Spectral-luminescent properties of condensation products of 8-aminoquinoline,aromatic aldehydes,and dimedone

Hydrobenzophenanthrolinone derivatives were synthesized by three-component condensation of 8-aminoquinoline, aromatic aldehydes, and dimedone. The structures of the obtained substances were confirmed by NMR and IR spectroscopy and mass spectrometry. Spectral-luminescent investigations of the synthesized compounds showed that they were characterized by high oscillator strengths for allowed electronic transitions S _n ← S ₀ (n = 1–3). Low fluorescence quantum yields in EtOH (Φ_fl ~ 10^–4–10^–3) and an increase of the Φfl values in toluene (~10^–2) at room temperature and with lowering the temperature to 77 K (Φ_fl ~ 10^–1) for a number of the compounds under study were satisfactorily explained within the framework of Marcus theory.     

Coulomb excitation of 74Ge beam

⁷⁴Ge beam was Coulomb-excited on a ^natPb target. Ten E2 matrix elements including diagonal matrix elements for 5 low-lying states have been determined using the least-squares search code GOSIA. The expectation values of the rotational invariants 〈Q ²〉 and 〈cos3δ〉 show the small and triaxial deformation of the two lowest members of the ground-state band , while the 0₂ ⁺ and 2₂ ⁺ states are found to be almost spherical. Received: 31 August 2000 / Accepted: 4 December 2000     

Fluorescence and Electronic Structure of the Laser Dye DCM in Solutions and in Polymethylmethacrylate

The photophysical properties and polarization of the fluorescence of the laser dye 4-dicyanomethylene-2-methyl-6-(p(dimethylamino)styryl)-4H-pyran (DCM) in solutions of different polarities and in polymethylmethacrylate (PMMA) at 293 and 77 K were investigated by stationary and pulsed fluorescent spectroscopy. Based on the data of polarized fluorescence, an oscillator model has been suggested, according to which the electronic absorption spectrum of DCM in the 240–500-nm range is formed by at least three electron transitions. The quantum yield of fluorescence _f increases linearly with increase in the polarity of a solvent in a toluene dimethylsulfoxide (DMSO) mixture from 0.08 (toluene) to 0.80 (DMSO). An increase of _f to 0.90 was also observed on increase in the rigidity of the medium by freezing a solution of DCM in n-propanol at 77 K or introducing of a dye to the polymeric matrix of PMMA at room temperature ( _f = 0.76). The fluorescence-decay kinetics of DCM in toluene, n-propanol, and PMMA at 293 K follows a biexponential law, whereas in n-hexane and vaseline oil at 293 K and in n-propanol at 77 K it follows a monoexponential law. The mechanisms underlying radiationless deactivation of the electron-excitation energy in solutions and in polymeric media are discussed.     

The effect of aluminum alloying on strength properties and deformation mechanisms of the 〈123〉 Hadfield steel single crystals

The role of aluminum alloying on strength properties and deformation mechanisms (slip, twinning) of 〈123〉 single crystals of Hadfield steel under tensile loading at T = 300 K is demonstrated. It is found out that aluminum alloying suppresses twinning deformation in the 〈123〉 single crystals and, during slip, results in a dislocation structure change from a uniform dislocation distribution to a planar dislocation structure. __________ Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 10, pp. 3–7, October, 2007.     

A lower bound for the volume-averaged mean-square magnetostatic stray field

Based on a micromagnetics model, we develop a method through which quantitative information on the volume-averaged mean-square magnetostatic stray field 〈|H ^b _d|²〉 _v due to non-zero divergences of the magnetization M within the bulk of a ferromagnetic body can be obtained by analysis of magnetic-field-dependent small-angle neutron scattering data. In the limit of high applied magnetic field H _a, when the direction of M deviates only sligthly from H _a, we have estimated a lower bound for 〈|H ^b _d|²〉 _v as a function of the external field, and we have applied the method to bulk samples of nanocrystalline electrodeposited Ni and Co and coarse-grained polycrystalline cold-worked Ni. The root-mean-square magnetostatic stray field, which is inherent to a particular magnetic microstructure, shows a pronounced field dependence, with values ranging from about 5 to 50mT. Even at applied fields as large as 1.7T, the quantity μ〈|H ^b _d|²〉^1/2 _v of nanocrystalline Co is still 24mT, which suggests that contributions to the total magnetostatic field originating from the bulk are significant in nanocrystalline ferromagnets; therefore, 〈|H ^b _d|²〉 _v cannot be ignored in the interpretation of e.g. measurements of magnetization or spin-wave resonance. A comparison of 〈|H ^b _d|²〉 _v with the volume-averaged mean-square anisotropy field reveals that both quantities are of comparable magnitude. Received 25 April 2002 Published online 31 October 2002 RID="a" ID="a"e-mail: anmi@nano.uni.saarland.de     

Effect of uniaxial strain on the structure of self-localized excitons in alkali halide crystals

We have used luminescence spectroscopy to establish the effect of low-temperature (100 K) elastic uniaxial strain on the configuration of a self-localized exciton (SLE) in alkali halide crystals (AHCs) at the instant of radiative relaxation. In face-centered (fc) alkali halide crystals, redistribution of the luminescence intensity occurs from the asymmetric SLE configuration to the symmetric SLE configuration (type III → II → I), while conversely in body-centered (bc) alkali halide crystals the redistribution occurs in favor of the asymmetric (polarized) SLE configuration (type I → II). External strain along the 〈100〉 direction leads to effective slip of the anions in the alkali halide crystals along the 〈110〉 direction, coinciding with the direction of compression of the SLE, which promotes creation of preferentially the symmetric SLE configuration, while strain along the 〈110〉 direction, acting perpendicularly to the length of the SLE, leads to elongation of the SLE, which promotes creation of the asymmetric SLE configuration with a higher degree of polarization. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 74, No. 1, pp. 67–72, January–February, 2007.     

Probing the strange quark condensate by di-electrons from φ-meson decays in heavy-ion collisions at SIS energies

QCD sum rules predict that the change of the strange quark condensate 〈ˉss〉 in hadron matter at finite baryon density causes a shift of the peak position of the di-electron spectra from φ-meson decays. Due to the expansion of hadron matter in heavy-ion collisions, the φ peak suffers a smearing governed by the interval of density in the expanding fireball, which appears as an effective broadening of the di-electron spectrum in the φ region. The emerging broadening is sensitive to the in-medium change of 〈ˉss〉. This allows to probe directly in-medium modifications of 〈ˉss〉 via di-electron spectra in heavy-ion collisions at SIS energies with HADES. Received: 22 November 2002 / Accepted: 30 January 2003 / Published online: 29 April 2003     

Nulling Phenomenon of the New Radio Pulsar J0810+37 at a Frequency of 111 MHz

Pulsar J0810+37 with a period of 1.2483 s is detected at a frequency of 111 MHz during the pulsar search at the Big Scanning Antenna (BSA) radio telescope of the Lebedev Physical Institute [1]. In this paper, we present the results of the detailed study of radio emission from J0810+37 which exhibits a rare nulling effect of different durations in a very wide time interval with an average nulling fraction in “switch-on” days 〈NF〉 = 38%; considering “switch-off” days, 〈NF〉 = 74%, since radio emission from this source is interrupted on average by 2–3 days, and then it again revives on average for 1–2 days. The “switch-off” periods reach 7 days.     

Rigorous Results on Spontaneous Symmetry Breaking in a One-Dimensional Driven Particle System

We study spontaneous symmetry breaking in a one-dimensional driven two-species stochastic cellular automaton with parallel sublattice update and open boundaries. The dynamics are symmetric with respect to interchange of particles. Starting from an empty initial lattice, the system enters a symmetry broken state after some time T ₁ through an amplification loop of initial fluctuations. It remains in the symmetry broken state for a time T ₂ through a traffic jam effect. Applying a simple martingale argument, we obtain rigorous asymptotic estimates for the expected times 〈 T ₁〉 ∝ Lln L and ln 〈 T ₂〉 ∝ L, where L is the system size. The actual value of T ₁ depends strongly on the initial fluctuation in the amplification loop. Numerical simulations suggest that T ₂ is exponentially distributed with a mean that grows exponentially in system size. For the phase transition line we argue and confirm by simulations that the flipping time between sign changes of the difference of particle numbers approaches an algebraic distribution as the system size tends to infinity.     

Charge radius change in the heavy tin isotopes until A = 132 from laser spectroscopy

Laser spectroscopy measurements have been carried out on the very neutron-rich tin isotopes with the COMPLIS experimental setup. Using the 5s ²5p ²³ P ₀ → 5s ²5p6s ³ P ₁ optical transition, hyperfine spectra of ^126-132Sn and ^{125m, 127m, 129m-131m}Sn where recorded for the first time. The variation of the mean-square charge radius ( δ〈r ²〉) between these nuclei and nuclear moments of the isomers and the odd isotopes were thus measured. An odd-even staggering which inverts at A = 130 is clearly observed. This indicates a small appearance of a plateau on the δ〈r ²〉 which has to be confirmed by measuring the isotope shift beyond A = 132. Received: 21 March 2002 / Accepted: 16 May 2002 / Published online: 31 October 2002 RID="a" ID="a"e-mail: leblanc@ipno.in2p3.fr     

A Discrete, Deterministic Construction of the Phase in Feynman Paths

In the path-integral formulation of quantum mechanics, the phase factor e ^iS(x〈t〉) is associated with every path x〈t〉. Summing this factor over all paths yields Feynman's propagator as a sum-over-paths. In the original formulation, the complex phase was a mathematical device invoked to extract wave behaviour in a particle framework. In this paper we show that the continuous phase itself can have a discrete origin in time reversal and that the propagator can be drawn by a single deterministic path. ¹On leave from Department of Mathematics, Ryerson University, Toronto, Ontario Canada.     

Synthesis,Electrochemical, and Optical Properties of New Fluorescent,Substituted Thieno[3,2-b][1]Benzothiophenes

The synthesis, electrochemical and optical properties of three fluorescent substituted thieno[3,2-b][1]benzothiophenes (TBT) derivatives, including 3-methoxythieno[3,2-b][1]benzothiophene (3-MeO-TBT), 2,3-dimethylthieno[3,2-b][1]benzothiophene (2,3-diMe-TBT), and 6-methoxythieno[3,2-b][1]benzothiophene-2-carboxylate (6-MeO-TBT-2-COOMe), were investigated. The oxidation potential values varied between 1.40 and 1.20 V/SCE according to the electronic substituent effect, and electropolymerization attempts, performed in 0.1 M LiClO₄ acetonitrile solution, led to the formation of very thin films of poly(3-MeO-TBT) and poly(2,3-di-Me-TBT). Electronic absorption spectra, fluorescence excitation and emission spectra, fluorescence quantum yields (Φ_F) , lifetimes (τ_F), and other photophysical parameters of the three new TBT derivatives were measured in DMSO solutions at room temperature. For the methyl-and methoxy-substituted TBT derivatives, the fluorescence emission peak were slightly red shifted relative to that of unsubstituted TBT (Δλ_em = 1–12 nm) whereas, in the case of 6-MeO-TBT-2-COOMe, a rather strong red-shift (Δλ_em = 73 nm) was attributed to the existence of a “push-pull” electronic interaction of the MeO and COOMe groups. All Φ_F values were rather high, varying between 0.11 and 0.35, according to the substituent effect. Fluorescence decays were mono-exponential and τ_F values were very short, ranging between 0.11 and 0.30 ns for the substituted TBT derivatives until study.     

Large-scale synthesis of crystalline β-SiC nanowires

Large quantities of high-purity crystalline β-SiC nanowires have been synthesized at relatively low temperature via a new simple method, the chemical-vapor-reaction approach, in a home-made graphite reaction cell. A mixture of milled Si and SiC powders and C₃H₆ were employed as the starting materials. The results show that the nanowires with diameters of about 10–35 nm are single crystalline β-SiCwithout any wrapping of amorphous material, and the nanowire axes lie along the 〈111〉 direction. Some unique properties are found in the Raman scattering from the β-SiC nanowires, which are different from previous observations of β-SiC materials. A possible growth mechanism for the β-SiC nanowires is proposed. Received: 27 August 2002 / Accepted: 28 August 2002 / Published online: 4 December 2002 RID="*" ID="*"Corresponding author. Fax: +86-29/8491-000, E-mail: zjli-sohu@sohu.com     

One-dimensional Anderson model with dichotomic correlation in the presence of external electric field

A one-dimensional diagonal tight binding electronic system with dichotomic correlated disorder in the presence of external d.c field is investigated. It is found numerically that the conductance distribution obeys fairly well to log-normal distribution in weak disorder strength in localized regime, which indicates validity of single parameter scaling theory in this limit. Contrary to the universal cumulant relation C ₁ = 2C ₂ in the absence of d.c. field, we demonstrated numerically that C ₁ ≫ 2C ₂ in the presence of the field in localized regime. We interpret this result as suppression of the fluctuation effects by the external field. In addition, it is obtained that the quantity NF _c , here N is the system size and F _c is the crossover field, decreases as the as the system energy E increases. Moreover, we find numerically a simple linear relation between the average logarithm of the conductance 〈ln(g)〉 and the field strength as 〈ln(g)〉 = C(N, λ)F, here C(N, λ) is a constant for particular values of N and λ, which is the Poisson parameter of the dichotomic process.     

亚单层黄色有机发光器件制备与光电性能研究

采用掺杂薄层作为亚单层有机发光技术,利用沉积在有机发光器件发光层中的亚单层分子[2-methyl-6-[2-(2,3,6,7-tetrahydro-1H,5H-benzo[ij] quinolizin-9-yl) ethenyl]-4H-pyran-4-ylidene] propane-dinitrile （DCM2）作为探针,同时改变DCM2层的位置,制备了四种亚单层结构的有机发光器件,对有机发光器件中激子的形成与扩散进行了研究,通过对各器件不同条件下的电致发光谱、发光强度和发光效率的对比研究,得到在N,N′-bis-(1-naphthyl)-N,N′-diphenyl-1,1′-biph-enyl-4,4′-diamine（NPB）/(8-hydroxyquinoline) aluminium（Alq）异质结界面处引入亚单层DCM2可以使DCM2分子获得的激子数量最多,获得了高效率的黄色有机发光器件.从其中总结规律,对有机发光器件制作有一定的指导作用.     

Decay reactions of rare gas cluster ions: Kinetic energy release distributions and binding energies

We have carried out measurements on metastable fragmentation of mass selected argon cluster ions which are produced by electron impact ionization of a neutral argon cluster beam. From the shape of the fragment ion peaks (MIKE scan technique) one can deduce information about the distribution of kinetic energy that is released in the decay reaction. In this study, for Ar ₅ ⁺ to Ar ₁₅ ⁺, it is Gaussian and thus we can calculate from the peak width the mean kinetic energy release 〈KER〉 of the corresponding decay reactions. Using finite heat bath theory we calculate from these data the binding energies of the decaying cluster ions. Received 20 November 2000     

Effect of polar dopant on energetic and positional disorders in tris(8-hydroxyquinolinato) aluminum (Alq3)

The influence of polar dopant on the charge carrier transport in amorphous tris (8-hydroxyquinolinato) aluminum (Alq₃) was studied by time-of-flight measurement. The 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran (DCM) was doped into Alq₃ with various concentration from 0.5 to 24 wt. %. The electron mobility was reduced by about one order by DCM doping in Alq₃. The electric-field dependence electron mobility in Alq₃:DCM films separated into two discrete regions of critical fields E_c ^1/2. The value of E_c ^1/2ranged from 360 to 405 (V/cm)^1/2 depending on the DCM concentration in Alq₃ films. The energetic disorder in Alq₃:DCM films increased from 0.01 eV to 0.09 eV with DCM doping concentration. The positional disorder in Alq₃:DCM films also increased from 0.3 to 6.5 with DCM doping concentration up to 24 wt. %. These results indicated the strong Coulombic and dipole–dipole interactions between DCM and Alq₃ molecules. The interactions between randomly located DCM molecules, Alq₃ dipoles and oriented dipoles are the major caused of positional disorder. PACS 73.50.-h; 73.61.Ph; 71.20.Rv     

Influence of local excitation of octupolar Oligophenylenevinylenes on their dipole moments

Absorption and fluorescence spectra of octupolar centrosymmetric oligophenylenevinylene dyes (E,E)-bis[2-(4-hexyloxyphenyl)ethenyl]-(E,E)-3,6-bis-[2-(4-N,N-dipropylaminophenyl)ethenyl]pyrazine and (E,E,E,E)-2,3,5,6- tetra-[2-(4-hexyloxyphenyl)ethenyl]pyrazine were measured in various solvents. An electro-optical absorption method was used to determine their dipole moments as μ _g  = 6.1∙10^–30 and 3.4∙10^–30 C∙m in the equilibrium ground state and the increased values ∆ ^a μ = 11.9∙10^–30 and 8.2∙10^–30 C∙m upon excitation into a Franck–Condon state. Quantum-chemical calculations showed that the molecules had non-planar configurations. The π,π-conjugated system was localized on the most planar part of the molecule that was responsible for light absorption in the range 300–450 nm due to a change in the geometry of the molecules in the ground state. Localized excitation of the molecules caused their dipole moments ∆ ^a μ to change significantly.     

Fluorescence spectroscopy of potential electroluminescent materials: Substituent effects on DSB and segmented PPV derivatives

The absorption and fluorescence of substituted distyrylbenzene (DSB) derivatives and segmented poly(phenylene vinylene) (PPV) derivatives are characterized by long-wavelength absorption maxima and absorption coefficients of λ_a = 380–450 nm, ε = 20,000–60,000 M⁻¹ cm¹ and fluorescence maxima, quantum yields, and decay times of λ_r = 440–530 nm, Φ_f = 0.2–0.9, and Τ = 0.8–2.5 ns, respectively. Alkoxy substituents at the central phenylene ring of DSB groups increase the bathochromic shift in the spectra in comparison to DSB, without a significant decrease in the high DSB fluorescence quantum yield. Both phenyl and cyano substitutions at the vinylene bridge lead to a further bathochromic shift of the fluorescence and a decrease in the quantum yield to ca. 0.4. The DSB derivatives and the related segmented PPV derivatives show nearly the same absorption spectra, fluorescence spectra, and radiative rate constantsk _f= Φ_f/Τ, indicating the efficacy of the segmentation of the polymer chain. The radiative rate constants determined by the Φ_f and Τ values and by the Strickler/Berg formula are in reasonable agreement. This supports the possibility of interpreting the properties of the polymers in terms of their DSB units. The decrease in the emission anisotropy can be ascribed to multistep energy transfer processes between different oriented segments.     

Fission lifetimes of Th nuclei measured by crystal blocking

Crystal blocking lifetime measurements have been made for highly excited Th nuclei with neutron number well removed from the stability line. Thin W crystals were bombarded with ³²S ions in the energy range 170-180 MeV and the yield of fission fragments was measured for emission close to a 〈111〉 axis. The fission blocking dips are compared to the appropriately scaled ones for elastic scattering of the ³²S beam ions and no significant difference is seen between the dips. This implies that the fraction of nuclei fissioning with lifetimes longer than 10 as is less than 2%. Fission lifetimes are increased by viscosity in the nuclear mass flow and comparison with a statistical model calculation indicates that the viscosity parameter, η, must be lower than for Th and U nuclei near β-stability. The effect of the N = 126 magic number is discussed. Received: 2 October 2002 / Accepted: 16 January 2003 / Published online: 29 April 2003