Collect. Czech. Chem. Commun.
2010, 75, 1023-1040
https://doi.org/10.1135/cccc2010064
Published online 2010-10-04 08:43:08
Synthesis, crystal structures and electrochemistry of ferrocenyl-substituted 1,3,4-oxadiazoles
Jiří Tauchman, Jakub Trnka, Ivana Císařová and Petr Štěpnička*
Charles University in Prague, Faculty of Science, Department of Inorganic Chemistry, Hlavova 2030, 128 40 Prague 2, Czech Republic
References
1a. Usp. Khim. 1964, 33, 1184 (English version: Russ. Chem. Rev. 1964, 33, 508).
< E. P., Grekov A. P.: https://doi.org/10.1070/RC1964v033n10ABEH001476>
1b. Adv. Heterocycl. Chem. 1967, 7, 183.
< A., Möckel K.: https://doi.org/10.1016/S0065-2725(08)60591-7>
1c. Curr. Org. Chem. 2008, 12, 850.
< Ž., Sollner Dolenc M.: https://doi.org/10.2174/138527208784911860>
1d. Krasovitskii B. M., Bolotin B. M.: Organic Luminiscent Materials. Wiley-VCH, Weinheim 1988.
2. J. Heterocycl. Chem. 1970, 7, 739.
< F. D., Moynahan E. B.: https://doi.org/10.1002/jhet.5570070352>
3. J. Prakt. Chem. 1967, 35, 149.
< H.-J., Pannier R., Wende A.: https://doi.org/10.1002/prac.19670350308>
4. Chem. Mater. 2008, 20, 540.
< C. C., Chen H.-C., Lee C., Leung M., Lin K.-R., Hsieh K.-H.: https://doi.org/10.1021/cm702217u>
5. J. Organomet. Chem. 2003, 675, 1.
< A. A. O., Izumi T.: https://doi.org/10.1016/S0022-328X(03)00216-X>
6. J. Am. Chem. Soc. 1955, 77, 1148.
< C.: https://doi.org/10.1021/ja01610a019>
7a. J. Chem. Soc. 1961, 4604.
< J. M., Pauson P. L.: https://doi.org/10.1039/jr9610004604>
7b. Polyhedron 2010, 29, 134.
< P., Císařová I., Nižňanský D., Bakardjieva S.: https://doi.org/10.1016/j.poly.2009.06.034>
8. Inorg. Chem. 2008, 47, 886.
< T., Noguchi D., Nakayama T., Inagaki Y., Shiota Y., Yoshizawa K., Ohkubo K., Fukuzumi S.: https://doi.org/10.1021/ic7016038>
9. J. Org. Chem. 1999, 64, 6989.
< T., Ishikawa T.: https://doi.org/10.1021/jo9909756>
10. Nakamoto K.: Infrared and Raman Spectra of Inorganic and Coordination Compounds, 5th ed., Part B, Chap. IV-6, p. 285. Wiley, New York 1997.
11. Izv. Akad. Nauk SSSR, Ser. Khim. 1998, 2309 (English version: Russ. Chem. Bull. 1998, 47, 2238).
L. I., Luiksaar S. I., Poddubnyi I. S., Krayushkin M. M.:
12. Cryst. Res. Technol. 2008, 43, 99 (structure determined from X-ray powder diffraction data).
< F., Reck G., Kraus W., Orgzall I., Schulz B.: https://doi.org/10.1002/crat.200711053>
13. Funct. Mater. 1996, 3, 460.
V. P., Patsenker L. D., Lokshin A. I., Tolmachev A. V.:
14a. Acta Crystallogr., Sect. E: Struct. Rep. Online 2003, 59, o1135.
< G., Orgzall I., Schulz B.: https://doi.org/10.1107/S1600536803014867>
14b. The geometric parameters were calculated from the data deposited with the Cambridge Crystallographic Data Centre (refcode: OJIFES).
15a. Inorg. Chem. 2005, 44, 4679.
< Y.-B., Wang H.-Y., Ma J.-P., Shen D.-Z., Huang R.-Q.: https://doi.org/10.1021/ic050218s>
15b. The geometric parameters were calculated from the data deposited with the Cambridge Crystallographic Data Centre (refcode: LARMIB).
16a. Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 2003, 59, o634.
< G., Orgzall I., Schulz B., Dietzel B.: https://doi.org/10.1107/S0108270103021413>
16b. The geometric parameters were calculated from the data deposited with the Cambridge Crystallographic Data Centre (refcodes: BEBMAX and BEMAX01; two polymorphs).
17a. J. Appl. Crystallogr. 2003, 36, 7.
< A. L.: https://doi.org/10.1107/S0021889802022112>
17b. The program is available via the Internet at http://www.cryst.chem.uu.nl/platon/.
18. Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 2000, 56, 1011.
< S., Yamin B. M., Boshaala A. M. A., Tarafder M. T. H., Crouse K. A., Fun H.-K.: https://doi.org/10.1107/S0108270100007010>
19. Some intermolecular C–H···O contacts are also detected.
20. J. Appl. Crystallogr. 1999, 32, 115.
< A., Burla M. C., Camalli M., Cascarano G. L., Giacovazzo C., Guagliardi A., Moliterni A. G. G., Polidori G., Spagna R.: https://doi.org/10.1107/S0021889898007717>
21. Sheldrick G. M: SHELXL97, Program for Crystal Structure Refinement from Diffraction Data. University of Göttingen, Göttingen 1997.