Electron proton resonance spectroscopy

TPR, Temperature-programmed reaction XPS, X-ray photoelectron spectroscopy IR, infrared spectroscopy H NMR, proton nuclear magnetic resonance spectroscopy UV-vis, ultraviolet-visible spectroscopy ESR, electron spin resonance spectroscopy TPD, temperature-programmed desorption EXAFS, extended X-ray absorption fine structure spectroscopy Raman, Raman spectroscopy C NMR, carbon-13 nuclear magnetic spectroscopy. 

The formation of highly conjugated systems, with their associated colouring, on the thermal and thermal-oxidative degradation of PVC is conveniently followed by electron proton resonance and ultraviolet spectroscopy [3]. 

Electron Proton Resonance with Near Infrared Spectroscopy... 

Rao and co-workers [82] used an inverted emulsion process for the synthesis of the emeraldine salt of PAM using a novel oxidising agent, benzoyl peroxide. The polymerisation was carried out in a non-polar solvent in the presence of four different protonic acids as dopants and an emulsifier (sodium lauryl sulfate). The polymer salts were characterised spectroscopically by ultraviolet-visible, Fourier-transform infrared, Fourier-transform Raman and electron paramagnetic resonance spectroscopy. Thermogravimetric analysis, was used to determine the stability of the salts and the activation energy for the degradation. The conductivity of the salts was found to be in the order of 10 S/cm. 

Poppl A, Kevan L. 1996. A practical strategy for determination of proton hyperfine interaction parameters in paramagnetic transition metal ion complexes by two-dimensional HYSCORE electron spin resonance spectroscopy in disordered systems. J Phys Chem 100 3387-3394. 

The [Fe =0(TMP+ )]+ complex exhibited a characteristic bright green color and corresponding visible absorbance in its UV-vis spectrum. In its NMR spectrum, the meta-proton doublet of the porphyrin mesityl groups were shifted more than 70 ppm downfield from tetramethylsilane (TMS) because they were in the presence of the cation radical, while the methyl protons shift between 10 and 20ppm downfield. In Mossbauer spectroscopy, the isomer shift, 5 of 0.06 mm/s, and A q value of 1.62mm/s were similar to those for other known Fe(IV) complexes. Electron paramagnetic resonance (EPR), resonance Raman (RR), and EXAFS spectroscopies provided additional indications of an Fe =0 n-cation radical intermediate. For instance,... 

For NMR, the intensity of the signal (which may be measured by electronically measuring the area under individual resonance signals) is directly proportional to the number of nuclei undergoing a spin-flip and proton NMR spectroscopy is a quantitative method. 

The circulating electrons in the 7t-system of aromatic hydrocarbons and heterocycles generate a ring current and this in turn affects the chemical shifts of protons bonded to the periphery of the ring. This shift is usually greater (downfield from TMS) than that expected for the proton resonances of alkenes thus NMR spectroscopy can be used as a test for aromaticity . The chemical shift for the proton resonance of benzene is 7.2 ppm, whereas that of the C-1 proton of cyclohexene is 5.7 ppm, and the resonances of the protons of pyridine and pyrrole exhibit the chemical shifts shown in Box 1.12. 

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