Generation of methylenephosphine oxides by thermal fragmentation of derivatives of the 2-phosphabicyclo [2.2.2] octa-5,7-diene oxide ring system
✍ Scribed by György Keglevich; Kálmán Újszászy; Louis D. Quin; Gyöngyi S. Quin
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 410 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
✦ Synopsis
Differential thermal analysis and differential scanning calorimetry showed that the title compounds decomposed at 240-260°C with release of the fragment
RP(0) = CH,. Mass spectral studies also showed this to be a fragmentation pathway. The extruded methylenephosphine oxide could be trapped with ethanol, hydroquinone, or by reaction with the surface OH groups of silica gel.
📜 SIMILAR VOLUMES
Stereost ruct u re of 8-C h loro-5,6di( met hoxycarbonyI)-4,7=di met hyl-2-et hoxy-2phosphabicyclo[2.2.2]octa-5,7-diene 2-Oxide
The stable 7-phosphanorbornadiene derivative, 2,3-benzo-1,4,5,6,7-pentaphenyl-7-phosphabicyclo[2.2.1]hepta-2,5-diene-7-oxide (1) was synthesized in 45% yield via the Diels-Alder reaction of pentaphenylphosphole oxide and benzyne. The reaction occurs specifically to give a single isomer, which was ch