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Metal-organic frameworks (MOFs), with their high porosities and surface areas, show great utility in the field of gas adsorption. To unlock this porosity, MOFs are generally fully activated by removing all adsorbed guests using high temperatures and low pressures. However, this is energy intensive and can be unfeasible if the MOF is part of a composite, where the maximum temperature of the composite is below the activation temperature. To investigate the effect of activation temperature on adsorption, a series of in situ single-crystal X-ray diffraction (scXRD) studies were performed on Ni-MOF-74 loaded with the gas nitric oxide (NO) under different conditions. These experiments uncovered anomalous adsorption results where partially activated samples adsorb ∼14% more NO per framework material than did the fully activated sample. The scXRD experiments revealed a new NO binding site that is only present if the open metal sites are partially occupied by water molecules. To shed more light on the respective binding of the two different NO sites in Ni-MOF-74, these were studied in situ under different treatment conditions, such as the exposure to vacuum at different temperatures. This study yields insights into the nature of binding sites in MOFs, how these are affected by activation, and helps to pave the way for the improved design of processing conditions.
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http://dx.doi.org/10.1021/jacs.5c10395 | DOI Listing |
Langmuir
September 2025
Laboratory of Electrochemistry-Corrosion, Metallurgy and Inorganic Chemistry, Faculty of Chemistry, USTHB, BP 32, 16111, Algiers, Algeria.
Azo dyes, prevalent in various industries, including textile dyeing, food, and cosmetics, pose significant environmental and health risks due to their chemical stability and toxicity. This study introduces the synthesis and application of a copper hydrogen-π-bonded benzoate framework (Cu-HBF) and its derived marigold flower-like copper oxide (MFL-CuO) in a synergetic adsorption-photocatalytic process for efficiently removing cationic azo dyes from water, specifically crystal violet (CV), methylene blue (MB), and rhodamine B (RhB). The Cu-HBF, previously available only in single crystal form, is prepared here as a crystalline powder for the first time, using a low-cost and facile procedure, allowing its application as an adsorbent and also serving as a precursor for synthesizing well-structured copper oxide (MFL-CuO).
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Understanding and controlling the nucleation and growth processes of gold clusters are crucial for advancing the nucleation theory and targeted cluster synthesis. While mass spectrometry has revealed the intermediate species formed during the growth process, the overall structural evolution remains unclear due to a lack of crystallographic information. In this study, we examined a new synthetic method for thiolate-protected gold clusters in their embryonic stage.
View Article and Find Full Text PDFDalton Trans
August 2025
Centro de Química Estrutural, Departamento de Engenharia Química, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais 1, 1000-049 Lisboa, Portugal.
In this work, new copper(I) complexes of borane-functionalized bis(3,5-dimethylpyrazolyl)methane ligands were synthesized, characterized and used as catalysts for the cycloaddition of phenylacetylene and azides. Reaction of the allylated bis(3,5-dimethylpyrazolyl)methane proligand (La) with CuCl or [Cu(NCMe)]BF gave rise to the neutral copper chloride complex [(La)CuCl] (1a) or the binuclear cationic copper complex [(La)Cu(NCMe)]2(BF4)2 (2a2), respectively. The same reactions using a borane-functionalized bis(3,5-dimethylpyrazolyl)methane proligand (Lb) led to the isolation of complexes [(Lb)CuCl] (1b) and [(Lb)Cu(NCMe)2]BF4 (2b).
View Article and Find Full Text PDFNat Commun
August 2025
State Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai, 200032, China.
Branched PFOA and PFOS have shorter half-lives, lower toxicity, and weaker serum protein binding than linear ones, offering better environmental and health safety. Yet methods to access such branched motifs remain under developed. We now introduce a one-step dehydroxy-perfluoro-tert-butylation of alcohols, in which perfluoro-tert-butyl phenyl sulfone serves both to activate the C-O bond and to deliver the perfluoro-tert-butyl group.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), The MOE Key Laboratory of Spectrochemical Analysis & Instrumentation, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xi
Soft biomaterials, characterized by structural disorder and weak interactions, pose significant challenges for structural characterization by conventional methods, which typically rely on long-range crystalline order or strong electron scattering. Here, we report a computationally assisted polarized Raman spectroscopy strategy that enables direct, in situ determination of three-dimensional (3D) molecular structures and their intermolecular interactions, correlating molecular-scale orientations with macroscopic morphologies. We validated our approach using the well-characterized α-glycine crystal, achieving structural precision comparable to that of single-crystal X-ray diffraction (RMSD = 0.
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