The construction of cluster-based crystalline chalcogenide structures through the traditional solvothermal method relies on synergistic control of precursors, template cations and auxiliary solvents. Generally, the combination of metal precursors plays a crucial role in controlling the size of clusters, while organic templates and auxiliary solvents usually contribute to the type of clusters and architecture of the framework. Decades of synthetic efforts have been mainly devoted to expanding organic amine templates for constructing new structures. However, the important role of auxiliary solvents in enriching the chalcogenide family is usually disregarded. Reported here are several new crystalline In-Se compounds (ISP-1 to 4) with different dimensions, obtained by elaborately regulating auxiliary solvents under the direction of the same organic template, piperidine. Of these four structures, ISP-1 is constructed by irregular supertetrahedral clusters, giving a novel 2D structure with a corner-shared single Se atom and InSe five-member ring as linkers; ISP-2 has a 1D structure composed by interlinked InSe five-member rings; ISP-4 is constructed by supertetrahedral T2 clusters exhibiting an uncommon zeolite-like network.
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http://dx.doi.org/10.1039/d2dt00174h | DOI Listing |
J Phys Chem A
December 2024
Research Center for Computational Design of Advanced Functional Materials (CD-FMat), National Institute of Advanced Industrial Science and Technology (AIST), Central 2, Umezono 1-1-1, Tsukuba 305-8568, Japan.
Three new schemes of induced solvent charges for the auxiliary polarization formulation of the fragment molecular orbital method are proposed and compared to the original approach. It is found that the charge balance of the solute and solvent embeddings is crucial for maintaining a proper gap between occupied and virtual orbitals of fragments for zwitterionic systems in solution. The original instability is eliminated with the new scheme of fragment-specific solvent charges.
View Article and Find Full Text PDFChemSusChem
December 2024
Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.
We report the use of carboxyl-functionalised alkylimidazolium salts as thermomorphic acid catalysts for the hydrolysis of cellulose and starch in water, free from organic solvents and auxiliary substances. The imidazolium salts are insoluble in water at room temperature and dissolve to form homogeneous solutions upon heating. Following catalysis at elevated temperatures the solution is cooled and the imidazolium salt precipitates from the aqueous layer to afford an aqueous glucose solution.
View Article and Find Full Text PDFInt J Biol Macromol
November 2024
School of Environmental and Chemical Engineering, Xi'an Key Laboratory of Textile Chemical Engineering Auxiliaries, Engineering Research Center of Biological Resources Development and Pollution Control Universities of Shaanxi Province, Key Laboratory of Textile Dyeing Wastewater Treatment Universities of Shaanxi Province, Xi'an Polytechnic University, Xi'an 710048, PR China. Electronic address:
The carboxyl groups on MIL-88B(Fe) are crucial for the covalent immobilization of snailase, and the enzyme can convert common ginsenoside Rb1 into the rare ginsenoside compound K (CK) with higher bioavailability. The present study proposed glutamate-modified MIL-88B(Fe) for the immobilization of snailase to improve enzymatic activity and loading capacity. The surface topography characterized by SEM and CLSM indicated snailase was successfully encapsulated and uniformly distributed in the Sna@MIL-88B(Fe).
View Article and Find Full Text PDFComput Struct Biotechnol J
December 2024
Laboratory of Biomolecular Interactions and Transport, Department of Gene Expression, Institute of Molecular Biology and Biotechnology, Faculty of Biology, Adam Mickiewicz University, Uniwersytetu Poznanskiego 6, Poznan 61-614, Poland.
Protein hydration plays a vital role in many biological functions, and molecular dynamics simulations are frequently used to study it. However, the accuracy of these simulations is often sensitive to the water model used, a phenomenon particularly evident in intrinsically disordered proteins. Here, we investigated the extent to which the choice of water model alters the behavior of complex networks of tunnels within proteins.
View Article and Find Full Text PDFRSC Adv
November 2024
Department of Organic Chemistry, University of Chemistry and Technology Prague Technická 5, Prague 6 Prague 166 28 Czech Republic
Three series of spiropyran photoswitches with an auxiliary chiral centre at position 3' of the indoline unit were synthesized. Using one example, a novel methodology for synthesis of an optically active spiropyran photoswitch with a defined chirality at position 3' is demonstrated. Furthermore, a new acid-mediated strategy for spiropyran purification affording moderate to excellent yields (up to 96%) is reported herein.
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