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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

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✦ 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.


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✍ Christine Gottardo; Stephen Fratpietro; Alan N. Hughes; Mark Stradiotto 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 158 KB 👁 1 views

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