Magnetic vibrational circular dichroism spectra of the title compounds are presented for the mid-IR region. The metalloporphytin E. modes have larger A terms than seen previously by an order of magnitude and are 2-3 times larger than in tetraphenylporphine. Comparison to the vibronic model is made.
The photoelectron spectra of tetraphenylporphine and some metallotetraphenylporphyrins
โ Scribed by Suresh C. Khandelwal; John L. Roebber
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- English
- Weight
- 423 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
โฆ Synopsis
Meso-tetraphenylprophine
and its complexes with the dipositive cations of bfg, Xfn, Fe, Cu, and Zn have very similnr photoelectron spectra. Eight major peaks appear in the 6.3 to 2C eV nnge which have positions, shapes and intensities showing only minor variations from compound to compound. Several of the obierved photoelectron bands arc assigned with the help of previously published optical and EPR spectral studies of solutions of the porphyrin cation radicals and thcoretical calculztions.
๐ SIMILAR VOLUMES
The He(l) photoelectron (PI.) spectra of 1,2,4-trnrinc, its three monomcthyl isomers. two dimethyl isomers, and trimethyl-1.2,4-trlazinc arc reported. The spectra arc interpreted hy comparison with the results of MO calculations ar.d cmpuiul correlat Ion proccdurcs.