Icosahedral noble-metal 13-atom nanoclusters (NCs) can form connected structures, which can be regarded as superatomic molecules, by vertex sharing. However, there have been very few reports on the superatomic molecules formed using silver (Ag) as the base element. In this study, we synthesized [AgPd(PPh)Cl] (Pd = palladium, PPh = triphenylphosphine, Cl = chloride), in which two icosahedral 13-atom NCs are connected, and elucidated its geometric and electronic structures to clarify what type of superatomic molecules can be synthesized. The results revealed that [AgPd(PPh)Cl] is a synthesizable superatomic molecule. Single crystal x-ray diffraction analysis showed that the metal-metal distances in and between the icosahedral structures of [AgPd(PPh)Cl] are slightly shorter than those of previously reported [AgPt(PPh)Cl], whereas the metal-PPh distances are slightly longer. On the basis of several experiments and density functional theory calculations, we concluded that [AgPd(PPh)Cl] and previously reported [AgPt(PPh)Cl] are more stable than [Ag(PPh)Cl] because of their stronger superatomic frameworks (metal cores). These findings are expected to lead to clear design guidelines for creation of new superatomic molecules.
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http://dx.doi.org/10.1063/5.0057005 | DOI Listing |
Inorg Chem
December 2024
Key Laboratory of Structure and Functional Regulation of Hybrid Materials, Anhui University, Ministry of Education, Institutes of Physical Science and Information Technology, Anhui University, Department of Chemistry and Center for Atomic Engineering of Advanced Materials, Anhui University, Hefei, Anhui 230601, P. R. China.
The investigation of bonding interactions between superatoms continues to be a largely unexplored area of study. In this study, we present the synthesis and characterization of two F-type superatomic molecules [AuAg(CHNOS)(DPPB)] and [AuAg(CHNS)(DPPM)] ( and for short, respectively). The overall structures were confirmed via X-ray crystallography, revealing the horizontal expansion of the biicosahedral AuAg yielding [AuAg(CHNOS)(DPPB)] and vertical expansion of the biicosahedral AuAg yielding [AuAg(CHNS)(DPPM)].
View Article and Find Full Text PDFJ Phys Chem A
December 2024
Department of Chemistry, Anhui University, Hefei 230601, P. R. China.
Searching for a useful way to build stable hypercoordinate carbon species is a great way to enrich carbon-based chemical rules. Here, we extend the super valence bond model into superatom-atom superbonding to theoretically predict a two-dimensional (BCB)N monolayer, which is the first design of a stable nonplanar hexacoordinate carbon containing material, featuring a sandwich BCB configuration. Chemical bonding analyses indicate that its stability originates from the unique super CO structures, where each tricoordinate B unit has six delocalized electrons acting as a super oxygen (SP), and the BCB unit mimics the bonding pattern of the CO molecule via the superatom-atom super double bond.
View Article and Find Full Text PDFNanoscale
November 2024
Department of Chemistry, National Institute of Technology Durgapur, Mahatma Gandhi Avenue, Durgapur 713209, India.
The reported copper nanoclusters (Cu NCs) of either Cu or Cu or mixed valence (MV) Cu/Cu or Cu/Cu characters are found to be stabilized with a discrete set of ligand donors; hence, analogous Cu NCs with a common architecture supported by the same or nearly the same donor set that exhibit different MV states of Cu, such as Cu/Cu and Cu/Cu, are unknown. Such a series of highest nuclearity copper clusters supported by aromatic thiol-S donor ligands, namely [(L4)CuI15Cu(μ-S)](PF) (1), [(L4)CuI15Cu(μ-S)]ClO·8CH (2) and [(L4)CuI15Cu(DMF)](PF)·CHOH·2CH (3), where L = 2-((3-X-thiophen)-(2-yl-methylene)amino)-4-(trifluoromethyl)benzenethiol (X = H/Me), have been synthesized and their electronic structural properties have been examined and reported herein. The Cu NCs, 1 and 2, feature a central sulfido-S (S) bridged tetracopper SCu core inside a sphere-shaped CuS truncated octahedron.
View Article and Find Full Text PDFJ Phys Chem Lett
November 2024
Guangdong Basic Research Center of Excellence for Structure and Fundamental Interactions of Matter, Guangdong Provincial Key Laboratory of Quantum Engineering and Quantum Materials, School of Physics, South China Normal University, Guangzhou 510006, China.
Dalton Trans
October 2024
Facultad de Ingeniería, Arquitectura y Diseño, Universidad San Sebastián, Bellavista 7, Santiago, 8420524, Chile.
Low-valent palladium nanoparticles are efficient species promoting catalytic activity and selectivity in a number of chemical reactions. Recently, an atom-centered cuboctahedral Pd motif has been characterized as a ligand-protected [Pd(Tr)] cluster featuring a 1s superatomic shell structure. In this report, we describe the ligand-cluster of and endohedral-cage interaction in [Pd(Tr)], which accounts for a favorable situation in the overall cluster.
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