Zinc(II)-MOF: A Versatile Luminescent Sensor for Selective Molecular Recognition of Flame Retardants and Antibiotics.

An exceptional Zinc(II)-organic framework with the formula [{Zn(L4-py)(bdc)}·DMF]n (Zn-MOF) has been constructed solvothermally using a novel linker L4-py {2,7-bis(3-(pyridin-4-ylethynyl)phenyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone}, coligand H2bdc (1,4-benzenedicarboxylic acid), and ZnBF4·xH2O. The ligand L4-py has been fabricated after functionalization of NDA (1,4,5,8-naphthalenetetracarboxylic dianhydride) core with 3-(pyridin-4-ylethynyl)phenyl group. The single-crystal X-ray analysis reveals that Zn-MOF exhibits a comprehensive three-dimensional (3D) framework architecture and features (4)-connected uninodal dia; 4/6/c1; sqc6 topology with point symbol {66} and two-dimensional (2D) + 2D, parallel polycatenation. Notably, Zn-MOF displayed excellent fluorescence phenomenon and stability in water as well as in methanol solvents and was harnessed as a versatile sensor, demonstrating selective and sensitive molecular recognition of flame retardants and antibiotics. Notably, Zn-MOF displayed 57 and 49.5% quenching efficiency for the flame-retardant pentabromophenol (PBP) and 3,3',5,5'-tetrabromobisphenol A (TBPA), respectively. Whereas an outstanding 90% quenching efficiency was observed for antibiotics, tetracycline (TC) and secnidazole (SD). The mechanistic investigations of this luminescence quenching suggest that this might be primarily occurring via the Fourier resonance energy transfer (FRET) and photoinduced electron transfer (PET) mechanisms, which might be assisted by the competitive absorption and host-guest interactions. The π-electron-rich framework structure of sensor Zn-MOF activates this mechanism.

Metal-Organic Framework-Based Selective Molecular Recognition of Organic Amines and Fixation of CO2 into Cyclic Carbonates.

Synthesis and structural depiction of two new metal-organic frameworks (MOFs), namely, [{Zn(L)(oba)}·4H2O]α (Zn-MOF-1) and [{Cd1/2(L)1/2(nipa)1/2(H2O)1/2}·(DMF)1/2(H2O)]α (Cd-MOF-2) (where L = N2,N6-di(pyridin-4-yl)naphthalene-2,6-dicarboxamide, 4,4'-H2oba = 4,4'-oxybisbenzoic acid, and 5-H2nipa = 5-nitroisophthalic acid) are reported. Both Zn-MOF-1 and Cd-MOF-2 have been prepared by reacting ligand L and coligand 4,4'-H2oba or 5-H2nipa with the respective dihydrates of Zn(OAc)2 and Cd(OAc)2 (OAc = acetate). Crystal structure X-ray analysis discloses that Zn-MOF-1 displays an overall 2D → 3D interpenetrated framework structure. The topological analysis by ToposPro suggests a (4)-connected uninodal sql topology with a point symbol of {44·62} having 2D + 2D parallel polycatenation. However, crystal packing of Cd-MOF-2 adapted a porous framework architecture and was topologically simplified as (3,4)-connected binodal 2D net. In addition, both Zn-MOF-1 and Cd-MOF-2 were proved to be multifunctional materials for the recognition of organic amines and in the fixation of CO2 to cyclic carbonates. Remarkably, Zn-MOF-1 and Cd-MOF-2 showed very good fluorescence stability in aqueous media and have shown 98 and 97% quenching efficiencies, respectively, for 4-aminobenzoic acid (4-ABA), among all of the researched amines. The mechanistic study of organic amines recognition proposed that fluorescence quenching happened mainly through hydrogen-bonding and π-π stacking interactions. Additionally, cycloaddition of CO2 to epoxide in the presence of Zn-MOF-1 and Cd-MOF-2 afforded up to 96% of cyclic carbonate within 24 h. Both Zn-MOF-1 and Cd-MOF-2 exhibited recyclability for up to five cycles without noticing an appreciable loss in their sensing or catalytic efficiency.

Hybrid aptamer-antibody linked fluorescence resonance energy transfer based detection of trinitrotoluene.

Combining synthetic macromolecules and biomolecular recognition units are promising in developing novel diagnostic and analysis techniques for detecting environmental and/or clinically important substances. Fluorescence resonance energy transfer (FRET) apta-immunosensor for explosive detection is reported using 2,4,6-trinitrotoluene (TNT) specific aptamer and antibodies tagged with respective FRET pair dyes in a sandwich immunoassay format. FITC-labeled aptamer was used as a binder molecule in the newly developed apta-immunoassay format where the recognition element was specific anti-TNT antibody labeled with rhodamine isothiocyanate. The newly developed sensing platform showed excellent sensitivity with a detection limit of the order of 0.4 nM presenting a promising candidate for routine screening of TNT in samples.

2-(Phenyl-selenon-yl)pyridine.

In the title compound, C11H9NO2Se, the pyridine and phenyl rings are almost perpendicular, with the dihedral angle between their mean planes being 79.16 (7)°. In the crystal, the mol-ecules pack so as to form ruffled sheets in the (110) plane connected by weak C-H⋯O inter-actions. In addition, there are weak π-π inter-actions between the mean planes of both the phenyl [centroid-centroid perpendicular distance of 3.591 (2) Šand slippage of 1.854 (2) Å] and pyridine rings [centroid-centroid perpendicular distance of 3.348 (2) Šand slippage of 1.854 (2) Å].

Coordination Polymers as a Functional Material for the Selective Molecular Recognition of Nitroaromatics and ipso-Hydroxylation of Arylboronic Acids.

We report the synthesis and structural characterization of two coordination polymers (CPs), namely; [{Zn(L)(DMF)4 } ⋅ 2BF4 ]α (1) and [{Cd(L)2 (Cl)2 } ⋅ 2H2 O]α (2) (where L=N2 ,N6 -di(pyridin-4-yl)naphthalene-2,6-dicarboxamide). Crystal packing of 1 reveals the existence of channels running along the b- and c-axis filled by the ligated DMF and lattice anions, respectively. Whereas, crystal packing of 2 reveals that the metallacycles of each 1D chain are intercalating into the groove of adjacent metallacycles resulting in the stacking of 1D loop-chains to form a sheet-like architecture. In addition, both 1 and 2 were exploited as multifunctional materials for the detection of nitroaromatic compounds (NACs) as well as a catalyst in the ipso-hydroxylation of aryl/heteroarylboronic acids. Remarkably, 1 and 2 showed high fluorescence stability in an aqueous medium and displayed a maximum 88% and 97% quenching efficiency for 4-NPH, respectively among all the investigated NACs. The mechanistic investigation of NACs recognition suggested that the fluorescence quenching occurred via electron as well as energy transfer process. Furthermore, the ipso-hydroxylation of aryl/heteroarylboronic acids in presence of 1 and 2 gave up to 99% desired product yield within 15 min in our established protocol. In both cases, 1 and 2 are recyclable upto five cycles without any significant loss in their efficiency.

Tween-embedded microemulsions--physicochemical and spectroscopic analysis for antitubercular drugs.

The microemulsion composed of oleic acid, phosphate buffer, ethanol, and Tween (20, 40, 60, and 80) has been investigated in the presence of antitubercular drugs of extremely different solubilities, viz. isoniazid (INH), pyrazinamide (PZA), and rifampicin (RIF). The phase behavior showing the realm of existence of microemulsion has been delineated at constant surfactant/co-surfactant ratio (K (m) = 0.55) with maximum isotropic region resulting in the case of Tween 80. The changes in the microstructure of Tween 80-based microemulsion in the presence of anti-TB drugs have been established using conductivty (sigma) and viscosity (eta) behavior. The optical microscopic images of the system help in understanding the effect of dilution and presence of drug on the structure of microemulsion. Partition coefficient, particle size analysis, and spectroscopic studies (UV-visible, Fourier transform infrared, and 1H NMR) have been performed to evaluate the location of a drug in the colloidal formulation. To compare the release of RIF, PZA, and INH from Tween 80 formulation, the dissolution studies have been carried out. It shows that the release of drugs follow the order INH>PZA>RIF. The kinetics of the release of drug has been analyzed using the Korsmeyer and Peppas equation. The results have given a fair success to predict that the release of PZA and INH from Tween 80 microemulsion is non-Fickian, whereas RIF is found to follow a Fickian mechanism.

Facile solubilization of organochalcogen compounds in mixed micelle formation of binary and ternary cationic-nonionic surfactant mixtures.

This study investigated the water solubility enhancements of organochalcogen compounds, viz. bis(diphenylmethyl)diselenide [(C6H5)2CHSe]2 and 3,3'-dibromo-4,4'-dimethyl-2-dipyridyl diselenide [C12H10N2Se2Br2] in micellar media. Two cationic and one nonionic surfactants possessing the same hydrocarbon tail, namely hexadecyltrimethylammonium bromide (C16Br), hexadecyltrimethylammonium chloride (C16Cl), and polyoxyethylene(20)mono-n-hexadecyl ether (Brij 58), in their single as well as equimolar binary and ternary mixed states have been used. Solubilization capacity has been evaluated in terms of the molar solubilization ratio and the micelle water partition coefficients. The association constants between the solubilizate molecules and that of micelle and the average number of solubilizate molecules per micelle have also been quantified. The results showed that cationic surfactants exhibit less solubilization as compared to nonionic surfactant. The mixing effects of surfactants on micelle formation and solubilization efficiencies have also been discussed. It has been observed that cationic-nonionic binary combinations showed better solubilization capacity as compared to pure cationic, nonionic, or cationic-cationic binary mixtures. An equimolar cationic-cationic-nonionic ternary surfactant system provides higher solubilization than cationic-cationic but lowers than their cationic-nonionic counterpart. In addition, Fourier transform infrared has been employed with fair success to predict the information regarding the aggregates and the mechanism of docking of the surfactant and the chalcogenides in the system. The analysis has provided valuable information for the selection of mixed surfactants for solubilizing water-insoluble compounds. Certainly the solubilization ability of these surfactants is not simply related to molar capacity. The results give sufficient encouragement to warrant more detailed investigation of the features of surfactant properties that affect solubilization.

Mixed surfactant based microemulsions as vehicles for enhanced solubilization and synthesis of organoselenium compounds.

We exploited the added degree of compositional freedom provided by mixed AOT/lecithin surfactants in reverse isooctane microemulsion to demonstrate that a small amount of added lecithin significantly enhances the solubility of organodiselenides over that in AOT reverse isooctane microemulsions alone. Conductivity results show that the added lecithin significantly increases the solubility of four different organodiselenides and raises the temperature required to induce percolation. FTIR, (1)H NMR, and UV-visible techniques were utilized to gain insight into the interactions of organodiselenides, AOT and lecithin headgroups with water in the micellar core. The information obtained from these experiments was used to design a novel synthetic route for preparing 4-chloro-2-(naphthalen-2-ylselanyl) pyrimidine in reverse microemulsion.

UV-FIA: UV-induced fluoro-immunochemical assay for ultra-trace detection of PETN, RDX, and TNT.

Fluorescence quenching based immunoassay format for the detection of a trace amount of some nitro-explosives with a high degree of selectivity is reported in this study. The immunoassay comprises anti-explosive antibodies functionalized microtitre strips specific to the targeted explosives, pentaerythritol tetranitrate (PETN), 1,3,5-trinitroperhydro-1,3,5-triazine (RDX), and 2,4,6-trinitrotoluene (TNT). UV induced photolysis of nitro-explosive bound to targeted antibodies generates primarily nitrite ions which after the quick reaction with the detector molecule, 2,3-diaminonaphthalene (DAN), a fluorophore, quenches its fluorescence intensity, however, proportionately undergo cyclization to produce a highly fluorescent product, 2,3-naphthotriazole (NAT). The synthesized product, NAT, was verified using various chromatographic and spectrophotometric techniques. This newly developed antibody-based detection method, utilizing DAN dye, demonstrated a high selectivity towards PETN, RDX, and TNT. This method can be used as an economical testing kit for direct quantification of explosives, implying the great potential for quick, low-cost trace detection of explosives.

Trace detection of some nitro-explosives using thermal mediated immunochemical defragmented method.

A new immunoassay format using thermally induced defragmentation of some nitro-explosives with a high degree of selectivity is reported. Specific antibodies against three widely used explosives, 2,4,6-trinitrotoluene (TNT), 1,3,5-trinitroperhydro-1,3,5-triazine (RDX), and pentaerythritol tetranitrate (PETN) were generated by designing suitable haptens using geometry optimization modules. These in-house generated antibodies were used in a newly developed thermal mediated immunochemical biosensing technique which involves the binding of specific antibodies to respective nitro-explosives on a microtiter strip, resulting in the formation of specific immunocomplex. Heating the specific immuno-complex formed on microtiter wells resulted in thermal lysis of nitro-explosives to generate nitrite ions. These ions react with Griess reagent to form a colored chromophore which correlates the concentration of individual explosive in the sample. The present work fulfills the need for an improved explosive detecting system that is highly specific and capable of quickly determining the presence of nitrate containing explosives from a mixture pool.

An insight into the micellization of dodecyldimethylethylammonium bromide (DDAB) in the presence of bovine serum albumin (BSA).

In this work, we report the effect of concentration of bovine serum albumin (BSA) on the micellization of a cationic surfactant, dodecyldimethylethylammonium bromide (DDAB). Several samples covering a wide range of concentrations of protein and surfactant have been investigated. The interactions between the moieties are investigated by measuring fluorescence quenching of BSA molecules. The aggregation number of DDAB micelles is found to be small in the presence of BSA. The formation of DDAB-BSA complex is confirmed by FTIR. Absorbance spectroscopy indicates that at higher concentration, the conformational stability of BSA in DDAB is higher. The viscosity data for protein-surfactant systems confirm conformational changes in protein chains induced by the surfactant. The cmc values for DDAB increase with increasing concentration of BSA. At higher temperatures the micellization-complexation becomes enthalpy-dominated.

Self-assembly of cetylpyridinium chloride in water-DMF binary mixtures: a spectroscopic and physicochemical approach.

The aggregation behavior of cetylpyridinium chloride (CPyCl) in N,N-dimethylformamide (DMF)-water mixed solvents was investigated using electrical conductivity and spectroscopic techniques. Micellar and thermodynamic parameters (DeltaG(m)(0), DeltaH(m)(0), DeltaS(m)(0) and Delta(m)C(p)(0)) were obtained from the temperature dependence of critical micelle concentrations in various aqueous mixtures of DMF. The differences in the Gibbs energies of micellization of CPyCl between water and binary solvents were determined to evaluate the influence of the cosolvent. The effect of cosolvent on the Krafft temperature (K(T)) and on the aggregation number was also analyzed. Micellar micropolarity was examined spectrophotometrically using two different probes, methyl orange (MO) and methylene blue (MB), and was found to increase with DMF addition, accompanied by an enhanced solvation. The mechanism of docking of surfactant and the probe molecules in the system were obtained by using Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) spectroscopy.

Synthesis and capping of water-dispersed gold nanoparticles by an amino acid: bioconjugation and binding studies.

We report a novel strategy for the synthesis of aqueous stable, carboxylated gold nanoparticles (GNPs) by using glutamic acid as the reducing agent. The ratio of chloroaurate ions, AuCl(-)(4) to glutamic acid was optimized in the reaction medium to obtain monodispersed GNPs. Glutamic acid reduced gold nanoparticles were characterized by UV-visible, FTIR, dynamic light scattering and transmission electron microscopy, which demonstrated high stability in aqueous solution over a period of time indicating stabilization via surface-bound amino acid. Functionalized nanoparticles were conjugated with protein molecules through electrostatic attraction between the surface-terminated negatively charged carboxylate groups (COO(-)) of glutamic acid and the positively charged amino groups (NH(+)(3)) of the protein. The conjugation efficiency of the GNP:protein conjugates was confirmed qualitatively and quantitatively through gel electrophoresis and critical flocculation concentration analysis. The interaction between functionalized GNPs with protein molecules was investigated using fluorescence spectroscopy showing the fluorescence quenching of the tryptophan residues of protein molecules after conjugation. Circular dichroism (CD) studies of the conjugates confirmed that the protein undergoes a more flexible conformational state on the boundary surface of GNPs after conjugation. There was substantial conformational transition from alpha-helix to beta-sheet structure after conjugation of protein to GNPs.

Micellar behavior of aqueous solutions of dodecyldimethylethylammonium bromide, dodecyltrimethylammonium chloride and tetradecyltrimethylammonium chloride in the presence of alpha-, beta-, HPbeta- and gamma-cyclodextrins.

Conductivity, static fluorescence and (1)H NMR measurements have been carried out to study the micellar behavior of aqueous solutions of dodecyldimethylethylammonium bromide (DDAB), dodecyltrimethylammonium chloride (DTAC) and tetradecyltrimethylammonium chloride (TDAC) in absence and presence of alpha-cyclodextrin (alpha-CD), beta-cyclodextrin (beta-CD), hydroxypropyl-beta-cyclodextrin (HPbeta-CD) and gamma-cyclodextrin (gamma-CD). The conductivity measurements were carried out at 298.15 K. The influence of cyclodextrins on the micellar parameters, such as cmc* (apparent critical micellar concentration), beta (degree of ionization) have been analyzed. Thermodynamics of the systems was discussed in terms of the change in standard free energy of micellization, DeltaG(m)(0). Micellization was found to be less spontaneous in presence of cyclodextrins. The fluorescence intensity of the surfactant solutions is enhanced by the addition of cyclodextrins. The association constants obtained from conductivity and fluorescence data suggest the binding of gamma-CD with the surfactants to be strongest among all the cyclodextrins used. (1)H NMR chemical shift changes provide powerful means for probing the cyclodextrin-micellar interactions and inclusion of surfactant is shown by the change in the chemical shift of some of the guest and host protons in comparison with the chemical shifts of the same protons in the free compounds.

Toxicological responses of surfactant functionalized selenium nanoparticles: A quantitative multi-assay approach.

The utilization of selenium nanomaterials (Se Nps) in material and biological science is quickly growing, crafting an imperative need for toxicological evaluation of the exposure prospective and environmental consequences of Se Nps. The combination of quantitative multi-assay approach into environmental toxicological analysis has provided novel opportunities to build up effective markers and scrutinize the means of venomous nature of Se Nps in the current study. In the present work, we analyzed the toxicological effect of bare and surface functionalized Se Nps by using multi assay viz. seed germination studies as a function of concentration of SeNps and by using antifungal assays. The influence of SeNps on bacterial activities were also investigated by using the S. aureus, E. coli, P. aeruginosa and S. typhi bacterial strains as widespread marker species for antibacterial studies. The ocular assessment of chlorophyll content was maximum for Brij coated Se NPs (98%) as compared to bare (20%), SDS (45%) and CTAB (38%) coated SeNps. The existence of chromosomal aberrations in root meristems of A. cepa(A. cepa) with computed MI values of 16, 25, 33 and 52% for bare, CTAB, SDS and Brij coated particles has indicated the genotoxic effects of SeNps. The biocompatible nature of Brij coated Se Nps was observed from the faster mobility of DNA in gel electrophoresis studies. The investigational studies in the current work appraise the toxicity and measure the competence of obtained data to characterize possibilities of probable threats, prominence of data requirement and breaches that must be filled to diminish the ambiguities about the safe use of Se Nps.

Chemical Sensing Applications of ZnO Nanomaterials.

Recent advancement in nanoscience and nanotechnology has witnessed numerous triumphs of zinc oxide (ZnO) nanomaterials due to their various exotic and multifunctional properties and wide applications. As a remarkable and functional material, ZnO has attracted extensive scientific and technological attention, as it combines different properties such as high specific surface area, biocompatibility, electrochemical activities, chemical and photochemical stability, high-electron communicating features, non-toxicity, ease of syntheses, and so on. Because of its various interesting properties, ZnO nanomaterials have been used for various applications ranging from electronics to optoelectronics, sensing to biomedical and environmental applications. Further, due to the high electrochemical activities and electron communication features, ZnO nanomaterials are considered as excellent candidates for electrochemical sensors. The present review meticulously introduces the current advancements of ZnO nanomaterial-based chemical sensors. Various operational factors such as the effect of size, morphologies, compositions and their respective working mechanisms along with the selectivity, sensitivity, detection limit, stability, etc., are discussed in this article.

Analysis of Tween based microemulsion in the presence of TB drug rifampicin.

The purpose of present study was to formulate microemulsion composed of oleic acid+phosphate buffer (PB)+Tween 80+ethanol and to investigate its potential as drug delivery system for an antitubercular drug rifampicin. The pseudo-ternary phase diagram has been delineated at constant surfactant/cosurfactant ratio (K(m) 0.55). Conductivity (sigma) and viscosity (keta) studies with variation in Phi (weight fraction of aqueous phase) and omega (molar concentration ratio) show the occurrence of structural changes from water-in-oil (w/o) microemulsion to oil-in-water (o/w). Along with the solubility and partition studies of rifampicin in microemulsion components, the changes in the microstructure of the microemulsion after incorporation of drug have been evaluated using pH, sigma and keta studies. The results have shown that the microemulsion remained stable after the incorporation of rifampicin (in terms of optical texture and phase separation). In addition, the particle size analysis indicates that the microemulsion changes into o/w emulsion at infinite dilution. Dissolution studies infer that a controlled release of rifampicin is expected from o/w emulsion droplet.

Behavior of acetyl modified amino acids in reverse micelles: a non-invasive and physiochemical approach.

The well-characterized, monodisperse nature of reverse micelles formed by sodium bis-(2-ethylhexyl)sulfosuccinate/water/isooctane and their usefulness in assimilating compounds of varied interests have been exploited to investigate the effect of acetyl modified amino acids (MAA) viz., N-acetyl-L-glycine (NAG), N-acetyl-L-aspartic acid (NAA) and N-acetyl-L-cysteine (NAC), on the water pool and physiochemical properties. Non-invasive techniques such as FTIR and UV-vis absorption spectroscopy have been employed to analyze the interactions of MAA with core water and the AOT headgroup. The micropolarities on both sides of AOT interface have further been investigated by UV-vis absorption probes, methyl orange (MO) and methylene blue (MB). The dynamics of water and temperature induced percolation process have also been studied. The MAA molecules have been found to assist the process with the increase in water content where as a contrary behavior has been observed with the increase in temperature. Conductivity results have been further rationalized in terms of scaling equations, which delineate the dynamic nature of the percolation process. The results have also been analyzed in the light of activation energy of the percolation process and thermodynamics of droplet clustering.

Facile synthesis, structural evaluation, antimicrobial activity and synergistic effects of novel imidazo[1,2-a]pyridine based organoselenium compounds.

A simple and efficient method has been described to synthesize the hitherto unknown imidazo[1,2-a]pyridine selenides (5a-l) by reaction of 2-chloroimidazo [1,2-a]pyridines with aryl/heteroaryl selenols, generated in situ by reduction of various diselenides with hypophosphorous acid. The crystal structures of 3-nitro-2-(phenylselanyl)-imidazo[1,2-a]pyridine (5a), 2-(mesitylselanyl)-3-nitro-imidazo[1,2-a]pyridine (5d) and 3-nitro-2-(pyridin-2-ylselanyl)-imidazo[1,2-a]pyridine (5e) were confirmed by X-ray crystallography and the DFT calculations were performed to determine various structural parameters which were correlated with the X-ray crystal structures. The synthesized compounds were subjected to antimicrobial evaluation and it was found that compounds 5a and 5j were active against gram negative bacterium Escherichia coli whereas compound 5e was active against different fungal strains. Time kill assay was performed to understand the microbial activity of synthesized organoselenium compounds and the toxicity of these compounds was evaluated against human cell lines. Synergistic effects of active compounds 5a and 5e were tested with existing antibiotic drugs which exhibited that the antibiotic combination with synthesized organoselenium compounds efficiently enhanced the antimicrobial activity.

On the temperature percolation in a w/o microemulsion in the presence of organic derivatives of chalcogens.

The course of temperature percolation in a w/o microemulsion system comprising water/bis(2-ethylhexyl) sulfosuccinate sodium, AOT/isooctane affected by the presence of additives has been investigated. Additives, viz., organic derivatives of chalcogens including dipyridyl diselenide (Py2Se2), diphenyl diselenide (Ph2Se2), and dipyridyl ditelluride (Py2Te2), have been assimilated in the reverse micellar system. Formulations have been studied in terms of (i) the concentration variation of additives, (ii) the change in omega (= [H2O]/[AOT]), and (iii) the change in the nonpolar continuum, S (= [oil]/[AOT]). Phenyl derivatives hinder the percolation, whereas the pyridyl derivative in moderate amounts favors the phenomenon. The estimated values of the critical exponents are lower than those predicted by the dynamic percolation theory. The association model has been implemented to access the thermodynamic parameters of droplet clustering. Pyridyl compounds are expected to alter the rigidity of the surfactant monolayer, which could help to promote the attractive interdroplet interaction. FT-IR spectroscopy has been used to elucidate the changes occurring in the core water in the presence of organic derivatives of chalcogens as the droplet size is increased. Results have been rationalized in terms of the alteration in the physicochemical behavior of the water/AOT/isooctane microemulsion in the presence of additives.