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Ft nmr avance 3 500 mhz

Manufactured by Bruker

The FT-NMR Avance III 500 MHz is a nuclear magnetic resonance (NMR) spectrometer manufactured by Bruker. It operates at a frequency of 500 MHz and utilizes Fourier transform (FT) technology for signal processing. The core function of this instrument is to analyze the molecular structure and properties of chemical samples through the detection and interpretation of nuclear magnetic resonances.

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3 protocols using ft nmr avance 3 500 mhz

1

Comprehensive Characterization of a Compound

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Elemental analysis of carbon and hydrogen, were carried out in a Vario Micro Cube. Infrared spectra were recorded using KBr pressed pellets with a Perkin-Elmer Spectrum GX FTIR spectrometer (MAGNA FTIR 750, Nicolet) in the region of 4000–400 cm−1 region. Paramagnetic 1H NMR spectra were recorded in a Bruker FT-NMR Avance III 500 MHz with deuterated solvents as internal standards. Matrix-assisted laser desorption/ionization-time of flight (MALDI–TOF) mass spectrometric data were acquired on a MALDI–TOF Synapt G2-S HDMS without additional matrix compound other than the sample itself. The absorption spectra were acquired at room temperature for diluted (2.0 × 10−6 M) DMSO (spectrophotometric grade) solutions on a Cary 500 Scan UV–vis–NIR spectrophotometer using a 1 cm quartz cell. Emission spectra were recorded at room temperature for diluted (2.0 × 10−6 M) DMSO (spectrophotometric grade) solutions on a Cary Eclipse Fluorescence spectrophotometer using a 1 cm quartz cell.
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2

NMR Spectroscopy in Acetonitrile Solvent

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NMR spectra were recorded on a Bruker FT–NMR Avance III 500 MHz instrument at 500.32 (1H) MHz in CD3CN at ambient temperature. Chemical shifts were referenced relative to the solvent signal for 1H nucleus.
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3

Spectroscopic Characterization of Organic Compounds

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The chemicals and instruments Reagents were purchased from Aldrich unless specified otherwise. All solvents were purified and degassed prior to use. NMR spectra were recorded on a Bruker FT-NMR Avance III 500 MHz instrument at 500.32 (1H). Chemical shifts were referenced relative to the solvent signal for 1H. ESI mass spectra were recorded on an LC/MSn ion trap mass spectrometer amaZon SL (Bruker, Bremen, Germany) with MeOH as a solvent. Elemental analysis was performed at Moscow State University with MicroCube Elementar analyzer.
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