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Crystal structure of pantoprazole sodium sesquihydrate Form I, C[subscript 16]H[subscript 14]F[subsc
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Crystal structure of tezacaftor Form A, C[subscript 26]H[subscript 27]F[subscript 3]N[subscript 2]O[
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Crystal structure of fulvestrant hydrate (ethyl acetate), C[subscript 32]H[subscript 47]F[subscript
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Crystal structure of ponazuril, C 18 H 14 F 3 N 3 O 6 S
The crystal structure of ponazuril has been solved and refined using synchrotron X-ray powder diffraction data, and optimized using density functional theory techniques. Ponazuril crystallizes in space group P2 1 /c (#14) with a = 8.49511(6), b = 12.38696(6), c = 18.84239(17) Å, β = 96.7166(4)°, V = 1969.152(12) Å 3 , and Z = 4. N–H∙∙∙O hydrogen bonds link the molecules into chains along the a-axis, with a graph set C1,1(6). The powder pattern has been submitted to ICDD for inclusion in the Powder Diffraction File™ (PDF®).
Crystal structure of deracoxib, C 17 H 14 F 3 N 3 O 3 S
The crystal structure of deracoxib has been solved and refined using synchrotron X-ray powder diffraction data, and optimized using density functional theory techniques. Deracoxib crystallizes in space group Pbca (#61) with a = 9.68338(11), b = 9.50690(5), c = 38.2934(4) Å, V = 3525.25(3) Å 3 , and Z = 8. The molecules stack in layers parallel to the ab-plane. N–H∙∙∙O hydrogen bonds link the molecules along the b-axis, in chains with the graph set C1,1(4), as well as more-complex patterns. N–H∙∙∙N hydrogen bonds link the layers. The powder pattern has been submitted to ICDD for inclusion in the Powder Diffraction File™ (PDF®).
Soluble Methane Monooxygenase Component Interactions Monitored by [superscript 19]F NMR
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Structural Dynamics of the Methyl-Coenzyme M Reductase Active Site Are Influenced by Coenzyme F 430 Modifications
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Structural Relationships and Absorption Spectroscopy of β-[NH 4 ][UF 5 ] and [NH 4 ][Pu 3 F 13 ]
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Local Structure Distortion Induced Broad Band Emission in the All-Inorganic BaScO[subscript 2]F:Eu[superscript 2+] Perovskite
Abstract not provided
Polymorphism in Weberite Na 2 Fe 2 F 7 and its Effects on Electrochemical Properties as a Na-Ion Cathode
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Oxygen Loss on Disordered Li-Excess, Mn-Rich Li-Ion Cathode Li 2 MnO 2 F through First-Principles Modeling
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Redox Behaviors in Li-Excess Cation-Disordered Mn-Nb-O-F Rocksalt Cathode
Lithium-excess cation-disordered rocksalt oxide (DRX) is a new choice of high energy Li-ion cathode materials. DRX cathode can deliver an exceptionally high capacity of >250 mAh/g, implying the participation of cationic transition metal and anionic oxygen redox in the electrochemistry. Understanding the explicit roles of both redox reactions in the newly developed cathode is of critical importance to further development of these materials. Herein, we synthesize a representative Mn-redox-based fluorinated DRX material, Li1.2Mn0.625Nb0.175O1.95F0.05 (LMNOF). Using a comprehensive suite of electroanalytical methods, we probe the cationic and anionic redox processes and their evolution upon cycling exclusively from the electrochemical point of view. This work sheds light on understanding of cationic and anionic redox and their roles in the capacity loss for high-capacity fluorinated DRX cathode, meanwhile, showcases an explicit approach to study the electrochemistry of novel electrode materials using such non-disruptive electroanalytical methods.
Catalytic Reactions and Energy Conservation in the Cytochrome bc 1 and b 6 f Complexes of Energy-Transducing Membranes
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Forcing Dicyanamide Coordination to f-Elements by Dissolution in Dicyanamide-Based Ionic Liquids
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