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Developing tunable motifs for heterometallic interactions should be beneficial for fabricating functional materials based on cooperative electronic communications between metal centers. Reported here is the efficient formation of cyclic heterometallic interactions from a complex containing an artificial tripeptide with metal binding sites on its main chain and side chains. X-ray structural analysis and X-ray absorption spectroscopy revealed that the cyclic metal-metal arrangements arise from the amide groups connecting four square-planar Cu centers and four octahedral Ni centers in a cyclic manner. UV/Vis spectral studies suggested that this efficient formation was achieved by the selective formation of the square-planar Cu centers and a crystallization process. Magnetic measurements using SQUID clarified that the cyclic complex represented the S=2 spin state at low temperatures due to effective antiferromagnetic interactions between the Ni and Cu centers.
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http://dx.doi.org/10.1002/anie.202013373 | DOI Listing |
Adv Mater
August 2025
School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, 610031, China.
MXene delivers promising features that are highly compatible with oxygen electrocatalysis, such as excellent electroconductivity, high specific surface area, superhydrophilicity, and tailorable chemically functionalized surfaces, thus being recognized as the ideal platform for developing high-performance catalysts for practical applications in industrial devices. A comprehensive understanding of oxygen catalytic mechanism on MXene ontology and a systematic refining of the general principles toward various physicochemical property regulation strategies are, respectively, the basis and effective alleyway to hitting the target, yet it is currently insufficient and need to be further explored in-depth. Herein, the fundamental effects of MXene on oxygen catalytic activity are sorted out thoroughly, and on this basis, the current mainstream strategies for tuning the property of MXene-based electrocatalysts are classified into four categories, including anion-tuning, cation-tuning, defect/vacancy regulation, and heterometallic dual-site collaboration, where the intrinsic mechanism of each strategy affecting the structure-activity relationship of catalysts is revealed accordingly.
View Article and Find Full Text PDFDalton Trans
September 2025
Department of Chemistry, Molecular Sciences Research Hub, Imperial College London, 82 Wood Lane, White City, London W12 0BZ, UK.
The alkaline earth metals are notorious for their tendency to form ionic compounds of their dications. In recent years, however, chemists have found ways to kinetically skirt around the edges of these thermodynamic sinks, thereby providing access to new pastures of molecular alkaline earth element chemistry. Most prominently, novel low-oxidation state reagents have enabled the synthesis of a wide range of complexes with alkaline earth-metal interactions.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
August 2025
Department of Inorganic Chemistry and Technology, Jozef Stefan Institute, Jamova 39, 1000 Ljubljana, Slovenia.
The new mol-ecular complex [NiPb(CHNO)(CHNO)Cl(HO)] with the Schiff base 2-meth-oxy-6-[(methyl-imino)-meth-yl]phenol and -vanillin ligands, both deprotonated, crystallizes in the monoclinic space group 2/ with one mol-ecule per asymmetric unit. The heterometallic mol-ecule exhibits a whole-mol-ecule orientational disorder [occupancy ratio 0.711 (6): 0.
View Article and Find Full Text PDFACS Catal
August 2025
Dept. Chemistry, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA, U.K.
Intermetallic synergy can be useful to both enhance catalytic performance and access diverse chemistries, but understanding and predicting the most effective metal combinations remains a challenge. This perspective focuses on a common class of homogeneous heteronuclear catalysts which combine transition metals (M-(II/III)) with Group III, f-, or s-block metals (M'(I-III)) in phenoxy-imine-ether donor ligands. Independent investigations into these heteronuclear complexes across different fields of catalysis, including electrocatalysis, polymerization catalysis, and small-molecule asymmetric catalysis, have all demonstrated the benefits of intermetallic cooperativity.
View Article and Find Full Text PDFRSC Adv
July 2025
Department of Medicinal Chemistry, Faculty of Pharmacy, Zabol University of Medical Sciences Zabol Iran.
Reactive oxygen species (ROS) modulate redox balance and cellular processes such as proliferation, angiogenesis, metabolism, immune modulation, and metastasis. Metal-based polymeric complexes have shown potential in disrupting oxidative pathways relevant to tumor development. A comprehensive investigation was conducted on the interaction between a Cu/Mn/Na polymer and catalase, as well as its cytotoxic behavior.
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