1980
DOI: 10.1021/ja00528a060
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Poly(dimethylphosphazene), (Me2PN)n

Abstract: the m/e 28 peak is nitrogen, of course, and some could be ethyne-úí? formed by facile isomerization31•32 of ethenylidene which would arise by loss of nitrogen from 3.Work on the kinetics and key intermediates is underway. If the initial steps proposed prove correct, this is further testimony to the lack of reactivity of the diazirine ring.

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Cited by 107 publications
(70 citation statements)
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“…Polymerization of noncyclic phosphazene monomers that already bear organic side groups destined for the polymer. This approach was pioneered by WisianNeilson and Nielson [21][22][23][24], Flindt and Rose [25] and by Matyjaszewski et al [26,27]. It uses organophosphoranimines as monomers and includes the following process:…”
Section: Basic Polymer Synthesis Processesmentioning
confidence: 99%
“…Polymerization of noncyclic phosphazene monomers that already bear organic side groups destined for the polymer. This approach was pioneered by WisianNeilson and Nielson [21][22][23][24], Flindt and Rose [25] and by Matyjaszewski et al [26,27]. It uses organophosphoranimines as monomers and includes the following process:…”
Section: Basic Polymer Synthesis Processesmentioning
confidence: 99%
“…Azido(bis(trimethylsilyl)amino](mesityl)phosphine (5). A freshly prepared sample of 1 (5.0 g, 14.5 mmol) was treated with Me 3 SiN 3 (2.5g, 21.7 mmol) at O°C.…”
Section: Cismentioning
confidence: 99%
“…Alternative methods of polyphosphazene synthesis also exist (12)(13)(14)(15) and several of these approaches are discussed elsewhere in this volume. Finally, chemistry conducted at the surface of polyphosphazenes allows the tailoring of those surfaces to achieve the development of specific chemical, physical, or biological characteristics (16-…”
Section: Introduction To Polvnhosnhazenesmentioning
confidence: 99%