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Recent Advances in Coordination Supramolecular Chemistry

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Organometallic Chemistry".

Deadline for manuscript submissions: 31 January 2025 | Viewed by 2806

Special Issue Editors


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Guest Editor
Instituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Camino de Vera s/n, 46022 Valencia, Spain
Interests: supramolecular chemistry
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Guest Editor
School of Sciences, CHRIST University, Karnataka 560029, India
Interests: chemosensors development; molecular recognition; selective analytes detection; colorimetric and fluorimetric studies; DNA binding

Special Issue Information

Dear Colleagues,

Coordination chemistry has a central role in supramolecular chemistry, allowing the development of sophisticated metal–organic assemblies with an amazing variety of geometries and shapes. The different coordination properties of metals combined with the large collection of ligands results in an endless number of possible compounds.

The multiple applications of coordination supramolecular chemistry include: fluorescent chemosensors for selective detection of cations, anions, and biomolecules through various co-ordinations in biology, physiology, pharmacology, and environmental sciences; the study of interactions of nucleic acids with small molecule ligands; the deveopment of drugs in anticancer therapy; molecular hosts for different analytes, etc.

Despite the progress made in the aforementioned field, several problems and challenges still exist. Nothing could be further from the truth, as we will always need ‘‘new’’ assemblies through different coordination.

This Special Issue will bring together publications in the field of coordination supramolecular chemistry. The publications will show the vast range of applications that can be achieved with coordination chemistry compounds. We welcome original research, reviews, mini reviews, and perspective articles.

Dr. Vicente Martí-Centelles
Dr. Avijit Kumar Das
Guest Editors

Manuscript Submission Information

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Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • supramolecular chemistry
  • self-assembly
  • metal–organic assemblies
  • molecular architectures
  • supramolecular materials
  • chemosensors
  • selective detection
  • colorimetric and fluorometric sensors

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Published Papers (2 papers)

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Research

15 pages, 4899 KiB  
Article
Supramolecular Solid Complexes between Bis-pyridinium-4-oxime and Distinctive Cyanoiron Platforms
by Igor Picek, Dubravka Matković-Čalogović, Goran Dražić, Gregor Kapun, Primož Šket, Jasminka Popović and Blaženka Foretić
Molecules 2024, 29(8), 1698; https://doi.org/10.3390/molecules29081698 - 9 Apr 2024
Viewed by 879
Abstract
The structural features and optical properties of supramolecular cyanoiron salts containing bis-pyridinium-4-oxime Toxogonin® (TOXO) as an electron acceptor are presented. The properties of the new TOXO-based cyanoiron materials were probed by employing two cyanoiron platforms: hexacyanoferrate(II), [Fe(CN)6]4– (HCF); and [...] Read more.
The structural features and optical properties of supramolecular cyanoiron salts containing bis-pyridinium-4-oxime Toxogonin® (TOXO) as an electron acceptor are presented. The properties of the new TOXO-based cyanoiron materials were probed by employing two cyanoiron platforms: hexacyanoferrate(II), [Fe(CN)6]4– (HCF); and nitroprusside, [Fe(CN)5(NO)]2– (NP). Two water-insoluble inter-ionic donor–acceptor phases were characterized: the as-prepared microcrystalline reddish-brown (TOXO)2[Fe(CN)6]·8H2O (1a) with a medium-responsive, hydrochromic character; and the dark violet crystalline (TOXO)2[Fe(CN)6]·3.5H2O (1cr). Complex 1a, upon external stimulation, transforms to the violet anhydrous phase (TOXO)2[Fe(CN)6] (1b), which upon water uptake transforms back to 1a. Using the NP platform resulted in the water-insoluble crystalline salt TOXO[Fe(CN)5(NO)]·2H2O (2). The structures of 1cr and 2, solved by single-crystal X-ray diffraction, along with a comparative spectroscopic (UV–vis–NIR diffuse reflectance, IR, solid-state MAS-NMR, Mössbauer), thermal, powder X-ray diffraction, and microscopic analysis (SEM, TEM) of the isolated materials, provided insight for the supramolecular binding, electron-accepting, and H-bonding capabilities of TOXO in the self-assembly of these functionalized materials. Full article
(This article belongs to the Special Issue Recent Advances in Coordination Supramolecular Chemistry)
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25 pages, 5547 KiB  
Article
Structures, Antioxidant Properties, and Antimicrobial Properties of Eu(III), Gd(III), and Dy(III) Caffeinates and p-Coumarates
by Grzegorz Świderski, Monika Kalinowska, Ewelina Gołębiewska, Renata Świsłocka, Włodzimierz Lewandowski, Natalia Kowalczyk, Monika Naumowicz, Adam Cudowski, Anna Pietryczuk, Edyta Nalewajko-Sieliwoniuk, Izabela Wysocka, Żaneta Arciszewska and Beata Godlewska-Żyłkiewicz
Molecules 2023, 28(18), 6506; https://doi.org/10.3390/molecules28186506 - 7 Sep 2023
Cited by 2 | Viewed by 1117
Abstract
In this study, we investigated the structures of lanthanide (Eu(III), Dy(III), and Gd(III)) complexes with p-coumaric (p-CAH2) and caffeic (CFAH3) acids using the FTIRKBr, FTIRATR, and Raman spectroscopic methods. The compositions of the solid [...] Read more.
In this study, we investigated the structures of lanthanide (Eu(III), Dy(III), and Gd(III)) complexes with p-coumaric (p-CAH2) and caffeic (CFAH3) acids using the FTIRKBr, FTIRATR, and Raman spectroscopic methods. The compositions of the solid phase caffeinates and p-coumarates were obtained on the basis of the amounts of hydrogen and carbon determined using an elemental analysis. The degree of hydration and the thermal decomposition of each compound were examined via a thermal analysis of TG, DTG, and DSC. Antioxidant spectroscopic tests were performed using the DPPH (1,1-diphenyl-2-picrylhydrazyl radical), FRAP (ferric reducing antioxidant activity), and ABTS (2,2’-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) (diammonium salt radical cation) methods. The antimicrobial activity of each compound against Escherichia coli, Bacillus subtilis, and Candida albicans was investigated. The electrical properties of the liposomes which mimicked the microbial surfaces formed in the electrolyte containing the tested compounds were also investigated. The above biological properties of the obtained complexes were compared with the activities of p-CAH2 and CFAH3. The obtained data suggest that lanthanide complexes are much more thermally stable and have higher antimicrobial and antioxidant properties than the ligands (with the exception of CFAH3 in the case of antioxidant activity tests). The Gd(III) complexes revealed the highest biological activity among the studied lanthanide complexes. Full article
(This article belongs to the Special Issue Recent Advances in Coordination Supramolecular Chemistry)
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