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Smart apex 2 ultra

Manufactured by Bruker
Sourced in Germany, United States

The SMART APEX II ULTRA is a versatile lab equipment product designed for various scientific applications. It provides core functionalities to support research and analysis activities. The detailed specifications and intended use of this product are not available in an unbiased and factual manner within the constraints of this request.

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3 protocols using smart apex 2 ultra

1

X-ray Diffraction Analysis of Complex Two

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X-ray diffraction data for Complex Two were collected at 173 K on a Bruker SMART APEX II ULTRA (Bruker AXS GmbH, Karlsruhe, Germany) diffractometer. Using the software package of APEX2 [16 ], data collection/reduction and semi-empirical absorption correction (SADABS) [17 ] were conducted. All of the calculations for the structure determination were carried out using the APEX2 package with the SHELXS-2014 (Version 6.22) [18 ] and SHELXL-2014 (Version 6.22) [19 ] programs. The non-hydrogen atoms of Compound Two were refined anisotropically. All hydrogen atoms were added in calculated positions and refined isotropically in a riding manner. The crystal structure figure was made using the Diamond program (Version 3.2) [20 ]. A summary of the refinement details and resulting factors for the crystal structures of Two are given in Table S1. CCDC number Two is as follows: CCDC-2259034.
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2

Characterization of Organic Compounds

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Specific rotation was measured with a Horiba SEPA-300 digital polarimeter (Kyoto, Japan, l = 5 cm) and IR spectra were collected on a Shimadzu FTIR-8100 spectrometer (Kyoto, Japan). For X-ray, a Bruker SMART-APEX II ULTRA (Billerica, MA, USA) was used. ESI-MS and HR-ESI-MS were carried out using a Thermo Fisher Scientific LTQ Orbitrap XL mass spectrometer (Waltham, MA, USA), and 1H (600 MHz) and 13C (150 MHz) NMR spectra were recorded on a JEOL JNM-ECA 600 spectrometer (Tokyo, Japan) with tetramethylsilane as an internal standard. Purification was run on a Shimadzu HPLC system equipped with a RID-10A refractive index detector and compound separation was performed on YMC-Pack ODS-A (Tokyo, Japan, 250 × 4.6 mm i.d.) and (250 × 20 mm i.d.) columns for analytical and preparative separation, respectively. Chromatography separation included normal-phase silica BW-200 (Fuji Silysia Chemical, Ltd., Kasugai, Japan, 150–350 mesh) and ODS reverse phase Chromatorex DM1020T (Fuji Silysia Chemical, Ltd., 100–200 mesh) columns as well as silica gel 60F254 (Merck, Darmstadt, Germany, 0.25 mm) and RP-18 WF254S (Merck, 0.25 mm) TLC plates with spots developed with heating of H2SO4-MeOH (1:9) sprayed plates.
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3

Detailed Characterization of Organic Compounds

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General, Measurement, and Materials. 1 H, 19 F, and 13 C{ 1 H} NMR spectra were recorded using Bruker AVANCE-400 NMR spectrometer and AVANCE-600 NMR spectrometer. Elemental analyses were carried out using a Perkin-Elmer 2400 CHN elemental analyzer and Yanaco CHN coder MT-6 or MT-5. Anhydrous toluene and THF were purchased from Kanto Chemical and used as dry solvents. Crystal Structure Determination Intensity data were collected on a Bruker SMART APEX II ULTRA with Mo Kα radiation. UV-vis absorption spectra in solution states were recorded on a Hitachi U-3900H spectrophotometer. Excitation and emission spectra in solution states were recorded on a Hitachi F-2700 fluorescence spectrophotometer. The PL quantum yields of the emission were measured using a Hamamatsu Photonics C9920-02 absolute PL quantum yield spectrometer. UV-vis absorption spectra and photoluminescence spectra for the vacuum-deposited films were recorded on a Hitachi U-3010 and JASCO FP-6500 spectrophotometer, respectively. The HOMO energy level was estimated by photoelectron yield spectroscopy (PYS) using a Riken Keiki AC-3 spectrometer. Out-of-plane and in-plane XRD measurements were performed using MiniFlex600 and SmartLab diffractometer (Rigaku Corporation, Cu Kα radiation), respectively. The incident angle ω was set to 0.3° for in-plane measurement.
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