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xtalab synergy r single source high flux rotating anode x ray diffractometer (Rigaku Corporation)

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Rigaku Corporation xtalab synergy r single source high flux rotating anode x ray diffractometer
Xtalab Synergy R Single Source High Flux Rotating Anode X Ray Diffractometer, supplied by Rigaku Corporation, used in various techniques. Bioz Stars score: 98/100, based on 606 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/x+ray+diffractometer/XtaLAB+Synergy-R/pmc13618343-57-6-5
Average 98 stars, based on 606 article reviews

xtalab synergy r single source high flux rotating anode x ray diffractometer - by Bioz Stars, 2026-10

98/100 stars

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Article Title: Development and comparative investigation of structural and functional properties of Ni-based metal–organic frameworks designed for photocatalytic hydrogen production
Article Snippet: Single-crystal data was measured with Rigaku XtaLAB Synergy-R single source high flux rotating anode X-ray diffractometer equipped with HyPix-Arc 100° detector and multilayer optics producing monochromatized Cu Kα (1.54187 Å) radiation.

Article Title: Versatile and efficient manganese catalysts with a secondary amine-based PN-ligand for ketone and aldehyde hydrogenation.
Article Snippet: 1 Supplementary Information

Article Title: Skeletal transformation to chiral nanocarbon molecules.
Article Snippet: X-ray data were obtained using a Rigaku XtaLAB Synergy-R/NLN diffractometer with a MicroMax007HFMR X-ray generator and a HyPix-6000HE detector.

X-ray Diffraction:

Article Title: Molecular Engineering of Interlayer Spacings in 2D Dion-Jacobson Perovskites for High-Fidelity Neuromorphic Computing.
Article Snippet: The development of memristive devices is important for energy-efficient neuromorphic computing.. While two-dimensional (2D) organic−inorganic hybrid perovskites offer structural tunability and improved stability, the correlation between their molecular-level interlayer architecture and resistive switching (RS) kinetics remains to be fully elucidated.. Herein, we modulate the inorganic layer spacing in Dion− Jacobson (DJ) phase 2D perovskites, BDAPbI4, HDAPbI4, and ODAPbI4, by tailoring the alkyl chain length of diammonium ligands.

Article Title: Integrated computational and automated flow synthesis platform for the rapid discovery of N-benzylpiperidine acetylcholinesterase inhibitors.
Article Snippet: .. Single-crystal X-ray diffraction was performed at 150.00 (2) K on a Rigaku XtaLAB Synergy R diffractometer (non-chiral compounds) or a Bruker D8 Venture diffractometer with Cu Kα radiation (chiral compounds). ..

Article Title: Orchestrating Anion-π + Interactions to Accelerate Metal-Free Room-Temperature Phosphorescence.
Article Snippet: .. Pyridinium salts o-pyI, 1–4, 1X (X = Br, OTf, and BARF) and −5 were characterized by single-crystal X-ray diffraction (SCXRD, XtaLAB Synergy-R, Rigaku), while micropowders of m-pyI and ppyI were analyzed using continuous rotation three-dimensional electron diffraction (3DED, XtaLAB Synergy-ED, Rigaku) (see Figures 3 and 4; Figures S12–S18; Tables S3–S8) [45]. ..

Article Title: Distortion-engineered C 1 -symmetric inorganic molecular cages enable tunable chiroptical nonlinear optics with broad infrared transparency
Article Snippet: .. The crystal structures of the title compounds were determined by single-crystal X-ray diffraction on the Rigaku Oxford X-ray diffractometer XtaLAB Synergy-R fitted with Mo- Kα radiation ( λ = 0.71073 Å), the Rigaku Mercury CCD diffractometer equipped with graphite-monochromatic Ga- Kα radiation ( λ = 1.3405 Å), and the Rigaku Oxford X-ray diffractometer XtaLAB SynergyCustom fitted with Cu- Kα radiation ( λ = 1.54178 Å). ..

Article Title: Drimane-Pyrone-Type Meroterpenoids and Co-Isolated Compounds from the Deep-Sea Fungus Penicillium rubens MABC05 and Their Anti-Ferroptotic and Cytotoxic Activities
Article Snippet: Semi-preparative high-performance liquid chromatography (HPLC) was undertaken on a Shimadzu LC-6AD pump (Shimadzu Co., Kyoto, Japan) equipped with a UV detector, employing a YMC-Pack ODS-A HPLC (YMC Co., Ltd., Kyoto, Japan) column (250 mm × 10 mm, S -5 μm, 12 nm). .. Single-crystal X-ray diffraction data were collected on two diffractometers: Cu K α data were acquired on a Rigaku XtaLAB Synergy-R diffractometer (Rigaku Corporation, Tokyo, Japan; Cu K α , λ = 1.54184 Å, 1.2 kW) and reduced using CrysAlisPro (version 1.171.44.91a); Mo Kα data were collected on a Bruker D8 VENTURE diffractometer (Bruker AXS Inc., Madison, WI, USA; Mo K α , λ = 0.71073 Å) and reduced using SAINT (version 8.40B). ..

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$(a) X-ray diffraction (XRD) patterns and (b) Fourier-transform infrared (FT-IR) spectra of whole quinoa flour samples subjected to different dry-heat treatment (DHT) temperatures. Characteristic diffraction peaks at 2θ ≈ 15°, 17°, 18°, and 23° indicate a typical A-type crystalline structure and the major FT-IR absorption regions (amide I band at 1700–1600 cm −1 and carbohydrate backbone at 1060–960 cm −1 ). Control, untreated quinoa flour; 110, 130, and 150 denote quinoa flour treated at 110 °C, 130 °C, and 150 °C for 1 h, respectively.$

Journal: Food Chemistry: X

Article Title: From raw material to functional food: Effect of dry-heat treatment on whole quinoa flour structure and dough rheology, with in vivo hypoglycemic validation at the optimal temperature

doi: 10.1016/j.fochx.2026.104360

Figure Lengend Snippet: (a) X-ray diffraction (XRD) patterns and (b) Fourier-transform infrared (FT-IR) spectra of whole quinoa flour samples subjected to different dry-heat treatment (DHT) temperatures. Characteristic diffraction peaks at 2θ ≈ 15°, 17°, 18°, and 23° indicate a typical A-type crystalline structure and the major FT-IR absorption regions (amide I band at 1700–1600 cm −1 and carbohydrate backbone at 1060–960 cm −1 ). Control, untreated quinoa flour; 110, 130, and 150 denote quinoa flour treated at 110 °C, 130 °C, and 150 °C for 1 h, respectively.

Article Snippet: X-ray diffraction patterns were obtained using a Smartlab SE X-ray diffractometer (Rigaku, Japan) operated in step-scan mode.

Techniques: Fourier Transform Infrared Spectroscopy, Control

$Structural characterization of tea polysaccharides from four dark teas. (a) Molecular weight distribution determined by gel permeation chromatography (GPC); (b) Monosaccharide composition analysed by PMP-HPLC; (c) UV–visible absorption spectra; (d) Zeta potential; (e) Thermogravimetric analysis (TGA); (f) Derivative thermogravimetry (DTG); (g) Fourier transform infrared (FT-IR) spectra; (h) X-ray diffraction (XRD) patterns; (i) Scanning electron microscopy (SEM) images at 500× and 5000× magnifications. LTPS, LFTPS, HTPS, and HFTPS represent polysaccharides extracted from raw dark tea (Maocha), flowered dark tea, pile-fermented dark tea, and pile-fermented and flowered dark tea, respectively.$

Journal: Food Chemistry: X

Article Title: Pile-fermentation and golden-flower fermentation reshape tea polysaccharides in Tibetan dark tea: structural characteristics and lipid-modulating effects in Caenorhabditis elegans

doi: 10.1016/j.fochx.2026.104390

Figure Lengend Snippet: Structural characterization of tea polysaccharides from four dark teas. (a) Molecular weight distribution determined by gel permeation chromatography (GPC); (b) Monosaccharide composition analysed by PMP-HPLC; (c) UV–visible absorption spectra; (d) Zeta potential; (e) Thermogravimetric analysis (TGA); (f) Derivative thermogravimetry (DTG); (g) Fourier transform infrared (FT-IR) spectra; (h) X-ray diffraction (XRD) patterns; (i) Scanning electron microscopy (SEM) images at 500× and 5000× magnifications. LTPS, LFTPS, HTPS, and HFTPS represent polysaccharides extracted from raw dark tea (Maocha), flowered dark tea, pile-fermented dark tea, and pile-fermented and flowered dark tea, respectively.

Article Snippet: Powder samples were evenly spread on the sample holder and analysed using an X-ray diffractometer (Rigaku Ultima IV) operated at 40 kV and 40 mA.

Techniques: Molecular Weight, GPC Assay, Zeta Potential Analyzer, Fourier Transform Infrared Spectroscopy, Electron Microscopy