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Institution

North Eastern Hill University

EducationShillong, Meghalaya, India
About: North Eastern Hill University is a education organization based out in Shillong, Meghalaya, India. It is known for research contribution in the topics: Population & Ruthenium. The organization has 2318 authors who have published 4476 publications receiving 48894 citations.
Topics: Population, Ruthenium, Ligand, Catalysis, Micelle


Papers
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Journal ArticleDOI
TL;DR: This survey of metal-metal (MM) bond distances in binuclear complexes of the first row 3d-block elements reviews experimental and computational research on a wide range of such systems and proposes for the first time the ranges and "best" estimates for MM bond distances of all types.
Abstract: This survey of metal–metal (MM) bond distances in binuclear complexes of the first row 3d-block elements reviews experimental and computational research on a wide range of such systems. The metals surveyed are titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, and zinc, representing the only comprehensive presentation of such results to date. Factors impacting MM bond lengths that are discussed here include (a) the formal MM bond order, (b) size of the metal ion present in the bimetallic core (M2)n+, (c) the metal oxidation state, (d) effects of ligand basicity, coordination mode and number, and (e) steric effects of bulky ligands. Correlations between experimental and computational findings are examined wherever possible, often yielding good agreement for MM bond lengths. The formal bond order provides a key basis for assessing experimental and computationally derived MM bond lengths. The effects of change in the metal upon MM bond length ranges in binuclear complexes suggest trends f...

95 citations

Journal ArticleDOI
TL;DR: In this article, the one-loop radiative corrections to the mass squared matrix of the CP-even Higgs bosons in the non-minimal supersymmetric standard model containing two Higgs doublets and a Higgs singlet chiral superfield were presented.

92 citations

Journal ArticleDOI
TL;DR: In this article, five new organotin(IV) complexes were synthesized and characterized using 1H NMR, 13C NMR, 119Sn NMR and infrared spectroscopic techniques, and the results demonstrate that the compounds containing Sn-Ph ligands are more effective than those with Sn-Bz ligands.
Abstract: Five new organotin(IV) complexes of composition [Bz2SnL1]n (), [Bz3SnL1H⋅H2O] (), [Me2SnL2⋅H2O] (), [Me2SnL3] () and [Bz3SnL3H]n () (where L1 = (2S)-2-{[(E)-(4-hydroxypentan-2-ylidene)]amino}-4-methylpentanoate, L2 = (rac)-2-{[(E)-1-(2-hydroxyphenyl)methylidene]amino}-4-methylpentanoate and L3 = (2S)- or (rac)-2-{[(E)-1-(2-hydroxyphenyl)ethylidene]amino}-4-methylpentanoate) were synthesized and characterized using 1H NMR, 13C NMR, 119Sn NMR and infrared spectroscopic techniques. The crystal structure of reveals a distorted trigonal-bipyramidal geometry around the tin atom where the oxygen atoms of the carboxylate ligand and a water ligand occupy the axial positions, while the three benzyl ligands are located at the equatorial positions. On the other hand, the analogous derivative of enantiopure L3H () consists of polymeric chains, in which the ligand-bridged tin atoms adopt the same trans-Bz3SnO2 trigonal-bipyramidal configuration and are now coordinated to a phenolic oxygen atom instead of H2O. In , the OH hydrogen of the ketoimine substituent has moved to the nearby nitrogen atom while in the salicylidene derivative , the OH is located almost midway between the phenolic oxygen atom and the nitrogen atom of the C[DOUBLE BOND]N group. For the dibenzyltin derivative , a polymeric chain structure is observed as a result of a long intermolecular Sn⋅⋅⋅O bond involving the exocyclic carbonyl oxygen atom from the tridentate ligand of a neighbouring tin-complex unit. The tin atom in this complex has distorted octahedral coordination geometry. In contrast, the racemic dimethyltin(IV) complexes and display discrete monomeric structures with a distorted octahedral- and trigonal-bipyramidal geometry, respectively. The structures show that the coordination mode of the Schiff base ligand depends primarily on the number of bulky benzyl ligands (R) at the tin atom, as indeed found in the structures of related complexes where R = phenyl. With three bulky R groups, the tridentate chelating O,N,O coordination mode is preferred, whereas with fewer or less bulky R ligands, only the carboxylate and hydroxy groups are involved, which leads to polymers. Larvicidal efficacies of two of the new tribenzyltin(IV) complexes ( and ) were assessed on the second larval instar of Anopheles stephensi mosquito larvae and compared with two triphenyltin(IV) analogues, [Ph3SnL1H]n and [Ph3SnL3H]n. The results demonstrate that the compounds containing Sn–Ph ligands are more effective than those with Sn–Bz ligands. Copyright © 2016 John Wiley & Sons, Ltd.

92 citations

Journal ArticleDOI
TL;DR: In this paper, the authors derived new analytic formulas and obtained substantially different numerical predictions for the running masses of quarks and charged leptons at higher scales in the SM, 2HDM and MSSM.
Abstract: Including contributions of scale-dependent vacuum expectation values, we derive new analytic formulas and obtain substantially different numerical predictions for the running masses of quarks and charged leptons at higher scales in the SM, 2HDM and MSSM. These formulas exhibit significantly different behaviours with respect to their dependence on gauge and Yukawa couplings from those derived earlier. At one-loop level, the masses of the first two generations are found to be independent of the Yukawa couplings of the third generation in all three effective theories in the small mixing limit. Analytic formulas are also obtained for the running of $\tan\beta(\mu)$ in 2HDM and MSSM. Other numerical analyses include a study of the third generation masses at high scales as functions of the low-energy values of $\tan\beta$ and the SUSY scale $M_{\mathrm{S}}=M_Z-10^4$ GeV.

90 citations


Authors

Showing all 2368 results

NameH-indexPapersCitations
Vivek Sharma1503030136228
Patrick J. Carroll5850513046
Majeti Narasimha Vara Prasad5622715193
Arun Sharma5537111364
Michael Schmittel5338710461
Birgitta Bergman5218710975
Harikesh Bahadur Singh463077372
Lal Chand Rai401344513
B. Dey403548089
Hiriyakkanavar Ila364075633
Jürgen-Hinrich Fuhrhop352085130
Sreebrata Goswami341423228
Gagan B.N. Chainy331074151
J.P. Gaur31643957
Hiriyakkanavar Junjappa303494102
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202321
202254
2021352
2020308
2019293
2018306