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Avance 500 ft nmr spectrometer

Manufactured by Bruker
Sourced in Germany

The Avance 500 FT-NMR spectrometer is a high-performance nuclear magnetic resonance (NMR) spectroscopy instrument manufactured by Bruker. It is designed to conduct advanced analytical techniques for the structural elucidation and characterization of chemical compounds. The Avance 500 features a 500 MHz superconducting magnet and employs Fourier transform (FT) technology to acquire and process NMR data.

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4 protocols using avance 500 ft nmr spectrometer

1

Characterizing AEMA-g-WSC Polymer by NMR

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The 1 (link)H-13 (link)C heteronuclear single-quantum correlation (HSQC) spectrum of AEMA-g-WSC was determined in D2O solution using a Bruker Avance-500 FT-NMR Spectrometer (Bruker Biospin, Rheinstetten, Germany).
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2

Spectroscopic Analysis of Natural Compounds

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The optical rotation data were measured in MeOH with a Jasco P-2000 Polarimeter (JASCO Inc., Tokyo, Japan). The infrared spectra were acquired on Shimadzu IR Affinity-1S Fourier Transform Infrared Spectrophotometer. The UV spectra were obtained from LAMBDA 265 UV/Vis Spectrophotometer (PerkinElmer Inc., Waltham, MA, USA). The 1D and 2D-NMR spectra were recorded with a Bruker Avance 500 FT-NMR spectrometer (Bruker Inc., Bremen, Germany). The HR-ESI-MS data were generated at the Mass Spectrometry Laboratory of the Chung Hsing University with a Thermo LTQ Orbitrap XL™ Hybrid Ion Trap-Orbitrap Mass Spectrometer (Thermo Scientific Inc., Waltham, MA, USA). Column chromatography was performed using LiChroCART Si 5 µM gel (Merck, Darmstadt, Germany) and Sephadex LH-20 (GE Healthcare Life Sciences Inc., Marlborough, MA, USA). The TLC (thin-layer chromatography) analysis was carried out using aluminum pre-coated Si plates (Silica Gel 60 F-254; Merck). The spots were visualized using a UV lamp at λ = 254 nm and detected by spraying with 10% H2SO4 alcohol solution and heating at 125 °C. Semi-preparative HPLC was performed using a normal phase column (Luna 5μm Silica 100 Å, 250 × 10 mm; Phenomenex Inc.) on a Precision Instruments IOTA 2 Refractive Index Detector system.
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3

Comprehensive Analytical Techniques for Novel Compounds

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1H and 13C NMR spectra were recorded on a Bruker Avance 500 FT-NMR spectrometer. HR-MS (high-resolution mass spectra) were obtained by a Thermo Scientific Q Exactive mass spectrometer, operated in heated electrospray ionization (HESI) mode and coupled with the Thermo Scientific UltiMate 3000 system. UV-Vis absorption spectra were recorded on a Thermo Scientific Evolution 201 UV-Visible Spectrophotometer. Photo-emission, excitation spectra, and lifetimes were recorded on an Edinburg spectrometer FLS-980 equipped with a Xe light source and an MCP-PMT detector in cooled housing (−20 °C), which covers a range of 200–870 nm. Lifetime data were analyzed with the F980 software package. Emission traces were recorded on an FLS-980 using the multiple scan mode and the shutter was set to always open. UV-portable UV lamps were used as light sources in the photoactivation processes. The optical power densities of these UV light sources were measured by a CEL-NP2000 optical power meter (Beijing CeauLight Technology Co., Ltd.). All measurements were performed at room temperature (RT).
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4

Characterization of Natural Compounds

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General procedures: HR ESI MS were measured in Agilent 6530 Accurate-Mass Q-TOF LC/MS, Santa Clara, USA instrument. 1D-and 2D NMR spectra were recorded on a Bruker Avance 500 FT-NMR spectrometer and the data acquisition was analyzed by MestReNova software. The spectra were run as CD 3 OD solution and were referenced to as solutions for the internal standard ( 1 H 3.33; 13 C  49.0). Preparative column chromatography was conducted with silica gel 60, , RP-18 and Sephadex LH-20. UV light and vanillin-H 2 SO 4 reagent were used for spot visualization.
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