We have formed the long-sought He-clathrate. This was achieved by refilling helium into ice XVI, opening a new synthesis route for exotic forms of clathrate hydrates. The process was followed by neutron diffraction; structures and cage fillings were established. The stabilizing attractive van der Waals interactions are enhanced by multiple cage fillings with theoretically up to four helium atoms per large cage and up to one per small cage; He-clathrate hydrates can be considered as a solid-state equivalent of the clustering of small apolar entities dissolved in the liquid state of water. Unlike most other guests, helium easily enters and leaves the water cages at temperatures well below 100 K, hampering applications as a gas storage material. Despite the weak dispersive interactions, the inclusion of helium has a very significant effect on lattice constants; this is also established for helium inclusion in ice Ih and suggests that lattice parameters are arguably the most sensitive measure to gauge dispersive water-gas interactions.
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http://dx.doi.org/10.1021/acs.jpclett.8b01423 | DOI Listing |
J Org Chem
January 2025
Department of Chemistry and the UCR Center for Catalysis, University of California-Riverside, Riverside, California 92521, United States.
suite of internally functionalized FeL cage complexes has been synthesized with lipophilic end groups to allow dissolution in varied solvent mixtures, and the scope of their molecular recognition of a series of neutral, nonpolar guests has been analyzed. The lipophilic end groups confer cage solubility in solvents with a wide range of polarities, from hexafluoroisopropanol (HFIP) to tetrahydrofuran, and the hosts show micromolar affinities for neutral guests, despite having no flat panels enclosing the cavity. These hosts allow interrogation of the effects of an internal functional group on guest binding properties, as well as solvent-based driving forces for recognition.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Chemistry and Chemical Engineering, Donghua University, Shanghai, 201620, P. R. China.
High-nuclearity polyoxometalate (POM) clusters are attractive building blocks (BBs) for the synthesis of metal-organic frameworks (MOFs) due to their high connectivity and inherently multiple metal centers as functional sites. This work demonstrates a strategy of step-wise growth on ring-shaped [PWO] precursor, which produced two new high-nuclearity polyoxotungstates, a half-closed [HPWO] {W} and a fully-closed [HPWO] {W}. By in situ synthesis, unique MOFs of copper triazole-benzoic acid (HL) complexes incorporating the negatively-charged {W} and {W} as nodes, {Cu(HL)W} HNPOMOF-1 and {Cu(HL)W} HNPOMOF-2, were constructed by delicately tuning the reaction conditions, mainly solution pH, which controls the formation of {W} and {W}, and at the same time the protonation of triazole-benzoic acid ligand thus its coordination mode to copper ion that creates the highest nuclearity POM-derived MOFs reported to date.
View Article and Find Full Text PDFiScience
December 2024
Department of Chemistry and the UCR Center for Catalysis, University of California - Riverside, Riverside, CA 92521, USA.
Commun Biol
November 2024
Department of Structure of Macromolecules, Centro Nacional de Biotecnología (CNB-CSIC), Campus de Cantoblanco, Madrid, Spain.
J Mol Graph Model
December 2024
Department of Chemistry, Süleyman Demirel University, 32260 Isparta, Turkey. Electronic address:
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