The Photoelectron Spectra of 4, 13-Diaza- and 4, 16-Diaza [24] (1,2,4,5)cyclophanes
β Scribed by Yang Zhong-zhi; Edgar Heilbronner; Hee Chol Kang; Virgil Boekelheide
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- German
- Weight
- 340 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0018-019X
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β¦ Synopsis
Abstract
A tentative assignment is proposed for the He (I__a__) photoelectron (PE.) spectra of the title compounds. It is based on the assumption that the first four Οβbands occupy the same position in both spectra, as suggested by a qualitative correlation with the PE. spectrum of 2~4~cyclophane and by a previously proposed molecular orbital model. If this is accepted, then the bands due to electron ejection from the loneβpair orbitals are split by roughly 0.8 eV in the case of the 4, 13βdiaza isomer, whereas no split can be detected in the case of the 4, 16βdiaza isomer.
π SIMILAR VOLUMES
## Abstract The piperidine ring in the title compound is in the chair conformation, whereas the diketopiperazine ring has a boat form. The benzyl group is axially positioned and folded above the diketopiperazine ring. No dimerisation is observed.
## Abstract The molecular structures of the title compounds 3 and 5 were investigated by NMR and Xβray structural methods. The NMR results suggest two equivalent halves for both molecules. The Xβray study shows an approximate mirror plane for 3 and an approximate twofold axis for a significant port
## Abstract 4,5,7,13,15,16βHexamethylβ **(3)** and 4,5,7,8,12,13,15,16βoctamethyl[2.2]paracyclophane **(4)** have been oxidized to their radical cations in solution under relatively mild conditions. Substantial hyperfine splittings in the ESR. spectra of **3β.** and **4β.** arise from the methyl pr