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Mercury plus 300 mhz spectrometer

Manufactured by Bruker

The Mercury Plus 300 MHz spectrometer is a nuclear magnetic resonance (NMR) instrument designed for routine analytical and research applications. It provides a magnetic field strength of 7.05 Tesla, corresponding to a proton (1H) resonance frequency of 300 MHz. The spectrometer is equipped with a superconducting magnet and can be used to analyze a variety of liquid and solid samples.

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2 protocols using mercury plus 300 mhz spectrometer

1

Spectroscopic Characterization of Compounds

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Optical rotation and circular dichroism was measured on a JASCO P-2000 polarimeter and JASC0 J-815 CD spectrometer in MeOH, respectively. IR spectra were recorded on a Bomem MB-Series spectrometer, in a 100 to 3500 cm−1 spectral region, using KBr matrix HR-ESI-MS and spectrum was recorded in a ESI-MS Quattro LCZ (Micromass Manchester, UK). NMR spectra were recorded on a Varian Mercury Plus 300 MHz spectrometer (7.02 T), operated at 75 MHz for 13C and 300 MHz for 1H and 2D NMR and a Bruker (Avance III) 400 MHz instruments. Column chromatography was carried out in Silica gel (70–230 mesh, Merck) for vacuum liquid chromatography (VLC) and Silica gel C-18 (HF Bondesil C-18, Agilent) for flash chromatography (FC). Thin-layer chromatography (TLC) was performed on precoated silica gel aluminum sheets (Kieselgel 60 F254, 0.20 mm, Merck, Darmstadt, Germany) and visualized in UV 254 or 365 nm.
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2

Peptide Synthesis and Characterization

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Peptides were synthesized employing an Fmoc-based solid phase peptide synthesis strategy using 2-chlorotrityl chloride resin. Protected peptide (0.016 mmol) was lipidated by 1-hexadecanol (16C), 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE) or 1,2-dihexanoyl-sn-glycero-3-phosphoethanolamine (DHPE). All peptides were characterizated by high-resolution mass spectra (HR-MS) (Supplementary file 1). HR-MS were measured on a Thermo Orbitrap coupled to a Thermo Accela HPLC system using electrospray ionization (ESI).
The small nucleophiles, ethanolamine 1 and phosphoethanolamine 2 were purchased from Sigma. Other small nucleophiles, glycerophosphoethanolamine 8 and diacetyl glycerophosphoethanolamine 10 were synthesized as shown in Figure 1—figure supplement 1B. Subsequently, these compounds were characterizated by NMR and HR-MS (Supplementary file 2). 1H NMR spectra were recorded on a Varian Mercury Plus 300 MHz spectrometer (300 MHz), a Bruker DRX 400 (400.13 MHz) spectrometer. NMR spectra were calibrated to the solvent signals of DMSO-d6 (δ = 2.50 and 40.45 ppm). All reactions were carried out under an inert atmosphere in dry solvents unless otherwise noted.
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