xtalab synergy-s dualflex diffractometer equipped with a hypix-6000he hpc area detector (Rigaku Corporation)
Rigaku Corporation is a verified supplier 
90
Structured Review
Rigaku Corporation
xtalab synergy-s dualflex diffractometer equipped with a hypix-6000he hpc area detector
Xtalab Synergy S Dualflex Diffractometer Equipped With A Hypix 6000he Hpc Area Detector, supplied by Rigaku Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/xtalab+synergy+diffractometer+with+a+dualflex+hypix+detector/hypix+6000he+detector/10__1021_slash_acselectrochem__4c00186-89-27-19
Average 90 stars, based on 1 article reviews
Xtalab Synergy S Dualflex Diffractometer Equipped With A Hypix 6000he Hpc Area Detector, supplied by Rigaku Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/xtalab+synergy+diffractometer+with+a+dualflex+hypix+detector/hypix+6000he+detector/10__1021_slash_acselectrochem__4c00186-89-27-19
Average 90 stars, based on 1 article reviews
xtalab synergy-s dualflex diffractometer equipped with a hypix-6000he hpc area detector - by Bioz Stars,
2026-10
90/100 stars
Images
Related Articles
other:Article Title: High-resolution structural study on pyridin-3-yl ebselen and its <i>N</i>-methylated tosylate and iodide derivatives Article Snippet: C79, 43-51 C10—C11—C12—C8 −0.5 (5) C19—C14—S1—O4 158.2 (2) N1—C8—C12—C11 −178.3 (3) C15—C14—S1—O4 −24.3 (3) C9—C8—C12—C11 0.4 (4) C19—C14—S1—O3 36.0 (3) C19—C14—C15—C16 −0.8 (4) C15—C14—S1—O3 −146.4 (2) S1—C14—C15—C16 −178.3 (2) C19—C14—S1—O2 −81.8 (2) C14—C15—C16—C17 0.7 (4) C15—C14—S1—O2 95.7 (2) C15—C16—C17—C18 −0.1 (4) Hydrogen-bond geometry (Å, o) D—H···A D—H H···A D···A D—H···A C6—H6···O2 0.93 2.28 2.925 (4) 126 C9—H9···O1 0.93 2.09 2.734 (4) 125 C10—H10···O3i 0.93 2.37 3.216 (4) 152 C11—H11···O7i 0.93 2.46 3.338 (4) 158 C12—H12···Se1 0.93 2.61 3.085 (3) 112 C13—H13B···O3i 0.96 2.57 3.442 (4) 152 C13—H13C···O4ii 0.96 2.54 3.490 (4) 170 C15—H15···O1ii 0.93 2.63 3.379 (4) 138 O5—H5A···O3 0.82 (1) 1.99 (1) 2.786 (3) 166 (4) O5—H5A···S1 0.82 (1) 3.01 (2) 3.698 (2) 144 (3) O5—H5B···O7 0.82 (1) 1.99 (4) 2.758 (3) 155 (8) O6—H6A···O4 0.82 (1) 2.27 (2) 3.045 (3) 159 (5) O6—H6B···O5 0.82 (1) 1.99 (2) 2.782 (4) 162 (7) O7—H7A···O6iii 0.82 (1) 1.97 (1) 2.783 (4) 176 (5) O7—H7B···O5iv 0.82 (1) 1.97 (1) 2.786 (4) 172 (6) Symmetry codes: (i) x, y−1, z; (ii) −x+2, −y+1, −z+1; (iii) −x+2, −y+2, −z+2; (iv) −x+1, −y+2, −z+2. (2-multipole) Crystal data C12H8N2OSe Mr = 275.16 Monoclinic, P21/n a = 6.1074 (1) Å b = 14.2227 (3) Å c = 12.0621 (2) Å β = 103.588 (2)° V = 1018.43 (3) Å3 Z = 4 F(000) = 544.0 Dx = 1.795 Mg m−3 Mo Kα radiation, λ = 0.71073 Å Cell parameters from 30292 reflections θ = 3.3–56.9° μ = 3.66 mm−1 T = 100 K Plate, colourless 0.48 × 0.15 × 0.05 mm Article Title: Structural phase transition in a charge-transfer compound: tropylium hexafluoridoantimonate(V)–1,4-dimethylnaphthalene (1/1) Article Snippet: Molecular motion in crystals has attracted much attention for the development of stimuli-responsive materials.. The most studied are molecules with few atoms or highly symmetrical molecules.. To develop molecules with new motion characteristics, we synthesized a charge-transfer compound, namely, tropylium hexafluoridoantimonate(V)–1,4-dimethylnaphthalene (1/1), (C7H7)[SbF6] C12H12, and studied its structural phase transition. Article Title: High-resolution structural study on pyridin-3-yl ebselen and its <i>N</i>-methylated tosylate and iodide derivatives Article Snippet: 1-Methyl-3-(3-oxo-2,3-dihydro-1,2-benzoselenazol-2-yl)pyridin-1-ium iodide (2-MeIodide) Crystal data C13H11N2OSe+·I− Mr = 417.10 Triclinic, P1 a = 7.0926 (1) Å b = 8.1329 (1) Å c = 11.8376 (1) Å α = 84.618 (1)° β = 82.243 (1)° γ = 77.756 (1)° V = 659.70 (1) Å3 Z = 2 F(000) = 396 Dx = 2.100 Mg m−3 Mo Kα radiation, λ = 0.71073 Å Cell parameters from 41098 reflections θ = 3.0–51.1° μ = 5.18 mm−1 T = 100 K Needle, pale yellow 0.46 × 0.06 × 0.06 mm Article Title: High-resolution structural study on pyridin-3-yl ebselen and its <i>N</i>-methylated tosylate and iodide derivatives Article Snippet: C79, 43-51 Se1—C1—C2—C7 1.17 (9) C9—C8—C12—C11 −0.79 (12) C1—C2—C3—C4 −0.60 (12) O1—C7—N1—C8 −2.54 (13) C7—C2—C3—C4 −179.28 (8) C2—C7—N1—C8 178.26 (7) C2—C3—C4—C5 −0.34 (13) O1—C7—N1—Se1 −179.84 (7) C3—C4—C5—C6 0.70 (14) C2—C7—N1—Se1 0.97 (8) C4—C5—C6—C1 −0.11 (13) C9—C8—N1—C7 −1.69 (12) C2—C1—C6—C5 −0.83 (12) C12—C8—N1—C7 178.33 (8) Se1—C1—C6—C5 177.74 (6) C9—C8—N1—Se1 175.46 (6) C1—C2—C7—O1 179.39 (8) C12—C8—N1—Se1 −4.52 (10) C3—C2—C7—O1 −1.90 (13) C11—C10—N2—C9 −1.72 (13) C1—C2—C7—N1 −1.40 (10) C11—C10—N2—C13 178.35 (8) C3—C2—C7—N1 177.32 (7) C8—C9—N2—C10 1.26 (12) N1—C8—C9—N2 −179.95 (7) C8—C9—N2—C13 −178.82 (8) C12—C8—C9—N2 0.03 (12) 1-Methyl-3-(3-oxo-2,3-dihydro-1,2-benzoselenazol-2-yl)pyridin-1-ium toluenesulfonate trihydrate (2- Metosylate) Crystal data C13H11N2OSe+·C7H7O3S−·3H2O Mr = 515.43 Triclinic, P1 a = 6.9412 (3) Å b = 12.1279 (4) Å c = 13.5994 (3) Å α = 70.426 (3)° β = 83.774 (3)° γ = 83.585 (3)° V = 1068.83 (7) Å3 Z = 2 F(000) = 528 Dx = 1.602 Mg m−3 Cu Kα radiation, λ = 1.54184 Å Cell parameters from 5181 reflections θ = 3.5–75.2° μ = 3.70 mm−1 T = 100 K Rod, colourless 0.21 × 0.03 × 0.03 mm |