Restorative Dental Materials: Recent Advances in Photoinitiating Systems Based on Iodonium Salts

Topa

Ortyl

2020

Materials

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The photoinduced polymerization of monomers is currently an essential tool in various industries. The photopolymerization process plays an increasingly important role in biomedical applications. It is especially used in the production of dental composites. It also exhibits unique properties, such as a short time of polymerization of composites (up to a few seconds), low energy consumption, and spatial resolution (polymerization only in irradiated areas). This paper describes a short overview of the history and classification of different typical monomers and photoinitiating systems such as bimolecular photoinitiator system containing camphorquinone and aromatic amine, 1-phenyl-1,2-propanedione, phosphine derivatives, germanium derivatives, hexaarylbiimidazole derivatives, silane-based derivatives and thioxanthone derivatives used in the production of dental composites with their limitations and disadvantages. Moreover, this article represents the challenges faced when using the latest inventions in the field of dental materials, with a particular focus on photoinitiating systems based on iodonium salts. The beneficial properties of dental composites cured using initiation systems based on iodonium salts have been demonstrated.

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“…Photoinduced processes possess a lot of attractive features-mild reaction conditions, nearly no release of volatile organic compounds (VOCs), and room temperature operation with the use of convenient light sources [3]. Recently, there have been many developments in the field of photochemistry-especially in new monomers [4,5]-for monitoring on-line and/or in-situ processes of photopolymerisation [6][7][8], as well as completely new highly efficient photoinitiating systems, which are necessary for photopolymerisation processes [9][10][11].…”

Section: Introductionmentioning

confidence: 99%

Thioxanthone Derivatives as a New Class of Organic Photocatalysts for Photopolymerisation Processes and the 3D Printing of Photocurable Resins under Visible Light

2020

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In the present paper, novel thioxanthone-based compounds were synthesised and evaluated as a component of photoredox catalysts/photoinitiating systems for the free-radical polymerisation (FRP) of acrylates and the ring-opening cationic polymerisation (CP) of epoxy monomers. The performance of the obtained thioxanthones in two- and three-component photoinitiating systems, in combination with amines, iodonium or sulphonium salt, as well as with alkyl halide, for photopolymerisation processes upon exposure to light emitting diodes (LEDs) with a maximum emission of 405 nm and 420 nm, was investigated. The studied compounds act also as one-component free-radical photoinitiators. Fourier transform real-time infrared spectroscopy was used to monitor the kinetics of disappearance of the functional groups of the monomers during photoinitiated polymerisation. Excellent photoinitiating efficiency and high final conversions of functional groups were observed. Moreover, the influence of thioxanthone skeleton substitution on photoinitiating efficiency was discussed. The photochemical mechanism was also investigated through cyclic voltammetry. It was discovered that thioxanthone derivatives can be used as a metal-free photoredox catalyst active for both oxidative and reductive cycles. Furthermore, a photopolymerizable system based on novel thioxanthone derivatives in a stereolithography three-dimensional (3D) printing technology under visible sources of light was used. The effects of photoinitiator type system and monomer type in photoresins during 3D printing processes were explored. The outcome of this research is the development of high-performance visible photosensitive resins with improved photosensitivity obtained thanks to the development of entirely novel photoinitiating systems specifically adapted for this application.

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Applicability of quinolizino-coumarins for monitoring free radical photopolymerization by fluorescence spectroscopy

Cited by 32 publications

References 19 publications

Double Role of Diphenylpyridine Derivatives as Fluorescent Sensors for Monitoring Photopolymerization and the Determination of the Efficiencies of the Generation of Superacids by Cationic Photoinitiators

Double Role of Diphenylpyridine Derivatives as Fluorescent Sensors for Monitoring Photopolymerization and the Determination of the Efficiencies of the Generation of Superacids by Cationic Photoinitiators

Moving Towards a Finer Way of Light-Cured Resin-Based Restorative Dental Materials: Recent Advances in Photoinitiating Systems Based on Iodonium Salts

Thioxanthone Derivatives as a New Class of Organic Photocatalysts for Photopolymerisation Processes and the 3D Printing of Photocurable Resins under Visible Light

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