02652nas a2200241 4500008004100000245016400041210006900205260000800274300001200282490000700294520177000301100002602071700001902097700001702116700002102133700001502154700002302169700002702192700001502219700002502234700002702259856012402286 2016 eng d00aCutaneous exposure to clinically-relevant pigeon pea (Cajanus cajan) proteins promote T(H)2-dependent sensitization and IgE-mediated anaphylaxis in Balb/c mice0 aCutaneous exposure to clinicallyrelevant pigeon pea Cajanus caja cJAN a827-8410 v133 aEpicutaneous (EC) sensitization to food allergens may occur when the skin has been lightly damaged. The study here tested whether cutaneous exposure to pigeon pea protein(s) may cause allergic sensitization. BALB/c mice were either orally gavaged or epicutaneously sensitized by repeated application of pigeon pea crude protein extract (CPE) on undamaged areas of skin without any adjuvant; afterwards, both groups were orally challenged with the pigeon pea CPE. Anaphylactic symptoms along with measures of body temperature, MCPT-1, TSLP, pigeon pea-specific IgE and IgG(1), myeloperoxidase (MPO) activity, T(H)2 cytokines, T(H)2 transcription factors (TFs) and filaggrin expression were determined. Mast cell staining, eosinophil levels and histopathological analysis of the skin and intestines were also performed. In the epicutaneously-sensitized mice, elevated levels of specific IgE and IgG(1), as well as of MCPT-1, TSLP, T(H)2 cytokines and TFs, higher anaphylactic scores and histological changes in the skin and intestine were indicative of sensitization ability via both routes in the pigeon pea CPE-treated hosts. Elevated levels of mast cells were observed in both the skin and intestine; increased levels of eosinophils and MPO activity were noted only in the skin. Decreased levels of filaggrin in skin may have played a key role in the skin barrier dysfunction, increasing the chances of sensitization. Therefore, the experimental data support the hypothesis that in addition to oral exposure, skin exposure to food allergens can promote T(H)2-dependent sensitization, IgE-mediated anaphylaxis and intestinal changes after oral challenge. Based on this, an avoidance of cutaneous exposures to allergens might prevent development of food anaphylaxis.1 aGupta, Rinkesh, Kumar1 aKumar, Sandeep1 aGupta, Kriti1 aSharma, Akanksha1 aRoy, Ruchi1 aVerma, Alok, Kumar1 aChaudhari, Bhushan, P.1 aDas, Mukul1 aAnsari, Irfan, Ahmad1 aDwivedi, Premendra, D. uhttps://library.ncl.res.in/content/cutaneous-exposure-clinically-relevant-pigeon-pea-cajanus-cajan-proteins-promote-th201579nas a2200205 4500008004100000245008700041210006900128260000800197300001400205490000700219520088200226100001801108700002101126700002701147700001701174700001801191700002401209700002101233856011901254 2017 eng d00aUltrahigh ionic conduction in water-stable close-packed metal-carbonate frameworks0 aUltrahigh ionic conduction in waterstable closepacked metalcarbo cAUG a9710-97150 v563 aUtilization of the robust metal-carbonate backbone in a series of water-stable, anionic frameworks has been harnessed for the function of highly efficient solid-state ion conduction. The compact organization of hydrophilic guest ions facilitates water-assisted ion-conduction in all the compounds. The dense packing of the compounds imparts high ion-conducting ability and minimizes the possibility of fuel crossover, making this approach promising for design and development of compounds as potential components of energy devices. This work presents the first report of evaluating ion-conduction in a purely metal-carbonate framework, which exhibits high ion-conductivity on the order of 10(-2) S cm(-1) along with very low activation energy, which is comparable to highly conducting well-known crystalline coordination polymers or commercialized organic polymers like Nafion.1 aManna, Biplab1 aDesai, Aamod, V.1 aIllathvalappil, Rajith1 aGupta, Kriti1 aSen, Arunabha1 aKurungot, Sreekumar1 aGhosh, Sujit, K. uhttps://library.ncl.res.in/content/ultrahigh-ionic-conduction-water-stable-close-packed-metal-carbonate-frameworks01454nas a2200229 4500008004100000022001400041245009900055210006900154260000800223300001600231490000700247520070500254100001700959700001700976700001700993700002301010700001501033700001801048700002201066700002101088856011501109 2018 eng d a0020-166900aMetamagnetism in nanosheets of Co-II-MOF with T-N at 26 K and a giant hysteretic effect at 5 K0 aMetamagnetism in nanosheets of CoIIMOF with TN at 26 K and a gia cDEC a15044-150470 v573 aHerein, we have synthesized at room-temperature two-dimensional nanosheets of a MOF comprised of cobalt(II) ion with benzenedicarboxylic acid ligand, which exhibited unusual magnetic properties. Direct-current magnetic susceptibility revealed an anti-ferromagnetic (AFM) transition at 26 K (Neel temperature, T-N) followed by a canting of the spin moments along with the concomitant appearance of a sigmoidal-shaped magnetization versus field (M-H) curve at 15 K. Such a canted AFM ordering led to nonzero remnant magnetization with a remarkably high coercive field of similar to 10 kOe at 5 K. Metamagnetism was further: substantiated by the alternating-current magnetic susceptibility measurements.1 aGupta, Kriti1 aDadwal, Arun1 aRana, Shammi1 aJha, Plawan, Kumar1 aJain, Anil1 aYusuf, S., M.1 aJoy, Pattayil, A.1 aBallav, Nirmalya uhttps://library.ncl.res.in/content/metamagnetism-nanosheets-co-ii-mof-t-n-26-k-and-giant-hysteretic-effect-5-k01740nas a2200229 4500008004100000022001400041245006600055210006300121260000900184300001400193490000700207520104700214100001701261700002301278700001701301700002201318700001901340700001701359700002201376700002101398856009101419 2019 eng d a1948-718500aEmbedding S=1/2 Kagome-like lattice in reduced graphene oxide0 aEmbedding S12 Kagomelike lattice in reduced graphene oxide cJUN  a2663-26680 v103 a

An elegant platform to explore frustrated magnetism is the kagome spin lattice. In this work, clinoatacamite, a naturally occurring S = 1/2 kagome-like antiferromagnetic insulator, is synthesized in water at ambient pressure for the first time from a cuprous chloride (CuCl) precursor whereby Cu(I) was spontaneously oxidized to Cu(II) in the form of clinoatacamite [Cu-2(OH)(3)Cl] with a simultaneous reduction of graphene oxide (GO) to reduced graphene oxide (rGO) in one pot. A stable nanocomposite of phase-pure clinoatacamite nanocrystals embedded in the rGO matrix was isolated. The clinoatacamite-rGO nanocomposite was determined to be magnetically active with a markedly enhanced coercive field of similar to 2500 Oe at S K as well as electronically active with a conductivity value of similar to 200 S.m(-1) at 300 K. Our results illustrate an avenue of combining exotic magnetic and electronic lattices without impeding their individual characteristics and synergistically generating a new class of magnetic semiconductors.

1 aGupta, Kriti1 aJha, Plawan, Kumar1 aDadwal, Arun1 aDebnath, Anil, K.1 aJaiswal, Ishan1 aRana, Shammi1 aJoy, Pattayil, A.1 aBallav, Nirmalya uhttps://library.ncl.res.in/content/embedding-s12-kagome-lattice-reduced-graphene-oxide02382nas a2200241 4500008004100000022001400041245016300055210006900218260000800287300001200295490000800307520150800315100002301823700002401846700001701870700001801887700002701905700001901932700001701951700002401968700002101992856012702013 2019 eng d a0008-622300aIn-situ generated Mn3O4-reduced graphene oxide nanocomposite for oxygen reduction reaction and isolated reduced graphene oxide for supercapacitor applications0 aInsitu generated Mn3O4reduced graphene oxide nanocomposite for o cDEC a285-2910 v1543 a

We have generated in situ nanocomposite of Mn3O4 and reduced graphene oxide (rGO) upon employing wet-chemical reduction of graphene oxide (GO) by Mn(II) salt as mild-reducing agent for the first time and examined the oxygen reduction reaction (ORR) activity in 0.1 M KOH electrolyte. The half-wave potential (E-1/2) of the nanocomposite catalyst (20% Mn3O4-rGO/C) was found to be around -0.153 V which is only similar to 87 mV negative from the commercially available catalyst (20% Pt/C). Remarkably, after 5000 linear sweep voltammetry cycles the E-1/2 shifted marginally by 20 mV; and the number of electrons transferred during ORR was estimated to be close to 4. Such an efficient electrocatalytic performance of the nanocomposite was primarily attributed to the synergistic interaction between Mn3O4 and rGO. The fabricated all-solid-state supercapacitor of rGO (extracted from the nanocomposite) in aqueous polyvinyl alcohol-sulfuric acid (PVA-H2SO4) gel polymer electrolyte (GPE) showed C-s value of similar to 310 F/g at a current density of 1 A/g along with long durability (10,000 charge-discharge cycles). All-solid-state flexible rGO supercapacitor exhibited high-flexibility and excellent durability (30,000 cycles with 100% retention of C-s). Our results provide an enormous opportunity in designing transition metal oxides decorated semiconducting reduced graphene oxide nanocomposite platforms for various electrochemical applications. (C) 2019 Elsevier Ltd. All rights reserved.

1 aJha, Plawan, Kumar1 aKashyap, Varchaswal1 aGupta, Kriti1 aKumar, Vikash1 aDebnath, Anil, Krishna1 aRoy, Debashree1 aRana, Shammi1 aKurungot, Sreekumar1 aBallav, Nirmalya uhttps://library.ncl.res.in/content/situ-generated-mn3o4-reduced-graphene-oxide-nanocomposite-oxygen-reduction-reaction-and01652nas a2200217 4500008004100000022001400041245011700055210006900172260000900241300001400250490000700264520090000271100001701171700001701188700002301205700001501228700001801243700002201261700002101283856013001304 2020 eng d a0020-166900aExploring magnetic XY behavior in a quasi-2D anisotropic triangular lattice of Cu(II) by functionalized graphene0 aExploring magnetic XY behavior in a quasi2D anisotropic triangul cMAY  a6214-62190 v593 a

Study on magnetism in two-dimensional (2D) spin-lattices is advancing rapidly. In this work, phase-pure botallackite (Bo) (Cu-2(OH)(3)Br), a quasi-2D S = 1/2 anisotropic triangular spin-lattice is stabilized over 2D reduced graphene oxide (rGO) nanosheets via simple oxidation-reduction reaction chemistry. In comparison to polycrystalline Bo, such an anchoring resulted in the oriented growth of Bo crystallites in the Bo-rGO system. The Bo-rGO nanocomposite was found to be magnetically active with a Neel transition at 8.9 K, crossing over to possible XY anisotropy at similar to 5 K-as revealed by complementary dc and ac susceptibility measurements-an unprecedented observation in the field assigned to an interfacial effect. This work demonstrates the potential usage of nonmagnetic 2D functionalized graphene to significantly modulate the magnetic properties of 2D spin-lattices.

1 aGupta, Kriti1 aDadwal, Arun1 aJha, Plawan, Kumar1 aJain, Anil1 aYusuf, S., M.1 aJoy, Pattayil, A.1 aBallav, Nirmalya uhttps://library.ncl.res.in/content/exploring-magnetic-xy-behavior-quasi-2d-anisotropic-triangular-lattice-cuii-functionalized02422nas a2200193 4500008004100000022001400041245008600055210006900141260000800210300001600218490000800234520177600242100001702018700001702035700001902052700002202071700002102093856011402114 2020 eng d a1932-744700aIntegrating structurally perfect s=1/2 kagome-lattice with reduced graphene oxide0 aIntegrating structurally perfect s12 kagomelattice with reduced  cSEP a19753-197590 v1243 a

S = 1/2 kagome-lattice hydroxychlorides are promising candidates for realizing the elusive quantum spin liquid (QSL) state. Herbertsmithite [Cu3Zn(OH)(6)Cl-2], a naturally occurring hydroxychloride mineral from the class of atacamites {[Cu-4-xMx(OH)(6)X-2] where M = Zn, Cu, Co, Ni and X = Cl, Br, I}, is one of the most appealing systems to study the QSL state because of the presence of a structurally perfect S = 1/2 kagome-lattice. It is an electrical insulator. However, realizing phase-pure herbertsmithite without imposing harsh reaction conditions remained synthetically challenging. In this work, for the first time, we have synthesized phase-pure herbertsmithite as well as its structural analogue paratacamite, [ZnxCu4-x(OH)(6)Cl-2; 0.33 = x < 1], at ambient reaction conditions. Furthermore, taking graphene oxide (GO) as an additional precursor in the reaction mixture, we have successfully integrated phase-pure crystallites of herbertsmithite (H) and paratacamite (P) with nanosheets of semiconducting and diamagnetic reduced graphene oxide (rGO) by in situ oxidation-reduction reaction. The isolated H-rGO and P-rGO systems were found to be magnetic semiconductors inheriting strong spin frustration from H and P, and semiconductivity from rGO. The H-rGO system in particular exhibited negative Seebeck coefficient (n-type semiconductor) with a thermoelectric power factor of 0.1 mu W center dot m(-1)center dot K-2 at 400 K. We anticipate the simple chemical principles outlined in this work to be useful for studying a variety of complex QSLs including electron doping. Also, semiconducting and rather unconventional materials of such metal oxochlorides with rGO isolated here need further exploration in view of thermoelectric applications.

1 aGupta, Kriti1 aDadwal, Arun1 aNinawe, Pranay1 aJoy, Pattayil, A.1 aBallav, Nirmalya uhttps://library.ncl.res.in/content/integrating-structurally-perfect-s12-kagome-lattice-reduced-graphene-oxide02899nas a2200157 4500008004100000245005900041210005800100260004400158490000900202520236600211100001702577700001702594700001802611700002102629856009102650 2020 eng d00aMagnetism in bimetallic NiII-CoII coordination polymer0 aMagnetism in bimetallic NiIICoII coordination polymer bAmerican Institute of Physics Inc.cNOV0 v22653 a

Co-BDC ([Co2(OH)2BDC], H2BDC = 1,4-benzenedicarboxylic acid) is known to possess metamagnetism originating from the antiparallel spins and high magneto crystalline anisotropy of Co(II).1 Herein, we have introduced a bimetallic concept by incorporating Ni(II) along with Co(II) in the same coordination polymer to modulate the magneto crystalline anisotropy in the lattice which in turn, affects the overall magnetic response of the coordination polymer. The Curie-Weiss equation fit suggested antiparallel arrangement of the spins (θ ≈ -62.5 K) of Ni(II) and Co(II) arranged in alternate fashion. The cusp in magnetization was observed at 7 K (Tc) with a significant coercive field of ∼750 Oe at 5 K.

1 aGupta, Kriti1 aDadwal, Arun1 aJoy, Pattayil1 aBallav, Nirmalya uhttps://library.ncl.res.in/content/magnetism-bimetallic-niii-coii-coordination-polymer01803nas a2200241 4500008004100000022001400041245011400055210006900169260000900238300001200247490000800259520100700267100001701274700001901291700001501310700001701325700001301342700001801355700001801373700002201391700002101413856012701434 2021 eng d a2469-995000aPossible electron doping of geometrically perfect spin-1/2 kagome-lattice barlowite by reduced graphene oxide0 aPossible electron doping of geometrically perfect spin12 kagomel cSEP  aL1004180 v1043 aDoping of quantum spin liquid (QSL) insulators by electron or hole leads to intriguing phase transitions to metallic and superconducting states. The barlowite family with geometrically perfect S = 1/2 kagome planes and tunable interkagome coupling is an emerging platform to realize spin-ordered, valence bond crystal, QSL states. Theoretical investigations on electron doping revealed localized states in the band gap of barlowite unlike metallicity in cuprate (Nd2CuO4). We present successful anchoring of phase-pure barlowite crystallites onto reduced graphene oxide (rGO). The resulting barlowite-rGO system was found to be an electrical semiconductor with Arrhenius activation energy of 0.07 eV. Semiconducting properties of the barlowite-rGO system were further modulated with retention of structural integrity. We have attributed such a transformation of electrical transport response to plausible electron doping thereby making charge-doping experiments on barlowite and its analogs propitious.1 aGupta, Kriti1 aNinawe, Pranay1 aJain, Anil1 aDadwal, Arun1 aAnas, M.1 aMalik, V., K.1 aYusuf, S., M.1 aJoy, Pattayil, A.1 aBallav, Nirmalya uhttps://library.ncl.res.in/content/possible-electron-doping-geometrically-perfect-spin-12-kagome-lattice-barlowite-reduced04907nas a2200229 4500008004100000245007800041210007000119260000800189490000600197520417400203100001804377700001904395700002204414700001704436700001704453700001704470700001604487700002104503700002204524700002104546856011004567 2024 eng d00aUnconventional hole doping of S = ½ kagome antiferromagnet CoCu3(OH)6Cl20 aUnconventional hole doping of S ½ kagome antiferromagnet CoCu3OH cSEP0 v33 a

Geometrically perfect S = ½ kagome lattices with frustrated magnetism are typically electrical insulators. Electron or hole doping is predicted to induce an exotic conducting state including superconductivity. Herein, an unconventional strategy of doping an S = ½ kagome lattice CoCu3(OH)6Cl2 is adopted – a structural analogue of a well-known quantum spin liquid (QSL) candidate herbertsmithite (ZnCu3(OH)6Cl2) – by integrating it with reduced graphene oxide (rGO) via in situ redox chemistry. Such an integration drastically enhances the electrical conductivity, resulting in the transformation of an insulator to a semiconductor, corroborating the respective density of states obtained from the density functional theory calculations. Estimation of the magnetic moments, data on the Hall-effect measurements, Bader charge analysis, and photoemission signals, altogether provide a bold signature of remote hole doping in CoCu3(OH)6Cl2 by rGO. The remote doping provides an alternative to the site doping approach to impart exotic electronic properties in spin liquid candidates, specifically, the generation of topological states like Dirac metal is envisioned.

1 aMandal, Rimpa1 aNinawe, Pranay1 aAnanthram, K., S.1 aMhase, Akash1 aGupta, Kriti1 aSaha, Sauvik1 aUgale, Ajay1 aSingh, Kirandeep1 aTarafder, Kartick1 aBallav, Nirmalya uhttps://library.ncl.res.in/content/unconventional-hole-doping-s-%C2%BD-kagome-antiferromagnet-cocu3oh6cl200858nas a2200205 4500008004100000022001400041245018000055210006900235260000900304300001600313490000700329653003700336653004700373100002000420700001700440700002600457700001900483700002000502856013000522 2024 eng d a2155-543500aUnraveling the metal-ligand cooperativity in a phosphine-free Mn(II)-catalyzed transfer hydrogenation of nitriles to primary amines and dehydrogenation of dimethylamine borane0 aUnraveling the metalligand cooperativity in a phosphinefree MnII cOCT  a15777-157890 v1410aCATALYZED TRANSFER HYDROGENATION10aSTEREOSELECTIVE TRANSFER SEMIHYDROGENATION1 aChowdhury, Deep1 aGupta, Kriti1 aGamidi, Rama, Krishna1 aJindal, Garima1 aMukherjee, Arup uhttps://library.ncl.res.in/content/unraveling-metal-ligand-cooperativity-phosphine-free-mnii-catalyzed-transfer-hydrogenation