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Abstrakty
Coumarines are compounds originating from the nature, used in many areas such as cosmetics, seasonings, pharmaceutics, and photochemistry. There are many developed methods of coumarines synthesis, e.g. Pechman reaction, Perkin reaction, Knoevenagel condensation and many others. Since coumarine derivatives have been studied in our laboratory, we have investigated their synthesis through Knoevenagel condensation. 3-carboxycoumarines were synthesized from appropriate hydroxybenzealdehydes and then their methacrylate monomers were synthetised using 2-hydroxyethyl methacrylate. All compounds were identified by GC-MS and IR and gave satisfactory results in comparison with authentic samples. Described in this paper series of monomers were copolymerised with other monomers to give photo- and electroluminescent copolymers.
Czasopismo
Rocznik
Tom
Strony
90--92
Opis fizyczny
Bibliogr. 19 poz., rys., tab.
Twórcy
autor
autor
autor
- Department of Chemistry, Politechnika Krakowska, ul. Warszawska 24, 31-155 Kraków, Poland, (012) 628 25, e-mail: pcbogdal@cyf-kr.edu.pl
Bibliografia
- (1) O'Kennedy R., Thomes R.D., Coumarins: Biology, Applications and Mode of Action, Wiley & Sons, Chichester, 1997.
- (2) (a) Beneteau v., Besson T., Guillard J., Leonce S., Pfeifer B., Eur. J. Med. Chem., 1999, 34, I 053, (b) Beneteau V., Pierre A., Pfeifer B., Renard P., Besson T., Bioorg. Med. Chem. Lett., 2000,10, 2231 , (c) Lamazzi C., Leonce S., Pfeifer B., Renard P., Guillaumet G., Rees C.W., Bioorg. Med. Chem. Lett., 2000,10, 2183.
- (3) Maeda M., Laser Dyes, Academic Pres, New York.
- (4) Perkin W.H., J. Chem. Soc., 1868,53.
- (5) Pechmann H., Ber., 1884, 17, 929.
- (6) Pechmann H., Duisberg C., Ber., 1883, 16, 2119.
- (7) Knoevenagel, E., 1898, 31, 2585, 2596.
- (8) Sonn A., Ber. 1917, 50, 1292.
- (9) Weiss R., Merksammer E., Monatsh. 1928, 50, 115.
- (10) Badhwar I.C., Baker W., Mennon B.K., Venkatraman K., J. Chem. Soc., 1931, 1541.
- (11) Smith L. I. , Dobrowolny F.J., J. Am. Chem. Soc., 1926, 48, 1693.
- (12) Kostanecki S., Różycki A., Ber., 1901, 34, 102.
- (13) Chakravarti D., Majumdar B., J. Indian Chem. Soc. 1938, 15, 136.
- (14) Bogdał D., Stępień I., Sanetra J., Gondek E., Polimery 2003, 48, 111.
- (15) D. Bogdał, Polimery 1999,44,555; Bogdał D., Boroń A., Polirnery, 1999, 44, 646; Bogdał D., Pielichowski J., Pielichowski K., Warzała M., Łukasiewicz M., Polimery, 2000, 45, 363.
- (16) Loupy A., Petit A., Hamelin J., Texier-Boullet F., Jacquault P., Mathe D. Synthesis 1998, 1213.
- (17) Bogdał D.: Wiad. Chem. 1999, 53, 66.
- (18) Deshayes S., Liagre M., Loupy A., Luche J.L., Petit A.: Tetrahedron, 1999, 55, 10851.
- (19) (a) Bogdał D., Stępień I, Sanetra J., Gondek E., Polimery 2003,48, III , (b) Sanetra J.,Bogdał D., Warzała M., Boroń A., Chem. Mat., 2002, 14,89; (c) Sanetra J., Bogdał D., Nizioł S., Armatys P., Pielichowski J., Synth. Met., 2001, 121; (d) Bogdał D., Warzała M., Pielichowski J, Sanetra J., Polimery 1999, 44,146.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BPS3-0002-0111