Unsymmetrically substituted aliphatic diacetylenes containing amine functionalities

Synthetic Communications

Volumn 28, Issue 23, 1998, Pages 4333-4338

  Rodriguez Abad, Rafael ^a   Tsibouklis, John ^b  

^a UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

^b UNIVERSITY OF PORTSMOUTH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLENE DERIVATIVE; ALIPHATIC COMPOUND; ALKYNE DERIVATIVE; AMINE; HEPTANE; OCTANE; PHTHALIMIDE DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CRYSTAL STRUCTURE; INFRARED SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POLYMERIZATION; SOLID STATE; SYNTHESIS;

EID: 0031737175     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919808004467     Document Type: Article

References (14)

1. Wegner, G., Z. Naturforsch., 1969, 24B, 824-832.
2. Tsibouklis, J., Advanced Materials, 1995, 7(4), 407-408.
3. Tsibouklis, J. in "The polymeric Materials Encyclopedia: Synthesis, Properties and Applications", Vol. 5, (Ed. J.C. Salamone), CRC press, 1996, p.3787-3794.
4. Tsibouklis, J.; Werninck, A.R.; Shand, A.J. and Milburn, G.W.H., Chemtronics, 1988, 3, 211-214.
5. Tsibouklis, J.; Weminck, A.R.; Shand, A.J. and Milburn, G.W.H., Liquid Crystals, 1988, 3(10), 1393-1400.
6. Tieke, B.; Lieser, G. and Wegner, G., J. Polym. Sci., Polym. Chem. Ed., 1979, 17, 1631-1644.
7. Bartu, E. and Tsibouklis, J., Tetrahedron Letters, 1996, 37(28), 5023-5026.
8. Viehe, H.G."Chemistry of Acetylenes" Marcel Dekker, New York, 1969, p.614-617.
9. Chodkiewicz, W., Annales de chimie, 1957, 2, 819-869.
10. Tsibouklis, J.; Pearson, C.; Song, Y.; Warren, J.; Petty, M.; Yarwood, J.; Petty, M.C. and Feast, W.J., J.Mater.Chem., 1993, 3(1), 97-104.
11. Ohba, S.and Engbersen, J.F.J., Tetrahedron, 1991, 47, 9947-9952.
12. Tsibouklis, J.; Campbell, C.; Werninck, A.R.; Shand, A.J. and Milburn, G.W.H., Polymer Bulletin, 1992, 29, 661-668.
13. Under conditions utilising a small excess of hydroxylamine, some material (ca 1% yield) in which only one of the carbonyls had been attacked could be isolated.
14. The monomers can be stored, for limited periods of time, at low temperatures (<-18°C) in the dark; the melting points of the monomers could not be meaningfully recorded.