Collect. Czech. Chem. Commun. 2006, 71, 1383-1391
https://doi.org/10.1135/cccc20061383

Synthesis, Self-Assembling and Redox Properties of 2-[(ω-Sulfanylalkyl)amino]-1,4-naphthoquinones

Maryte Kažemekaitea, Vilma Railaitea,b, Arunas Bulovasa, Zita Talaikytea, Gediminas Niauraa, Valdemaras Razumasa,* and Eugenijus Butkusa,b,*

a Department of Bioelectrochemistry and Biospectroscopy, Institute of Biochemistry, Mokslininku 12, LT-08662 Vilnius, Lithuania
b Department of Organic Chemistry, Vilnius University, Naugarduko 24, LT-03225 Vilnius, Lithuania

References

1. Finklea H. O. in: Electroanalytical Chemistry (A. J. Bard and I. Rubinstein, Eds), pp. 108–335. Marcel Dekker, New York 1996.
2. Ye S., Yashiro A., Sato Y., Uosaki K.: J. Chem. Soc., Faraday Trans. 1996, 92, 3813. <https://doi.org/10.1039/ft9969203813>
3. Hong H.-G., Park W., Yu E.: J. Electroanal. Chem. 1999, 476, 177. <https://doi.org/10.1016/S0022-0728(99)00380-0>
4. Hong H.-G., Park W.: Langmuir 2001, 17, 2485. <https://doi.org/10.1021/la001466y>
5. Seo K., Jeon I. C., Hong H.-G., Park W.: Bull. Korean Chem. Soc. 2002, 23, 1671.
6. Mukae F., Takemura H., Takehara K.: Bull. Chem. Soc. Jpn. 1996, 69, 2461. <https://doi.org/10.1246/bcsj.69.2461>
7. Panetta C. A., Fan P. W.-J., Fattah R., Greever J. C., He Z. L., Hussey C. L., Sha D. Z., Wescott L. D.: J. Org. Chem. 1999, 64, 2919. <https://doi.org/10.1021/jo981185j>
8. Ohtsuka T., Nagata M., Komori H., Nahgo M.: Electrochemistry 1999, 67, 1184.
9. Katz E. Y., Borovkov V. V., Evstigneeva R. P.: J. Electroanal. Chem. 1992, 326, 197. <https://doi.org/10.1016/0022-0728(92)80512-3>
10. Gao P., Gosztola D., Leung L.-W. H., Weaver M. J.: J. Electroanal. Chem. 1987, 233, 211. <https://doi.org/10.1016/0022-0728(87)85017-9>
11. Kazakevičiene B., Valincius G., Niaura G., Talaikyte Z., Kažemekaite M., Razumas V.: J. Phys. Chem. B 2003, 107, 6661. <https://doi.org/10.1021/jp035048o>
12. Taylor Ch. E., Pemberton J. E., Goodman G. G., Schoenfisch M. H.: Appl. Spectrosc. 1999, 53, 1212. <https://doi.org/10.1366/0003702991945687>
13. Niaura G., Gaigalas A. K., Vilker V. L.: J. Raman Spectrosc. 1997, 28, 1009. <https://doi.org/10.1002/(SICI)1097-4555(199712)28:12<1009::AID-JRS196>3.0.CO;2-G>
14a. Kolesnikov V. T., Boldyrev B. G., Yarysh M. E.: Zh. Org. Khim. 1971, 7, 1031.
14b. Kolesnikov V. T., Boldyrev B. G., Yarysh M. E.: J. Org. Chem. U.S.S.R. (Engl. Transl.) 1971, 1051.
15. Kažemekaite M., Bulovas A., Talaikyte Z., Butkus E., Railaite V., Niaura G., Palaima A., Razumas V.: Tetrahedron Lett. 2004, 45, 3551. <https://doi.org/10.1016/j.tetlet.2004.03.059>
16. Bittner S., Gorohovsky S., Paz-Tal (Levi) O., Becker J. Y.: Amino Acids 2002, 22, 71. <https://doi.org/10.1007/s726-002-8202-3>
17. Ulrich H., Richter R.: Methoden der Organischen Chemie (Houben–Weyl), Band VII/3a, Chinone, Teil I, pp. 404–424. Georg Thieme, Stuttgart 1977.
18. Stewart J. J. O.: MOPAC 6.0. Fujitsu Ltd., Tokyo 1993.
19. Wheland C. M., Barnes C. J., Gregoire C., Pireaux J. J.: Surf. Sci. 2000, 67, 454.
20. Balakrishnan G., Mohandas P., Umapathy S.: J. Phys. Chem. 1996, 100, 16472. <https://doi.org/10.1021/jp960568n>
21. Dolish F. R., Fateley W. G., Bentley F. F.: Characteristic Raman Frequencies of Organic Compounds. John Wiley and Sons, New York 1974.