Poly(2,5-dihydroxy-1,4-phenylene benzobisthiazole)/poly(1,4-phenylene benzobisthiazole) copolymers: Chain packing and properties

Citation
Hh. Song et al., Poly(2,5-dihydroxy-1,4-phenylene benzobisthiazole)/poly(1,4-phenylene benzobisthiazole) copolymers: Chain packing and properties, J POL SC PP, 39(5), 2001, pp. 559-565
Citations number
25
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS
ISSN journal
08876266 → ACNP
Volume
39
Issue
5
Year of publication
2001
Pages
559 - 565
Database
ISI
SICI code
0887-6266(20010301)39:5<559:PBB>2.0.ZU;2-N
Abstract
Crystal-packing, optical, and electrical properties of poly(2,5-dihydroxy-1 ,4-phenylene benzobisthiazole) (DiOH-PBZT) and copolymers of DiOH-PBZT/poly (1,4-phenylene-benzobisthiazole) (PBZT) were examined. Intramolecular hydro gen bonds between the hydroxyl units and the neighboring nitrogen atoms, as evidenced by the IR spectra, led to the formation of a pseudoladder chain structure and changed the chain packing. The (200) and (010) planes were bo th affected by the copolymer composition, with the (200) plane spacing incr easing from 5.895 to 6.482 Angstrom and the (010) plane spacing decreasing from 3.539 to 3.404 Angstrom with the transition from the unsubstituted PBZ T homopolymer to the DiOH-PBZT homopolymer. The cell dimensions of the copo lymers were simple averages of those of the individual homopolymers, sugges ting the isomorphic crystal structure formation of the two units. The c-axi s spacing, how ever, remained unchanged. The increase in the conjugation le ngth of the copolymers as the dihydroxy content increased was confirmed by the bathochromic shift of the absorption band in the ultraviolet-visible sp ectra. The intrinsic conductivities of the copolymers were 3 orders of magn itude higher than that of the unsubstituted PBZT. (C) 2001 John Wiley & Son s, Inc.