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Oxygen absorption modes

The interpretation of the vibrational fine structure in the formaldehyde spectrum developed more slowly. Aside from the well developed progressions in a frequency of 1182 cm" which were assigned to the vi carbon-oxygen stretching mode, the other intervals observed in the spectrum were not readily interpreted. The hot bands did not form intervals which correlated with the ground state vibrational frequencies. Furthermore, the band structure in absorption and emission did not display the expected mirror image relationship. The major problem was the abnormally small vibrational spacing of 125 cm" which separated the first two bands in the spectrum. [Pg.175]

They found that the order for the M—0 stretching modes (M—0 force constants) was (02)Pd(02) > Pd(Oj) and (02)Ni(02) > Ni(02), and since the 0-0 force constant increased as the M-0 force constant decreased, reversibility could not be equated with shorter 0—0 bond length. To test the proposed isosceles model they predicted the various absorptions that would be expected on the basis of the symmetrical structure (a) and unsymmetrical structure (c), Fig. 8. If the isotopic ratio of 0 0 is 1 1, then three bands would be expected for structure (a), with relative intensities 1 2 1, and four bands would be expected for structure (c), with relative intensities 1 1 1 1, the two oxygen atoms now being in different environments. These workers 189) then obtained the IR spectrum for the cocondensation product from the reaction between nickel and O2 (4.2—10°K), in isotopic ratio 0 =1 1, and found three bands with relative inten-... [Pg.27]

From IR vibrational absorption experiments, there is a multitude of vibrational bands in Si that contain H, far more than the modes attributable to Si—H, Si—H2 and Si—H3. The presence of oxygen causes broadening and overlap of some of these modes, hindering their interpretation. Vibrational bands above 2000 cm-1 are attributed to vacancy-... [Pg.19]

Cation radicals of several metallated TPP and OEP complexes were reported to have unique IR active ring modes (21. These absorptions were observed in the region 1250-1290 cm for TPP complexes and 1520-1570 cm for OEP complexes. IR and raman active modes have also been observed for several different reduced oxygen species adsorbed on various metal substrates. Observations of the adsorption of oxygen on silver by surface enhanced raman spectroscopy (SERS) 22), show superoxide molecules (O2) have a frequency of 1053 cm, and peroxide (0 ) of 697 cm. This same study reported additional peaks were observed at 815 cm and 1286... [Pg.330]


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Absorption mode

OXYGEN ABSORPTION

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