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Ranjan K. Singh

Bio: Ranjan K. Singh is an academic researcher from Banaras Hindu University. The author has contributed to research in topics: Raman spectroscopy & Liquid crystal. The author has an hindex of 20, co-authored 134 publications receiving 1465 citations. Previous affiliations of Ranjan K. Singh include Schiller International University & University of Würzburg.


Papers
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Journal ArticleDOI
TL;DR: In this paper, a piperazine derivative, ethyl 4-phenylthiocarbamoylpiperazine-1-carboxylate and its Ni(II, Zn(II), and Cd(II) complexes have been synthesized and characterized by elemental analyses, magnetic susceptibility measurement, UV-visible, FTIR, Raman spectroscopic and DFT methods.

6 citations

Journal ArticleDOI
TL;DR: In this article, the authors investigated the mechanism that enables N-Acetylcysteine (NAC), an antioxidant drug, to act as an antitoxin of arsenic poisoning, and showed that a stable complex between NAC and arsenic is formed in three steps.

6 citations

Journal ArticleDOI
TL;DR: In this paper, the structural changes observed in the X-ray diffraction pattern has been further confirmed by Raman analysis, and major changes in the E(1TO), A1-1TO, and E+B1 phonon modes suggest the structural change from cubic to rhombohedral with increase in Ni concentration in PNNZT.
Abstract: Lead niobate zirconate titanate (PNZT) with general formula 0.5PbNb2O6–0.5Pb(ZrxTi1-x)O3 (where x = 0.15, 0.25, 0.35) and lead nickel niobate zirconate titanate (PNNZT) with general formula Pb(NixNb0.5-xZr0.25Ti0.25)O3 (where x = 0.167, 0.250, 0.333) have been prepared by conventional solid state reaction. The phase formation has been studied by X – ray diffraction analysis. Raman investigations have been carried out in the 200–1000 cm−1 wave number range. The structural changes observed in the X – ray diffraction pattern has been further confirmed by Raman analysis. The major changes in the E(1TO), A1(1TO) and E + B1 phonon modes suggest the structural change from cubic to rhombohedral with increase in Ni concentration in PNNZT. The optical band gap has been calculated from UV – Vis absorption spectra.

5 citations

Journal ArticleDOI
TL;DR: Insight is given into the intrinsic dependence of magnetic resonance contrast effects of NPs on particle size and surface coating layer mass ratio and thus demonstrates the development of efficient magnetic nanoparticles based contrast agents by fine tuning of particlesize and surface properties.
Abstract: Magnetic nanoparticles (MNPs) have widely demonstrated their applicability in many biomedical applications including magnetic resonance imaging (MRI), hyperthermia, and drug delivery. However, the effectiveness of MNPs can be limited for in vivo applications due to their hydrophobic surfaces leading to nanoparticle agglomeration and thus requires appropriate surface modification to enhance colloidal stability. Glycols are widely used coating material for surface modifications of MNPs to improve their physicochemical properties and biocompatibility. The present work reports the preparation of two different sized ethylene glycol coated gadolinium oxide nanoparticles (EG@Gd2O3 NPs) using two different synthesis approaches and their applicability as contrast agents in MRI. Thermo-gravimetric analysis and Fourier transform infrared spectroscopy confirmed the successful coating of ethylene glycol on the surface of NPs. We found that independent of the size of NPs, the globular shaped EG@Gd2O3 NPs exhibited similar crystal structures, magnetic properties, and cellular cytotoxicity behavior. However, a significant impact of size on MRI contrast enhancement properties was seen. It was revealed that the relaxivity of EG@Gd2O3 NPs increases with a decrease in particle size. Small sized EG@Gd2O3 NPs (∼12 nm) exhibited a high specific in vitro and ex vivo longitudinal relaxivity of 3.7 and 1.5 mM−1 s−1, respectively, thus clearly elucidating the potential of these NPs for use as local contrast enhancement agents. The present study gives insights into the intrinsic dependence of magnetic resonance contrast effects of NPs on particle size and surface coating layer mass ratio and thus demonstrates the development of efficient magnetic nanoparticles based contrast agents by fine tuning of particle size and surface properties.

5 citations

Journal ArticleDOI
TL;DR: The temperature-dependent Raman study revealed that the increased vibration of the long alkyl tail and the rotation around the long molecular axis are the two primary phenomena responsible for the crystal–SmG transition.
Abstract: We report on a temperature-dependent Raman study of terephthalidine-bis-butylaniline (TBBA) and terephthalidine-bis-heptylaniline (TB7A) in the temperature range 10-406 K and in the wavenumber regions 1120-1240 cm-1 and 1500-1700 cm-1. The variations of peak positions and linewidths of several Raman marker bands with temperature, which clearly show crystal-SmG transition at ~334 K, have been used to discuss the dynamics of this phase transition. The temperature-dependent Raman study revealed that the increased vibration of the long alkyl tail and the rotation around the long molecular axis are the two primary phenomena responsible for the crystal-SmG transition. Density functional theory (DFT) at the B3LPY/6-31G(d) level was employed to obtain the optimized geometry and the harmonic vibrational wavenumbers of TBBA. The eigenvectors of the modes corresponding to these marker bands were also calculated.

5 citations


Cited by
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Journal ArticleDOI
TL;DR: The limit of sensitivity in SERS is introduced in the context of single-molecule spectroscopy and the calculation of the ‘real’ enhancement factor, which illustrates the broad applications of this powerful technique.
Abstract: Surface-enhanced Raman spectroscopy (SERS) combines molecular fingerprint specificity with potential single-molecule sensitivity. Therefore, the SERS technique is an attractive tool for sensing molecules in trace amounts within the field of chemical and biochemical analytics. Since SERS is an ongoing topic, which can be illustrated by the increased annual number of publications within the last few years, this review reflects the progress and trends in SERS research in approximately the last three years. The main reason why the SERS technique has not been established as a routine analytic technique, despite its high specificity and sensitivity, is due to the low reproducibility of the SERS signal. Thus, this review is dominated by the discussion of the various concepts for generating powerful, reproducible, SERS-active surfaces. Furthermore, the limit of sensitivity in SERS is introduced in the context of single-molecule spectroscopy and the calculation of the 'real' enhancement factor. In order to shed more light onto the underlying molecular processes of SERS, the theoretical description of SERS spectra is also a growing research field and will be summarized here. In addition, the recording of SERS spectra is affected by a number of parameters, such as laser power, integration time, and analyte concentration. To benefit from synergies, SERS is combined with other methods, such as scanning probe microscopy and microfluidics, which illustrates the broad applications of this powerful technique.

706 citations

Journal ArticleDOI
TL;DR: In this paper, the authors presented an Austrian Federal Ministry of Science, Research and Economy and National Foundation for Research, Technology and Development (NFthis paper ) supported by the OMV Group, the EPSRC (DTA studentships for D.W. and T.E.O.), the World Premier Institute Research Center Initiative (WPI), MEXT, Japan (to K.L., GAN 701192 - VSHER), the German Research Foundation (to M.F.
Abstract: This work was supported by the Christian Doppler Research Association (Austrian Federal Ministry of Science, Research and Economy and the National Foundation for Research, Technology and Development), the OMV Group (to E.R.), the EPSRC (DTA studentships for D.W.W. and T.E.R), the Isaac Newton Trust, the German Research Foundation (to M.F.K.), the World Premier Institute Research Center Initiative (WPI), MEXT, Japan (to K.L.O.) and a Marie Curie Research fellowship (to K.H.L., GAN 701192 - VSHER).

383 citations

Reference BookDOI
08 Oct 2018
TL;DR: Xerographic photoreceptors charge acceptance and dark discharge photoinduced discharge photogeneration theories photogengeneration in organic solids charge transport theories charge transport in polymers and related materials experimental techniques photoreceptor preparation photoresceptors fatigue summary and future requirements.
Abstract: Xerographic photoreceptors charge acceptance and dark discharge photoinduced discharge photogeneration theories photogeneration in organic solids charge transport theories charge transport in polymers and related materials experimental techniques photoreceptor preparation photoreceptors fatigue summary and future requirements.

378 citations

Journal ArticleDOI
26 Nov 1994-BMJ
TL;DR: In the future of all-conquering genetic technology, who should be screened for what and by whom?
Abstract: Ed Lori B Andrews, Jane E Fullarton, Neil A Holtzman, Arno G Motulsky National Academy Press, £28.95, pp 338 ISBN 0-309-04798-6 Genetic screening tends to serve as a flypaper on which our hovering fears of a Brave New World alight and stick. In the future of all-conquering genetic technology, who should be screened for what and by whom? Here is a dense report, compiled by a committee of the great and the good, with hundreds of recommendations for action and inaction. How much …

332 citations

Journal ArticleDOI
01 May 2019-Talanta
TL;DR: CQDs, their structure, and PL characteristics are introduced and recent advances of the application of CQDs in biotechnology, sensors, and CL is comprehensively discussed.

286 citations