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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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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
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author Wall, Leo A.
Straus, Sidney
Florin, Roland E.
Mohler, Fred L.
Bradt, Paul
author_facet Wall, Leo A.
Straus, Sidney
Florin, Roland E.
Mohler, Fred L.
Bradt, Paul
author_sort Wall, Leo A.
collection PubMed
description 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.
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spelling pubmed-52871032019-06-18 Phosphinoborine Compounds: Mass Spectra and Pyrolysis Wall, Leo A. Straus, Sidney Florin, Roland E. Mohler, Fred L. Bradt, Paul J Res Natl Bur Stand A Phys Chem Article 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. [Gaithersburg, MD] : U.S. Dept. of Commerce, National Institute of Standards and Technology 1959 1959-08-01 /pmc/articles/PMC5287103/ /pubmed/31216142 http://dx.doi.org/10.6028/jres.063A.004 Text en https://creativecommons.org/publicdomain/zero/1.0/ The Journal of Research of the National Bureau of Standards Section A is a publication of the U.S. Government. The papers are in the public domain and are not subject to copyright in the United States. Articles from J Res may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Article
Wall, Leo A.
Straus, Sidney
Florin, Roland E.
Mohler, Fred L.
Bradt, Paul
Phosphinoborine Compounds: Mass Spectra and Pyrolysis
title Phosphinoborine Compounds: Mass Spectra and Pyrolysis
title_full Phosphinoborine Compounds: Mass Spectra and Pyrolysis
title_fullStr Phosphinoborine Compounds: Mass Spectra and Pyrolysis
title_full_unstemmed Phosphinoborine Compounds: Mass Spectra and Pyrolysis
title_short Phosphinoborine Compounds: Mass Spectra and Pyrolysis
title_sort phosphinoborine compounds: mass spectra and pyrolysis
topic Article
url 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
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