KOMLEKSNYE SOEDINENIYA GIDROKSIPROIZVODNOGO DINITROBENZOFUROKSANA. CHAST' 3. VZAIMODEYSTVIE TRIHLORIDA RODIYA S DINATRIEVYM KOMPLEKSOM 4,6-DINITRO-1-OKSOBENZ[6,5-C]-2,1,3-OKSADIAZOLDIOLA-5,7 V VODNO-ACETONOVOY SREDE
Abstract and keywords
Abstract (English):
To clarify the composition and structure of rhodium complex synthesized in aqueous -acetone medium under the interaction of rhodium trichloride and disodium 4,6-dinitro-1-oxobenzo[6,5-c]-2,1,3-oxodiazoldiol-5,7 complex, mass spectrometry and 13 C NMR methods were applied can conclude that a structural unit consisting of compounds are distinguished [Rh 4 +3(C 6N 4O 8) 4 С l 16] , where the atom by furoxane cycle and N 3 = O group at C 6 carbon atom coordinating rhodium is ligand. The layers are binded by complex of rhodium( III ). In turn, in [Rh 4 +3(C 6N 4O 8) 4 С l 16] cations and rhodium cations surrounded viewed rhodium octahedral environment of the molecule which are water and chloride ions, whereby they are integrated in the chain. And so the octahedral environment of rhodium cations are molecules dioxidinitrobenzofuroxane, water and chloride ions. Connecting of cations by means of rhodium complex compound forms a cross-linked multilayer structure. The method of powder diffraction confirms identity of them. Virtual screening of biological activity showed marked immuno-stimulation properties in the treatment of system lupus erythematosus .

Keywords:
гидроксипроизводные динитробензофураксана, динатриевый комплекс 4,6-динитро-1-оксобенз[6,5-c]-2,1,3-оксадиазолдиола-5,7, трихлорид родия, комплексообразование, синтез, водно-ацетоновая среда, фрагментация, dinitrobenzofuroxane hydroxyderivatives, disodium 4,6-dinitroо-1-oxobenz[6,5-c]-2,1,3-oxadiazoldiole-5,7 complex, rhodium trichloride, complexing, synthesis, water -acetone medium, fragmentation
References

1. E.V. Guseva, L.R. Galimzyanova, A.M. Sayfutdinov, V.I. Morozov, Vestnik Kazanskogo Tehnologicheskogo Universiteta, 12, 26-29 (2012)

2. E.I. Gazizova. Diss. kand. him. nauk, Kazanskiy gosudarstvennyy tehnologicheskiy universitet, Kazan', 2008. 131s.

3. R. Sil'versteyn, G. Bassler, T. Morril, Spektrometricheskaya identifikaciya organicheskih soedineniy. Mir, Moskva, 1977. 590s.

4. X. Gyunter, Vvedenie v kurs spektroskopii YaMR. Mir, Moskva, 1984.462s.

5. L.A. Kazicina, N.B. Kupletskaya, Primenenie UF-, IK- i YaMR-spektroskopii v organicheskoy himii. Mir, Vyssh. Shkola, 1971. 264s.

6. L.M. Sven, F. Eva, G. Frank, M. Jens, L. Bemhard, Inorganic Chemistry, 37, 3195-3203 (1998).

7. V.C Jyothi Bhasu, M. Munavar Chaudri, J. Housden, J. Matrials Science, 26, 2199-2207 (1991.

8. Takakis Ioannis M., Tsantali George G., Haas George W., Giblin Daryl, L. Michael, J. Mass Spectrom., 34, 1137-1153 (1999).

9. I.V. Galkina, E.V. Tudriy, O.N. Kataeva, L.M. Yusupova, V.I. Galkin. Neobychnaya reakciya fosforilirovaniya dihlordinitrobenzofuroksana trifenilfosfinom // Tez. dokl. XVIII Mendeleevskogo s'ezda po obschey i prikladnoy himii. - M., 2007. - T. 1. - S. 168.

10. D. Tudella, C. Muro, V. Fernandez, Zeiteschrift fűr anorganischen und allgemeine Chemie, 538, 201-206 (1986).

11. G.A. Kuznecova, Kachestvennyy rentgenofazovyy analiz: metodicheskie ukazaniya [Elektronnyy resurs]. - Rezhim dostupa: http://www.fineprint.com, svobodnyy. - Provereno 30.03.2013.

12. Gloriozova T.A., Filimonov D.A., Lagunin A.A., Poroykov V.V., Him.-farm. zhurnal, 32,12,33-39 (1998).

13. A.V. Sadym, A.A.Lagunin, D.A. Filimonov, V.V. Poroykov Him.-farm. zhurnal, 36,10,21-26 (2002).

14. E.I. Gazizova, L.M. Yusupova, O.N. Kataeva, Vestnik Kazan. tehnol. un-ta, 6, 31-36 (2007).

Login or Create
* Forgot password?