Relative partial photoionization cross sections and photoelectron branching ratios have been obtained for the valence bands of osmium tetroxlde in the ionization energy range I2 to 18 eV. The photon energies used ranged between 24 and 100 eV. The ionization cross sections of the 21, and 2a, orbitals
Variable energy photoelectron spectroscopy: electronic structure and electronic relaxation
β Scribed by Edward I. Solomon; Lipika Basumallick; Peng Chen; Pierre Kennepohl
- Publisher
- Elsevier Science
- Year
- 2005
- Tongue
- English
- Weight
- 591 KB
- Volume
- 249
- Category
- Article
- ISSN
- 0010-8545
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β¦ Synopsis
Use of variable photon energy with polarization available from synchrotron radiation has revolutionized the use of photoelectron spectroscopy (PES) in the study of transition metal complexes. The intensity dependence of PES peaks allows their definite assignment, a quantitation of the covalent mixing of the metal and ligand valence orbitals over the entire valence band, and an experimental determination of electronic relaxation. The last effect is the change in electronic structure with ionization, which is found to be large for transition metal complexes. Variable energy PES (VEPES) provides a powerful method to study bonding and its change with ionization and this provides fundamental insight into redox processes in inorganic and bioinorganic chemistry.
π SIMILAR VOLUMES
The spectroscopic-potentials-adjusted INDO (SPINDO) has been used to calculate the electronic structure of toluene. Reasonable agreement between the orbital energies and the photoelectron spectrum has been obtained, which indicates the usefulness of the new procedure. The molecular orbitals of tolue