A rhodamine hydrazide–4-nitroindole-3-carboxaldehyde based turn on Hg2+ chemosensor: cytoplasmic live cell imaging,logic gate and memory device applications and computational studies

A new, highly sensitive probe L² for the selective detection of Hg²⁺ in organo-aqueous (H₂O:CH₃CN, 1:1, v/v, HEPES buffer, pH 7.2) medium has been synthesized from rhodamine 6G-hydrazide and 4-nitroindole-3-carboxaldehyde. It was thoroughly characterized by physicochemical techniques including single crystal X-ray diffraction studies. The reaction of L² with Hg²⁺ gives a 1:1 stoichiometry resulting in a 146 fold fluorescence enhancement and a binding constant (K_f) of 3?×?10⁴ M^?1. The spirolactam form of the probe is non-fluorescent; however, it shows dual channel (absorbance and fluorescence) recognition of Hg²⁺ via CHEF effect through the opening of the spirolactam ring. The quantum yields of L² (0.00045) and L²-Hg²⁺ (0.29) show the higher stability of complex in the excited state over the free ligand. The 44.5?nM LOD value demonstrates the detection of Hg²⁺ at a very low concentration range. Cell imaging studies show the cytoplasmic recognition of Hg²⁺ by L². Experimental results are comparable with theoretical values obtained by DFT studies. The fluorescence emission of the complex was completely quenched by I^- and from the reversibility studies an advance level INHIBIT logic gate and memory device can be framed.     

Detection and incorporation of amino endgroups in free-radical polymerization of methyl methacrylate

Amino endgroups have been incorporated in poly(methyl methacrylate) by two methods: (a) initiation with systems producing amine radicals and (b) chain transfer with amines. A new dye-partition technique with the use of disulfine blue was developed for qualitative and in some cases quantitative estimation of amino endgroups in the polymer.     

Secondary Neutral Pion-nucleon Flux Ratio at the Top of the Atmosphere

The CERN Intersecting Storage Ring data on the inclusive reaction p + p → π° + X has been fitted with a phenomenological form where W_c(a,b,z) is the generalized confluent function defined by . M(a, b, z) being the well known Kummer's function. Using this form and primary proton spectrum of Goddard Space Flight Center Group the secondary neutral pion-nucleon flux ratio at the top of the atmosphere has been estimated. The derived result has been compared with those expected from p + p → π^± + X data, via different models.     

Ammonium and potassium fluoromonooxalatomanganates(II), A[MnF(C2O4)] (A = NH4 or K) and sodium fluoromonooxalatomanganate(II) dihydrate,Na[MnF(C2O4)] · 2H2O

Summary Light pink-white microcrystalline ammonium and potassium fluoromonooxalatomanganates(II), A[MnF(C₂O₄)] (A = NH₄ or K), and sodium fluoromonooxalatomanganate(II) dihydrate, Na[MnF(C₂O₄)] · 2H₂O, have been synthesized by two different methods. Either KMnO₄ is reduced in the presence of 40% HF and alkali metal oxalate, A₂C₂O₄ (A = NH₄, Na or K), or MnO(OH) in 40% HF reacts with A₂C₂O₄. Characterisation was made by elemental analyses, determination of oxidation states, magnetic susceptibility measurements and infrared spectral studies.     

Structure of hydrated clusters of tetrahydroisoquinoline [THIQ-(H2O)(n=1,3)] investigated by jet spectroscopy

The hydrated clusters of tetrahydroisoquinoline have been investigated by laser-induced fluorescence (LIF), UV-UV hole burning, and IR-UV double-resonance spectroscopy in a seeded supersonic jet. Clusters of different sizes and isomeric structures have different 0-0 transitions (origins) in the LIF spectrum. UV-UV hole burning spectroscopy has been used to identify different cluster species and their vibrational modes. The structures of the clusters have been predicted by comparing the observed OH and NH frequencies in the IR-UV double-resonance spectra with the results calculated at different levels of sophistication. It is found that the water molecules form linear and six- and eight-membered cyclic H-bonded structures at the nitrogen center of 1:1, 1:2, and 1:3 clusters, respectively.     

Quantum deformation of the confined Hulthen problem

A scheme for studyingq deformed quasi exactly solvable problem has been applied to the Schrödinger Hulthen problem (l=0). It is found that for the confined Hulthen problem, the confining parameter can be related to the deformation parameterq.     

Reactivity investigations of some chosen peroxo-vanadium(V), manganese(III) and chromium(VI) compounds

An interpretative account of the results of reactions in aqueous medium of a highly peroxygenated vanadium(V) complex, K [V(O_{2 3}]·3H₂O, with different organic and inorganic substrates is presented. The reactions were monitored by solution EPR spectroscopy and isolation of products at different stages of the reactions. Redox reactions between diperoxide, K[VO(O₂)₂(H₂O)] and VOSO₄ were conducted. The results of the investigation suggest that secondary oxygen exchange-reaction occurs which not only depends on but also utilises the intermediates in the primary reaction during diperoxovanadate-dependent oxidation of VOSO₄. In an interesting reactiontris(acetylacetonato)-manganese(III), Mn(acac)₃, on being reacted with a hydrogen peroxide adduct, KF·H₂O₂, and bpy and phen afforded crystalline [Mn(acac)₂(bpy)] and [Mn(acac)₂(phen)], respectively. The X-ray structural analysis of [Mn(acac)₂(phen)] showed that the compound crystallised in orthorhombic space groupPbcn. The structure consists of a pseudooctahedral Mn(II) ion being bound to two acac⁻(C₅H₅O ₂ ⁻ ) and a phen ligand with the molecule lying on two-fold axis. Reactivity profiles of two new chromium(VI) reagents viz., pyridinium fluorochromate, C₅H₅NH[CrO₃F] (PFC), and quinolinium fluorochromate C₉H₇NH [CrO₃F] (QFC), have been presented. The compounds are capable of acting as both electron-transfer and oxygen-atom-transfer agents. The X-ray analysis of PFC crystals reveals that the compound crystallises in the orthorhombic space group CmcZ₁. The structure consists of discrete pyridinium cations and CrO₃ F anions with no significant hydrogen bonding. This results in total disorder of the pyridinium cation. The tetrahedral [CrO₃ F]⁻ ion lies on a crystallographic mirror plane.     

Higher-order solution for dust acoustic solitary waves in an unmagnetized dusty plasma

The effect of higher-order nonlinearity on dust acoustic solitary waves is studied taking into account the dust-charge variation. The model of charge fluctuation, taken here, is of the formI _e+I _i=0,I _e andI _i being the electronic and ionic currents. The dust charge is determined self consistently from the current-balance equation. It is found that the higher-order correction modifies the amplitude and width of the dust acoustic solitary waves. The effect of dust-charge streaming is also discussed.     

Spectra of K3Mn(CN)6

The polarised optical spectra of single crystal of K₃Mn(CN)₆ is reported at liquid nitrogen temperature. A new system of transition is located along with its hot components which is verified by temperature variation studies. The crystal field parameters to reproduce the bands are given.