A Highly Sensitive and Selective Fluorescent Chemodosimeter for Hg<Superscript>2+</Superscript> in Neutral Aqueous Solution

A fluorescent assay of Hg²⁺ in neutral aqueous solution was developed using N-[p-(dimethylamino)benzamido]-N′-phenylthiourea (1). 1’s fluorogenic chemodosimetric behaviors towards various metal ions were studied and a high sensitivity as well as selectivity was achieved for Hg²⁺. It was because of a strongly fluorescent 1,3,4-oxadiazoles which was produced by the Hg²⁺ promoted desulfurization reaction. The spectra of ESI mass and IR provided evidences for this reaction. According to fluorescence titration, a good linear relationship ranging from 1.0 × 10⁻⁷ to 2.0 × 10⁻⁵ mol l⁻¹ was obtained with the limit of detection as 3.1 × 10⁻⁸ mol l⁻¹. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Spectroscopic properties of Nd<Superscript>3+</Superscript>:CaNb<Subscript>2</Subscript>O<Subscript>6</Subscript> crystal

The absorption spectra, fluorescence spectrum and fluorescence decay curve of Nd³⁺ ions in CaNb₂O₆ crystal were measured at room temperature. The peak absorption cross section was calculated to be 6.202×10⁻²⁰ cm² with a broad FWHM of 7 nm at 808 nm for E//a light polarization. The spectroscopic parameters of Nd³⁺ ions in CaNb₂O₆ crystal have been investigated based on Judd-Ofelt theory. The parameters of the line strengths Ω _t are Ω ₂=5.321×10⁻²⁰ cm²,Ω ₄=1.734×10⁻²⁰ cm²,Ω ₆=2.889×10⁻²⁰ cm². The radiative lifetime, the fluorescence lifetime and the quantum efficiency are 167 μs, 152 μs and 91%, respectively. The fluorescence branch ratios are calculated to be β ₁=36.03%,β ₂=52.29%,β ₃=11.15%,β ₄=0.533%. The emission cross section at 1062 nm is 9.87×10⁻²⁰ cm².     

Renormalization group functions of the φ<Superscript>4</Superscript> theory from high-temperature expansions

It has been previously shown that calculation of the renormalization group (RG) functions of scalar ϕ⁴ theory reduces to analysis of thermodynamic properties of the Ising model. Using high-temperature expansions for the latter, RG functions of the four-dimensional theory can be calculated for arbitrary coupling constant g with an accuracy of 10⁻⁴ for the Gell-Mann-Low function β(g) and with an accuracy of 10⁻³–10⁻² for anomalous dimensions. The expansions of the renormalization group functions up to the 13th order in g ^−1/2 have been obtained.     

Improved (1s)<Superscript>2</Superscript> variational model for helium

The ground-state energy of neutral helium is estimated variationally with a trial wavefunction of the form ϕ≈e ^−γ(rA/a _o)ⁿe^−γ(rB/a _o)ⁿ. This model represents a modification of traditional textbook examinations of this problem via inclusion of the power “n” as a second nonlinear variational parameter in addition to the usual effective nuclear charge γ and leads to an upper-limit on the ground state energy of −2.86107 E _h (E _h =1 hartree) in comparison with the traditional (n=1) result of −2.84766 E _h . This result represents a reduction of the percentage overestimate from the true ground-state energy (−2.90373 E _h ) of from 1.93 to 1.47. In comparison with the maximum accuracy obtainable from an uncorrelated trial wavefunction, −2.86168 E _h , the present trial wavefunction reduces the percentage overestimate from 0.49 (n=1) to 0.021. The optimum values of (n, γ) are determined to be ≈(0.897, 1.825).     

Longitudinal dynamics of <Superscript>197</Superscript>Au<Superscript>32+</Superscript> and <Superscript>197</Superscript>Au<Superscript>79+</Superscript> ions in NICA injection chain

The main objective of the NICA project developed at the Joint Institute for Nuclear Research (JINR) is to conduct experimental studies with colliding heavy ion beams in an energy range of 1–4.5 GeV/nucleonucleon with luminosity on the level of 1 × 10²⁷ cm⁻² s⁻¹. In this paper the operation regime of the collider injection chain providing the bunch with experimentally desirable parameters at the output of the Nuclotron is considered for gold ions as an example.     

A Coumarin-Based Fluorescent Chemosensor for Zn<Superscript>2+</Superscript> in Aqueous Ethanol Media

A coumarin-based fluorescent chemosensor 1 for Zn²⁺ was designed and synthesized. Compound 1 exhibits lower background fluorescence due to intramolecular photoinduced electron transfer. However, upon mixing with Zn²⁺ in 30% (v/v) aqueous ethanol, a “turn-on” fluorescence emission is observed. The fluorescence emission increases linearly with Zn²⁺ concentration in the range 0.5–10 μmol L⁻¹ with a detection limit of 0.29 μmol L⁻¹. No remarkable emission enhancement was, however, observed for other metal ions. The proposed chemosensor was applied to the determination of Zn²⁺ in water samples with satisfactory results.     

The Sensitive Determination of Nucleic Acids Using Fluorescence Enhancement of Eu<Superscript>3+</Superscript>-BenzoylacetoneCetyltrimethylammonium Bromide-Nucleic Acid System

A new quantitative method for micro amounts of nucleic acids in aqueous solution is proposed using Eu³⁺-benzoylacetone (BA) complex as fluorescent probe in the presence of cetyltrimethyl-ammonium bromide (CTMAB). Under the optimum condition, the ratio of the fluorescence intensities with and without nucleic acids is proportional to the concentration of nucleic acid in the range of 1.0 × 10⁻⁹ to 5.0 × 10⁻⁶ g/mL for herring sperm DNA (hsDNA), 3.0 × 10⁻⁹ to 1.0 × 10⁻⁶ g/mL for calf thymus DNA(ctDNA) and 8.0 × 10⁻⁹ to 1.0 × 10⁻⁶ g/mL for yeast RNA (yRNA), and their detection limits are 0.33, 0.21 and 0.99 ng/mL, respectively. Actual sample (DNA of Arabidopsis thaliana) was determined satisfactorily. In addition, the interaction mechanism is also investigated.     

Theoretical study of NO<Stack><Subscript>3</Subscript><Superscript>−</Superscript></Stack> interacting with carbon nanotube

This paper deals with quantum mechanical interaction of no ₃⁻ with (5,5) and (8,0) swcnts. To perform this we have made an ab initio calculation based on the density functional theory. In these framework the electronic density plays a central role and it was obtained of a self-consistent field form. It was observed through binding energy that NO₃⁻ molecule interacts with each nanotube in a physisorption regime. We propose these swcnts as a potential filter device due to reasonable interaction with NO₃⁻ molecule. Besides this type of filter could be reusable, therefore after the filtering, the swcnts could be separated from NO₃⁻ molecule.      

Cluster radioactivity leading to doubly magic <Superscript>100</Superscript>Sn and <Superscript>132</Superscript>Sn daughters

Decay of neutron-deficient ^{128 − 137}Gd parents emitting ⁴He to ³²S clusters are studied within the Coulomb and proximity potential model. The predicted half-lives are compared with other models and most of the values are well within the present experimental limit for measurements (T _1/2 < 10³⁰ s). The lowest T _1/2 value for ²⁸Si emission from ¹²⁸Gd indicates the role of doubly magic ¹⁰⁰Sn daughter in cluster decay process. It is also found that neutron excess in the parent nuclei slows down the cluster decay process. Geiger–Nuttal plots for all clusters are found to be linear with different slopes and intercepts. The α-decay half-lives of ^{148 − 152}Gd parents are computed and are in agreement with experimental data. The role of doubly magic ¹³²Sn daughter in cluster decay process is also examined for various neutron-rich Ba, Ce, Nd, Sm and Gd parents emitting clusters ranging from ⁴He to ³²Si. Alpha-like structures are most probable in the decays leading to ¹⁰⁰Sn, while non-α-like structures are probable in the decays leading to ¹³²Sn. The neutron–proton asymmetry in parent and daughter nuclei is responsible for the reduced decay rate in the decay leading to ¹³²Sn.     

Direct calculation of transition intensities in LiYF<Subscript>4</Subscript>: Nd<Superscript>3+</Superscript>

Duan’s simple model is extended to analyze the mixing of the 4f ^{N − 1}5d configuration with the 4f ^N states. The explicit static coupling and traditional dynamic coupling are considered, and the parameters are fitted according to the absorption spectrum in LiYF₄: Nd³⁺. The parameter values obtained are as follows: T ₃₂ = −28i × 10⁻⁷, T ₅₂ = −1151i × 10⁻⁷, A ₃₂² = 192i × 10⁻¹² cm, A ₅₂⁴ = i × 10⁻¹² cm, A ₇₂⁶ = 54i × 10⁻¹² cm, and A ₇₆⁶ = −680i × 10⁻¹² cm. Compared to the experimental measurements, the present model yields better results than those obtained from the Judd-Ofelt theory. The text was submitted by the authors in English.     

Microscopic study of low-lying yrast spectra in <Superscript>100–108</Superscript>Mo isotopes

Variation-after-projection (VAP) calculations in conjunction with Hartree-Bogoliubov (HB) ansatz have been carried out for A=100−108 molybdenum (Mo) isotopes. In this framework, the yrast spectra with J _max ^π ≥10⁺, B(E2) transition probabilities, quadrupole (β₂) and hexadecapole (β₄) deformation parameters, moment of inertia (I) and square of cranking frequency (ω²) for even-even Mo isotopes have been obtained. The results of the calculation give an indication that it is important to include the hexadecapole-hexadecapole component of the two-body interaction for obtaining various nuclear structure quantities in these Mo isotopes.     

Spectroscopy of the <Superscript>10</Superscript>Li isotope in stopped pion absorption reactions on a <Superscript>14</Superscript>C radioactive target

A search for the ¹⁰Li formation was performed in missing mass spectra measured in stopped pion absorption reactions ¹⁴C(π ⁻, pt)X and ¹⁴C(π ⁻, dd)X. Three excited states of ¹⁰Li were found. The broad state with a resonance energy of E _R = 6.13 ± 0.11 MeV has the highest excitation energy in comparison with levels observed earlier.     

Thermo-optic coefficients of monoclinic KLu(WO<Subscript>4</Subscript>)<Subscript>2</Subscript>

The three thermo-optic coefficients of the biaxial laser host KLu(WO₄)₂ are measured at 633 nm by a deflection method. Their values at 300 K amount to ∂ n _g /∂ T=−7.4×10⁻⁶ K⁻¹; ∂ n _m /∂ T=−1.6×10⁻⁶ K⁻¹ and ∂ n _p /∂ T=−10.8×10⁻⁶ K⁻¹. Nearly athermal propagation directions are found for polarizations along the N _m and N _p dielectric axes.     

Effect of Sr<Superscript>2+</Superscript> ion substitution with trivalent ions (Sc<Superscript>3+</Superscript>, In<Superscript>3+</Superscript>, La<Superscript>3+</Superscript>, Bi<Superscript>3+</Superscript>) on its ferroelectric instability in SrTiO<Subscript>3</Subscript>

The vibration frequencies of unstable ferroelectric and antiferrodistortion modes and the dependences of the energy on the ion displacement amplitude have been calculated within the generalized Gordon-Kim model for distortions along eigenvectors of these modes in the mixed compounds Sr_{1 − x} A _x Ti_{1 − x} /₄□ _x/4O₃ and Sr_{1 − y} A _2y /₃□ _y/3TiO₃ (A = Sc³⁺, In³⁺, La³⁺, Bi³⁺; □ is the vacancy). To compensate an excess positive charge, vacancies are introduced into the Ti⁴⁺ or Sr²⁺ site. Calculations have been performed in the “daverage” crystal approximation for impurity concentrations of 0.25 and 0.50. To this end, a set of 40 atomic superlattices with various orderings of heterovalent ions Sr²⁺ and impurity A ³⁺ has been considered. It has been found that each impurity type, independently of charge balance, induces ferroelectric instabilities in doped compounds. In the case of doping with In³⁺ and La³⁺ for concentration x = 0.25, the possibility of rotating the polarization vector has been shown.     

Associated single photons and doubly-charged scalars at linear <Emphasis Type="Italic">e</Emphasis><Superscript>−</Superscript><Emphasis Type="Italic">e</Emphasis><Superscript>−</Superscript> colliders

Doubly-charged scalars, predicted in many models having exotic Higgs rep-resentations, can in general have lepton-number violating (LFV) couplings. We show that by using an associated monoenergetic final state photon seen at a future linear e ⁻ e ⁻ collider, we can have a clear and distinct signature for a doubly-charged resonance. The strength of the ΔL = 2 coupling can also be probed quite effectively as a function of the recoil mass of the doubly-charged scalar.      

A high-stability semiconductor laser system for a <Superscript>88</Superscript>Sr-based optical lattice clock

We describe a frequency-stabilized diode laser at 698 nm used for high-resolution spectroscopy of the ¹S₀–³P₀ strontium clock transition. For the laser stabilization we use state-of-the-art symmetrically suspended optical cavities optimized for very low thermal noise at room temperature. Two-stage frequency stabilization to high-finesse optical cavities results in measured laser frequency noise about a factor of three above the cavity thermal noise between 2 Hz and 11 Hz. With this system, we demonstrate high-resolution remote spectroscopy on the ⁸⁸Sr clock transition by transferring the laser output over a phase noise-compensated 200-m-long fiber link between two separated laboratories. Our dedicated fiber link ensures a transfer of the optical carrier with frequency stability of 7×10⁻¹⁸ after 100 s integration time, which could enable the observation of the strontium clock transition with an atomic Q of 10¹⁴. Furthermore, with an eye toward the development of transportable optical clocks, we investigate how the complete laser system (laser+optics+cavity) can be influenced by environmental disturbances in terms of both short- and long-term frequency stability.     

Studies on Interaction of Norfloxacin,Cu<Superscript>2+</Superscript>, and DNA by Spectral Methods

The interactions of norfloxacin (NFA), DNA, and Cu²⁺ are studied by fluorescence and UV-spectra method. According to the experimental results, it can be concluded that NFA can form a steady binary complex with Cu²⁺. There is a linear relationship between the Fluorescence intensity of the norfloxacin–Cu²⁺–DNA system and the concentration of DNA. And when the concentration of the NFA is 1.95×10⁻⁵ mol L⁻¹, they possess a good linearity in the concentration of DNA ranged from 4.7×10⁻⁶ to 2.8×10⁻⁵ mol L⁻¹.It is a good method due to the high sensitivity and selectivity.     

A cobalt-doped transparent glass ceramic saturable absorber Q-switch for a LD pumped Yb<Superscript>3+</Superscript>/Er<Superscript>3+</Superscript> glass microchip laser

We fabricate a transparent glass ceramic contains magnesium-aluminum spinel nanocrystallites doped with Co²⁺ ions. The ground-state and excited-state absorption cross section of this glass ceramic at 1.54 μm are estimated to be (2.8 ± 0.3) × 10⁻¹⁹ cm² and (4.8 ± 0.5) × 10⁻²⁰ cm², respectively. For the first time, the passively Q-swithched operation of LD pumped 1.54 μm microchip Yb³⁺/Er³⁺ glass laser is realized with transparent glass ceramic as saturable absorber. The Q-switched pulses of 3.846 kHz in repetition rate, 6.2 ns in duration and 6.3 μJ in energy are obtained. At last, the dependences of pulse width and repetition rate on pump power are also investigated.     

Detection of trielectronic recombination of In<Superscript>+</Superscript> ion

The trielectronic recombination of an In⁺ (4d ¹⁰5s ^{2 1} S ₀) ion in collisions with slow electrons, including the two-electron excitation of the 5s2 core of the ion with the simultaneous capture of the triply excited 5p ³ intermediate autoionizing state with its subsequent radiative stabilization 5p ³ → 5s5p ² + hν has been detected and experimentally examined for the first time. The maximum effective cross section of trielectronic recombination is 1.6 × 10⁻¹⁶ cm², which is comparable to the effective cross sections for both dielectronic recombination and electron excitation of the In⁺ ion.