Repozytorium

Organotin adducts of indomethacin: synthesis, crystal structures and spectral characterization of the first organotin complexes of indomethacin.

Autorzy

A. Galani

Dimitra Kovala-Demertzi

N. Kourkoumelis

A. Koutsodimou

V. Dokorou

Zbigniew Ciunik

U. Russo

Mavroudis A. Demertzis

Rok wydania

2004

Czasopismo

Polyhedron

Numer woluminu

23

Strony

2021-2030

DOI

10.1016/j.poly.2004.05.004

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

The complexes [Me2(Indo)SnOSn(Indo)Me2]2, (1) [Bu2(Indo)SnOSn(Indo)Bu2]2, (2), where Hindo is indomethacin, have been prepared and structurally characterized by means of 119Sn Mössbauer, vibrational, and NMR (1H and 13C) spectroscopy. The crystal structures of the complexes [Me2(Indo)SnOSn(Indo)Me2]2 · 2C4H8O2, 3 and 2 have been determined by X-ray crystallography. Each structure is centro-symmetric and features a central rhombus Sn2O2 unit with two additional tin atoms linked at the O atoms. Pairs of tin atoms are bridged by bidentate carboxylate ligands and by a monoatomic bridging oxygen. C–H→π, π→π, stacking interactions, inter and intramolecular hydrogen bonds stabilize the structures 2 and 3. Complexes 2 and 3 are self-assembled via π→π, C–H-π and stacking interactions.The complexes [Me2(Indo)SnOSn(Indo)Me2]2, (1) [Bu2(Indo)SnOSn(Indo)Bu2]2, (2), where Hindo is indomethacin, have been prepared and structurally characterized by means of 119Sn Mössbauer, vibrational, and NMR spectroscopy. The crystal structures of the complexes [Me2(Indo)SnOSn(Indo)Me2]2 · 2C4H8O2, 3 and 2 have been determined by X-ray crystallography. Complexes 2 and 3 are self-assembled via π→π, C–H-π and stacking interactions.

Słowa kluczowe

Indomethacin, Diorganotin, Crystal structures, Spectroscopic studies

Adres publiczny

https://doi.org/10.1016/j.poly.2004.05.004

Strona internetowa wydawcy

http://www.elsevier.com

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