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Maldi tof ms performance

Manufactured by Shimadzu
Sourced in Japan

The MALDI-TOF MS Performance is a mass spectrometry instrument that utilizes Matrix-Assisted Laser Desorption/Ionization (MALDI) technology and Time-of-Flight (TOF) mass analysis. It is designed to provide accurate and reliable mass measurements of a wide range of biomolecules, including proteins, peptides, and oligonucleotides.

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3 protocols using maldi tof ms performance

1

Comprehensive Spectroscopic Analysis of Organic Compounds

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1H and 13C NMR spectra were recorded on a Bruker-Avance 400 MHz spectrometer by using CDCl3 as the solvents. Elemental analyses were performed with a PerkinElmer 240C elemental analyzer by investigation of C, H, and N. MS spectra were measured on Agilent Technologies 6224 spectrometer and MALDI-TOF MS Performance (Shimadzu, Japan). UV-visible spectra were carried out on a Shimadzu UV-2550 spectrophotometer. Fluorescence measurements were measured on a Cary Eclipse Fluorescence Spectrophotometer. The absolute fluorescence quantum yield for the solid sample was obtained using an Edinburgh FLS920 steady state spectrometer using an integrating sphere. Density functional theory (DFT) calculations were done employing the Gaussian 09W suit of programs at the B3LYP/6-31G(d) level. XRD patterns were measured on a Bruker D8 Focus Powder X-ray diffraction instrument.
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2

Characterization of novel HQTPE compound

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All 1H and 13C NMR spectra were recorded in DMSO-d6 solutions at 298 K using a Bruker (400 MHz) spectrometer with tetramethylsilane as an internal standard. Mass spectra were recorded on matrix-assisted laser desorption ionization time-of-flight MS (MALDI-TOF MS), Performance (Shimadzu, Japan). Perkin Elmer CE-440 was used for micro elemental analyses. Infrared spectra were recorded by Perkin Elmer (Spectrum 100) FT-IR Spectrometer. UV-vis spectra were recorded using Perkin Elmer (Lambda 750) UV/Vis/NIR Spectrometer in ethyl acetate solvent. Fluorescence emission, quantum yield, and lifetime measurements were performed by SHIMADZU Spectro fluorophotometer RF-6000. Aggregations of HQTPE were examined by scanning electron microscopy (SEM) by a Hitachi SU-8010 SEM instrument fitted with a field-emission source and operating at 10 kV. Samples were prepared for SEM by mounting a portion of the cover slide on a silicon stub. Electrochemical measurements were performed on a CH-Instruments Model CHI660D using a one-compartment cell under air atmosphere. The three-electrode system consisted of a platinum counter electrode, an Ag/AgCl reference electrode, and a platinum working electrode.
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3

Spectroscopic Analysis of Molecular Compounds

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All of the solvents and chemicals were purchased in analytical grade and were used as received. Column chromatography used 300–400 mesh silica gels. Ultrapure water was produced by a Milli-Q Direct 16 system of Millipore. UV-Vis absorption spectra were gained on a Shimadzu UV-2550 spectrophotometer (Shimadzu, Kyoto, Japan). Fluorescence spectra were obtained on a Cary Eclipse fluorescence spectrophotometer from Agilent. 1H- and 13C-NMR spectra were recorded with a Mercury plus instrument at 400 and 100 MHz by using DMSO-d6 as the solvents. MS spectra were recorded on a MALDI-TOF MS Performance (Shimadzu, Japan).
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