Evidence map›Paper›PMID 35806254›Full record

ArticleInternational journal of molecular sciences2022

Isocyanonaphthol Derivatives: Excited-State Proton Transfer and Solvatochromic Properties.

Anita Adamoczky, Tibor Nagy, Péter Pál Fehér, Veronika Pardi-Tóth, Ákos Kuki, Lajos Nagy, Miklos Zsuga, Sándor Kéki

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Application ofMolecules (Basel, Switzerland) · 2022
    Article
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

8 authors.

Anita AdamoczkyDepartment of Applied Chemistry, Faculty of Sciences and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Tibor NagyDepartment of Applied Chemistry, Faculty of Sciences and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0001-8568-914X
Péter Pál FehérResearch Centre for Natural Sciences, Magyar Tudósok Körútja 2., H-1117 Budapest, Hungary.ORCID 0000-0002-6927-4523
Veronika Pardi-TóthDepartment of Applied Chemistry, Faculty of Sciences and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Ákos KukiDepartment of Applied Chemistry, Faculty of Sciences and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Lajos NagyDepartment of Applied Chemistry, Faculty of Sciences and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Miklos ZsugaDepartment of Applied Chemistry, Faculty of Sciences and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Sándor KékiDepartment of Applied Chemistry, Faculty of Sciences and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0002-5274-6117

Funding

National Research, Development and Innovation Fund of Hungary TKP2021-NKTA-34NKFI K-132236NKFI K-132685
6 · The paper itself

Abstract

Fluorescent probes that exhibit solvatochromic or excited-state proton-transfer (ESPT) properties are essential tools for the study of complex biological or chemical systems. Herein, the synthesis and characterization of a novel fluorophore that reveals both features, 5-isocyanonaphthalene-1-ol (ICOL), are reported. Various solvatochromic methods, such as Lippert−Mataga and Bilot−Kawski, together with time-dependent density functional theory (TD-DFT) and time-resolved emission spectroscopy (TRES), were applied to gain insights into its excited-state behavior. To make comparisons, the octyloxy derivative of ICOL, 5-isocyano-1-(octyloxy)naphthalene (ICON), was also prepared. We found that internal charge transfer (ICT) takes place between the isocyano and −OH groups of ICOL, and we determined the values of the dipole moments for the ground and excited states of both ICOL and ICON. Furthermore, in the emission spectra of ICOL, a second band at higher wavelengths (green emission) in solvents of higher polarities (dual emission), in addition to the band present at lower wavelengths (blue emission), were observed. The extent of this dual emission increases in the order of 2-propanol < methanol < N,N-dimethylformamide (DMF) < dimethyl sulfoxide (DMSO). The presence of the dual fluorescence of ICOL in these solvents can be ascribed to ESPT. For ICOL, we also determined ground- and excited-state pKa values of 8.4 ± 0.3 and 0.9 ± 0.7, respectively, which indicates a considerable increase in acidity upon excitation. The TRES experiments showed that the excited-state lifetimes of the ICOL and ICON spanned from 10.1 ns to 5.0 ns and from 5.7 ns to 3.8 ns, respectively. In addition, we demonstrated that ICOL can be used as an effective indicator of not only the critical micelle concentration (cmc) of ionic (sodium lauryl sulfate (SLS)) and nonionic surfactants (Tween 80), but also other micellar parameters, such as partition coefficients, as well as to map the microenvironments in the cavities of biomacromolecules (e.g., BSA). It is also pointed out that fluorescence quenching by pyridine can effectively be utilized for the determination of the fractions of ICOL molecules that reside at the water−micelle interface and in the interior spaces of micelles.

Indexed as

MicellesProtonsFluorescent DyesMethanolSolventsSpectrometry, FluorescenceFluorescent DyesMethanolMicellesProtonsSolvents5-isocyano-1-(octyloxy)naphthalene5-isocyanonaphthalene-1-oldual emissionexcited-state proton transferfluorescencephotoacid

Identifiers

PMID35806254
PMCPMC9266744

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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.