Publications by authors named "Sarou-Kanian V"

Oxalate ligands are found in many classes of materials, including energy storage materials and biominerals. Determining their local environments at the atomic scale is thus paramount to establishing the structure and properties of numerous phases. Here, we show that high-resolution O solid-state NMR is a valuable asset for investigating the structure of crystalline oxalate systems.

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Gliomas account for 50% of brain cancers and are therefore the most common brain tumors. Molecular alterations involved in adult gliomas have been identified and mainly affect tyrosine kinase receptors with amplification and/or mutation of the epidermal growth factor receptor (EGFR) and its associated signaling pathways. Several targeted therapies have been developed, but current treatments remain ineffective for glioblastomas, the most severe forms.

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The structure of MOF (M = Nb, Ta) compounds was precisely modeled by combining powder X-ray diffraction, solid-state NMR spectroscopy, and semiempirical dispersion-corrected DFT calculations. It consists of stacked (MOF) layers along the direction formed by heteroleptic corner-connected MX (X = O, F) octahedra. F NMR resonance assignments and occupancy rates of the anionic crystallographic sites have been revised.

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Lithium-ion batteries are at the core of the democratisation of electric transportation and portative electronic devices. However, fast and/or low temperature charge induce performance loss, mainly through lithium plating, a degrading mechanism. In this report, Li operando Nuclear Magnetic Resonance spectroscopy is used to detect the onset of metastable lithium deposits in an NMC622/graphite cell at 0 °C and fast charge.

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Article Synopsis
  • Critical bone defect repair is challenging, and calcium-deficient apatites (CDA) are being studied as biocompatible materials that aid in bone healing.
  • Previous research showed that using activated carbon cloths (ACC) coated with CDA or strontium-doped CDA can accelerate bone repair in rats, especially in the short term.
  • This study further examines the long-term effectiveness of these patches, finding that strontium-doped patches notably enhance bone quality and integrate well without harmful debris, suggesting they are effective biomaterials for bone reconstruction.
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Intensive research on improving the catalytic properties of zeolites is focused on modulating their acidity and the distribution of associated Al sites. Herein, by studying a series of ZSM-5 zeolites over a broad range of Al content, we demonstrate how the nature of the mineralizing agent (F or OH ) used in hydrothermal syntheses directly impacts Al sites distribution. The proportions of Al sites, probed by Al NMR, depend on the Si/Al ratio for F , but remain identical for OH (from Si/Al=30 to 760).

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Crystallization of oxide glasses rich in Zn, Ga, and Ge is of interest for the synthesis of new transparent ceramics. In this context, we report the identification and detailed structural characterization of a new solid solution CaGaZnGeO (0 ≤ ≤ 1). These compounds adopt the trigonal langasite structure type, offering three possible crystallographic sites for the coordination of isoelectronic Zn, Ga, and Ge.

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Gliomas are the most common primary brain tumors in adults. Significant progress has been made in recent years in identifying the molecular alterations involved in gliomas. Among them, an amplification/overexpression of the EGFR (Epidermal Growth Factor Receptor) proto-oncogene and its associated signaling pathways have been widely described.

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Article Synopsis
  • The study explores the use of activated carbon fiber cloth (ACC) and its coated version with calcium-deficient hydroxyapatite (ACC/CDA) as potential tissue patches to enhance bone healing.
  • In a rat model, the research compared natural bone healing to healing with these patches and assessed bone formation at different time points using advanced imaging techniques.
  • Results indicated that both patches were highly biocompatible and that ACC/CDA significantly accelerated bone regeneration due to its structural support and osteogenic properties, suggesting potential applications in human medicine.
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The measurement of dipolar and J- couplings between Si and O isotopes is challenging owing to (i) the low abundance of both isotopes and (ii) their close Larmor frequencies, which only differ by 19%. These issues are circumvented here by the use of isotopic enrichment and dedicated triple-resonance magic-angle spinning NMR probe. The surface of Si-enriched silica was labelled with O isotope and heated at 80 and 200 °C.

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Human malignant gliomas are the most common type of primary brain tumor. Composed of glial cells and their precursors, they are aggressive and highly invasive, leading to a poor prognosis. Due to the difficulty of surgically removing tumors and their resistance to treatments, novel therapeutic approaches are needed to improve patient life expectancy and comfort.

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The synthesis and characterization of a polyrotaxanated covalent organic network (CON) based on the association between the viologen and pillar[5]arene (P[5]OH) units are reported. The mechanical bond allows for the irreversible insertion of n-type redox centers (P[5]OH macrocycles) within a pristine structure based on p-type viologen redox centers. Both redox units are active on a narrow potential range and, in water, the presence of P[5]OH greatly increases the electroactivity of the material.

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Across the evolutionary history of insects, the shift from nitrogen-rich carnivore/omnivore diets to nitrogen-poor herbivorous diets was made possible through symbiosis with microbes. The herbivorous turtle ants Cephalotes possess a conserved gut microbiome which enriches the nutrient composition by recycling nitrogen-rich metabolic waste to increase the production of amino acids. This enrichment is assumed to benefit the host, but we do not know to what extent.

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We present an algorithm suitable for automatically correcting rolling baseline coming from time-domain truncation induced by the dead time in pulse-acquire one-dimensional MAS NMR spectra. It relies on an iterative estimation of the baseline restricted in the time-domain by the dead time duration combined with a histogram filter allowing adaptive selection of the baseline points. This method does not make any assumption regarding the NMR resonances line shapes or widths and does not modify the acquired free induction decay points.

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It has already been shown that sono-electrodeposition can be used to coat activated carbon fiber cloth (ACC) with calcium phosphates (CaP) and we recently demonstrated that cathodic polarization at -1 V/Hg/HgSO was the best parameter to obtain a carbonated calcium deficient hydroxyapatite (CDA) coating with optimal uniformity and homogeneity. In the present study, we investigated whether this technique was suitable to dope this carbonated CDA coating by partial substitution with another bivalent cation such as strontium. We show here that a strontium-substituted carbonated CDA coating can be produced and quantitatively controlled up to at least 10 at.

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Aluminium batteries constitute a safe and sustainable high-energy-density electrochemical energy-storage solution. Viable Al-ion batteries require suitable electrode materials that can readily intercalate high-charge Al ions. Here, we investigate the Al intercalation chemistry of anatase TiO and how chemical modifications influence the accommodation of Al ions.

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Drosophila flies are versatile animal models for the study of gene mutations in neuronal pathologies. Their small size allows performing in vivo Magic Angle Spinning (MAS) experiments to obtain high-resolution H nuclear magnetic resonance (NMR) spectra. Here, we use spatially-resolved H high-resolution MAS NMR to investigate in vivo metabolite contents in different segments of the fly body.

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Magic-angle-spinning (MAS) enhances sensitivity and resolution in solid-state nuclear magnetic resonance (NMR) measurements. MAS is obtained by aerodynamic levitation and drive of a rotor, which results in large centrifugal forces that may affect the physical state of soft materials, such as polymers, and subsequent solid-state NMR measurements. Here, we investigate the effects of MAS on the solid-state NMR measurements of a polymer electrolyte for lithium-ion battery applications, poly(ethylene oxide) (PEO) doped with the lithium salt LiTFSI.

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A crystallographic approach incorporating multinuclear high field solid state NMR (SSNMR), X-ray structure determinations, TEM observation, and density functional theory (DFT) was used to characterize two polymorphs of rubidium cryolite, RbAlF. The room temperature phase was found to be ordered and crystallizes in the (no. 70) space group with = 37.

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Crystallization from glass can lead to the stabilization of metastable crystalline phases, which offers an interesting way to unveil novel compounds and control the optical properties of resulting glass-ceramics. Here, we report on a crystallization study of the ZrF-TeO glass system and show that under specific synthesis conditions, a previously unreported TeZrOF zirconium oxyfluorotellurite antiglass phase can be selectively crystallized at the nanometric scale within the 65TeO-35ZrF amorphous matrix. This leads to highly transparent glass-ceramics in both the visible and near-infrared ranges.

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Nuclear magnetic resonance is one of the rare techniques able to probe selectively the ions inside the nanoporous network in supercapacitor devices. With a magnetic resonance imaging method able to detect all ions (adsorbed and nonadsorbed), we record one-dimensional concentration profiles of the active ions in supercapacitors with an electrode configuration close to that used in industry. Larger anionic concentration changes are probed upon charge and discharge in a carbide-derived carbon (CDC) with micropores smaller than 1 nm compared to a conventional nanoporous carbon (CC) with a larger distribution of pore sizes, up to 2 nm.

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We report the study of high-temperature melts (1600-2300 °C) and related glasses in the SrO-Al2O3-SiO2 phase diagram considering three series: (i) depolymerized ([SrO]/[Al2O3] = 3); (ii) fully polymerized ([SrO]/[Al2O3] = 1); and (iii) per-aluminous ([SrO]/[Al2O3] < 1). By considering the results from high-temperature 27Al NMR and high-temperature neutron diffraction, we demonstrate that the structure of the polymerized melts is controlled by a close-to-random distribution of Al and Si in the tetrahedral sites, while the depolymerized melts show smaller rings with a possible loss of non-bridging oxygens on AlO4 units during cooling for high-silica compositions. A few five-fold coordinated VAl sites are present in all compositions, except per-aluminous ones where high amounts of high-coordinated aluminium are found in glasses and melts with complex temperature dependence.

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Al site distribution in the structurally complex and industrially important ZSM-5 zeolite is determined by studying the spectroscopic response of Al(OSi) units and using a self-consistent combination of up-to-date solid-state NMR correlations (Si-Al and H-Al D-HMQC) and quantum chemistry methods (DFT-D). To unravel the driving forces behind specific Al sitting positions, our approach focuses on ZSM-5 containing its more efficient OSDA, tetrapropylammonium.

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RhL complexes of phosphonate-derivatized 2,2'-bipyridine (bpy) ligands L were immobilized on titanium oxide particles generated in situ. Depending on the structure of the bipy ligand-number of tethers (1 or 2) to which the phosphonate end groups are attached and their location on the 2,2'-bipyridine backbone (4,4'-, 5,5'-, or 6,6'-positions)-the resulting supported catalysts showed comparable chemoselectivity but different kinetics for the hydrogenation of 6-methyl-5-hepten-2-one under hydrogen pressure. Characterization of the six supported catalysts suggested that the intrinsic geometry of each of the phosphonate-derivatized 2,2'-bipyridines leads to supported catalysts with different microstructures and different arrangements of the RhL species at the surface of the solid, which thereby affect their reactivity.

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The intrinsic ionic conductivity of polyethylene oxide (PEO)-based block copolymer electrolytes is often assumed to be identical to the conductivity of the PEO homopolymer. Here, we use high-field Li nuclear magnetic resonance (NMR) relaxation and pulsed-field-gradient (PFG) NMR diffusion measurements to probe lithium ion dynamics over nanosecond and millisecond time scales in PEO and polystyrene (PS)-b-PEO-b-PS electrolytes containing the lithium salt LiTFSI. Variable-temperature longitudinal (T) and transverse (T) Li NMR relaxation rates were acquired at three magnetic field strengths and quantitatively analyzed for the first time at such fields, enabling us to distinguish two characteristic time scales that describe fluctuations of the Li nuclear electric quadrupolar interaction.

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