The intramolecular addition of hydroxyl group of 3-(3-hydroxyl)propylidene-2,5\_piperazinedione to 3-position and the same substitution of 3-(3-hydroxy)propyl derivative to 6-position gave the corresponding 3-spiro-and 3,6bridged 2,5\_piperazinediones, respectively. Recently, much attention is bein
Syntheses and PE-Spectroscopic Investigations of 2,6- and 3,5-Bridged 1,4-Dimethylidenecyclohexanes
✍ Scribed by Teh-Chang Chou; Holger Lange; Rolf Gleiter; Tibor Gögh; Miroslav Kríž; Max H. Pfenninger; Marian Valentíny; Camille Ganter
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- German
- Weight
- 834 KB
- Volume
- 78
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Three 1,4‐dimethylidenecyclohexanes, bridged in the 2,6‐ and 3,5‐positions by two ethano (4), one ethano and one propano (5), and two propano bridges (6) have been synthesized. The interaction of the two exocyclic methylidene groups has been investigated by He(I) photoelectron (PE) spectroscopy. It revealed a slightly larger energy difference (0.8 eV) for 4 and 5 as compared to the parent 1,4‐dimethylidenecyclohexane (7) (0.7 eV). The interpretation of the PE spectra was based on the comparison with PE data of related systems and with the results of semiempirical calculations on 4–6.
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