ISSN:
0449-296X
Schlagwort(e):
Physics
;
Polymer and Materials Science
Quelle:
Wiley InterScience Backfile Collection 1832-2000
Thema:
Chemie und Pharmazie
Notizen:
The syntheses of N-2-phenylallylacrylamide (I) and N-ethyl-2-phenallylacrylamide (II) are described. Both monomers can be polymerized with radical initiators to form cyclopolymers although complete cyclization does not occur. Lewis acids (ZnCl2 in the case of I, Et1.5AlCl1.5 in the case of II) result in the formation of higher molecular weight polymers in a shorter period of time. Polymers of I and II have been hydrolyzed to polyampholytes. The copolymerization of α-methylstyrene-acrylamide in the presence of azobisisobutyronitrile (AIBN) and ZnCl2 leads to the formation of a 1:1 copolymer, whereas styrene-acrylamide under the same conditions give a copolymer slightly dependent upon the monomer feed composition. Attempted cyclopolymerization of N-allylacrylamide (monomer I without the phenyl group) with ZnCl2-AlBN was not successful, only crosslinked polymer being obtained. An explanation is offered for the fact that I does not form a perfect cyclopolymer, although the α-methylstyrene-acrylamide system forms a 1:1 copolymer.
Zusätzliches Material:
10 Tab.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1002/pol.1972.170101203