UV-Vis spectroscopy is used to study the charge transfer complexes of thiacrown ethers - with fullerene. The size of TCE1-6 and the nature of the heteroatoms (N, O and S) have been systematically changed to examine the effect of these factors on the HOMO/LUMO energy levels, the optical energy gap and the interactions between TCE's and C60. The negative and positive values of ΔS designate the structural forming method and the randomness of the free solvent molecules, respectively. Thermodynamics and stability data show that the complexes have a 1:1 ratio that has been emphasized by density functional theory calculations. Additionally, they show a synergetic interplay of donor-acceptor, π-π, and -π interactions, which are the basis for the affinity of our novel receptors toward C. The proposed system of enzyme model suggests a development concept in the future design of enzyme model organic photovoltaic systems.
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http://dx.doi.org/10.1021/acsomega.0c01877 | DOI Listing |
Int J Mol Sci
February 2022
Butlerov Institute of Chemistry, Kazan Federal University, Kremlevskaya Str. 18, 420008 Kazan, Russia.
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 , OS-thiacrown-ether , and OS-bridged thiacalixtube ). The study was conducted in bulk liquid phase and Langmuir monolayers.
View Article and Find Full Text PDFChem Asian J
March 2022
Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, 1-1 Minami-Osawa, Hachioji, Tokyo, 192-0397, Japan.
Thiacrown ethers have attracted much attention in host-guest chemistry. Herein, we present the polymethylation reactions of unsaturated thiacrown ethers. Unsaturated thiacrown ethers having sulfonium groups were synthesized by the reaction of corresponding unsaturated thiacrown ethers with methyl triflate.
View Article and Find Full Text PDFACS Omega
October 2020
Department of Chemistry, Mutah University, Al Karak 61710, Jordan.
UV-Vis spectroscopy is used to study the charge transfer complexes of thiacrown ethers - with fullerene. The size of TCE1-6 and the nature of the heteroatoms (N, O and S) have been systematically changed to examine the effect of these factors on the HOMO/LUMO energy levels, the optical energy gap and the interactions between TCE's and C60. The negative and positive values of ΔS designate the structural forming method and the randomness of the free solvent molecules, respectively.
View Article and Find Full Text PDFPhys Chem Chem Phys
August 2020
Institute of Chemistry, University of Silesia, Szkolna 9, 40-006 Katowice, Poland.
In this work, we report the synthesis, unexpected glass-forming properties, molecular dynamics and conformational analysis of two thiacrown ethers: 6-methyl-2,3-dihydro-1,4-benzodithiine (1), with a six-membered heterocyclic ring, and macrocyclic 2,3-(4'-methylbenzo)-1,4-dithia-7-oxacyclononane (2). Based on the calorimetric studies, we showed that compound 1 is a viscous liquid at room temperature undergoing vitrification at 192 K. Compound 2 is a crystalline solid at room temperature characterized by a melting point at 331 K; however, it can be vitrified with ease after being melted by cooling down to 224 K.
View Article and Find Full Text PDFCarbohydr Res
September 2020
Department of Chemistry, Faculty of Science, University of Kufa, An-Najaf, Iraq.
Polymeric macrocycles are important as complexation agents in chemistry. The multivalent binding of heteroatoms inside the macrocycle to metals and organic pollutants has gained much interest. A protecting group strategy was applied to synthesise functionalized crown ether based on glucose.
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