Md. Akhtarul Alam

Amido-Schiff base derivatives as colorimetric fluoride sensor: Effect of nitro substitution on the sensitivity and color change

A series of Schiff bases synthesized by the condensation of benzohydrazide and -NO2 substituted benzaldehyde have been used as selective fluoride ion sensor. Test paper coated with these synthetic Schiff bases (test kits) can detect fluoride ion selectively with a drastic color change and detection can be achieved by just using the naked-eye without the help of any optical instrument. Interestingly, the position of -NO2 group in the amido Schiff bases has an effect on the sensitivity as well as on the change of color of species.

Reusable amine-based structural motifs for green house gas (CO2) fixation.

A series of compounds with an amine based structural motif (ASM) have been synthesized for efficient atmospheric CO(2) fixation. The H-bonded ASM-bicarbonate complexes were formed with an in situ generated HCO(3)(-) ion. The complexes have been characterized by IR, (13)C NMR, and X-ray single-crystal structural analysis. ASM-bicarbonate salts have been converted to pure ASMs in quantitative yield under mild conditions for recycling processes.

An efficient size-selective anion binding cleft-shaped receptor: A novel [F2(H2O)3]2− cluster with pseudo-encapsulated F− ion

A cleft-shaped receptor 1 was synthesized and its anion binding properties have been investigated. Receptor 1 can selectively recognize fluoride ion by naked-eye color change and UV-vis spectral changes in aqueous-acetonitrile solvent. The single crystal X-ray analysis of 1 with fluoride ion shows that there are two types of fluoride ions in the unit cell, one of which is pseudoencapsulated within the cleft-shaped cavity and the other type forms a dimer through [F2(H2O)3]2−fluoride-water cluster.

Reduced Schiff-base assisted novel dihydrogenphosphate–water polymer

Reduced Schiff bases with a common p-nitro-o-phenylenediamine moiety have been synthesised and their structures have been characterized by single-crystal structural analysis. Schiff bases having self-complementary H-bond donors and H-bond acceptors can form a “scissors” like structure through intermolecular H-bonding interaction. Reduced Schiff bases interact with biologically important dihydrogenphosphate ion and form stable complexes. Furthermore, dihydrogenphosphate and water form an unprecedented self-assembled dihydrogenphosphate–water [H2PO4·H2O]nn− 1D supramolecular polymer upon complexation with reduced Schiff bases.

Selective chromo-fluorogenic molecular sensor for dual channel recognition of Cu2+ and F−: effect of functional group on selectivity

The sensor HNHCB (3-hydroxy-naphthalene-2-carboxylic acid (4-cyano-benzylidene)-hydrazide) comprises a –CONH– group, –OH group, –CHN– linkage and an electron withdrawing –CN group that can act as both an anion (fluoride) and a cation (copper) sensor by two distinct output modes. It can detect fluoride by naked eye color change and copper by fluorescence enhancement. Interestingly, the nature of the substituent in HNHCB has an effect on the selectivity. The detection limit can be as low as 160 nM for Cu2+ and 1.3 μM for F−. DFT calculations have been performed to demonstrate the structure of HNHCB and its copper complex. Biological applications of HNHCB have been evaluated in HEK 293 and it was found to exhibit membrane permeability for the detection of Cu2+. The sensor HNHCB is also sensitive towards fluoride in commercially available toothpaste.

Interaction of a synthesized pyrene based fluorescent probe with CT-DNA: spectroscopic, thermodynamic and molecular modeling studies

The present study demonstrates the synthesis of a new pyrene based water soluble fluorescent probe and its interaction with Calf-thymus DNA. The interaction has been studied using various biophysical methods like absorption and fluorescence spectroscopy, optical melting, isothermal titration colorimetry and circular dichroic studies. Experimental results indicate the binding mode between the probe and DNA to be principally intercalative having a binding energy in the range of −7 to −8 kcal mol−1 and the binding process is favored by both negative enthalpy change and positive entropy change. A salt dependent study revealed that the binding is favored by both small ionic interaction and large nonionic interactions. All the data obtained from biophysical studies have been validated by a molecular modeling study.

Binding mode dependent signaling for the detection of Cu2 +: An experimental and theoretical approach with practical applications

Two amido-schiff bases (3-Hydroxy-naphthalene-2-carboxylic acid pyren-1-ylmethylene-hydrazide and Naphthalene-2-carboxylic acid pyren-1-ylmethylene-hydrazide) have been synthesized having a common structural unit and only differs by a -OH group in the naphthalene ring. Both of them can detect Cu2+ ion selectively in semi-aqueous medium in distinctly different output modes (one detects Cu2+ by naked-eye color change where as the other detects Cu2+ by fluorescence enhancement). The difference in the binding of Cu 2+ with the compounds is the reason for this observation. The detection limit is found to be micromolar region for compound which contains -OH group whereas the compound without -OH group detects copper in nano-molar region. DFT calculations have been performed in order to demonstrate the structure of the compounds and their copper complexes. Practical utility has been explored by successful paper strip response of both the compounds. The biological applications have been evaluated in RAW 264.7.