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6520 accurate mass q tof spectrometer

Manufactured by Agilent Technologies

The 6520 Accurate-Mass Q-TOF spectrometer is a high-performance mass spectrometer designed for accurate mass measurements. It utilizes quadrupole time-of-flight (Q-TOF) technology to provide precise mass determination and high-resolution analysis of complex samples.

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4 protocols using 6520 accurate mass q tof spectrometer

1

Comprehensive Analytical Characterization

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Elemental analyses were performed by the Campbell Microanalytical Laboratory, Chemistry Department, University of Otago, New Zealand. High resolution mass spectra (HR-MS) were performed on an Agilent 6520 Accurate-Mass Q-TOF spectrometer. Thermogravimetric analyses were performed on a Mettler Toledo thermal analyzer using a ramp rate of 7 °C min–1 up to a maximum temperature of 700 °C. Ultraviolet-visible (UV-Vis) absorption spectra were recorded on an Agilent Cary 60 UV-Vis spectrophotometer in the range 220–1000 nm. Near infra-red (NIR) absorption spectra were recorded on a PerkinElmer Lambda 1050 UV/Vis/NIR spectrophotometer in the range 800–1330 nm. Electronic absorption spectra are discussed in the ESI (Fig. S13, Table S4). Infrared spectra (KBr disk) were recorded on a Bruker Tensor 27 FTIR spectrometer. Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) was performed on a PerkinElmer Optima 4300 DV Optical Emission Spectrometer. Wavelengths chosen for analysis were 228.616 nm for Co and 206.200 nm for Zn, with five replicate measurements performed at each wavelength. The sample (3.0 mg) was digested in 1 mL reverse aqua regia and diluted with water prior to analysis.
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2

Spectroscopic Characterization of Compounds

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Optical rotations ([α]D), UV spectra, ECD spectra and NMR spectra were acquired as previously described [19 (link)]. Spectra of 1H and 13C were referenced to the residual deuterated solvent peaks at δH 2.50 and δC 39.5 (DMSO-d6), and at δH 7.26 and δC 77.2 (CDCl3). Heteronuclear multiple bond correlation (HMBC) experiments were optimized for nJCH = 8.3 Hz. HRESIMS data were acquired on an Agilent 6520 Accurate Mass Q-TOF spectrometer. High performance liquid chromatography (HPLC) purifications were performed using a PerkinElmer Series 200 HPLC pump and autosampler, with a Flexar photodiode array detector and the associated Chromera version 3.4.1 software; with delivery module, detector, software and extraction and chromatography solvents and as described previously [19 (link)].
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3

Characterization of Xylose Dehydrogenase

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Xylose dehydrogenase
from C. crescentus NA 1000 (XylB) was
produced in our
lab as previously described.26 (link) Alcohol
dehydrogenase from C. kluyveri was
purchased from Sigma-Aldrich. All other chemicals were purchased from
commercial sources as reagent grade. IR spectra were obtained in FT-IR
Spectrum One. The frequency of absorption maximums (ν) is expressed
in cm–1 and the samples were analyzed in a KBr tablet.
UV spectra were acquired on Molecular Devices Spectramax PLUS 384.
High-resolution mass spectra (HRMS) were recorded on an Agilent 6520
Accurate Mass Q-TOF spectrometer with an ESI source. 1H
and 13C NMR spectra, using D2O as the solvent,
were recorded on a Varian System 500 spectrometer equipped with a
5 mm HCN cold probe with field z-gradient, operating at 500.13 and
125.76 MHz for 1H and 13C, respectively. The
sample temperature was maintained constant at 298 K.
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4

Elemental and Spectroscopic Characterization

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Elemental analyses were performed by the Campbell Microanalytical Laboratory, Chemistry Department, University of Otago, New Zealand. High resolution mass spectra (HR-MS) were performed on an Agilent 6520 Accurate-Mass Q-TOF spectrometer on acetonitrile solutions.
Variable temperature ultraviolet-visible (UV-Vis) absorption spectra were recorded on an Agilent Cary 60 UV-Vis spectrophotometer in the range 220-1000 nm. Infrared spectra (KBr disk) were recorded on a Bruker Tensor 27 FTIR spectrometer. Band intensities are described as strong (s), medium (m), weak (w) or shoulder (sh).
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