Polymeric amines by chemical modifications of alternating aliphatic polyketones
Alternating, aliphatic polyketones were chemically modified by using di-amines to obtain polymeric products having pendant amino groups. The used reaction, Paal-Knorr, involves the formation of pyrrole rings along the polyketone backbone. The corresponding kinetics and final conversions are clearly...
Saved in:
Published in | Journal of applied polymer science Vol. 107; no. 1; pp. 262 - 271 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
05.01.2008
Wiley |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Alternating, aliphatic polyketones were chemically modified by using di-amines to obtain polymeric products having pendant amino groups. The used reaction, Paal-Knorr, involves the formation of pyrrole rings along the polyketone backbone. The corresponding kinetics and final conversions are clearly dependent, among others, on statistical factors (two adjacent carbonyls must react in order to obtain ring formation) as well as on the steric hindrance (sterically hindered amino groups react very slow). The corresponding reaction products (polymeric amines) display very interesting physical properties in aqueous solution. These have been characterized by using dynamic light scattering, Cryo-electron microscopy, fluorescence techniques, etc. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 |
---|---|
Bibliography: | http://dx.doi.org/10.1002/app.27029 istex:9B8FB7A42CEEA11BC5E0D433DF8D9CEF852BA8C2 ArticleID:APP27029 ark:/67375/WNG-V3DQDST5-3 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0021-8995 1097-4628 |
DOI: | 10.1002/app.27029 |