Synthesis, characterisation, and DC conductivity of polyaniline-lead oxide composites

The polyaniline-PbO composites of various mass fractions were prepared by in situ polymerisation. The prepared samples were characterised by FTIR, and the dominant peaks confirmed the formation of polyaniline-PbO composites. The SEM study shows a granular agglomerated morphology, and increases with an increase in the lead oxide mass % in polyaniline. Direct current (DC) conductivity (σ _DC) was studied as a function of temperature (T). From these studies, it was found that conductivity increased at higher temperatures due to the polarons hopping from one localised state to another. DSC studies reveal, the decrease in peak temperature from 273°C (pure PANI) to 169.2°C, 193.5°C, 218.4°C, 235.2°C, and 224.2°C, respectively for the various mass fractions (10 %, 30 %, 20 %, 40 %, and 50 %) of polyaniline-PbO composites.     

Influence of additives on the clouding behavior of amphiphilic drug solutions

The present work focuses on the clouding phenomenon in an amphiphilic drug [amitriptyline (AMT), which is a tricyclic antidepressant] solution. A 50-mM AMT solution prepared in 10 mM of sodium phosphate (SP) buffer was taken where the cloud point (CP) was found to decrease with increasing pH. The same CP decreasing trend (with pH increase) followed in the presence of a fixed concentration (50 mM) of added salts [NaBr, and tetra-n-butylammonium bromide (TBuAB)]. The addition of increasing amounts of quaternary bromides (tetramethylammonium bromide, tetraethylammonium bromide, tetra-n-propylammonium bromide, TBuAB, and tetra-n-pentylammonium bromide) to 50 mM of AMT solution (prepared in 10 mM of SP buffer) caused continuous increase in CP, which was found to be dependent upon the alkyl chain length of that particular salt. The similar type of CP increase was also observed in the presence of conventional (cetyltrimethylammonium bromide and tetradecyltrimethylammonium bromide) and gemini surfactants [bis(hexadecyldimethylammonium)hexane, bis(hexadecyldimethylammonium)pentane, and bis(hexadecyldimethylammonium)butane]. The overall behavior was discussed in terms of electrostatic interactions, micellar growth, and mixed micelle formation.     

Synthesis and characterization of new synthetic oxygen carriers. A kinetic study of the reaction of the binuclear iron(III)–copper(II) complex with H<Subscript>2</Subscript>O<Subscript>2</Subscript>

New oxygen carriers have been synthesized by the interaction of the Cu^II/Ni^II derivative of the bis(5-nitroindazolyl)methane complex with 14-membered 1,8-dihydro-1,3,6,8,10,13-hexaazacyclotetradecane (M-mac), where M=Fe^III, Ni^II, Co^II, to yield binuclear complexes. These complexes have been characterized by physico-chemical methods: elemental analysis, i.r., ¹H-n.m.r., ¹³C-n.m.r., 2D cosy n.m.r., e.p.r., u.v.–vis. spectroscopy and cyclic voltammetry. A representative binuclear Fe^III–Cu^II complex was chosen to interact with H₂O₂ to elucidate the mechanistic pathway of oxygen binding in solution spectrophotometrically, and also by cyclic voltammetry. Hydrogen peroxide exhibits two mechanisms for binding, either (i) homolysis or (ii) heterolytic cleavage. The mode of H₂O₂ binding can be hazardous in (i) due to the threat of oxidative damage to the cellular structure, proteins and metabolites, or eco-friendly as in (ii) which produces innocuous products such as water and dioxygen. This study aims to combat the problems associated with H₂O₂ binding in nature by producing a parallel study on model compounds.     

On Jordan Triple Higher Derivable Mappings on Rings

Let R be a ring and \({\mathbb{N}}\) be the set of all non-negative integers. A family of maps \({D=\{d_n\}_{n \in\mathbb{N}}}\) is said to be Jordan triple higher derivable if \({d_n(aba)=\sum \nolimits_{p+q+r=n} d_p(a)d_q(b)d_r(a)}\) holds for all \({a,b \in R}\), where d ₀ = I _R , (the identity map on R). In this paper, we determine Jordan triple higher derivable map on a ring R, which contains a nontrivial idempotent which is automatically additive. An immediate application of our main result shows that every Jordan triple higher derivable map becomes higher derivation on R.     

Novel Pyrazoline‐based Organometallic Compounds Containing Ferrocenyl and Quinoline units: Synthesis,Characterization and Microbial susceptibilities

Some novel pyrazoline‐based organometallic compounds were synthesized as new leads in antimicrobial chemotherapy. The structures of compounds were elucidated by different spectroscopic techniques and elemental analyses. All compounds were investigated for in vitro antimicrobial studies against fifteen ATTC bacterial and fungal strains. The microbial susceptibility of these compounds revealed that all the tested compounds gave good minimum inhibitory concentration (MIC) values against the tested organisms that are either similar or even better than the reference drugs amoxicillin and fluconazole, which gave MIC values 8‐64 μg/ml against bacterial and 64 μg/ml against fungal strains, respectively. Among all compounds, compound ( 4d ) 1‐(5‐(4‐chlorophenyl)‐3‐ferrocenyl‐4,5‐dihydropyrazol‐1‐yl)‐2‐quinolin‐8‐yloxy) ethanone, emerged out the most promising antimicrobial organometallic derivative with MIC values against all the strains ranging from 8‐32 μg/ml. Other compounds gave a range of MIC values between 16‐64 μg/ml against S. bovis, 16‐32 μg/ml against E. coli, and C. tropicalis except compound ( 4d) which gave MIC 8 μg/ml against S. bovis and E. coli, whereas 32 μg/ml against C. tropicalis. Collectively, these compounds gave a lower MIC value between 32‐64 μg/ml against both of the biofilm forming strains namely, P. aeruginosa and S. mutans. The results of microbial susceptibility concluded that these novel organometallic compounds are new leads in antimicrobial chemotherapy and can be very useful for further optimization work on microbial chemotherapy.     

Spectroscopic Physicochemical and Photophysical Investigation of Biologically Active 2-oxo-quinoline-3-carbonitrile Derivative

4-(2,3,4-trimethoxyphenyl)-8-methoxy-2-oxo-1,2,5,6 tetrahydrobenzo [h] quinoline-3-carbonitrile (TMTQ) dye was synthesized by one-pot multicomponent reactions (MCRs) of 2,3,4 trimethoxybenzaldehyd, ethyl cyanoacetate, 6-methoxy-1,2,3,4-tetrahydro-naphthalin-1-one and ammonium acetate under microwave irradiation. The structures of the synthesized compound was established by spectroscopic (FT-IR, ¹H–NMR, ¹³C–NMR, EI-MS) and elemental analysis. In addition, spectroscopic and physicochemical parameters, including electronic absorption, excitation coefficient, Stokes shift, oscillator strength, transition dipole moment and fluorescence quantum yield have investigated in order to explore the analytical potential of synthesized compounds. TMTQ dye undergoes solubilization in different micelles and may be used as a probe and quencher to determine the critical micelle concentration (CMC) of CTAB and SDS. In addition we extent of TMTQ anti-bacterial properties TMTQ was first tested in vitro by the disk diffusion assay against two Gram-positive and two Gram-negative bacteria, and then the minimum inhibitory concentration (MIC) was determined with the reference of standard drug Tetracycline.     

Hierarchical Equations of Motion Simulation of Temperature‐Dependent Two‐Dimensional Electronic Spectroscopy of the Chlorophyll a Manifold in LHCII

We simulated two‐dimensional electronic spectra (2DES) of the chlorophyll a manifold of light‐harvesting complex II (LHCII) at various temperatures (77, 110, 150, 190, 230, 273, and 293 K) using the hierarchical equations of the motion‐phase matching approach. We confirm the main excitation energy transfer pathways assignments within the chlorophyll a manifold of LHCII measured in a recent work (J. Phys. Chem. B 2019, 123, 6765–6775). The calculated transfer rates are also in general agreement with the measured rates. We also provided theoretical confirmation for the experimental assignments, as uphill and downhill energy transfer processes, of 2D spectral features that were reported in recent experimental reports. These temperature‐dependent features were also ascertained to follow the detailed‐balance principle.     

A Comprehensive Outlook of Synthetic Strategies and Applications of Redox‐Responsive Nanogels in Drug Delivery

Increasing recognition of the role of oxidative stress in the pathogenesis of many clinical conditions and the existence of defined redox potential in healthy tissues has led to extensive research in the development of redox‐responsive materials for biomedical applications. Especially, considerable growth has been seen in the fabrication of polymeric nanogel–based drug delivery carriers utilizing redox‐responsive cross‐linkers bearing a variety of functional groups via various synthetic strategies. Redox‐responsive polymeric nanogels provide an advantage of facile chemical modification post synthesis and exhibit a remarkable response to biological redox stimuli. Due to the interdisciplinary nature of the subject, a more profound combined conceptual knowledge from a chemical and biological point of view is imperative for the rational design of redox‐responsive nanogels. The present review provides an insight into the design and fabrication of redox‐responsive nanogels with particular emphasis on synthetic strategies utilized for the development of redox‐responsive cross‐linkers, polymerization techniques being followed for nanogel development and biomedical applications. Cooperative effect of redox trigger with other stimuli such as pH and temperature in the evolution of dual and triple stimuli‐responsive nanogels is also discussed.     

Poly (3,4‐ethylenedioxythiophene) γ‐Fe2O3 polymer composite–super paramagnetic behavior and variable range hopping 1D conduction mechanism–synthesis and characterization

The present paper reports the preparation of poly (3,4‐ethylenedioxythiophene) (PEDOT) ferrimagnetic conducting polymer composite by incorporation of ferrite particles in the polymer matrix by emulsion polymerization. Synthesis of PEDOT–γ‐Fe₂O₃ composite was carried out by chemical oxidative polymerization of EDOT with ferrite particles in the presence of dodecylbenzenesulfonic acid (DBSA) that works as dopant as well as surfactant in aqueous medium. The resulting conducting composite possesses saturation magnetization (Ms) value of 20.56 emu/g with a conductivity of 0.4 Scm^?1, which was determined by VSM and four probe technique, respectively. B‐H curve reveals that ferrimagnetic particles of γ‐Fe₂O₃ show super‐paramagnetic behavior at room temperature which was also observed in PEDOT–γ‐Fe₂O₃ composite. The resulting conducting ferrimagnetic composite shows microwave absorption loss of 18.7–22.8 dB in the frequency range of 12.4–18 GHz. Thermogravimetric analysis of the composite revealed that the composite is thermally stable up to 230°C. The characterization of the PEDOT–γ‐Fe₂O₃ composite was carried out using XRD and FTIR spectroscopy. Copyright © 2007 John Wiley & Sons, Ltd.     

Brownian dynamics simulations of polyelectrolyte adsorption in shear flow with hydrodynamic interaction

The adsorption of single polyelectrolyte molecules in shear flow is studied using Brownian dynamics simulations with hydrodynamic interaction (HI). Simulations are performed with bead-rod and bead-spring chains, and electrostatic interactions are incorporated through a screened Coulombic potential with excluded volume accounted for by the repulsive part of a Lennard-Jones potential. A correction to the Rotne-Prager-Yamakawa tensor is derived that accounts for the presence of a planar wall. The simulations show that migration away from an uncharged wall, which is due to bead-wall HI, is enhanced by increases in the strength of flow and intrachain electrostatic repulsion, consistent with kinetic theory predictions. When the wall and polyelectrolyte are oppositely charged, chain behavior depends on the strength of electrostatic screening. For strong screening, chains get depleted from a region close to the wall and the thickness of this depletion layer scales as N(1/3)Wi(2/3) at high Wi, where N is the chain length and Wi is the Weissenberg number. At intermediate screening, bead-wall electrostatic attraction competes with bead-wall HI, and it is found that there is a critical Weissenberg number for desorption which scales as N(-1/2)kappa(-3)(l(B)|sigmaq|)(3/2), where kappa is the inverse screening length, l(B) is the Bjerrum length, sigma is the surface charge density, and q is the bead charge. When the screening is weak, adsorbed chains are observed to align in the vorticity direction at low shear rates due to the effects of repulsive intramolecular interactions. At higher shear rates, the chains align in the flow direction. The simulation method and results of this work are expected to be useful for a number of applications in biophysics and materials science in which polyelectrolyte adsorption plays a key role.