Publications by authors named "Harun A R Pramanik"

A Schiff-base fluorescent probe - 2-((E)-(quinolin-8-ylimino)methyl)quinolin-8-ol (H7L) was synthesized and evaluated as a chemoselective Zn2+ sensor. Upon treatment with Zn2+, the complexation of H7L with Zn2+ resulted in a red shift with a pronounced enhancement in the fluorescence emission intensity in ethanol solution. Moreover, other common alkali, alkaline earth and transition metal ions failed to induce response or minimal spectral changes.

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A Schiff-base fluorescent probe - N, N(/)-bis(salicylidene) trans 1, 2 - diaminocyclohexane (H 2 L) was synthesized and evaluated as a chemoselective Zn(2+) sensor. Upon treatment with Zn(2+), the complexation of H 2 L with Zn(2+) resulted in a bathochromic shift with a pronounced enhancement in the fluorescence intensity in ethanol solution. Moreover, other common alkali, alkaline earth and transition metal ions failed to induce response or minimal spectral changes.

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A Schiff-base fluorescent compound - N, N'-bis(salicylidene)-1,2 - phenylenediamine (LH2) was synthesized and evaluated as a chemoselective Zn(2+) sensor. Addition of Zn(2+) to ethanol solution of LH2 resulted in a red shift with a pronounced enhancement in the fluorescence intensity. Moreover, other common alkali, alkaline earth and transition metal ions failed to induce response or minimal spectral changes.

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Article Synopsis
  • A new room-temperature liquid-crystalline salicylaldimine Schiff base and its lanthanide(III) complexes were synthesized and analyzed using various techniques including FTIR, NMR, and UV/Vis, confirming the ligand's coordination to metal ions.
  • The ligand demonstrates a stable hexagonal columnar phase at room temperature, while the complexes display a lamellar columnar phase at 120°C, with both showing significant thermal stability.
  • Notably, the compounds emit distinct colors under UV light, with the samarium complex giving off orange light and the terbium complex glowing green, supported by computational modeling indicating a nine-coordinate structure for the lanthanide complexes.
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Two new mixed-ligand iron(III) complexes, [Fe(L(n))(acac)(C(2)H(5)OH)] incorporating coordinated ethanol from the reaction solvent were accessed from the reaction of [Fe(acac)(3)] with [ONO] donor dibasic tridentate unsymmetrical Schiff base ligands derived from condensation of 2-hydroxy-1-napthaldehyde with 2-aminophenol (H(2)L(1)) or 2-aminobenzoic acid (H(2)L(2)). The thermal study (TGA-DTA) provided evidence for weakly bound ethanol which is readily substituted by neutral N-donor molecule imidazole, benzimidazole or pyridine to produce an array of newer complexes, [Fe(L(n))(acac)X] (n=1, 2; X=Im, Bim, Py). The compounds were characterized by elemental analyses, FT-IR, UV-vis, solution electrical conductivity, FAB mass, (1)H and (13)C NMR spectroscopy.

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