Phosphazene azides: A new means for polymer cross-linking and property modification

Thomas J. Hartle; Michael B. McInstosh; Harry R. Allcock

Phosphazene azides: A new means for polymer cross-linking and property modification

Thomas J. Hartle
, Michael B. McInstosh
, Harry R. Allcock

Research output: Contribution to journal › Conference article › peer-review

Abstract

Cyclic phosphazene trimers containing the azido group with aryloxy, alkoxy, or diakylamino cosubstituents were synthesized through reaction of NaN₃ with the appropriate chlorophosphazene. The ability of the phosphazene azides to form nitrenes and undergo insertion into C-H bonds was also studied.

Original language	English (US)
Pages (from-to)	908-909
Number of pages	2
Journal	American Chemical Society, Polymer Preprints, Division of Polymer Chemistry
Volume	40
Issue number	2
State	Published - Aug 1 1999

All Science Journal Classification (ASJC) codes

Polymers and Plastics

Cite this

@article{46d3871909bd43c6a5ec2e63cd9ec728,

title = "Phosphazene azides: A new means for polymer cross-linking and property modification",

abstract = "Cyclic phosphazene trimers containing the azido group with aryloxy, alkoxy, or diakylamino cosubstituents were synthesized through reaction of NaN3 with the appropriate chlorophosphazene. The ability of the phosphazene azides to form nitrenes and undergo insertion into C-H bonds was also studied.",

author = "Hartle, \{Thomas J.\} and McInstosh, \{Michael B.\} and Allcock, \{Harry R.\}",

year = "1999",

month = aug,

day = "1",

language = "English (US)",

volume = "40",

pages = "908--909",

journal = "American Chemical Society, Polymer Preprints, Division of Polymer Chemistry",

issn = "0032-3934",

number = "2",

}

TY - JOUR

T1 - Phosphazene azides

T2 - A new means for polymer cross-linking and property modification

AU - Hartle, Thomas J.

AU - McInstosh, Michael B.

AU - Allcock, Harry R.

PY - 1999/8/1

Y1 - 1999/8/1

N2 - Cyclic phosphazene trimers containing the azido group with aryloxy, alkoxy, or diakylamino cosubstituents were synthesized through reaction of NaN3 with the appropriate chlorophosphazene. The ability of the phosphazene azides to form nitrenes and undergo insertion into C-H bonds was also studied.

AB - Cyclic phosphazene trimers containing the azido group with aryloxy, alkoxy, or diakylamino cosubstituents were synthesized through reaction of NaN3 with the appropriate chlorophosphazene. The ability of the phosphazene azides to form nitrenes and undergo insertion into C-H bonds was also studied.

UR - https://www.scopus.com/pages/publications/0032662781

UR - https://www.scopus.com/pages/publications/0032662781#tab=citedBy

M3 - Conference article

AN - SCOPUS:0032662781

SN - 0032-3934

VL - 40

SP - 908

EP - 909

JO - American Chemical Society, Polymer Preprints, Division of Polymer Chemistry

JF - American Chemical Society, Polymer Preprints, Division of Polymer Chemistry

IS - 2

ER -

Phosphazene azides: A new means for polymer cross-linking and property modification

Abstract

All Science Journal Classification (ASJC) codes

Other files and links

Fingerprint

Cite this