Syntheses of New Unsymmetrical 2,5‐Disubstituted‐1,3,4‐oxadiazoles and 1,2,4‐Triazolo[3,4‐b]‐1,3,4‐thiadiazoles Bearing Thieno[2,3‐c]pyrazolo Moiety

New series of (thieno[2,3‐c]pyrazolo‐5‐yl)‐[1,2,4]triazolo[3,4‐b][1,3,4]thiadiazoles 10a , 10b , 10c and (thieno[2,3‐c]pyrazol‐5‐yl)‐1,3,4‐oxadiazol‐3(2H)‐yl)ethanones 6a , 6b , 6c has been synthesized from thieno[2,3‐c]pyrazole‐5‐carbohydrazide 3 by multistep reaction sequence. (5‐Aryl‐1,3,4‐oxadiazol‐2‐yl)‐1H‐thieno[2,3‐c]pyrazoles 4a , 4b , 4c were also synthesized from thieno[2,3‐c]pyrazole‐5‐carbohydrazide 3 by cyclization with various aromatic carboxylic acids. The hydrazide 3 was obtained by reaction of thieno[2,3‐c]pyrazole‐5‐carboxylate 2 with hydrazine hydrate in good yield, and compound 2 was obtained by the reaction of 5‐chloro‐3‐methyl‐1‐phenyl‐1H‐pyrazole‐4‐carbaldehyde 1 and 2‐ethyl thioglycolate in presence of sodium alcoholate in good yield.     

New Synthesis and Reactions of Ethyl 5‐amino‐4‐cyano‐1‐phenyl‐1H‐pyrazole‐3‐carboxylate

Synthesis of ethyl 5‐amino‐4‐cyano‐1‐phenyl‐1H‐pyrazole‐3‐carboxylate 5 has been achieved via abnormal Beckmann rearrangement of o‐chloroaldehyde 1 . Reaction of o‐aminocarbonitrile 5 with concentrated H₂SO₄ furnished expected o‐aminocarboxamide pyrazole 6 . Key intermediates o‐aminocarbonitrile 5 and o‐aminocarboxamide 6 were successfully utilized for the synthesis of pyrazolopyrimidine derivatives. The replacement of Cl in o‐chlorocarbonitrile 3 with secondary amine furnished new synthon 13 , which was further used for the synthesis of polysubstituted heterocycles. The obtained new products were well characterized by IR, ¹H and ¹³C NMR, and mass spectra.     

Spectroscopy of Charge Transfer Complexes of Aniline Blue

Charge transfer (CT) complexes of aniline blue (AB) were prepared with standard organic acceptors such as TCNQ, TCNE, DDQ, and chloranil and studied with UV-VIS-NIR spectra showing σ→π* and π→π* transitions along with free-carrier absorption due to scattering of light particles which has been found involving phonon–photon, electron–photon, and electron–electron scattering. Infrared spectra contain half power beta density due to hopping conduction and an asymmetric band corresponding to A(k) = A₀k exp(?bk) as absorption associated with diffraction of IR light from the crystalline particles.     

FTIR and thermal studies on gel grown neodymium tartrate crystals

The growth of neodymium tartrate crystals was achieved in silica gel by single diffusion method. Optimum conditions were established for the growth of good quality crystals. Fourier transform infrared (FT-IR) spectroscopic study indicates the presence of water molecules and tartrate ligands and suggests that tartrate ions are doubly ionised. The thermal behaviour of the material was studied using thermogravimetry (TG), differential thermal analysis (DTA), derivative thermogravimetry (DTG) and differential scanning calorimetry (DSC). Thermogravimetric analysis support the suggested chemical formula of the grown crystal to be Nd₂(C₄H₄O₆)₃·7H₂O, and the presence of seven water molecules as water of hydration. It is shown that the material is thermally stable up 45 °C beyond which it decomposes through many stages till the formation of neodymium oxide (Nd₂O₃) at 995 °C. The decomposition pattern is reported to be typical of a hydrated metal tartrate.     

Polyaniline thin film optical waveguides for integrated optics and VLSI prepared by vacuum evaporation technique

Polyaniline is emerging as an important polymer material which offers challenging opportunities for both fundamental research and new technological applications in waveguides. Metal doped polyaniline has been prepared initially in the form of powder by a solution growth technique. The emeraldine salt with doped metal was also prepared by solution growth technique. This powder was used for vacuum evaporation on optically flat glass substrate. The dark green doped (Fe, Al) polyaniline thin films were prepared by vacuum evaporation technique (10^?4 torr). Deposited waveguide thin films have been characterized structurally, using X‐ray diffraction (XRD), optically etc. Effective refractive index of the thin film waveguide was also calculated theoretically and experimentally. Waveguide parameters, namely refractive index, propagation loss and depth of vacuum deposited polyaniline thin films optical waveguide have been determined. The optical spectra and structure and waveguide parameters of vacuum deposited polyaniline thin films are strongly affected by the type of doping. It is possible to reduce the losses by addition of Fe to the vacuum deposited polyanine thin film and modify the effective refractive index (O_eff) according to particular requirements. Results are compared with the results in the literature. Copyright © 2002 John Wiley & Sons, Ltd.     

Morphology of PbI2 Crystals Grown by Gel Method

The single crystals of Lead Iodide have been grown by gel method. X‐ray diffraction studies on these crystals shows that the lattice parameters of grown crystals are almost matching with reported values. The results of detailed studies made on the microstructures of Lead Iodide crystals, have been described. The observations of the faces of these crystals revealed that they have grown by layer as well as spiral mechanisms. The probable role of these parameters is explained along with the surface microstructures on these various shaped crystals.     

Study of transport properties co – evaporated lead telluride (PbTe) thin films

Thin films of lead telluride (PbTe) of thicknesses ranging from 1000 Å to 2500 Å have been prepared by co‐evaporation (three temperature) technique, onto precleaned amorphous glass substrates at various temperatures. The deposited samples were annealed and annealed samples were used for characterization. Resistivity of these samples was measured by four‐probe technique as a function of thickness and temperature. Activation energy for charge transport have been evaluated and found in the range of 0.09 to 0.106 eV. Thermoelectric power has been measured and found to be positive indicating that the samples are p‐type semiconducting material. Mobility variation with temperature has been estimated (evaluated) and correlated with scattering mechanism in the entire range of temperature studied. The X‐ray diffraction analysis confirmed that films are polycrystalline having cubic structure cell and lattice parameters are reported.     

Synthesis of Poly(N-ethylaniline) Nanoparticles Synthesis and Characterization of Organically Soluble Conducting Poly(N-ethylaniline) Nanoparticles using Acrylic Acid as a Soft Template

In this paper, we report the synthesis of poly(N-ethylaniline) (PNETA) by using tartaric acid (TA) as an organic acid dopant by aqueous polymerization method of N-ethylaniline using ammonium per sulphate (APS) as an oxidant and acrylic acid (AA) as a soft template. This is a new polymerization method for the direct synthesis of the emeraldine salt form of poly(N-ethylaniline) in bulk quantity, which is soluble in organic solvents such as m-cresol and N-methyl pyrrolidinone. The prepared polymers were characterized by UV, FTIR, XRD, TGA, SEM and conductivity measurement studies. The results are discussed with reference to HCl doped poly(N-ethylaniline). It is observed that PNETA/TA/AA polymer is comparatively more soluble in m-cresol than that doped with HCl in its salt form. The formation of emeraldine salt phase and dopping process was confirmed by FTIR and UV-Vis spectroscropy. We demonstrate the effect of organic dopant on the morphology and conductivity of the PNETA. It was found that, PNETA doped with TA synthesized using acrylic acid (AA) as a soft template display higher doping level, crystallinity and solubility in common organic solvent. On the contrary, HCl doped polymer was lowered at doping level and amorphous in nature which reflects the role of organic dopant and soft template. X-ray diffraction studies indicate that the PNETA/TA/AA doped samples exhibit higher crystallinity, which indicates enhanced polymer sub-chain alignment as compared to HCl doped polymer. This is also manifested by the FTIR studies. SEM result also revealed the continuous morphology and sub-micrometer size, evenly distributed particles of the PNETA/TA/AA doped polymer.