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Single quadrupole detector

Manufactured by Waters Corporation
Sourced in Italy

The Single Quadrupole Detector is a mass spectrometry instrument that uses a quadrupole mass analyzer to separate and detect ions based on their mass-to-charge ratio. It provides accurate and reliable detection capabilities for analytical applications.

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4 protocols using single quadrupole detector

1

Mass Spectrometry Analysis of CAGE-oct

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Mass spectra were
obtained by gently warming CAGE-oct until it melted and then directly
injecting it into a Waters single quadrupole detector at 4.2 kV capillary
voltage using electrospray ionization (both positive and negative
modes were obtained).
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2

Characterization of Novel Organic Compounds

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All reactants used were purchased from Sigma Aldrich (Milan, Italy). The 1H NMR and 13C NMR spectra were recorded on a Bruker Anova spectrometer (Billerica, MA, USA) at 400 MHz. The FT-IR measurements were recorded on a Nicolet 5PC FTIR (Rodano, MI, Italy) analyzing products directly on the ATR accessory in the 4000–400 cm−1 range. The relative intensity of reported FT-IR signals is defined as s = strong, m = medium, and w = weak. ESI-MS analysis was performed using a Waters Acquity Ultraperformance ESI-MS spectrometer with Single Quadrupole Detector (Sesto San Giovanni, MI, Italy). Elemental analyses were performed on a CHNS Thermo Fischer (Rodano, MI, Italy). UV–vis spectra were recorded on a Thermo Scientific Evolution 260 Bio instrument (Rodano, MI, Italy). HR-MS were recorded on a Thermo Scientific Orbitrap LTQ-XL (Rodano, MI, Italy). The light intensity measurement was carried out with an Optical Power Meter (Newport 840-C, Monza, Italy) equipped with a Mod. 818-UV detector (active area 1 cm2). The determination was at 420 nm.
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3

Purification and Characterization of Organic Compounds

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Reactants and reagents were purchased from
MilliporeSigma, Oakwood
Chemicals, or Fisher Scientific and used without further purification.
NMR spectra were measured on either a Varian (1H 500 MHz, 13C 125 MHz), Bruker (1H 600 MHz, 13C
150 MHz), or Jeol (1H 400 MHz, 13C 100 MHz)
spectrometer. Spectra were calibrated with the solvent’s residual
signals (CDCl3, 7.26 ppm for 1H and 77.1 ppm
for 13C; CD3OD, 3.31 ppm for 1H and
49.0 ppm for 13C). NMR signals were assigned using standard
two-dimensional NMR experiments (HSQC, COSY, HMBC). Purification occurred
on CombiFlash RF and Biotage system with Silicycle silica columns.
Mass-spectrometry data was recorded and analyzed using a single quadrupole
detector 2 from Waters, and high-resolution mass-spectrometry data
were recorded and analyzed on a Waters Ultima using the LC/MS Calibrant
Mix from Agilent as the internal standard. TLC was eluted using hexane/ethyl
acetate or MeOH/CH2Cl2 as solvents and visualized
with charring after dipping in a 5% H2SO4 solution
in absolute ethanol.
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4

Synthesis and Characterization of Thiosemicarbazone Metal Complexes

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All common laboratory chemicals were purchased from commercial sources and used without further purification: 8-hydroxy-2-quinolinecarboxaldehyde, ≥96% (Sigma-Aldrich, St. Louis, MO, USA); thiosemicarbazide, ≥99.9% (Fluka, Buchs, Switzerland); 4-methyl-3-thiosemicarbazide, 97% (Fluorochem, Hadfield, UK); 4,4-dimethyl-3-thiosemicarbazide, ≥98.0% (TCI, Tokyo, Japan); 4-phenyl-3-thiosemicarbazide, 99% (Sigma-Aldrich); gallium nitrate hydrate, 99.9% (Sigma-Aldrich); indium nitrate hydrate, 99.9% (Sigma-Aldrich). NMR was recorded on a Bruker Anova spectrometer at 400 MHz (Billerica, MA, USA), with chemical shift reported in δ units (ppm). NMR spectra were referenced relative to residual NMR solvent peaks. The solvent used in the spectra’s acquisitions is DMSO-d6. The FT-IR measurements were recorded on Nicolet 5PC FT-IR (Rodano, MI, Italy) in the 4000–400 cm−1 range, equipped with the ATR accessory. Elemental analyses were performed using the Thermofisher Scientific Flashsmart CHNS Elemental Analyzer (Rodano, MI, Italy). ESI-MS were recorded on a Waters Acquity Ultraperformance ESI-MS spectrometer with a Single Quadrupole Detector (Sesto San Giovanni, MI, Italy). UV/Vis spectra were collected using a Thermofisher Scientific Evolution 260 Bio Spectrophotometer (Rodano, MI, Italy), using quartz cuvettes of 1 cm path length.
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