Crystal and molecular structure of acetamidrazone derivatives

Springer Science and Business Media LLC - Tập 31 - Trang 149-154 - 2001
S. Ianelli1, G. Pelosi1, G. Ponticelli2, M.T. Cocco3, V. Onnis3
1Dipartimento di Chimica Generale ed Inorganica, Chimica Analitica, Chimica Fisica, Centro di Studio per la Strutturistica Diffrattometrica del CNR, Parma, Italy
2Dipartimento di Chimica Inorganica ed Analitica, Università degli studi di Cagliari—Cittadella di Monserrato, Monserrato, Cagliari, Italy
3Dipartimento di Tossicologia, Università degli Studi di Cagliari, Cagliari, Italy

Tóm tắt

N 1-acetylacetamidrazones and N 1-benzoylacetamidrazones (1a–d) were characterized by 1H and 13C NMR spectroscopy. The actual tautomeric form present has been shown to be the amide hydrazone. NMR spectra of N 1-acetylacetamidrazones (1a,b) showed the existence of Z and E isomers in solution, while N 1-benzoylacetamidrazones (1c,d) were present as Z isomers. The crystal structures of the amidrazones have been determined at 173 and 293 K, respectively. The amidrazones 1c and 1d crystallize in the monoclinic system: in particular for 1c space group P21/c, with a = 11.016(5), b = 20.594(14), c = 13.657(7) Å β = 98.29(3)° V = 3066(3) Å3 and D c = 1.243 g/cm3 for Z = 4; for 1d space group P21/a, with a = 9.410(5), b = 10.449(3), c = 14.295(11) Å β = 101.04(5)° V = 1380(1) Å3 and D c = 1.220 g/cm3 for Z = 4. The X-ray diffraction analysis carried out on 1c has shown the presence of three molecules in the asymmetric unit which differ for the orientation of the phenyl ring.

Tài liệu tham khảo

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