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Advance 3 600

Manufactured by Bruker
Sourced in Germany

The Advance III 600 is a high-performance nuclear magnetic resonance (NMR) spectrometer manufactured by Bruker. It is designed to provide researchers with advanced analytical capabilities for a wide range of applications, including chemical analysis, materials science, and life sciences. The Advance III 600 features a 14.1 Tesla superconducting magnet and can operate at a proton frequency of 600 MHz, enabling high-resolution NMR measurements. The instrument is equipped with a robust and flexible design to accommodate various sample types and experimental configurations.

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4 protocols using advance 3 600

1

Comprehensive Analytical Characterization

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The 300 MHz 1H and the 75 MHz 13C-{1H} NMR spectra were measured on a Bruker AVIII 300 and the 600 MHz 1H NMR spectra were performed using a Bruker Advance III 600. The 500 MHz 1H NMR spectra were obtained using a Bruker AV DRX 500. MALDI–TOF spectra were performed on a Bruker Ultraflex TOF mass spectrometer, the molecular masses being recorded in linear mode. Dithranol was used as a matrix and sodium trifluoroacetate (NaTFA) as ionization reagent. The samples were dissolved in DMF. DSC measurements were performed using a Mettler Toledo DSC 822. The GC–MS analyses were carried out on Thermo Finnigan Trace DSQ GC/MS-System with THF as solvent. HPLC analyses were performed on BioTek Konton 525 equipped with UV detector (at 260 nm, diode array detector HPLC 540) at room temperature (column: Chiralcel OD-H, eluent: methanol/water 8:2, flow rate: 0,4 mL/min). Optical rotations were measured with a Perkin-Elmer 341 polarimeter in THF as solvent, with a concentration of 10 mg ml−1. GPC analysis were carried out at 60 °C with N,N-dimethylformamide as eluent with a flow rate of 1 mL/min using a ViscotekGPCmax VE2001 system and a Viscotek VE 3500 RI detector. The system was calibrated with polystyrene standards with a molecular range from 1,280 g/mol to 1,373,000 g/mol.
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2

Solid-state 13C NMR Characterization of Coal

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After more than three
decades of the development of the NMR theory, 13C solid-state
NMR technology is considered to be the most advantageous tool for
the structural characterization of natural organic matter.19 (link),50 (link)−53 (link) The 13C NMR spectra of the five coal samples were measured
using a Bruker Advance III 600 spectrometer produced by Bruker Company
(Germany) at the Institute of Coal Chemistry (Chinese Academy of Sciences).
The samples were characterized at a contact time condition of 3 ms
and a pulse repetition delay of 3 s under a rotation frequency of
4 kHz. Moreover, we combined the total sideband suppression technology
to obtain the semi-quantitative compositional information.54 (link) To better quantitatively understand the relative
content of the different carbon types, we deconvoluted the 13C NMR spectra and calculated the NMR parameters (Table 3).
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3

NMR Analysis of EGCG Metabolites

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1H NMR spectra
were obtained on Advance III 600 (Bruker, Ettingen, Germany) with
a cryoprobe. EGCG and EGCG-sulfate extracted from metabolites of human
SULT were dissolved in acetonitrile-d3 (99.8% atom% D contains 0.03% (v/v) TMS, Sigma-Aldrich, St. Louis,
MO, USA).
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4

NMR and Mass Spectrometry Analysis

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1 H, 13 C, COSY, HMQC and HMBC spectra were measured on a Bruker DPX-300, DRX-400, DRX-500, or Bruker Advance III 600 (Bruker Corporation, Germany) spectrometer. All spectra were acquired at 298 K. Chemical shifts are given in -units (ppm) and are referenced to TMS. Coupling constants (J) are reported in Hz. Numbering of atoms is placed in schemes. Optical rotations were measured with an Autopol VI (Rudolph Research Analytical, USA) digital polarimeter in appropriate solvents, at temperature 25 o C and 589 nm sodium line, in 1 dm cuvette and are given at 10 -1 .deg.cm².g -1 . Concentrations (c) are given in g/100 mL. Low resolution ESI-MS were carried out using an Esquire 6000 ESI-Ion Trap from Bruker Daltonics. ESI high resolution mass spectra were measured with a LTQ Velos Orbitrap XL (Thermo Fisher Scientific, UK) instrument equipped with LockSpray in ES+ and ES-modes with mobile phase of 80% methanol. MALDI high resolution mass analysis was carried out in positive reflectron mode using a MALDI TOF UltrafleXtremeTM MALDI TOF/TOF (Bruker Daltonics, Germany) instrument equipped with 1 kHz smartbeam II laser. 2,5-Dihydroxybenzoic acid was a matrix substance. Nominal and exact m/z values are reported in Daltons.
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