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8453 diode array uv vis spectrometer

Manufactured by Agilent Technologies

The 8453 diode array UV-Vis spectrometer is a laboratory instrument designed to measure the absorption of ultraviolet and visible light by samples. It utilizes a diode array detector to simultaneously capture the full spectrum of the sample, providing rapid and accurate measurements.

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3 protocols using 8453 diode array uv vis spectrometer

1

Spectroscopic Characterization of Biomolecules

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1H and 13C NMR spectra were obtained using a Bruker 300 instrument, and chemical shifts are reported in ppm on the δ scale relative to TMS, TSP, or solvent. Electrospray iodization (ESI) high resolution mass spectra (HRMS) were obtained on JEOL double sector JMS-AX505HA mass spectrometer (University of Notre Dame, IN). Analytical SE-HPLC was performed on an Agilent 1200 (Agilent, Santa Clara, CA) equipped with a diode array detector (λ = 254 and 280 nm), with the themostat set at 35°C. All absorbance measurements for the protein concentration and ligand protein ratio were obtained on an Agilent 8453 diode array UV-Vis spectrometer equipped with an 8-cell transport system (designed for 1 cm cells).
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2

FTIR and UV-Vis Spectroscopy of Mq3 Complexes

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The FTIR spectra of solid samples of the Mq3 complexes studied and of the free ligands were recorded at T = 298.1 K using a FTIR Spectrum BX equipped with an ATR Pike Tech-nologies GladiaATR™ sample holder. The UV-Vis spectra of all Mq3 complexes and of the free ligands in CH2Cl2, at T = 298.1 K, were recorded with an Agilent 8453 diode array UV-Vis spectrometer, using a quartz cell with a path length of 10.00 mm. Temperature control was achieved by means of a Julabo F25 HP refrigerated circulator.
The concentration of the samples was in the order of 10 -5 M.
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3

Spectroscopic and Photochemical Analysis

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The acetonitrile solvent was of HPLC grade and purchased from Merck. Mg(ClO 4 ) 2 was from Sigma Aldrich, and used without further purification.
The absorption spectra were recorded on an Agilent 8453 diode array UV-Vis spectrometer. The fluorescence spectra and the fluorescence decay curves were recorded with an FLS920 Edinburgh Instruments combined steady state and fluorescence lifetime spectrometer. Two pulsed diode lasersan EPL-375 (emitting at 378 nm, pulse width ∼90 ps) and an EPL-470 (emitting at 473 nm, pulse width ∼100 ps) were used as light sources when the decay curves were recorded. NMR spectra were recorded on a Bruker Avance DRX-500 spectrometer. The mass spectra were obtained using a Waters Q-TOF Premier mass spectrometer (Manchester, UK) in positive electrospray mode.
In the photolysis experiments, the samples were irradiated by using an Osram XBO OFR 150 W xenon arc lamp, placing a BG3/4g band-pass filter in front of the lamp, with a transmission range of ∼300-420 nm. The photon flux incident on the samples was determined by chemical actinometry, via measuring the yield of photoconversion of o-nitrobenzaldehyde into o-nitrosobenzoic acid. 32, 33 The optical spectroscopic and photochemical experiments were carried out at 25 °C, in aerated solutions.
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