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Bachcha Singh

Bio: Bachcha Singh is an academic researcher from Banaras Hindu University. The author has contributed to research in topics: Mesophase & Liquid crystal. The author has an hindex of 13, co-authored 89 publications receiving 545 citations.


Papers
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Journal ArticleDOI
TL;DR: In this paper, the binding sites of acr with Mg were identified by experimental and computational methods, and experimental and theoretical results suggest that Mg coordinated with the oxygen atom of C O group of ac r. In-vitro cytotoxicity studies revealed significant decrease in the toxic level of ac R-Mg complex as compared to pure acr.

3 citations

Journal ArticleDOI
TL;DR: The complexes [M(L1)nCl2] and [Cu(L2)SO4(H2O)2] have been prepared and analyzed using analytical, molar conductance, magnetic susceptibility, electronic, ESR and NMR spectral data as mentioned in this paper.
Abstract: The complexes [M(L1)nCl2] and [Cu(L2)SO4(H2O)2] [M= Co(II), Ni(II), Cu(II) and Cd(II); L1=acetophenone oxaloyldihydrazone (CONHN═C(CH3)C6H5)2, n=2 and L2=4-hydroxyacetophenone oxaloyldihydrazone (CONHN= C(CH3)C6H4OH–4)2 have been prepared. Analytical, molar conductance, magnetic susceptibility, electronic, ESR and NMR spectral data have been used to investigate the structure and bonding of the complexes. X-ray powder diffraction data indicate the shape and size of the unit cell of the copper(II) complex. Some of the complexes were screened against E. coli and Aspergillus niger for biological activity.

2 citations

Journal ArticleDOI
TL;DR: In this article, a new series of acid dimers, N-(4′-carboxybenzylidene)-4-alkoxybenzoyloxyaniline (4-HOOCC6H4CH˭N), where R = CmH2m + 1 and m = 6, 8, 10, 12, 14, and 16, have been synthesized.
Abstract: In this study, a new series of acid dimers, N-(4′-carboxybenzylidene)-4-alkoxybenzoyloxyaniline [(4′-HOOCC6H4CH˭N)-4-C6H4OCOC6H4OR, where R = CmH2m + 1 and m = 6, 8, 10, 12, 14, and 16], have been synthesized. The compounds have been characterized by elemental analyses and FTIR, UV-visible, 1H, and 13C NMR spectra. The mesomorphic properties of these acid dimers were studied by differential scanning calorimetry and polarizing optical microscopy. The mesomorphic nature of these compounds depends on hydrogen bonding and on the alkoxy chain length. The compounds with m = 6 and 8 show a characteristic enantiotropic nematic mesophase, whereas those with m = 12 and 14 exhibit monotropic behavior. The compounds with m =10 and 16 exhibit non-mesomorphic behavior.

2 citations

Journal ArticleDOI
TL;DR: In this article, a new ligand, 2,6−diacetylpyridine•2,thenoylpicolynoyl dihydrazone (H2dapthph), has been prepared.
Abstract: A new ligand, 2,6‐diacetylpyridine‐2‐thenoylpicolynoyl dihydrazone (H2dapthph), has been prepared. Complexes of the type [Ln(H2dapthph)Cl2]Cl (Ln = La, Pr, Nd, Sm, Eu, Gd, Tb and Dy) have been synthesized and characterized by analytical, molar conductance, FAB mass, IR, NMR, electronic and emission spectral data. The bonding sites of the hydrazone are deduced from IR and NMR spectra and the ligand is found to bond to the metal ion in a hexadentate fashion. Electronic spectra of the complexes have been analyzed and the spectral parameters viz. nephelauxetic ratio (β), bonding parameter (b1/2), Sinha parameter (δ%), angular overlap covalency (η) and oscillator strength (P) were calculated and discussed. The symmetry around the Ln(III) ions is indicated from emission spectra of the Eu(III) complex.

2 citations


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Journal ArticleDOI
01 Jan 1889

595 citations

Book ChapterDOI
01 Jan 1991
TL;DR: The nature of metal complexes of heterocyclic thiosemicarbazones reported in the literature through 1989 have been reviewed with an emphasis on variations in stoichiometry and stereochemistry as discussed by the authors.
Abstract: The nature of metal complexes of heterocyclic thiosemicarbazones reported in the literature through 1989 have been reviewed with an emphasis on variations in stoichiometry and stereochemistry. A brief introduction is followed by a survey of the biological activity of the uncomplexed thiosemicarbazones. Next is a section on the chemical nature of thiosemicarbazones including a discussion of preparative methods, modes of coordination and isomerism. This is followed by a discussion of structural information and biological activity of the iron(III), iron(II), copper(II), cobalt(III), cobalt(II) and nickel(II) complexes of heterocyclic thiosemicarbazones. Short sections on the biological activity of other chelating thiosemicarbazones and metal complexes are also included.

435 citations

Journal ArticleDOI
TL;DR: A facile one-step, low-temperature, nonhydrolytic approach to in situ synthesizing amino-functionalized TiO2 nanoparticles (abbreviated as NH2 -TiO2 NPs) is developed by chemical bonding of amino (-NH2 ) groups, via TiN bonds, onto the surface of TiO1 NPs.
Abstract: Titanium oxide (TiO2 ) has been commonly used as an electron transport layer (ETL) of regular-structure perovskite solar cells (PSCs), and so far the reported PSC devices with power conversion efficiencies (PCEs) over 21% are mostly based on mesoporous structures containing an indispensable mesoporous TiO2 layer. However, a high temperature annealing (over 450 °C) treatment is mandatory, which is incompatible with low-cost fabrication and flexible devices. Herein, a facile one-step, low-temperature, nonhydrolytic approach to in situ synthesizing amino-functionalized TiO2 nanoparticles (abbreviated as NH2 -TiO2 NPs) is developed by chemical bonding of amino (-NH2 ) groups, via TiN bonds, onto the surface of TiO2 NPs. NH2 -TiO2 NPs are then incorporated as an efficient ETL in n-i-p planar heterojunction (PHJ) PSCs, affording PCE over 21%. Cs0.05 FA0.83 MA0.12 PbI2.55 Br0.45 (abbreviated as CsFAMA) PHJ PSC devices based on NH2 -TiO2 ETL exhibit the best PCE of 21.33%, which is significantly higher than that of the devices based on the pristine TiO2 ETL (19.82%) and is close to the record PCE for devices with similar structures and fabrication procedures. Besides, due to the passivation of the surface trap states of perovskite film, the hysteresis of current-voltage response is significantly suppressed, and the ambient stability of devices is improved upon amino functionalization.

197 citations

Journal ArticleDOI
TL;DR: In this article, the authors summarized the published innovations in nanomaterial-based optical sensors for the detection of Hg 2+ according to different sensing strategies, including colorimetric, fluorescent and surface enhanced Raman scattering detection.
Abstract: As one of the most toxic heavy metals, mercury ion (Hg 2+ ) has become a concern focus for its severe threats to environment and human health. As a result, it is of great importance to develop novel methods to realize the recognition and quantification of Hg 2+ . The past decades witness the development of nanomaterial-based optical sensors for Hg 2+ detection, showing the benefits of simplicity, rapidity, high sensitivity and selectivity, and cost-effectiveness. The reported methods have allowed the detectability down to nanomolar concentrations or much lower levels, and proved their practical applications for detecting and quantifying Hg 2+ in synthetic solutions or natural water samples. In this review, we summarize the published innovations in nanomaterial-based optical sensors for the detection of Hg 2+ according to different sensing strategies, including colorimetric, fluorescent and surface enhanced Raman scattering detection. Moreover, some challenges and significant attempts related to these methods are also discussed.

191 citations

Journal ArticleDOI
TL;DR: The experimental results suggest that the adsorption efficiency of DOX is dominated by the strong complexation, electrostatic interactions between DOX molecules and the Cu-BC samples, which hold the significant potential for enhancing the effectiveness to remove DOX from water.

146 citations