To enhance the superatom family, the new superatom analogue Be of group IVA elements has been developed. Be can exhibit multiple valence states (+2 and +4), similar to carbon-group elements, and is capable of forming stable ionic compounds with other atoms such as carbon, chalcogen, (super)halogen, and hydroxyl. This resembles how tin and lead atoms combine with these elements to form stable molecules. Their special stability can be rationalized from the perspective of a cluster shell model. Sn or Pb could be the nearest atomic analogue to Be in group IVA, as the +2 oxidation state is more stable than the +4 oxidation state. This comparative investigation highlights the resemblance between Be and carbon-group elements, which encourages additional exploration within the superatom family.
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http://dx.doi.org/10.1021/acs.inorgchem.3c04200 | DOI Listing |
Phys Chem Chem Phys
November 2024
College of Physics and Electronic Engineering, Northwest Normal University, Lanzhou 730070, China.
Chevrel-type superatoms refer to the ligated transition metal chalcogenide clusters MEL, where the octahedral M is face-capped with cubic chalcogen E (E = S/Se/Te). Most transition metals can form such superatoms and many organic and inorganic ligands can be substituted in solution reactions, which allows these atomic precision species to be easily functionalized and their properties to be tunable. No test was reported for substituting the chalcogens with pnicogens in this class of materials.
View Article and Find Full Text PDFACS Omega
June 2024
College of Information Technology, Jilin Normal University, Siping 136000, China.
Superatoms are crucial in the assembly of functional and optoelectronic materials. This study investigates the endohedral metallo-boron nitride [boron nitride (BN)] fullerenes U@BN, Cm@BN, and U@BN in theory. Our findings confirm that U@BN, Cm@BN, and U@BN are superatoms and their electronic configurations are 1P1S1D1F2P2S2D2F3P, 1P1S1D1F1G1H2S2P2D2F, and 1P1S1D1F2P2S2D2F, respectively.
View Article and Find Full Text PDFNatl Sci Rev
July 2024
College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.
Phys Chem Chem Phys
May 2024
Department of Chemistry, York University, Toronto, ON, Canada M3J 1P3.
Transition metal nanoclusters can exhibit unique and tunable properties which result not only from their chemical composition but also from their atomic packing and quantized electronic structures. Here, we introduce a promising family of bimetallic TM@Ti, TM@Zr, and TM@Hf nanoclusters with icosahedral geometry, where TM represents an atom from groups 3 to 12. Density functional theory calculations show that their stability can be explained with familiar concepts of metal cluster electronic and atomic shell structures.
View Article and Find Full Text PDFJ Am Chem Soc
April 2024
School of Chemistry and Chemical Engineering, State Key Laboratory of Crystal Materials, Shandong University, Ji'nan 250100, People's Republic of China.
Atomically precise superatomic copper nanoclusters (Cu NCs) have been the subject of immense interest for their intriguing structures and diverse properties; nonetheless, the variable oxidation state of copper ions and complex solvation effects in wet synthesis systems pose significant challenges for comprehending their synthesis and crystallization mechanism. Herein, we present a solvent-mediated approach for the synthesis of two Cu NCs, namely, superatomic and pure-Cu(I) . They initially formed as a hetero-phase and then separated as a homo-phase via modulating binary solvent composition.
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