A Brief Review on Fluorescent Copper Sensor Based on Conjugated Organic Dyes

The design and development of the fluorescence reporting molecules for the trace recognition of the metallic ions in the aqueous, mixed organic aqueous media, environmental specimen, living things e.g., body fluids, serum, urine etc is the evergreen research area. Among several methodologies utilized for these purposes, the fluorescent techniques have wonderful impact in the era of metal sensor development due to their acclamatory features of non-invasive detection process and appreciable sensitivity. The utilization of small organic molecules for the sensation of metallic ions through the fluorescent techniques harvested the wonderful results having some interesting features of chromogenic response on metal binding, robustness in the preparation and applicability to establish the metallic accumulation level inside the live cells via bioimaging studies. The detailed knowledge and background about the several reported chemosening strategies have the utmost importance in order to understand or to design the novel molecules for metal sensing purposes. The objective of the presents review was to compile the best ever used copper sensing strategies via fluorescent means in the running decade. We have summarized the values of optical positions of the spectral lines, spectral shifting upon metal binding, binding/association/dissociation constants, chromogenic changes in the reaction mixture, proposed complexation mechanism of the ligand with the copper, ligand sensitivities toward the copper recognition, binding stoichiometries and the detailed bioimaging results where applicable.     

Nanoparticulate cerium dioxide and cerium dioxide-titanium dioxide composite thin films on glass by aerosol assisted chemical vapour deposition

Two series of composite thin films were deposited on glass by aerosol assisted chemical vapour deposition (AACVD)—nanoparticulate cerium dioxide and nanoparticulate cerium dioxide embedded in a titanium dioxide matrix. The films were analysed by a range of techniques including UV-visible absorption spectroscopy, X-ray diffraction, scanning electron microscopy and energy dispersive analysis by X-rays. The AACVD prepared films showed the functional properties of photocatalysis and super-hydrophilicity. The CeO₂ nanoparticle thin films displaying photocatalysis and photo-induced hydrophilicity almost comparable to that of anatase titania.     

The design and construction of a VUV Ar-arc source and a VUV monochromator

The design and construction of a VUV source and a VUV monochromator is reported. The reliability of the VUV source suggests that it can be used as a VUV high radiance transfer secondary standard. A VUV window is used to isolate the high pressure argon-arc source from the VUV monochromator. The spectrum is therefore limited by the transmission cut-off of the window. Alternatively, a differential pump could be used to extend the wavelength range to the extreme UV and eliminate the uncertainties associated with the aging effects of the VUV window. The apparatus is to be used to measure the VUV spectra of certain glass samples.We wish to acknowledge the financial support by SERC under research grant number GR/E 01973.     

Dimensionality estimate of the manifold in chemical composition space for a turbulent premixed H2 + air flame

The dimensionality ( ) of manifolds of active chemical composition space has been measured using three different approaches: the Hausdorff geometrical binning method, Principal Component Analysis, and the Grassberger‐Procaccia cumulative distribution method. A series of artificial manifolds is also generated using a Monte Carlo approach to discern the advantages and limitations of the three methods. Dimensionality is quantified for different levels of turbulent intensity in a simulation of the interactions of a 2D premixed hydrogen flame with a localized region of turbulence superimposed over the cold region upstream of the flame front. The simulations are conducted using an adaptive mesh refinement code for low Mach number reacting flows. By treating the N_s species and temperature of the local thermo‐chemical state as a point in multidimensional chemical composition space, a snapshot of a flame region is mapped into chemical composition space to generate the manifold associated with the 2‐D flame system. An increase in was observed with increasing turbulent intensity for all three methods. Although each method provides useful information, the Grassberger‐Procaccia method is subject to fewer artifacts than the other two thereby providing the most reliable quantification of . © 2004 Wiley Periodicals, Inc. Int J Chem Kinet 36: 326–336, 2004     

Tetracyclic triterpenoids from the leaves of Azadirachta indica and their insecticidal activities

A new tetranortriterpenoid, meliatetraolenone [24,25,26,27-tetranor-apotirucalla-(apoeupha)-6alpha-O-methyl, 7alpha-senecioyl(7-deacetyl)-11alpha,12alpha,21,23-tetrahydroxy-21,23-epoxy-2,14,20(22)-trien-1,16-dione] (1) was isolated from the methanolic extract of fresh leaves of Azadirachta indica along with the known compound odoratone (3) which was hitherto unreported from this source. Their structures have been elucidated by spectral studies including 2D NMR. The insecticidal activities of 1 as well as those of odoratone (3) are reported. 1 and odoratone both showed mortality on fourth instar larvae of mosquitoes (Anopheles stephensi) with LC(50) values of 16 and 154 ppm, respectively.     

Phonetographic profiles and F0-SPL characteristics of untrained versus trained vocal groups

The phonetogram has been recommended as an international tool for voice analysis. However, the capability of this technique to distinguish between different vocal groups has not been clearly established. The purpose of this study was to examine untrained versus trained vocalists using the phonetogram and the fundamental frequency by intensity (F₀/SPL) information derived through that method. In this study, “musical” or “controlled” ranges of phonation were stressed rather than “physiological” ranges. Results indicated that (a) characteristic phonetographic profiles may be established for untrained versus trained vocalists, and (b) trained vocalists show significantly increased capability in terms of F₀ range and maximum, minimum, and comfortable SPL production. Elicitation of “controlled” phonations may be the key to revealing the underlying vocal capabilities of seemingly different vocal groups.     

Use of amorphous zirconium phosphate for the treatment of radioactive waste

Ion-exchange experiments were carried out for the removal of¹³⁷Cs, and⁹⁰Sr/⁹⁰Y radioisotopes by different cationic forms of amorphous zirconium phosphate. The effect of temperature and concentration on the percent uptake and distribution coefficients (K _d ) values (milli-equivalents of ion per gram of exchanger/milli-equivalents of ion per ml of solution) were determined. Experiments were made in simulated pond water at pH 11.4.     

Interaction of C-Si, C-Sn, and Si-Si sigma-bonds with chalcogen lone pairs

The ability of neighboring C-Si, C-Sn, and Si-Si groups in conformationally constrained cyclic molecules to reduce the lowest ionization energies of sulfur, selenium, and tellurium compounds has been determined by charge-transfer spectroscopy of complexes with tetracyanoethylene. For selected compounds, ionization energies were determined by gas-phase photoelectron spectroscopy. The lowest ionization energies measured by photoelectron spectroscopy, with one exception, correlate with the charge-transfer spectroscopic data. In addition, theoretical analysis has provided insight into the photoelectron spectra and the geometry-dependent interaction between C-Si or C-Sn bonds and chalcogen lone pairs. Substantial lowering of ionization energies is found which is anticipated to have important consequences in the chemistry of these and related species.     

Theoretical studies on conjugated phenyl-cored thiophene dendrimers for photovoltaic applications

Pi-conjugated dendrimers are an important class of materials for optoelectronic devices, especially for light-harvesting systems. We report here a theoretical investigation of the optical response and of the excited-state properties of three-arm and four-arm phenyl-cored dendrimers for photovoltaic applications. A variety of theoretical methods are used and evaluated against each other to calculate vertical transition energies, absorption and excitation spectra with vibronic structure, charge transport, and excitonic behavior upon photoexcitation and photoemission processes. Photophysical phenomena in these dendrimers are, in general, better explained with ab initio methods rather than with semiempirical techniques. Calculated reorganization energies were found to correlate well with the device photocurrent data where available. The excitons formed during photoexcitation are calculated to be more delocalized than the ones formed after vibrational relaxation in the excited states for fluorescence emission. The localization of excitons in emission processes is a result of geometrical changes in the excited state coupled with vibronic modes. Correlated electron-hole pair diagrams illustrate breaking of pi-conjugation in three-arm dendrimers due to meta linkage of arms with the core, whereas four-arm dendrimers are not affected by such breaking due to presence of ortho and para branching. Yet, ortho branching causes large twist angles between the core and the arms that are detrimental to pi-electron system delocalization over the structure.