The standard heterogeneous rate constants for the reduction of a series of viologen derivatives with a range of inter-ring torsion angles were measured at Bi and Pt electrodes. The electrode potentials for the first one-electron reduction of the viologens vary from -684 mV to -1070 mV vs. Ag/0.01 m Ag; this enabled a comparison of the behaviour of metallic (Pt) and semi-metallic (Bi) electrodes over a wide range of applied potentials. The differential capacitance (6.5 μF cm) of Bi/MeCN,TBAPF interfaces at the potential of zero charge (=-0.60 V) is at least an order of magnitude greater than that calculated on the basis of the bulk Bi carrier density (3×10 cm) and the differential capacitance (9.5 μF cm) of Pt/MeCN interfaces at their (-0.43 V) is of the same order. The series of viologen derivatives exhibited simple one-electron redox behaviour and showed similar rate constants at Pt (1.8×10-1.6×10 cm s) and Bi electrodes (1.1×10-1.9×10 cm s) after application of the Frumkin correction. These results demonstrate that the density of states at the Bi surface is much higher than in bulk. Finally, the Frumkin-corrected standard rate constants were observed to be inversely correlated with the inter-ring torsion angle of the viologens.
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http://dx.doi.org/10.1002/celc.201600536 | DOI Listing |
Chemistry
December 2024
Hunan Normal University, Department of Chemistry, Hunan Normal University, 410081, Changsha, CHINA.
Host-stabilized charge transfer (HSCT) has been widely utilized in macrocycle-derived supramolecular assemblies and architectures. However, there has been less research attention focused on the direct fabrication of pure organic photocatalysts using HSCT. Herein, four viologen derivatives (m-PV2+, m-BPV2+, d-PV2+, and d-BPV2+) with different electron donor-acceptor (D-A) structures were synthesized.
View Article and Find Full Text PDFSoft Matter
December 2024
Department of Chemistry, IIT Madras, Chennai, 600 036, India.
pH responsive self-assembled supramolecular systems in water hold tremendous promise spanning across the various realms of science and technology. Herein, we report the design and synthesis of benzyl viologen (BV) based amphiphiles and their ability to form pH responsive aggregates with a water soluble anionic dye (electron donor), a polyelectrolyte (PE), and a surfactant. To counter the low solubility of viologen derivatives, β-cyclodextrin (β-CD) was employed as a solubility promoter and the host-guest complexes were characterized by NMR spectroscopy.
View Article and Find Full Text PDFMolecules
August 2024
Key Laboratory for Advanced Materials, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, China.
Stimulus-responsive materials hold significant promise for antitumor applications due to their variable structures and physical properties. In this paper, a series of peptides with a responsive viologen derivative, Pep-CV ( = 1, 2, 3) were designed and synthesized. The process and mechanism of the interaction were studied and discussed.
View Article and Find Full Text PDFInorg Chem
September 2024
Key Laboratory of Surface & Interface Science of Polymer Materials of Zhejiang Province, School of Chemistry and Chemical Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, P. R. China.
Different types of electron transfers (ETs) underlie the versatile use of various solid viologen-derived compounds, which is still insufficiently understood and difficult to control. Here, we demonstrate an effective strategy for modulating the key ET process in crystalline metalloviologen compounds (MVCs). By adjusting the coordinated transition metal ions bearing different electronic structures (e.
View Article and Find Full Text PDFChemphyschem
December 2024
Department for Innovation in Biological, Agro-Food and Forest systems, Università della Tuscia (DIBAF), L.go dell'Università, s.n.c., Viterbo, 01100, Italy.
Supramolecular contacts responsible for chemical interaction of cucurbit[7]uril (CB[7]) macrocycle on a Tolyl-Viologen-Phenylene-Imidazole (T-VPI) molecular thread, at acid pH (T-VPI-H) or after Ag cation addition (T-VPI-Ag), are analytically addressed in a computational framework combining Quantum Theory of Atoms in Molecules (QTAIM) with Density Functional Theory (DFT). In this respect, the crystallographic structure (CCDC number 2217466) is taken as reference condition for addressing the nature of the chemical interactions driving the shuttling of the CB[7] between T and P stations recently observed in dilute water solutions. Beside the host(CB[7]) vs guest(T-VPI-H or T-VPI-Ag) complexation, the coordination sphere of the Ag cation is also investigated by means of local electronic energy density - H(r) - descriptors.
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