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Uv 2600 spectrophotometer

Manufactured by Edinburgh Instruments

The UV-2600 spectrophotometer is a high-performance analytical instrument designed for accurate and precise UV-vis spectroscopic measurements. It features a wavelength range of 185 to 900 nm and can be used to quantify the absorption, transmission, and reflectance of a wide range of samples.

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2 protocols using uv 2600 spectrophotometer

1

Comprehensive Optoelectronic Characterization

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The current–luminance–voltage characteristics were measured by using a computer-controlled source meter (Keithley 2400) equipped with a light intensity meter LS-110 under ambient atmosphere without encapsulation. The EL spectra were measured by a Spectrascan PR650 spectrophotometer. The EQEs were calculated from the luminance, current density, and EL spectrum, assuming a Lambertian distribution. The photophysical properties, including UV/vis absorption, photoluminescence (PL), and excitation spectra were measured by a Shimadzu UV-2600 spectrophotometer, and an Edinburgh Instruments FLS 980 spectro-fluorometer. Additionally, the PL transient decay curves of the films were performed on Quantaurus-Tau fluorescence lifetime measurement system (C11367-03, Hamamatsu Photonics Co.). All the results of devices were measured in the forward-viewing direction and all the measurements were carried out under an ambient atmosphere without encapsulation.
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2

Host-Guest Binding Studies by 1H-NMR Titration

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Synthetic procedures are described below. All other chemicals were purchased from commercial suppliers and used without further purication. Dry solvents were puried using an MBraun SPS-800. NMR spectra were recorded on a Bruker DRX 500, AMX 400 or DRX 300, ESI-MS data were obtained from an HR-ToF Bruker Daltonik GmbH Impact II. UV-vis spectra were recorded on a Shimadzu UV-2600 spectrophotometer and uorescence measurements were performed on an Edinburgh Instruments Spectrouorometer FS5. Synthesis PDI-Py 2 ligand 50 and supramolecular heteroleptic square 2, 44 were prepared according to literature procedures.
Host-guest binding studies 1 H-NMR titrations. To a stock solution of 2 (600 mL, 0.42 mM) or 1 (600 mL, 0.83 mM) in DMF-d 7 was added a stock solution of each of the respective substrates (100 mM, 3 mL per equivalent). A total of 60 eq. was added in 10 steps and the change was followed by 1 H-NMR spectroscopy. Chemical shis of PDI-hydrogens d and e, as well as the signals of the respective substrate were followed. Fitting the binding curve was done using the tool: http://supramolecular.org/ with the NMR 1 : 1 model and the Nelder-Mead method.
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