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The spectra obtained with a third-order Q-box using the LS method. All energies in MeV. Taken from Ref. .

The spectra of 1,1-dichloroethane, CH3CHCI2, showing the effect of two halogen atoms on the same carbon on the resonance frequencies of the protons. The CH3 group absorbs at 2.06 ppm, while the proton on the chlorine-containing carbon is highly deshielded and absorbs at 5.89 ppm. The 7ab coupling constant is 6.0 Hz.

The spectra of 3,3 -dimethylnaphthidine products recorded during chronoampero-metric measurements at an Sn02 OTE.

The spectra of a few metal-poor stars are shown above

The spectra of a PENBTE film measured at different potentials from 0.4 V

The spectra of a sample of PMMA on a Ge. substrate obtained by transmission, specular reflection, and ATR spectroscopy.

The spectra of a three layered sample as the sample is translated axially through the laser focus,

The spectra of acetic acid. The acid proton absorbance at 11.8 ppm is characteristic of carboxylic acids.

The spectra of butylamine. The amine protons give rise to the sharp singlet at 1.1 ppm. The adjacent methylene protons are shifted to about 2.7 ppm by the electronegative nitrogen, while the other alkyl methylene and methyl protons appear at their usual chemical shift positions.

The spectra of carbon tetrachloride and carbon disulfide liquids, cell length 0.1 nun.

The spectra of cyclohexanone. The only characteristic absorbance for ketones in the proton NMR spectrum is that of the protons adjacent to the carbonyl group, which are shifted to 2.4 ppm by slight deshielding.

The spectra of ethylbenzene, showing the characteristic aromatic ring and benzylic proton absorbances typical of alkyl-substituted aromatic compounds.

The spectra of four neptunium oxidation states showing quadrupole

The spectra of Hyperion, Ariel, Titania, Oberon, and Umbriel .

The spectra of ms-DLE in the presence of FeCy and DAD DCMU

The spectra of nitropropane.

The spectra of one-way drawn PET film in the directions parallel and perpendicular to the direction of draw and through the thickness direction of the film. Reproduced with permission from Ref. 1986

The spectra of oriented pha.se-I PVDF annealed under strain relaxation. Parallel, perpendicular, and calculated thickness-direction spectra are shown.

The spectra of oriented phase-I PVDF annealed under tension. Parallel, perpendicular, and calculated thickness-direction spectra are shown.

The spectra of peroxidase in a cell with an optically transparent electrode. peroxidase reduced at 0.05 V.

The spectra of phenol, CeHs-OH, an aromatic alcohol. The hydroxyl proton is deshielded by the aromatic ring and appears at a chemical shift of 5.6 ppm.

The spectra of phenol, CgHs—OH, an aromatic alcohol. The hydroxyl proton is deshielded by the aromatic ring and appears at a chemical shift of 5.6 ppm.

The spectra of PVAc interface at saturation surface coverage

The spectra of real ei parts of the pseudodielectic function e Si i E2 for the multilayer structure. Circles and triangles - experimental data straight line - calculated spectra.

The spectra of several HABIs.



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