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D8 quest system

Manufactured by Bruker

The D8 QUEST system is a versatile X-ray diffractometer designed for a wide range of applications in materials science and other research fields. The system is capable of performing high-quality X-ray diffraction measurements to characterize the structural properties of various materials.

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3 protocols using d8 quest system

1

Crystallographic Analysis of Samples

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The
crystal samples were assembled on the glass fiber through the oil
drop method. The graphite-monochromatic Cu Kα radiation (λ
= 0.71073 Å) was used for measurements. Crystallographic data
were collected on a Bruker D8 QUEST system. The spherical harmonics
program (multi-scan type) was used for the absorption corrections.
The direct method (SHELXS 97) or intrinsic phasing method (ShelXT)
was used for structural analysis.33 (link) All
nonhydrogen atoms were anisotropically refined through the least square
method on F2. Selected bond lengths (Å) and angles
(°) are listed in Table S1.
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2

Single Crystal Structure Determination

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Single crystal experiments were carried out on a BRUKER D8 QUEST system with graphite-monochromated Mo Kα radiation (λ = 0.71073 Å). The crystal samples were placed in inert oil, mounted on a glass fiber attached to a brass mounting pin, and transferred to the cold dinitrogen gas steam (100 K). Crystal data were collected and integrated using a Bruker Apex II system. The structures were solved by direct method (SHELXS-2014) and refined against F2 using SHELXL-201452 (link).
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3

Structural Characterization of Crystalline Compounds

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The intensity data were recorded on a Bruker D8 QUEST system with Cu-Kα radiation (λ = 1.54178 Å). The crystal structures were solved by means of Direct Methods and refined employing full-matrix least squares on F2 (SHELXTL-97). The diffraction data were treated by the “SQUEEZE” method as implemented in PLATON.17 (link) All non-hydrogen atoms were refined anisotropically, and hydrogen atoms of the organic ligands were generated theoretically onto the specific atoms and refined isotropically with fixed thermal factors. The unidentified solvent molecules and counter ions were not included for all the structures. CCDC 1864223–1864225 contain the supplementary crystallographic data for this paper.
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