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Avance 250 mhz spectrometer

Manufactured by Bruker
Sourced in Germany

The Avance 250 MHz spectrometer is a nuclear magnetic resonance (NMR) instrument manufactured by Bruker. It operates at a frequency of 250 MHz and is designed to analyze the chemical composition and structure of materials through the observation of nuclear spin interactions.

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6 protocols using avance 250 mhz spectrometer

1

NMR Analysis of Curcumin-Loaded Hydrogel

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Gel-H.P dialyzed for 24 h against distilled water and then lyophilized. The lyophilized hydrogel dissolved in D2O and was applied for NMR analysis using a Bruker Avance 250 MHZ spectrometer. Gel-H.P.Cur was immersed in DMSO for 48 h and then the NMR of released curcumin in DMSO was studied.The NMR data was processed using MestReNova software.
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2

Synthesis and Characterization of Compounds 5-7

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All reagents were purchased from Sigma-Aldrich (St. Louis, MO, USA), Alfa Aesar (Lancaster, UK) and TCI (Tokyo, Japan) and used without further purification. NMR spectra were recorded with a Bruker Avance 500 MHz spectrometer (Bruker, Rheinstetten, Germany) operating at 500 MHz (1H) and 125 MHz (13C) or with a Bruker Avance 250 MHz spectrometer (Bruker, Rheinstetten, Germany) operating at 250 MHz (1H) and 62.5 MHz (13C). Chemical shifts are reported in ppm relative to DMSO-d6 (1H: δ = 2.50 ppm, 13C: δ = 39.52 ± 0.06 ppm). Elemental analyses were performed using a PerkinElmer 2400 CHNS 100V Organic Elemental Analyzer (Waltham, MA, USA). Compounds 5–7 were synthesised as described previously [27 (link),28 (link),29 (link)].
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3

Synthesis and Characterization of Magnetic Nanoparticles

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All materials and reagents were purchased from chemical sources and used as received. The Fourier transform infrared spectroscopy (FT-IR) was performed using a Bruker Vertex 70 FT-IR spectrometer. 1H and 13C NMR spectra were recorded using a Bruker Avance 250 MHz spectrometer. The powder X-ray diffractometry (XRD) patterns were obtained using an X'Pert Pro Panalytical diffractometer applying a 30 mA current and a 40 kV voltage with Cu-Kα radiation (λ = 1.5418 Å). The morphology and size of the prepared nanoparticles were investigated using SEM images obtained from the FESEM-TESCAN MIRA3 instrument. Nanocatalysts' chemical composition was determined by EDX using SEM analysis. The specimen's magnetic susceptibility was determined via a vibrating sample magnetometer (Meghnatis Daghigh Kavir, Co. Iran) in a magnetic field of 20 kOe. Thermogravimetric analysis (TGA) was performed using the Shimadzu DTG-60 device at 0 to 700 °C. In addition, thin-layer chromatography (TLC) analysis was performed to determine the products' purity and monitor the reaction progress in a silica gel 60 F254 aluminum sheet.
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4

NMR Characterization of Hydrogels

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Hydrogels were dialyzed for 24 h against distilled water and then were lyophilized. The lyophilized hydrogels were dissolved in D2O and used as NMR samples on a Bruker Avance 250 MHZ spectrometer. NMR data processing was performed using MestReNova software.
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5

NMR Spectroscopy with Laser Irradiation

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All irradiation experiments were performed on a Bruker AVANCE 250 MHz spectrometer. Light was directed into the sample using a multimode optical fibre with 1000 μm core diameter. To ensure inert conditions, the NMR tubes were filled in a glove box and equipped with a conical insert that could host the optical fibre. Thus, the sample volume could be kept isolated from the outside atmosphere. As light source we used a 700 mW laser diode (638 nm), which was mounted on the far end of the optical fibre. The outer cladding of the fibre was removed for about 5 cm on the sample side and the glass surface was roughened to ensure uniform irradiation of the sample, as previously reported.47 (link)
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6

NMR Characterization of Nanoparticles

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1 H-NMR spectra were recorded on a Bruker AVANCE 250 MHz spectrometer. All spectra were measured in deuterium oxide (D2O), using dimethyl sulfoxide (DMSO) as an internal standard, with 16 scans per sample under a 12 s pulse delay. For these experiments, the relative concentration of D2O, DMSO and nanoparticle dispersion was kept constant.
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