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Phosphinoborine Compounds: Mass Spectra and Pyrolysis

The mass spectra of tetramethylphosphinoborine trimer, [P(CH(3))(2)B(CH(3))(2)](3) (I) and a a compound, P(5)(CH(3))(9)B(5)H(9), (II) prepared from dimethylphosphinoborine were observed, and the compounds were pyrolyzed at 300 to 500° C. Most peaks in the spectrum of (I) came from the P—B, B—C, and...

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Detalles Bibliográficos
Autores principales: Wall, Leo A., Straus, Sidney, Florin, Roland E., Mohler, Fred L., Bradt, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: [Gaithersburg, MD] : U.S. Dept. of Commerce, National Institute of Standards and Technology 1959
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287103/
https://www.ncbi.nlm.nih.gov/pubmed/31216142
http://dx.doi.org/10.6028/jres.063A.004
Descripción
Sumario:The mass spectra of tetramethylphosphinoborine trimer, [P(CH(3))(2)B(CH(3))(2)](3) (I) and a a compound, P(5)(CH(3))(9)B(5)H(9), (II) prepared from dimethylphosphinoborine were observed, and the compounds were pyrolyzed at 300 to 500° C. Most peaks in the spectrum of (I) came from the P—B, B—C, and P—C cleavages. The mass spectrum of (II) was much more complicated with evidence for methyl group redistribution. The pyrolysis of both compounds indicates a very complicated mechanism with many unidentifiable compounds. Trends in the formation of volatile products indicate that both compounds are completely decomposed in 4 hr at 450° C. Compound (I) produces trimethylboron, which disappears rapidly above 400° C. Neither (I) nor (II) formed ethane or elemental phosphorus.