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dc.contributor.authorGutmańska, K-
dc.contributor.authorPodborska, A-
dc.contributor.authorMazur, T-
dc.contributor.authorSławek, A-
dc.contributor.authorSivasamy, R-
dc.contributor.authorMaximenko, A-
dc.contributor.authorOrzeł, L-
dc.contributor.authorOszajca, J-
dc.contributor.authorStochel, G-
dc.contributor.authorDev, A V-
dc.contributor.authorVijayakumar, C-
dc.contributor.authorSzaciłowski, `K-
dc.contributor.authorDołęga, A-
dc.date.accessioned2025-11-20T07:52:27Z-
dc.date.available2025-11-20T07:52:27Z-
dc.date.issued2025-06-03-
dc.identifier.citationChemistry-A European Journal; 31(31):e202500215en_US
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/chem.202500215-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/5032-
dc.description.abstractCyanothiazoles, small and quite overlooked molecules, possess remarkable optical properties that can be fine-tuned through coordination with transition metals. In this study, we investigate a promising application of cyanothiazoles, where their combination with copper(I) iodide forms a new class of complexes exhibiting outstanding optical properties. X-ray crystallography of copper(I) iodide complexes with isomeric cyanothiazoles revealed key structural features, such as π─π stacking, hydrogen bonding, and rare halogen⋅⋅⋅chalcogen I⋅⋅⋅S interactions, enhancing stability and reactivity. Advanced spectroscopy and computational modeling allowed precise identification of spectral signatures in Fourier-transform infrared (FTIR), nuclear magnetic resonance (NMR), and ultraviolet-visible (UV–Vis) spectra. Fluorescence studies, along with X-ray absorption near edge structure (XANES) synchrotron analyses, highlighted their unique thermal and electronic properties, providing a solid foundation for further research in the field.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.titleFrom Donor-Acceptor Ligands to Smart Coordination Polymers: Cyanothiazole-Cu(I) Complexes for Multifunctional Electronic Devicesen_US
dc.typeArticleen_US
Appears in Collections:2025

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