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9 protocols using absolute pl quantum yield spectrometer c11347 quantaurus qy

1

Comprehensive Characterization of Molecular Compounds

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1H and 13C NMR spectra were measured on a Bruker AV 500 spectrometer in appropriated deuterated solution at room temperature. UV–vis absorption spectra were measured on a Shimadzu UV-2600 spectrophotometer. Photoluminescence spectra were recorded on a Horiba Fluoromax-4 spectrofluorometer. Solution fluorescence quantum yields were measured using a Hamamatsu absolute PL quantum yield spectrometer C11347 Quantaurus-QY. Zeta potential measurements were conducted on dynamic light scattering (Malvern ZSE, UK). Isothermal titration calorimetry (ITC) was conducted on Malvern MicroCal ITC. Cells were observed under confocal laser-scanning microscope (CLSM) (LSM710, Zeiss, Germany).
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2

Spectroscopic Characterization of DCM-βgal

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DCM-βgal solution was prepared at a concentration of 100 µM in a 2 ml total volume of reaction buffer (pH 7.4, 30% DMSO and 70% PBS). 1 U ml−1 β-gal was added into DCM-βgal solution and the mixture was gently agitated and incubated at 37°C for 15 min. UV-vis absorption spectra for DCM-βgal and reaction product were respectively analyzed on a PerkinElmer Lambda 25 UV/vis Spectrometer. Photoluminescence (PL) spectra were analyzed on a PerkinElmer spectrfluorometer LS55 with a wavelength range of 550–800 nm. Fluorescence quantum yields were detected on a Hamamatsu absolute PL quantum yield spectrometer C11347 Quantaurus-QY.
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3

Absolute Fluorescence Quantum Yield Measurement

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The absolute fluorescence quantum yields were determined by a calibrated integrating sphere of a Hamamatsu absolute PL quantum yield spectrometer C11347 Quantaurus-QY, excitation wavelength: 365 nm. Spectrophotometric-grade solvents were used in the measurements without further purification.
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4

Photophysical Properties of Fluorescent Compounds

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All reagents and solvents were purchased from FUJIFILM Wako Pure Chemical Corporation or Tokyo Chemical Industry Co., Ltd. and used as received unless otherwise stated. Compounds 3 was synthesized according to the literature.35 (link) UV-vis absorption spectra in solution were recorded on a JASCO V-570 spectrophotometer. Diffuse-reflectance spectra were measured by a JASCO V-550 spectrophotometer. Emission spectra were measured by a JASCO FP8500 or Hitachi F7000 spectrophotometer. 1H and 13C NMR spectra were obtained at 25 °C on a JEOL ECS-400 FT-NMR spectrometer with tetramethylsilane as an internal standard of the chemical shift. Infrared (IR) spectra were recorded on a JASCO FT/IR-410 spectrometer. Electrospray ionization time of flight mass (ESI-TOF-MS) spectrometry were carried out with JEOL JMS-T100CS spectrometer using methanol/dichloromethane as a solvent system. CHN elemental analysis was performed at Center for Instrumental Analysis of Kyushu Institute of Technology. Absolute photoluminescence quantum yields were determined by using a Hamamatsu Absolute PL Quantum Yield Spectrometer C11347 Quantaurus-QY (400–1100 nm) which equipped with an integrating sphere.
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5

Steady-State and Delayed Photophysical Analysis

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The steady-state, delayed PL spectra and phosphorescence lifetime were measured on an Edinburgh FLSP 980 fluorescence spectrophotometer equipped with a xenon arc lamp (Xe900) and a microsecond flash-lamp (uF900). Absolute PL quantum yields were measured using a Hamamatsu absolute PL quantum yield spectrometer C11347 Quantaurus_QY. Delayed emission of NA/PCP (Δt = 1 s) was recorded on an Ocean Optics Spectrometer (QE Pro).
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6

Measuring Solid Film Fluorescence QY

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Solid film fluorescence quantum yields were measured, using a Hamamatsu absolute PL quantum yield spectrometer C11347 Quantaurus_QY (Hamamatsu City, Shizuoka Prefecture, Japan) and a matched integrating sphere. Data showed averaged values of three detected readings from the machine.
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7

Detailed Spectroscopic Characterization of Compounds

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All the chemicals and reagents were purchased from a commercial source and used as received without further purification. 1H and 13C NMR spectra were measured on a Bruker AV 500 (500 MHz) spectrometer in CD2Cl2 with tetramethylsilane (TMS, δ = 0). High-resolution mass spectra (HRMS) were recorded on a GCT premier CAB048 mass spectrometer operating in MALDI-TOF mode. Single-crystal X-ray diffraction intensity data were collected on a Bruker–Nonices Smart Apex CCD diffractometer with graphite monochromated MoKα radiation. Processing of the intensity data was carried out using the SAINT and SADABS routines, and the structure and refinement were conducted using the SHELTL suite of X-ray programs (version 6.10). UV–vis absorption spectrum was measured on a Shimadzu UV-2600 spectrophotometer. PL spectra were recorded on a Horiba Fluoromax-4 spectrofluorometer. Solution fluorescence quantum yields were measured using a Hamamatsu absolute PL quantum yield spectrometer C11347 Quantaurus_QY. High-performance liquid chromatography spectra were measured using Waters alliance e2695 separation module.
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8

Spectroscopic Analysis of Sunflower Oil

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The organic solvents used for spectroscopy measurement were spectra grade, and the water was Milli-Q water (Millipore, Burlington, MA, USA). Sunflower oil, stabilized with about 0.02% of d-δ-tocopherol, was obtained from Wako. The UV-Vis absorption spectra were performed on a JASCO V-770 spectrophotometer (JASCO Group, Tokyo, Japan), and the fluorescence spectra and quantum yields were obtained using a Hamamatsu Photonics Quantaurus-QY Absolute PL quantum yield spectrometer C11347 (Hamamatsu Photonics, Yokohama, Japan). Dynamic light scattering (DLS) measurements were performed on a Zetasizer Nano ZS analyzer (Malvern Instruments Ltd., Malvern, UK).
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9

Comprehensive Characterization of Organic Compounds

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All reagents were purchased from commercial sources (Innochem (Beijing, China), TCI (Shanghai, China), Sigma-Aldrich (Shanghai, China), Adamas-beta (Shanghai, China), Aladdin (Shanghai, China)) and used without further purification. All solvents and inorganic salts were purchased from Beijing Reagent, Sinopharm Chemical Reagent Beijing or General-Reagent, and used without further processing. Human cervical carcinoma cells (HeLa cells), human hepatocarcinoma cells (HepG-2 cells), human non-small cell lung cancer cell (A549 cells), and Human Umbilical Vein Endothelial Cells (HU-EVC cells) were purchased from the Center of Cells, Peking Union Medical College.
1H NMR and 13C NMR spectra were obtained with Bruker Avance III 400 and Ascend 600 MHz spectrometers (Karlsruhe, Germany), respectively, using CDCl3 or DMSO-d6 as a solvent, and tetramethylsilane (TMS) was used as an internal standard. Electrospray Ionization Mass Spectrometry (ESI-MS) was conducted using a Thermo Fisher Scientific Q-Exactive spectrometer (Waltham, MA, USA). Absorption spectra were recorded on a Hitachi U-3900 ultraviolet–visible (UV-Vis) spectrophotometer (Tokyo, Japan). Fluorescence spectra were recorded on a Hitachi F-4600 spectrofluorometer (Tokyo, Japan). Absolute fluorescence quantum yields were measured in a Quantaurus-QY absolute PL quantum yield spectrometer C11347 (Hamamatsu, Shizuoka, Japan).
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