Evidence map›Paper›PMID 38732024›Full record

ArticleInternational journal of molecular sciences2024

Molecular Design Using Selected Concentration Effects in Optically Activated Fluorescent Matrices.

Aneta Lewkowicz, Katarzyna Walczewska-Szewc, Martyna Czarnomska, Emilia Gruszczyńska, Mattia Pierpaoli, Robert Bogdanowicz, Zygmunt Gryczyński

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Aneta LewkowiczInstitute of Experimental Physics, Faculty of Mathematics, Physics, and Informatics, University of Gdansk, ul. Wita Stwosza 57, 80-308 Gdańsk, Poland.ORCID 0000-0002-4308-2291
Katarzyna Walczewska-SzewcInstitute of Physics, Faculty of Physics, Astronomy and Informatics, Nicolaus Copernicus University in Toruń, ul. Grudziądzka 5, 87-100 Toruń, Poland.
Martyna CzarnomskaInstitute of Experimental Physics, Faculty of Mathematics, Physics, and Informatics, University of Gdansk, ul. Wita Stwosza 57, 80-308 Gdańsk, Poland.
Emilia GruszczyńskaInstitute of Experimental Physics, Faculty of Mathematics, Physics, and Informatics, University of Gdansk, ul. Wita Stwosza 57, 80-308 Gdańsk, Poland.
Mattia PierpaoliDepartment of Metrology and Optoelectronics, Faculty of Electronics, Telecommunication, and Informatics, Gdańsk University of Technology, Gabriela Narutowicza 11/12, 80-233 Gdańsk, Poland.ORCID 0000-0002-7508-1824
Robert BogdanowiczDepartment of Metrology and Optoelectronics, Faculty of Electronics, Telecommunication, and Informatics, Gdańsk University of Technology, Gabriela Narutowicza 11/12, 80-233 Gdańsk, Poland.ORCID 0000-0002-7543-2620
Zygmunt GryczyńskiDepartment of Physics and Astronomy, Texas Christian University, 2995 S. University Dr., Fort Worth, TX 76109, USA.

Funding

National Science Center OPUS 2021/41/B/HS5/03250
6 · The paper itself

Abstract

Molecular physics plays a pivotal role in various fields, including medicine, pharmaceuticals, and broader industrial applications. This study aims to enhance the methods for producing specific optically active materials with distinct spectroscopic properties at the molecular level, which are crucial for these sectors, while prioritizing human safety in both production and application. Forensic science, a significant socio-economic field, often employs hazardous substances in analyzing friction ridges on porous surfaces, posing safety concerns. In response, we formulated novel, non-toxic procedures for examining paper evidence, particularly thermal papers. Our laboratory model utilizes a polyvinyl alcohol polymer as a rigid matrix to emulate the thermal paper's environment, enabling precise control over the spectroscopic characteristics of 1,8-diazafluoro-9-one (DFO). We identified and analyzed the cyclodimer 1,8-diazafluoren-9-one (DAK DFO), which is a non-toxic and biocompatible alternative for revealing forensic marks. The reagents used to preserve fingerprints were optimized for their effectiveness and stability. Using stationary absorption and emission spectroscopy, along with time-resolved emission studies, we verified the spectroscopic attributes of the new structures under deliberate aggregation conditions. Raman spectroscopy and quantum mechanical computations substantiated the cyclodimer's configuration. The investigation provides robust scientific endorsement for the novel compound and its structural diversity, influenced by the solvatochromic sensitivity of the DFO precursor. Our approach to monitoring aggregation processes signifies a substantial shift in synthetic research paradigms, leveraging simple chemistry to yield an innovative contribution to forensic science methodologies.

Indexed as

Spectrum Analysis, RamanFluorescent DyesForensic SciencesHumansSpectrometry, FluorescenceFluorescent Dyesabsorption spectracyclodimer 1,8-diazafluoren-9-onefluorescence spectrafriction ridge analysis

Identifiers

PMID38732024
PMCPMC11084466

What OpenQuestion holds

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Registered trials

None linked

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.