ORGANIC SYNTHESIS AND CHARACTERIZATION OF ELECTRICALLY CONDUCTING POLY (o-TOLUIDINE) DOPED WITH ORGANIC ACID

Abstract. Poly(o-toluidine) doped with acrylic acid and without it was synthesized by using chemical oxidative polymerization technique. With the help of this method the polymer, poly(o-toluidine) was synthesized in the form of emeraldine salt. The oxidizing agent used for this method is the ammonium persulphate .The polymer products were characterized by UV-Visible and FTIR spectroscopy. The polymer, poly(o-toluidine) doped with acrylic acid was highly soluble in common organic solvents like m-cresol, NMP, DMF etc. The FTIR studies demonstrate that the acrylic acid doped poly(o-toluidine) shows broad and intense band at 3250-3000 cm -1 and 1160-1100 cm -1 account for the higher degree of doping. These results are well supported by conductivity measurements

Synthesis and evaluation of analgesic, anti-asthmatic activity of (E)-1-(8-hydroxyquinolin-7-yl)-3-phenylprop-2-en-1 ones

Abstract Seventeen (E)-1-(8-hydroxyquinolin-7-yl)-3-phenylprop-2-en-1 one derivatives were synthesized via aldol condensation of substituted benzaldehydes with quinoline chalcones starting from 8-hydroxy quinoline. Molecular docking studies were performed on COX-2 protein for analgesic activity and PDE 4 enzyme for anti-asthmatic activity. Docking studies for analgesic activity reveal that the compounds 2 , 4 , 12 , 14 , and 15 showed significant interaction in terms of hydrogen bonding, hydrophobic attachment and van der Waal interaction with COX-2. The docking studies and pharmacological screening indicate that substitution of hydroxyl and conjugated ketone groups on the aldehyde ring and the quinoline ring accelerates analgesia with better binding to active site. Eddy's hot plate method was used to evaluate analgesic activity of the synthesized compounds. Compounds showed a substantial increase in reaction time when compared with standard pentazocin. Compounds 2 , 4 , 7 , 9 and 13 showed significant binding interactions with PDE 4 enzyme and hence were selected for evaluation of anti-asthmatic activity using the goat tracheal chain method. Studies reveal that substitution of the methoxy group at 4th & 5th positions for compounds 2 , 4 & 7 leads to significant percentage inhibition of histamine induced contraction. The synthesized compounds are thus found to be potent as analgesic and anti-asthmatic agents

hemia_200

Abstract. Polydiphenylamine (PDPA) doped with acrylic acid was synthesized by oxidative chemical polymerization. This is a new chemical polymerization method developed for the direct synthesis of emeraldine salt form of polydiphenylamine which exhibits remarkably improved solubility in a common organic solvent. These polymers have been characterized by the physical techniques such as UV-visible, FTIR, XRD and conductivity measurement. The results are discussed with reference to the H 2 SO 4 doped polydiphenylamine. The use of functionalized acrylic acid (AA) made it possible to obtain the polymer in doped state with enhanced solubility in organic solvent such as N-methyl pyrrolidinone (NMP) and m-cresol directly without converting to emeraldine base form. The UV-visible spectra of acrylic acid doped PDPA in m-cresol showed a free carrier tail commencing at 950 nm, which may be attributed to secondary doping due to extended coil conformation. Whereas in NMP spectra excitonic peak at ~ 320 nm and 610 nm typical for emeraldine base form indicates that NMP dose hinders the doping ability of dopant. The FTIR spectra shows a broad and intense band at ~ 3400 cm -1 and 1150-1050 cm -1 in acrylic acid doped PDPA account for the higher doping level than H 2 SO 4 doped polydiphenylamine polymers. This is further manifested by the X-ray studies and conductivity measurement. The X-ray diffractograms of acrylic acid doped polymer show an enhancement in the crystallinity indicating better ordered chain alignment. These results are well supported by the conductivity measurements, where the conductivity of acrylic acid doped polymers is greater than that of H 2 SO 4 doped polymers

Ultrasound assisted N-bromosuccinimde catalyzed one pot condensation approach for synthesis of Bis(indolyl)methanes from primary alcohols

A simple, efficient protocol for one pot synthesis of bis(indolyl)methanes from primary alcohols is investigated with N-bromosuccinimde as a catalyst under ultrasound irradiation. Alcohols can be converted into carbonyl compounds by removal of hydrogen in presence of N-bromosuccinimde as an oxidant and can react in situ with indole to give desired bis(indolyl)methanes. In the reported one pot multicomponent condensation reaction N-bromosuccinimde promotes the oxidation of alcohol to aldehyde, facilitating the subsequent condensation with indole to afford bis(indolyl) methanes in good to excellent yields. The inexpensiveness and easy handling are some of important feature of N-bromosuccinimde. The by-product N-succinimide can be easily recovered and recycled to N-bromosuccinimide

Polyindole-ZnO Nanocomposite: Synthesis, Characterization and Heterogeneous Catalyst for the 3,4-Dihydropyrimidinone Synthesis under Solvent-free Conditions

<div><p>A Polyindole-ZnO nanocomposite particle was synthesized by using a chemical oxidative polymerization method. Synthesized nanocomposite was characterized by UV-Visible, FTIR, SEM, XRD, EDAX and electrical conductivity measurements. The band at ∼3400 cm⁻¹ and 735 cm⁻¹ in FTIR spectra confirmed the polyindole formation. XRD spectral studies exhibits major diffraction in between 30–40° (2θ) indicates the partial crystalline nature of the polyindole-ZnO nanocomposite. SEM image reveals agglomerated granular particulate nature with ZnO embedded in the polyindole matrix. The application of Polyindole-ZnO nanocomposite as a polymer-supported catalyst was studied for the synthesis of one pot multicomponent Biginelli condensation.</p> </div