ISOMERISM AND SYMMETRY OF STACKED POLYMERIC PHTHALOCYANINES AND RELATED POLYMERS

Authors
Citation
G. Knothe, ISOMERISM AND SYMMETRY OF STACKED POLYMERIC PHTHALOCYANINES AND RELATED POLYMERS, Makromolekulare Chemie. Theory and simulations, 2(6), 1993, pp. 917-927
Citations number
23
Categorie Soggetti
Polymer Sciences
ISSN journal
10185054
Volume
2
Issue
6
Year of publication
1993
Pages
917 - 927
Database
ISI
SICI code
1018-5054(1993)2:6<917:IASOSP>2.0.ZU;2-7
Abstract
The number of isomers i(r,t) for stacked polymeric phthalocyanines in which each phthalocyanine ring is tetrasubstituted or octasubstituted with two different substituents (each benzene moiety substituted with both substituents) is determined to be lim(x-->infinity) i(r,t) = 2m/1 6 where m is the number of substituted phthalonitrile molecules incorp orated into the polymer and x is the number of phthalocyanine macrocyc les (degree of polymerization; m = 4x). Specifically, for a stacked po lymeric phthalocyanine with x = 2, there exist 26 isomers, and when x = 3, there exist 298 isomers. The stacked polymeric phthalocyanines wi th substituted phthalocyanine rings possess different symmetry groups (D2h, D2d, C4h, C4, C2v or C(s); or E as sole symmetry operation). The results are valid for stacking of other macrocycles similar to phthal ocyanine such as porphyrins.