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 1 paper.
0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.2field-weighted citation impact, top 25% of its field
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
1 citing paper in PubMed, 11 citations in OpenAlex.
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
13 authors at 6 institutions in 1 country.
Anton MuravevArbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, Arbuzov Str. 8, 420088 Kazan, Russia.ORCID 0000-0002-2245-3460
Ayrat YakupovButlerov Institute of Chemistry, Kazan Federal University, Kremlevskaya Str. 18, 420008 Kazan, Russia.
Tatiana GerasimovaArbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, Arbuzov Str. 8, 420088 Kazan, Russia.
Daut IslamovArbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, Arbuzov Str. 8, 420088 Kazan, Russia.
Vladimir LazarenkoNational Research Centre "Kurchatov Institute", Kurchatov Square 1, 123182 Moscow, Russia.
Alexander ShokurovFrumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Leninsky Pr. 31, 119071 Moscow, Russia.ORCID 0000-0003-4562-8603
Alexander OvsyannikovArbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, Arbuzov Str. 8, 420088 Kazan, Russia.
Pavel DorovatovskiiNational Research Centre "Kurchatov Institute", Kurchatov Square 1, 123182 Moscow, Russia.
Yan ZubavichusSynchrotron Radiation Facility SKIF, Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Nikolskii Pr. 1, 630559 Koltsovo, Russia.ORCID 0000-0003-2266-8944
Alexander NaumkinFrumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Leninsky Pr. 31, 119071 Moscow, Russia.ORCID 0000-0001-5696-5723
Sofiya SelektorFrumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Leninsky Pr. 31, 119071 Moscow, Russia.ORCID 0000-0002-3720-1717
Svetlana SolovievaArbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, Arbuzov Str. 8, 420088 Kazan, Russia.ORCID 0000-0001-7106-6777
Igor AntipinButlerov Institute of Chemistry, Kazan Federal University, Kremlevskaya Str. 18, 420008 Kazan, Russia.ORCID 0000-0002-9882-7035
A.E. Arbuzov Institute of Organic and Physical Chemistry · RUFrumkin Institute of Physical Chemistry and Electrochemistry · RUKazan Federal University · RUKurchatov Institute · RUA. N. Nesmeyanov Institute of Organoelement Compounds · RUBoreskov Institute of Catalysis · RU
Funding
The Ministry of Education and Science of the Russian Federation 0671-2020-0063
6 · The paper itself
Abstract
Sulfur-containing groups preorganized on macrocyclic scaffolds are well suited for liquid-phase complexation of soft metal ions; however, their binding potential was not extensively studied at the air-water interface, and the effect of thioether topology on metal ion binding mechanisms under various conditions was not considered. Herein, we report the interface receptor characteristics of topologically varied thiacalixarene thioethers (linear bis-(methylthio)ethoxy derivative
Indexed as
Confined SpacesMercuryLigandsMetalsSaltsSulfidesSulfurWaterLigandsMercuryMetalsSaltsSulfidesSulfurWaterAg+ and Hg2+ complexesLangmuir monolayersthiacalix[4]arenesthiacrown-ethersX-ray photoelectron spectroscopy
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.
Thiacalixarenes with Sulfur Functionalities at Lower Rim: Heavy Metal Ion Binding in Solution and 2D-Confined Space. · full record | OpenQuestion