Synthesis,extraction, and anti‐bacterial studies of some new bis‐1,2,4‐triazole derivatives part I |
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Authors: | Nurhan Gumrukcuoglu Serpil Ugras Halil Ibrahim Ugras Umit Cakir |
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Affiliation: | 1. Vocational School of Health Sciences, KTü, Trabzon, Turkey;2. Department of Biology, Faculty of Arts and Sciences, Giresun University, Giresun 28049, Turkey;3. Department of Chemistry, Faculty of Arts and Sciences, Giresun University, Giresun 28049, Turkey;4. Department of Chemistry, Faculty of Arts and Sciences, Bal?kesir University, Balikesir 10160, Turkey |
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Abstract: | A series of new bis triazole Schiff base derivatives (4) were prepared in good yields by treatment of 4‐amino‐3,5‐diphenyl‐4H‐1,2,4‐triazole (3) with bisaldehydes (1). Schiff bases (4) were reduced with NaBH4 to afford the corresponding bisaminotriazoles (5). All the new compounds were characterized by IR, 1H NMR and 13C NMR spectral data. Their overall extraction (log Kex) constants for 1 : 1 (M : L) complexes and CHCl3/H2O systems were determined at 25 ± 0.1°C to investigate the relationship between structure and selectivity toward various metal cations. The extraction equilibrium constants were estimated using CHCl3/H2O membrane transfer with inductively coupled plasma‐atomic emission spectroscopy spectroscopy. The stability sequence of the triazole derivatives in CHCl3 for the metal cations was exhibited a characteristic preference order of extractability to metal ions [Fe(III) > Cu(II) > Pb(II) > Co(II) > Ni(II) > Mn(II) > Zn(II) > Mg(II) > Ca(II)]. The compounds were tested for anti‐microbial activity applying agar diffusion technique for 11 bacteria. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012 |
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Keywords: | 4‐Amino‐4H‐1,2,4‐triazole bis‐1,2,4‐triazoles bisSchiff bases extraction ability‐selectivity anti‐bacterial activity |
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