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Avance spectrometer

Manufactured by Brucker

The Avance spectrometer is a versatile nuclear magnetic resonance (NMR) instrument designed for high-resolution structural analysis. It offers advanced capabilities for various applications in chemistry, materials science, and life sciences. The core function of the Avance spectrometer is to provide precise and reliable measurements of molecular structures and dynamics through the detection and analysis of nuclear magnetic resonances.

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2 protocols using avance spectrometer

1

Spectroscopic Characterization of Quinolinium Compounds

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All reagents were purchased from Sigma Aldrich or Alfa Aesar and purity was checked by H1 NMR (300MHz). Solvents were ACS grade. 4-chloro-1-methylquinolinium iodide (Q) was obtained from Dr. N. Shank. UV-Vis spectra were recorded on a CARY-300 Bio UV-visible spectrophotometer, Fluorescence spectra were recorded on a CARY Eclipse fluorimeter, 1H and 13C NMR spectra were run on a Brucker Avance spectrometer at 500 and 75.47 MHz, respectively. Chemical shifts are reported as δ values (ppm) with reference to the residual solvent peaks. ESI-MS spectra were taken in a Finnigan ESI/APCI Ion Trap Mass Spectrometer on positive ion mode.
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2

Characterization of Insoluble Compounds

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Polyvinylidene fluoride (PVDF) (MW ~530,000) and Dimethylformamide (DMF) were purchased from Merck; Vulcan XC72 Carbon Black (CB) was used, and 0.05 mm thick conductive graphite paper (RERAS, purchased from China and used as electrode substrate) was used to prepare cathode materials.
Melting points were measured on a Kruess KSP 11 Melting Point Analyzer. 1H NMR spectra were recorded on a Brucker Avance spectrometer at 300 or 500, respectively, in DMSO-d6 or CDCl3 solutions. Chemical shifts were expressed in parts per million (δ, ppm) relative to solvent signal (DMSO-d6: 2.50 ppm CDCl3: 7.26 ppm for 1H NMR) [46 (link)]. Compounds 3ag are too insoluble to record a qualitative 13C NMR spectrum. Elemental CHN analysis was carried out on a Euro Vector EA 3000 analyzer. FTIR spectra were recorded on a Perkin-Elmer Spectrum 100 FTIR spectrometer. The UV–Vis absorption spectra were acquired with a Perkin-Elmer 35 UV/Vis spectrometer using 1 cm length quartz cuvettes with a concentration of compound c = 2.5 × 10−5 M. Low-resolution mass spectra were acquired on a Waters EMD 1000MS mass detector (ESI + mode, voltage 30 V) with an Xterra MS C18 5 μm 2.1 × 100 mm column and gradient eluent mode using 0.1% HCOOH in deionized water and MeCN or MeOH.
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