Turn-on Fluorescence Chemosensor for Zn2+ Ion Using Salicylate Based Azo Derivatives and their Application in Cell-Bioimaging.

The synthesis and optical studies of salicylate based azo derivatives (DPSAD and IPSAD) are reported. The receptors act as a versatile fluorogenic chemosensor for Zn2+ causing a selective enhancement of fluorescence over other competing cations. The complex formed between receptors and Zn2+ are identified on the basis of absorption and fluorescence titration and further confirmed by ESI-MS. DFT/TD-DFT calculations support the observed optical changes happens only upon complexation with Zn2+ ion. Moreover, receptors are further applied to intracellular sensing and imaging studies. Graphical Abstract Salicylate based azo derivatives (DPSAD and IPSAD) as fluorogenic chemosensor for the detection of Zn2+ ion.

Highly enantioselective asymmetric Henry reaction catalyzed by novel chiral phase transfer catalysts derived from cinchona alkaloids.

A new type of di-site chiral phase transfer catalyst has been designed and synthesized from cinchona alkaloids as a chiral precursor. The prepared catalysts are applied in the asymmetric Henry reaction to a wide range of aldehydes using mild concentrations of a base and solvent and under room-temperature conditions. Under the optimized reaction conditions, the highest chemical yields up to 99% along with an excellent enantiomeric excess (ee) up to 99% were obtained using the prepared cinchona alkaloid based chiral phase transfer catalysts.

Construction of direct Z-scheme g-C3N4/BiYWO6 heterojunction photocatalyst with enhanced visible light activity towards the degradation of methylene blue.

Construction of the Z-scheme heterojunction photocatalyst achieved highly improved photocatalytic ability by its high redox ability of the photoinduced e--h+ pairs. In the study, Z-scheme g-C3N4/BiYWO6 heterojunction photocatalyst is prepared by the single-step hydrothermal method. Further, its photocatalytic ability was assessed by degrading methylene blue under visible light exposure. Particularly, the optimized 30 wt% of g-C3N4 in the g-C3N4/BiYWO6 composite exposes almost complete degradation after 90 min, that is ~ 3.0 times greater than the bare BiYWO6 and g-C3N4 with the rate constant value 0.032 min-1. Experimentally, the radical trapping studies indicate O2·- and ·OH radicals are playing a vital role in the photocatalytic degradation process. Also, the Z-scheme g-C3N4/BiYWO6 heterojunction photocatalyst exhibits excellent photoelectrochemical property and it is stable after 5 cycles, which indicates its good reusability nature. These enhancements are due to the newly formed heterostructure that facilitates the migration and separation efficiency of the photoproduced e--h+ pairs. Hence, the synthesized Z-scheme g-C3N4/BiYWO6 heterostructure could be an excellent material for wastewater remediation works.

A Z-scheme BiYO3/g-C3N4 heterojunction photocatalyst for the degradation of organic pollutants under visible light irradiation.

Photocatalysis is one of the fascinating fields for the wastewater treatment. In this regard, the present study deals with an effective visible light active BiYO3/g-C3N4 heterojunction nanocomposite photocatalyst with various ratios of BiYO3 and g-C3N4 (1:3, 1:1 and 3:1), synthesised by a wet chemical approach. The as-synthesised nanocomposite photocatalysts were investigated via different physicochemical approaches like Fourier transform infrared (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), transmission electrons microscopy (TEM), UV-vis diffuse reflectance spectroscopy (DRS), photoluminescence (PL) and photoelectrochemical studies to characterise the crystal structure, morphology, optical absorption characteristics and photoelectrochemical properties. The photocatalytic degradation ability of the prepared photocatalytic samples was also analysed through the degradation of RhB in the presence of visible light irradiation. Of all the synthesised photocatalysts, the optimised CB-1 composite showed a significant photocatalytic efficiency (88.7%), with excellent stability and recyclability after three cycles. O2•- and •OH radicals were found to act a major role in the RhB degradation using optimised CB-1 composite, and it possessed ~ 1 times greater photocurrent intensity than the pristine g-C3N4 and BiYO3. In the present work, a direct Z-scheme heterojunction BiYO3/g-C3N4 with a considerably improved photocatalytic performance is reported.

Construction of direct FeMoO4/g-C3N4-2D/2D Z-scheme heterojunction with enhanced photocatalytic treatment of textile wastewater to eliminate the toxic effect in marine environment.

A novel FeMoO4/g-C3N4-2D/2D Z-scheme heterojunction photocatalyst was prepared via wet chemical method. The observed structural morphology of FeMoO4/g-C3N4 reveals the 2D-iron molybdate (FeMoO4) nanoplates compiled with the 2D-graphitic carbon nitride (g-C3N4) nanosheets like structure. The photocatalytic activity of the g-C3N4, FeMoO4, and FeMoO4/g-C3N4 composites were studied via the degradation of Rhodamine B (RhB) as targeted textile dye under visible light irradiation (VLI). The optimal FeMoO4/g-C3N4 (1:3 ratio of g-C3N4 and FeMoO4) composite show an enhanced degradation performance with rate constant value of 0.02226 min-1 and good stability even after three cycles. Thus, the h+ and O2•－are the key radicals in the degradation of RhB under VLI. It is proposed that the FeMoO4/g-C3N4 Z-scheme heterojunction effectively enhances the transfer and separation ability of e-/h+ pairs, by the way increasing the photocatalytic efficiency towards the RhB degradation. Thus, the newly constructed Z-scheme FeMoO4/g-C3N4 heterojunction photocatalyst is a promising material for the remediation of wastewater relevant to elimination of toxic effect in marine environment.

One-pot synthesis of bismuth yttrium tungstate nanosheet decorated 3D-BiOBr nanoflower heterostructure with enhanced visible light photocatalytic activity.

A visible light driven BiOBr/BixY1-xWO6 nanocomposite photocatalyst of various compositions are prepared by the addition of different amounts of KBr (0.5, 1.0, 1.5, 2.0 mmol) in BixY1-xWO6 by a one-pot hydrothermal method. Furthermore, the photocatalytic properties of the as-prepared materials are analyzed by the decomposition of methylene blue under visible light illumination. In particular, the BiOBr/BixY1-xWO6 nanocomposite prepared by taking 1.5 mmol of KBr present a superior photocatalytic ability (78.3%) with the rate constant value 0.016 min-1, a low bandgap (Eg = 2.51 eV) as well as photoluminescence emission intensity than other photocatalysts prepared in this study. The radical scavenging studies revealed that OH and h+ performed an imperative role in the decomposition of methylene blue. Furthermore, the optimized photocatalyst is stable even after four cycles, which exposes the excellent photostability and reusability properties of the photocatalyst. In addition, a plausible mechanism of decomposition of methylene blue under visible light irradiation is also proposed.

One-step synthesis of rod-on-plate like 1D/2D-NiMoO4/BiOI nanocomposite for an efficient visible light driven photocatalyst for pollutant degradation.

Visible light active 1D/2D-NiMoO4/BiOI nanocomposite photocatalyst has been constructed by single step solvothermal method. Various compositions of NiMoO4/BiOI nanocomposites are prepared by loading different amounts of nickel molybdate (NiMoO4) (1, 2, 3 wt%) to the bismuth oxy iodide (BiOI) and investigated by XRD, FTIR, SEM, EDAX, TEM, UV-vis DRS, and PL analysis. Among the as-prepared photocatalysts, 1 wt% NiMoO4 incorporated BiOI (NMBI-1) showed superior photocatalytic activity with a rate constant of 0.0442 min-1 for methylene blue degradation. While the bandgap values of pure BiOI and NiMoO4 are 1.94 and 2.43 eV, respectively, the optimized NMBI-1 exhibited a lower bandgap energy of 1.64 eV, and showed about 2 and 3.7 times higher photodegradation ability than the pure NiMoO4 and BiOI, respectively, towards MB removal under visible light. The NMBI-1 nanocomposite photocatalyst is stable even after four cycles, indicating an excellent photostability and recyclability. Charge carriers on the interface of NiMoO4 and BiOI easily transferred via the newly formed heterojunction, thereby increasing the photocatalytic performance. Photochemically formed h+ and.OH are found to be the major species in the MB removal under visible light illumination. Therefore, the 1D/2D-NiMoO4/BiOI nanocomposite photocatalyst materials may be considered for the wastewater remediation processes.

A facile synthesis of visible light driven Ni3V2O8 nano-cube/BiVO4 nanorod composite photocatalyst with enhanced photocatalytic activity towards degradation of acid orange 7.

Photocatalysis is one of the promising method to degrade harmful organic pollutants under visible light exposure. In this work, a novel Ni3V2O8/BiVO4 nanocomposite has been prepared by one-pot hydrothermal method, and investigated through X-ray diffraction, FT-IR, UV-visible diffuse reflectance spectroscopy, scanning and transmission electron microscopy and photoluminescence techniques. Subsequently, the photocatalytic performance of Ni3V2O8/BiVO4 nanocomposite has been examined by degrading AO7 under visible light illumination. The photocatalytic efficiency of the optimized 1:2 ratio of Ni3V2O8/BiVO4 nanocomposite photocatalyst is found to be 87% with a rate constant value of 0.03387 min-1 which are higher than those of other prepared photocatalysts. This nanocomposite exhibits excellent stability even after 3 three cycles, and shows 1.135- and 1.17-times higher photocurrent intensity than pure BiVO4 and Ni3V2O8 respectively. The mechanism for the degradation of AO7 over Ni3V2O8/BiVO4 nanocomposite photocatalyst has been proposed.

Solvent-free benzylic oxidation of aromatics over Cu(II)-containing propylsalicylaldimine anchored on the surface of mesoporous silica catalysts.

A sustainable method was used to produce aromatic ketones by the solvent-free benzylic oxidation of aromatics over mesoporous Cu(II)-containing propylsalicylaldimine anchored on the surface of Santa Barbara Amorphous type material-15 (CPSA-SBA-15) catalysts. For comparison, mesoporous Cu(II)-containing propylsalicylaldimine anchored with Mobil Composition of Matter-41 (CPSA-MCM-41) was assessed for these reactions under similar reaction conditions. The washed CPSA-SBA-15(0.2) (W-CPSA-SBA-15(0.2)) catalyst was prepared using an easy chemical method for the complete removal of non-framework CuO nanoparticle species on the surface of pristine CPSA-SBA-15(0.2) (p-CPSA-SBA-15(0.2) prepared with 0.2 wt% of Cu, and its catalytic activity was evaluated with different reaction parameters, oxidants and solvents. In order to confirm the catalytic stability, the recyclability was assessed, and the performance of hot-filtration experiments was also evaluated. All the catalysts used for these catalytic reactions were characterized using many instrumental techniques to pinpoint the mesoporous nature and active sites of the catalysts. The proposed reaction mechanism has been well documented on the basis of catalytic results obtained for solvent-free oxidation of aromatics. Based on the catalytic results, we found that W-CPSA-SBA-15(0.2) is a very ecofriendly catalyst with exceptional catalytic activity.

Novel star-shaped D-π-D-π-D and (D-π)2-D-(π-D)2 anthracene-based hole transporting materials for perovskite solar cells.

Three types of novel star-shaped molecular architectures, D-π-D-π-D and (D-π)2-D-(π-D)2 anthracene (ANTTPA, AOME, AOHE) based hole transporting materials, are designed for hybrid perovskite solar cells using the Gaussian 09 computation program with the B3LYP/6-31g (d, p) basis set level. The HOMO energy level of the designed materials has a higher HOMO energy level compared to the perovskite HOMO energy level, which is more facile for hole transport from the hole transporting layer to the oxidized perovskite layer. Thereafter, anthracene-based derivatives were synthesized from Buchwald-Hartwig and Mizoroki-Heck cross coupling reactions. The behaviors of the transporting charges were determined by both UV-visible absorbance and emission spectroscopy through solvatochromism experiments. Furthermore, the electrochemical properties also proved that the synthesized compounds had an optimal HOMO energy level in the TiO2/perovskite/HTM interface. Our hole transport materials (HTMs) have a good film formation compared to the spiro-OMeTAD, which was confirmed from scanning electron microscopy images. The obtained theoretical and experimental data show the suitability of designing anthracene-based derivatives with the potential to be used as hole transporting materials in organic-inorganic hybrid perovskite solar cells.

A highly sensitive and selective Schiff-base probe as a colorimetric sensor for Co2+ and a fluorimetric sensor for F- and its utility in bio-imaging, molecular logic gate and real sample analysis.

In this work, we designed a novel Schiff-base probe from the condensation reaction of 3,5-diiodosalicylaldehyde with isoniazid. Treatment of the sensor molecule with different metal ions like K+, Ba2+, Ca2+, Mg2+, Fe2+, Mn2+, Co2+, Cu2+, Cd2+, Ni2+, Hg2+, Zn2+, Pb2+ and Al3+ in visual inspection and absorption measurements explained its colorimetric sensing ability. The sensor DISN displays a remarkable color variation from pale yellow to brownish-orange towards Co2+ ion. The absorption and emission spectra of DISN, upon treating with various anions including F-, Br-, Cl-, I-, HSO4-, NO3-, H2PO4-, and CN- were tested. The addition of the fluoride ion to the receptor caused not only the intense color variation from pale yellow to orange but also a significant fluorescence turn-on response. Job's plot method fixed the binding of Co2+ and F- to DISN separately, in 2:1 and 1:1 binding stoichiometry, respectively. The detection limit of 1.24 × 10-7 M and 0.108 × 10-6 M was attained for Co2+ and F-, respectively. The TD-DFT calculations further supported the photophysical properties involved in the free probe and its complexes. The YES and INHIBIT logic function was found to operate from modulation in the absorbance and fluorescence behavior of Co2+ and F- ions with DISN. Furthermore, DISN displays its practical applicability in filter-paper strips, live cell imaging, and real sample analyses.

Functionalized silicate sol-gel-supported TiO2-Au core-shell nanomaterials and their photoelectrocatalytic activity.

The N-[3-(trimethoxysilyl)propyl]ethylenediamine (EDAS) derived silicate matrix supported core-shell TiO(2)-Au nanoparticles (EDAS/(TiO(2)-Au)(nps)) were prepared by NaBH(4) reduction of HAuCl(4) precursor on preformed TiO(2) nanoparticles in the presence of EDAS monomer. The core-shell (TiO(2)-Au)(nps) nanoparticles were stabilized by the amine functional group of the EDAS silicate sol-gel network. The potential application of this EDAS/(TiO(2)-Au)(nps) modified electrode toward the photoelectrochemical oxidation of methanol was explored. The EDAS/(TiO(2)-Au)(nps) modified electrode showed a 12-fold enhancement in the catalytic activity toward photoelectrooxidation of methanol when compared to TiO(2) dispersed in EDAS silicate sol-gel matrix. This improved photoelectrochemical performance is explained on the basis of beneficial promotion of interfacial charge transfer processes of the EDAS/(TiO(2)-Au)(nps) nanocomposite. A methanol oxidation peak current density of 12.3 mA cm(-2) was achieved at an optimum loading of Au(nps) on TiO(2) particles. This novel amine functionalized EDAS silicate sol-gel stabilized core-shell (TiO(2)-Au)(nps) nanomaterial could be an excellent candidate for the photocatalytic and photoelectrochemical applications.