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Institution

University of Rajasthan

EducationJaipur, India
About: University of Rajasthan is a education organization based out in Jaipur, India. It is known for research contribution in the topics: Chemical shift & Derivative (chemistry). The organization has 15058 authors who have published 15733 publications receiving 117400 citations. The organization is also known as: Rajasthan University.


Papers
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Journal ArticleDOI
TL;DR: In this paper, the state-of-the-art on thin, conductive and flexible graphene films as an active electrode material in polymer photovoltaics is discussed.

36 citations

Journal ArticleDOI
TL;DR: In this article, the authors considered the soliton solution of the KdV equation for a warm-ion magnetized plasma with two Maxwellian electron components, and the effect of ion temperature, obliqueness and magnetization on the amplitude and width of soliton was discussed in detail.

36 citations

Journal ArticleDOI
Shreyasi Acharya1, Dagmar Adamová2, Souvik Priyam Adhya1, Alexander Adler3  +1051 moreInstitutions (102)
TL;DR: In this paper, the J/ψ meson was reconstructed via the dimuon decay channel at forward rapidity (2.5 < y < 4) down to zero transverse momentum.
Abstract: The inclusive J/ψ production in Pb–Pb collisions at the center-of-mass energy per nucleon pair $ \sqrt{s_{\mathrm{NN}}} $ = 5.02 TeV, measured with the ALICE detector at the CERN LHC, is reported. The J/ψ meson is reconstructed via the dimuon decay channel at forward rapidity (2.5 < y < 4) down to zero transverse momentum. The suppression of the J/ψ yield in Pb–Pb collisions with respect to binary-scaled pp collisions is quantified by the nuclear modification factor (R$_{AA}$). The R$_{AA}$ at $ \sqrt{s_{\mathrm{NN}}} $ = 5.02 TeV is presented and compared with previous measurements at $ \sqrt{s_{\mathrm{NN}}} $ = 2.76 TeV as a function of the centrality of the collision, and of the J/ψ transverse momentum and rapidity. The inclusive J/ψ RAA shows a suppression increasing toward higher transverse momentum, with a steeper dependence for central collisions. The modification of the J/ψ average transverse momentum and average squared transverse momentum is also studied. Comparisons with the results of models based on a transport equation and on statistical hadronization are carried out.[graphic not available: see fulltext]

36 citations

Journal ArticleDOI
TL;DR: A series of transition metal complexes of Fe(III), Co(II), and Cu(II) containing the bidentate N,O and N,S donor ligand, camphor semicarbazone (1,7,7-trimethylbicyclo [2,2,1]heptanesemicarbazones, TBHSC) and camphor thiosemicarbazoned (1.7, 7- trimethylbicycleclo[2, 2,1]-heptanethiose-micarazone,
Abstract: A series of transition metal complexes of Fe(III), Co(II) and Cu(II) containing the bidentate N,O and N,S donor ligand, camphor semicarbazone (1,7,7-trimethylbicyclo [2,2,1]heptanesemicarbazone, TBHSC) and camphor thiosemicarbazone (1,7,7- trimethylbicyclo [2,2,1]heptanethiosemicarbazone, TBHTSC) have been synthesized and characterized by elemental analysis, molar conductance measurement and various spectral studies (IR, electronic and FAB Mass) and thermogravimetric analysis (TGA). All the metal complexes (1-8) are [M(LH)Cl 2 ] and [M(LH) 2 Cl 2 ] type, where M = Fe(III), Co(II) and Cu(II); LH = TBHSC and TBHTSC. TBHSC and TBHTSC act as neutral bidentate ligands in all the complexes. FAB mass spectroscopic studies of the three representative complexes (1), (2), (4), (5) and (8) suggest their monomeric nature. The proposed geometries of the complexes were octahedral geometry for 1:2 complexes, square planar for 1:1 complexes and distorted octahedral for Cu(II) complexes (1:2). The free radical scavenging activity of newly synthesized ligands (TBHSC, TBHTSC) and their metal complexes have been determined at the concentration range of 50-1000 µg/ml by means of their interaction with the stable free radical 1,1-diphenyl-2-picrylhydrazyl (DPPH). All the compounds have shown encouraging antioxidant activities. The least IC 50 value (111.0 µg/ml) for compound (5) showed the potent scavenging property compared to other test compounds.

36 citations

Journal ArticleDOI
TL;DR: In this article, a catalyst-free aqueous mediated multicomponent domino reaction (MCR) capable of affording medicinally important spiro[indole-3,4′-pyrazolo] under sonication in excellent yield and in shorter time is reported.
Abstract: A novel and catalyst-free aqueous mediated multicomponent domino reaction (MCR) capable of affording medicinally important spiro[indole-3,4′-pyrazolo[3,4-e][1,4]thiazepines] under sonication in excellent yield and in shorter time is reported. This new protocol provides a new seven-membered ring system selectively instead of the expected five-membered ring system or other possible isomers. The structure and relative stereochemistry of spiro products was established by single crystal X-ray analysis of a representative compound and spectroscopic techniques. In comparison to conventional synthesis, the advantages of this method are that it is catalyst-free, has an easy workup and uses water as the solvent which is considered to be relatively environmentally benign, and this work offers a new way to create molecular complexity with maximum simplicity. The representative compounds were screened for their ability to inhibit the enzyme α-amylase.

36 citations


Authors

Showing all 15080 results

NameH-indexPapersCitations
Rakesh K. Jain2001467177727
J. Pluta12065952025
Sudhir Raniwala11359144168
Rashmi Raniwala11357944076
Sanjay Jain10388146880
Mirko Planinic9446731957
Manish Sharma82140733361
Nikola Poljak7839320795
Hari M. Srivastava76112642635
Radhey S. Gupta7137718078
Ashwani Kumar6670318099
Amit Kumar65161819277
Rashmi Gupta5242850962
Allan R. Oseroff481217029
Vinod K. Aswal465569917
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20233
202233
2021218
2020242
2019163
2018143