Macrocyclic ring-chain poly(ether ketone)s

Macromolecules

Volumn 33, Issue 23, 2000, Pages 8907-8909

  Colquhoun, Howard M ^a   Sestiaa, Lionel G ^a   Zolotukhin, Mikhail G ^a,c   Williams, David J ^b  

^a UNIVERSITY OF SALFORD   (United Kingdom)

^b IMPERIAL COLLEGE LONDON   (United Kingdom)

^c INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

MOLECULAR STRUCTURE; POLYCONDENSATION; RING OPENING POLYMERIZATION; SYNTHESIS (CHEMICAL);

POLYETHER KETONES;

AROMATIC POLYMERS;

EID: 0034316264     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma001261w     Document Type: Article

References (13)

1. (a) Brunelle, D. J. In New Methods of Polymer Synthesis; Ebdon, J. R., Eastmond, G. C., Eds.; Blackie: London, 1995; p 197.
2. (b) Wang, Y. F.; Chan, K. P.; Hay, A. S. React. Funct. Polym. 1996 30, 205.
3. (c) Hodge, P.; Colquhoun, H. M.; Williams, D. J. Chem. Ind. (London) 1998, 162.
4. (a) Colquhoun, H. M.; Dudman, C. C.; Thomas, M.; O'Mahoney, C. A.; Williams, D. J. J. Chem. Soc., Chem. Commun. 1990, 336.
5. (b) Chen, M.; Gibson, H. W. Mocromolecules 1996, 29, 5502.
6. (c) Yokoi, Y.; Yamamoto, K.; Tsuchida, E.; Hay, A. S. Macromolecules 1997, 30, 4502.
7. (d) Jiang, H. Y.; Chen, T. L.; Qi, Y. H.; Xu, J. P. Polym. J. 1998, 30, 300.
8. (e) Teasley, M. F.; Wu, D. Q.; Harlow, R. L. Macromolecules 1998, 31, 2064.
9. Friedel-Crafts chemistry has however been developed for other types of macrocycles-for example, the formation of polyketones by condensation of dibenzo-crown ethers with long-chain dicarboxylic acids. See: Ueda, M.; Kano, T.; Twaragai, T.; Sugita, H. Makromol. Chem., Rapid Commun. 1985, 6, 847.
10. A macrocyclic aromatic ether sulfone, with dicarboxylic acid functionality appended through short aliphatic chains, has been shown to give a low molecular weight ring-chain type polyamide on condensation with 4,4′-diaminodiphenyl-methane. See: Rodewald, B.; Ritter, H. Macromol. Rapid Commun. 1997, 18, 817.
11. o)].
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13. Alkylation of aromatic rings by chlorinated solvents during Friedel-Crafts polyaroylations has been reported. See: Clendinning, R. A.; Kelsey, D. R.; Botkin, J. H.; Winslow, P. A.; Youssefi, M.; Cotter, R. J.; Matzner, M.; Kwiatkowski G. T. Macromolecules 1993, 26, 2361.