Polyphosphazenes for Biomedical Applications 2008
DOI: 10.1002/9780470478882.ch10
|View full text |Cite
|
Sign up to set email alerts
|

Polyphosphazenes from Condensation Polymerization

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2016
2016
2020
2020

Publication Types

Select...
3
2

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(2 citation statements)
references
References 38 publications
0
2
0
Order By: Relevance
“…Poly(alkyl/aryl)phosphazenes, [NPR 2 ] n , whereby the organic substituent is directly attached via a P–C bond, can also be prepared via direct polymerisation routes. Initially developed by thermal (100–180 °C) condensation of (CF 3 CH 2 O)R 2 P NSiMe 3 type monomers, 25 this has since been expanded to cationic initiators and with monomers of the type BrR 2 P NSiMe 3 . 21 Recently, the polymerisation of halo(alkyl/aryl)phosphoranimines (XR 2 PNSiMe 3 , X = Br or Cl) initiated by organic phosphites ((MeO) 3 P) has also been shown to be an effective route to poly(alkyl/aryl)phosphazenes at ambient temperature ( Fig.…”
Section: Synthesis Of Polyphosphazenesmentioning
confidence: 99%
“…Poly(alkyl/aryl)phosphazenes, [NPR 2 ] n , whereby the organic substituent is directly attached via a P–C bond, can also be prepared via direct polymerisation routes. Initially developed by thermal (100–180 °C) condensation of (CF 3 CH 2 O)R 2 P NSiMe 3 type monomers, 25 this has since been expanded to cationic initiators and with monomers of the type BrR 2 P NSiMe 3 . 21 Recently, the polymerisation of halo(alkyl/aryl)phosphoranimines (XR 2 PNSiMe 3 , X = Br or Cl) initiated by organic phosphites ((MeO) 3 P) has also been shown to be an effective route to poly(alkyl/aryl)phosphazenes at ambient temperature ( Fig.…”
Section: Synthesis Of Polyphosphazenesmentioning
confidence: 99%
“…For example, Wisian–Nielson and Nielson devised a condensation polymerization that has yielded numerous polymers with direct phosphorus–carbon-linked side groups (Reaction ). , These reactions provide access to polymers that are difficult or impossible to obtain by macromolecular substitution. …”
Section: Polymer Synthesismentioning
confidence: 99%