Evidence map›Paper›PMID 31731521›Full record

ArticlePolymers2019

Applicability of 1,6-Diphenylquinolin-2-one Derivatives as Fluorescent Sensors for Monitoring the Progress of Photopolymerisation Processes and as Photosensitisers for Bimolecular Photoinitiating Systems.

Monika Topa, Filip Petko, Mariusz Galek, Kamil Machowski, Maciej Pilch, Patryk Szymaszek, Joanna Ortyl

Abstract read
In one paragraph

Article in Polymers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Monika TopaFaculty of Chemical Engineering and Technology, Cracow University of Technology, Warszawska 24, 30-155 Cracow, Poland.
Filip PetkoPhoto HiTech Ltd., Bobrzyńskiego 14, 30-348 Cracow, Poland.
Mariusz GalekPhoto HiTech Ltd., Bobrzyńskiego 14, 30-348 Cracow, Poland.
Kamil MachowskiPhoto HiTech Ltd., Bobrzyńskiego 14, 30-348 Cracow, Poland.
Maciej PilchFaculty of Chemical Engineering and Technology, Cracow University of Technology, Warszawska 24, 30-155 Cracow, Poland.
Patryk SzymaszekFaculty of Chemical Engineering and Technology, Cracow University of Technology, Warszawska 24, 30-155 Cracow, Poland.
Joanna OrtylFaculty of Chemical Engineering and Technology, Cracow University of Technology, Warszawska 24, 30-155 Cracow, Poland.ORCID 0000-0002-4789-7199

Funding

Foundation for Polish Science (Warsaw, Poland) REINTEGRATION/2016-1/4 (POIR.04.04.00-00-1E42/16-00)Foundation for Polish Science (Warsaw, Poland) TEAM TECH project Grant No. TEAM TECH/2016-2/15 (POIR.04.04.00-00-204B/16-00)National Science Centre Project SONATA [Grant No. UMO-2012/07/D/ST5/02300, 2012]PLGrid Infrastructure open infrastructure resources PLGrid Infrastructure
6 · The paper itself

Abstract

The applicability of new 1,6-diphenylquinolin-2-oneas derivatives as fluorescent molecular sensors for monitoring the progress of photopolymerisation processes by Fluorescence Probe Technique (FPT) has been tested. The progress of cationic, free-radical and thiol-ene photopolymerisation for commercially available monomers: triethylene glycol divinyl ether (TEGDVE), trimethylolpropane triacrylate (TMPTA) and trimethylpropane tris(3-mercaptopropropionate) (MERCAPTO) was monitored. It was found that new derivatives of 1,6-diphenylquinolin-2-one shifted their fluorescence spectra towards shorter wavelengths with the progress of polymerisation, which enabled monitoring the progress in terms of fluorescence intensity ratios as the progress indicator. Derivatives of 1,6-diphenylquinolin-2-one show sensitivity to changes in both polarity and viscosity in the surrounding microenvironment during photopolymerisation processes. Therefore, it was shown that they are good candidates to act as fluorescent sensors for monitoring the kinetics of very quick processes, such as photopolymerisation processes. Furthermore, the effect of the nature of substituents attached to the 1,6-diphenylquinolin-2-one ring on the characteristics of emission spectra was identified. Moreover, the sensitivity of fluorescent sensors was compared with commercially available model sensors, such as 7-diethylamino-4-methylcoumarin (Coumarin 1) and trans-2-(2',5'-dimethoxyphenyl)ethenyl-2,3,4,5,6-pentafluorobenzene (25ST). Moreover, it was also proven that selected derivatives of 1,6-diphenylquinolin-2-one exhibit an accelerating effect on the progress of cationic photopolymerisation of vinyl monomers (TEGDVE). Thus, the new 1,6-diphenylquinolin-2-one derivatives can be successfully used both as molecular fluorescence sensors to monitor the progress of photopolymerisation processes and as diaryliodonium salt photosensitisers to initiate cationic photopolymerisation processes in a UV-A range of 365 nm.

Indexed as

cationic photopolymerisationfluorescent molecular sensorsfree-radical photopolymerisationluminescence spectroscopyphotoinduced electron transferphotopolymerisationphotosensitizerthiol-ene photopolymerisation

Identifiers

PMID31731521
PMCPMC6918307

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.