Phosphonation of polysulfones via lithiation and reaction with chlorophosphonic acid esters
(2005) In Journal of Polymer Science. Part A, Polymer Chemistry 43(2). p.273-286- Abstract
- A noncatalytic route for the phosphonation of polysulfones was established in which lithiated sites on polysulfones were reacted with an excess of chlorophosphonic acid esters through an SNP(V) mechanism. Both the bisphenol A and biphenyl sulfone segments of the polysulfone main chain were modified according to whether brominated polysulfone or pristine polysulfone was used. Up to 50% of the repeating units of the polysulfones were modified by a careful selection of reaction parameters to avoid crosslinking. The phosphonated polysulfones in their acid form showed high thermal stability with decomposition temperatures of approximately 350 C under nitrogen. Polysulfones with phosphonated bisphenol A segments showed good membrane-forming... (More)
- A noncatalytic route for the phosphonation of polysulfones was established in which lithiated sites on polysulfones were reacted with an excess of chlorophosphonic acid esters through an SNP(V) mechanism. Both the bisphenol A and biphenyl sulfone segments of the polysulfone main chain were modified according to whether brominated polysulfone or pristine polysulfone was used. Up to 50% of the repeating units of the polysulfones were modified by a careful selection of reaction parameters to avoid crosslinking. The phosphonated polysulfones in their acid form showed high thermal stability with decomposition temperatures of approximately 350 C under nitrogen. Polysulfones with phosphonated bisphenol A segments showed good membrane-forming properties and are candidates for components in ionomer composite membranes for fuel cells. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/153041
- author
- Lafitte, Benoit LU and Jannasch, Patric LU
- organization
- publishing date
- 2005
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Polymer Science. Part A, Polymer Chemistry
- volume
- 43
- issue
- 2
- pages
- 273 - 286
- publisher
- John Wiley & Sons Inc.
- external identifiers
-
- wos:000225953600003
- scopus:12344279432
- ISSN
- 0887-624X
- DOI
- 10.1002/pola.20487
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Polymer and Materials Chemistry (LTH) (011001041)
- id
- 668a9bf6-9061-4623-bd8c-f7dc9a1616c4 (old id 153041)
- date added to LUP
- 2016-04-01 16:49:03
- date last changed
- 2022-04-15 07:16:05
@article{668a9bf6-9061-4623-bd8c-f7dc9a1616c4, abstract = {{A noncatalytic route for the phosphonation of polysulfones was established in which lithiated sites on polysulfones were reacted with an excess of chlorophosphonic acid esters through an SNP(V) mechanism. Both the bisphenol A and biphenyl sulfone segments of the polysulfone main chain were modified according to whether brominated polysulfone or pristine polysulfone was used. Up to 50% of the repeating units of the polysulfones were modified by a careful selection of reaction parameters to avoid crosslinking. The phosphonated polysulfones in their acid form showed high thermal stability with decomposition temperatures of approximately 350 C under nitrogen. Polysulfones with phosphonated bisphenol A segments showed good membrane-forming properties and are candidates for components in ionomer composite membranes for fuel cells.}}, author = {{Lafitte, Benoit and Jannasch, Patric}}, issn = {{0887-624X}}, language = {{eng}}, number = {{2}}, pages = {{273--286}}, publisher = {{John Wiley & Sons Inc.}}, series = {{Journal of Polymer Science. Part A, Polymer Chemistry}}, title = {{Phosphonation of polysulfones via lithiation and reaction with chlorophosphonic acid esters}}, url = {{http://dx.doi.org/10.1002/pola.20487}}, doi = {{10.1002/pola.20487}}, volume = {{43}}, year = {{2005}}, }