Atomic clusters often show unique, size-dependent properties and have become a fertile ground for the discovery of novel molecular structures and chemical bonding. Here we report an investigation of the B₁₉⁻ cluster, which shows chemical bonding reminiscent of that in [10]annulene (C₁₀H₁₀) and [6]circulene (C₂₄H₁₂). Photoelectron spectroscopy reveals a relatively simple spectrum for B₁₉⁻, with a high electron-binding energy. Theoretical calculations show that the global minimum of B₁₉⁻ is a nearly circular planar structure with a central B₆ pentagonal unit bonded to an outer B₁₃ ring. Chemical bonding analyses reveal that the B₁₉⁻ cluster possesses a unique double π-aromaticity in two concentric π-systems, with two π-electrons delocalized over the central pentagonal B₆ unit and another ten π-electrons responsible for the π-bonding between the central pentagonal unit and the outer ring. Such peculiar chemical bonding does not exist in organic compounds; it can only be found in atomic clusters.
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http://dx.doi.org/10.1038/nchem.534 | DOI Listing |
Langmuir
January 2025
Department of Chemical Engineering and Materials Research Institute, Pennsylvania State University, University Park, Pennsylvania 16802, United States.
The chemical reactivity of glass surfaces is often studied with elemental analysis techniques, and although such characterization methods provide insights on compositional changes from exposure to specific chemical conditions, molecule-specific chemical reactions are not determined unambiguously. This study demonstrates the use of reflection-absorption infrared spectroscopy (RAIRS) to detect molecular species on alkali-free boroaluminosilicate and alkali aluminosilicate glasses, using acetic acid vapor as a model reactant to probe reaction sites at the surface with or without pretreatment by aqueous solutions of varied pH. With the assistance of the theoretical calculation of spectral changes based on refractive indices of bulk materials, it was possible to identify the molecular species being removed and produced at the glass surface.
View Article and Find Full Text PDFNanomicro Lett
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Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-Ro, Seodaemun-Gu, Seoul, 03722, Republic of Korea.
Amidst the ever-growing interest in high-mass-loading Li battery electrodes, a persistent challenge has been the insufficient continuity of their ion/electron conduction pathways. Here, we propose cellulose elementary fibrils (CEFs) as a class of deagglomerated binder for high-mass-loading electrodes. Derived from natural wood, CEF represents the most fundamental unit of cellulose with nanoscale diameter.
View Article and Find Full Text PDFACS Appl Mater Interfaces
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Tianjin Key Laboratory for Marine Environmental Research and Service, School of Marine Science and Technology, Tianjin University, Tianjin 300072, China.
Marine biofouling and corrosion have become the main problems affecting the development of the marine industry. Silicone-based coatings have been widely used for antifouling and anticorrosion due to their low surface energy. However, the poor adhesion and low mechanical stability of these materials limit their application in complex marine environments.
View Article and Find Full Text PDFActa Crystallogr B Struct Sci Cryst Eng Mater
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Faculty of Pharmacy, Wroclaw Medical University, Borowska 211A, Wrocław, 50-556, Poland.
Two new crystals of amantadinium salts were obtained from fenamic and tolfenamic acid. The salt of fenamic acid is a model compound for interaction analysis, while amantadinium tolfenamate is a composition of a drug used in the treatment of symptoms of Parkinsonism and as a nonsteroidal anti-inflammatory drug. The crystal structures were studied and a theoretical analysis of the hydrogen bonds and weak interactions was carried out using quantum theory of atoms in molecules (QTAIM) and non-covalent interaction (NCI) methods.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, California 92093, United States.
The structure and dynamics of water at charged graphene interfaces fundamentally influence molecular responses to electric fields with implications for applications in energy storage, catalysis, and surface chemistry. Leveraging the realism of the MB-pol data-driven many-body potential and advanced path-integral quantum dynamics, we analyze the vibrational sum frequency generation (vSFG) spectrum of graphene/water interfaces under varying surface charges. Our quantum simulations reveal a distinctive dangling OH peak in the vSFG spectrum at neutral graphene, consistent with recent experimental findings yet markedly different from those of earlier studies.
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