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5 μm mixed c columns

Manufactured by Hewlett-Packard

The 5 μm mixed-C columns are analytical HPLC columns designed for the separation and analysis of a wide range of organic compounds. These columns feature a 5 μm particle size and a mixed-mode stationary phase, providing efficient chromatographic performance for various applications.

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2 protocols using 5 μm mixed c columns

1

Spectroscopic Characterization of Organic Compounds

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NMR spectra were recorded on a Bruker-600 MHz spectrometer. Chemical shifts for 1H NMR spectra were reported in parts per million relative to a singlet at 7.26 ppm for the residual chloroform in deuterated chloroform. Chemical shifts for 13C NMR were reported relative to the centerline of a triplet at 77.16 ppm for deuterated chloroform. Molecular weights and polydispersity indices were determined by GPC in THF (20 °C; flow rate 1 mL min–1) using Polymer Labs 5 μm mixed-C columns, a Hewlett-Packard 1100 instrument equipped with a laser refractometer LR40 (Viscotek), and Viscotek software (TriSEC GPC Version 3.0, Viscotek Corp.). Poly(ethylene glycol) standards (Polymer Laboratories) were used for molecular weight calibration. Samples were dissolved in THF (0.4% w/v) and passed through a 0.2 μm filter before injection. Steady-state fluorescence emission spectra were recorded on a Horiba FluoroMax-4 spectrofluorometer. High-resolution mass spectra were obtained from the University of Illinois at Urbana-Champaign (UIUC) Mass Spectrometry Facility. UV-Vis spectra were produced from a Hewlett-Packard 8452A diode-array spectrophotometer. Unless otherwise noted, materials were obtained from commercial suppliers and were used without further purification. All of the solvents were either HPLC or spectroscopic grade in the optical spectroscopic studies.
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2

Polymer Molecular Weight Analysis

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The number-average molecular weights of the polymers were determined by 1H nuclear magnetic resonance (NMR) spectroscopy using a Bruker ARX NMR spectrometer (500 MHz). For 1H NMR measurements, polymer samples were prepared in deuterated chloroform at a polymer concentration of 5 wt %. The polydispersity indices (PDIs) of the polymers were measured by size-exclusion chromatography (SEC) using an Agilent Technologies 12000 Series instrument equipped with a Hewlett-Packard G1362A refractive index detector and 3 PLgel 5 μm MIXED-C columns. Tetrahydrofuran was used as the mobile phase (kept at 35 °C, flowing at a rate of 1 mL/min). Calibration was performed using polystyrene standards (Agilent Easi Cal).
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