In this study, firstly, 3-(2,3-bis(hexadecylthio)propoxy)phthalonitrile (2) as a new phthalonitrile derivative was prepared. Then, new types of non-peripheral phthalocyanine derivatives [CuPc (3), ZnPc (4), and CoPc (5)] were synthesized by using this ligand. The synthesized new compounds were characterized by common spectroscopic methods such as FTIR, 1H-NMR, 13C-NMR, MALDI-TOF, UV-Vis and fluorescence spectroscopy. The H- or J-type aggregation behaviors of novel type metallophthalocyanines in the presence of valuable metal ions such as Ag(i) and Pd(ii) were investigated by UV-Vis and fluorescence spectroscopy. The quenching efficiency of the Ag(i) and Pd(ii) ions for ZnPc (4) was obtained using the Stern-Volmer equation and the quenching constant of ZnPc (4) towards Ag(i) and Pd(ii) ions was found to be 2.9 × 105 mol L-1 and 1.2 × 105 mol L-1, respectively. The binding constant (Ka) and binding stoichiometry (n) of Ag(i) and Pd(ii) ions for ZnPc (5) were calculated using a modified Benesi-Hildebrand equation, and were found to be 1.4 × 108 M-1 and 3.4 × 107 M-1, respectively. The binding ratio and free energy change of Ag(i) and Pd(ii) ions for ZnPc (4) were found to be 1.86, 1.54, -46.49 kJ mol-1 and -42.9 kJ mol-1, respectively. Also, the antioxidant properties of the synthesized novel type metallophthalocyanines and their Ag(i) and Pd(ii) ion doped aggregates were determined using three different methods: DPPH free radical scavenging activity, ferrous ion chelating activity and reducing power activity. Finally, the antibacterial and antifungal activities of phthalocyanine compounds synthesized within the scope of this study were determined by disc diffusion and macrobroth dilution methods and the effect of the doping of Ag(i) and Pd(ii) ions on the antibacterial activities of phthalocyanines was investigated.
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http://dx.doi.org/10.1039/d0dt04103c | DOI Listing |
Herein, the first example of a homoleptic Ag complex stabilized by a monodentate N-donor ligand is presented. Na[SO] oxidizes the linear Ag complex, Na[Ag(succ)] (1), to form a square planar argentate(iii) ion, [Ag(succ)], which crystallizes with a polymeric chain-structure, M[Ag(succ)] (2), when treated with alkali metal sulfate MSO (M = K, Rb, Cs). A mixed-valent Robin-Day class I system, [(HO)Ag][Ag(succ)] (2), forms in the absence of K/Rb/Cs ion.
View Article and Find Full Text PDFDalton Trans
September 2024
Department of Chemistry, Opole University, 48 Oleska Street, Opole 45-052, Poland.
N-Heterocyclic carbenes (NHCs) represent a pivotal class of ligands in coordination chemistry owing to their unique electronic properties. In particular, hemilabile N-heterocyclic carbenes have garnered significant attention over the past decade due to their capacity to transiently coordinate to metals and open coordination sites. However, hemilabile NHC ligands have been predominantly limited to N, O and P donors, while NHC ligands bearing versatile S-donors have been severely underdeveloped.
View Article and Find Full Text PDFMolecules
August 2024
Institut de Physique et Chimie des Matériaux de Strasbourg, Université de Strasbourg-CNRS UMR7504, 23 rue du Loess, BP 43, CEDEX 2, 67034 Strasbourg, France.
The design and study of rich, bulky phosphorus ligands is a key area of research for homogeneous catalysis. Here, we describe an original strategy using a hydrophosphination reaction to produce phosphines of interest for coordination chemistry and homogenous catalysis. In particular, the phosphine obtained by reacting diphenylphosphine with acenaphthylene (ligand ) gives a ligand that adopts an unusual spatial geometry.
View Article and Find Full Text PDFJ Phys Chem A
August 2024
Department of Chemistry, Anhui University, Hefei, Anhui 230601, P. R. China.
Metallophilic interactions are the widespread interactions in multimetal clusters to orientate closed-shell metal self-assembly form linear, facet, or block clusters. The closed-shell metal cation does not have empty valence orbitals, but is able to attract each other. It is still a conundrum to understand the resource in balancing the strong Coulomb repulsion between two cations.
View Article and Find Full Text PDFRSC Adv
June 2024
Chemistry Department, Faculty of Science, Damietta University New Damietta 34517 Egypt
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