Vibronic-spin-orbit interactions in heterocyclic analogues of fluorene with the N and O heteroatoms

The transition dipole moments P _0n ^s for the transitions from the electronic triplet state ³ B ²(ππ*) to vibrational sublevels of the vibrational out-of-plane modes n of the carbazole and dibenzofuran molecules are calculated. The values of the radiative deactivation rate constant k _rad ^s of the triplet sublevels T ^s are determined along with the components k _SO ^s and k _VSO ^s of this constant, which depend on the intramolecular spin-orbit (SO) and vibronic-spin-orbit (VSO) interaction. It is ascertained that k _rad ^z > k _rad ^y . For different structural units of the molecules (the heteroatom and the carbon atoms of the dibenzene fragment), the effect of the SO coupling on the constant k _VSO～Σ_{s, n} (P _0n ^s )² is studied. A competition between the effects on k _VSO from the SO coupling in the carbon atoms and in the light N and O heteroatoms is revealed. This competition accounts for the weak influence of the heteroatom on this component of the rate constant k _rad in these molecules. It is ascertained that the intensity distribution among the vibronic lines in the phosphorescence spectra of carbazole and dibenzofuran I _0n ～Σs (P _0n ^s )² is different due to the substantially different influence of the N and O heteroatoms on the deactivation of the triplet sublevel T ^y .     

Nonradiative <Emphasis Type="Italic">S-T</Emphasis> intersystem crossing in α and β chlorine derivatives of naphthalene

The rate constants K _ST ^s of nonradiative S ₁ ? T ₁ ^s transitions to triplet sublevels s in molecules of chlorine derivatives of naphthalene (1,4-dichloro- and monosubstituted α-chloro- and β-chloronaphthalene) have been calculated within the model of vibronically induced spin-orbit (VISO) couplings. The contribution of the spin-orbit couplings in Cl atoms and carbon framework of the molecule to VISO couplings is determined. A dependence of the heavy-atom effect on the constant K _ST ^s in relation to the type of sublevel T ^s and α and β positions of chlorine in the molecule is established and explained.     

Stability of Coulomb systems

The stability of m ₁ ⁺ m ₂ ⁺ m ₃ ^? m ₄ ^? Coulomb systems formed by particles of unit charge against dissociation is considered as a function of the particle mass. It is shown that, from the stability of the m ₁ ⁺ m ₂ ⁺ m ₃ ^? three-particle system, it follows that the m ₁ ⁺ m ₂ ⁺ m ₃ ^? m ₄ ^? four-particle system containing an additional particle of mass satisfying the condition m ₄ ^? ? m ₃ ^? is stable. The results of calculations of the stability domain for m ₁ ⁺ m ₂ ⁺ m ₃ ^? systems asymmetric in particle masses are reported. The stability of 39 asymmetric exotic four-particle molecules and mesic molecules against dissociation is established.     

Anisotropic characteristics of the kraichnan direct cascade in two-dimensional hydrodynamic turbulence

The statistical characteristics of the Kraichnan direct cascade for two-dimensional hydrodynamic turbulence are numerically studied (with spatial resolution 8192 × 8192) in the presence of pumping and viscous-like damping. It is shown that quasi-shocks of vorticity and their Fourier partnerships in the form of jets introduce an essential influence in turbulence leading to strong angular dependencies for correlation functions. The energy distribution as a function of modulus k for each angle in the inertial interval has the Kraichnan behavior, ~k ^–4, and simultaneously a strong dependence on angles. However, angle average provides with a high accuracy the Kraichnan turbulence spectrum E _k = C _Kη^2/3k^–3, where η is the enstrophy flux and the Kraichnan constant C _K ? 1.3, in correspondence with the previous simulations. Familiar situation takes place for third-order velocity structure function S ₃ ^L which, as for the isotropic turbulence, gives the same scaling with respect to the separation length R and η, S ₃ ^L = C ₃ηR ³, but the average over the angles and time differs from its isotropic value.     

<Emphasis Type="Italic">B</Emphasis>-meson decays into charmonium states in the ATLAS experiment

The paper presents several recent ATLAS results on the analyses of B-meson decays into charmonium states. These include the measurements of B⁺ mass and the fractions of J/ψ mesons produced in b-hadron decays in pp collisions at \(\sqrt s\) = 13 TeV in the center of mass system. The measured partial widths and polarizations in B _c ⁺ → J/ψD _s ^(*)+ decays and CP-violation parameters in B _s ⁰ → J/ψ? decays in pp collisions at 7 and 8 TeV in the center of mass system are also presented.     

Dipole moment functions for electronic transitions from ion-pair states of the second tier of molecular iodine

The emission spectra caused by the transitions from the ion-pair states and f0 _g ⁺ and G1_g of the I₂ molecule are obtained by excitation of individual rovibronic levels of the molecule by the method of optical-optical double resonance. The emission spectra from the state F0 _u ⁺ populated due to collisions I₂(f) + I₂(X) are also measured. By modeling the experimental emission spectra, the dipole moment functions for the electronic transitions f _g ⁺ -B0 _u ⁺ , A0 _u ⁺ , and B″0 _u ⁺ ; G1_g-A0 _u ⁺ and B″0 _u ⁺ ; and F0 _u ⁺ -X0 _g ⁺ and a′0 _g ⁺ of the iodine molecule are reconstructed.     

Integral characteristics of vibronic-spin-orbit interactions in a phosphorus-containing analogue of the fluorene molecule

The strengths (P ₀₀ ^s )² and F _VSO ² of the transitions from the triplet sublevels s = z, y, and x of the electronic state ³A″ of the phenyldibenzophosphole (DB(P-Ph)) molecule are calculated taking into account the intramolecular spin-orbit (SO) and joint vibronic-spin-orbit (VSO) interactions. The contributions to the vibronic transition strengths from the SO interactions in different structural elements of the molecule (the C atoms of the dibenzene framework, the P atom, and the Ph substituent) are determined. The effect of the nonplanar nuclear configuration of the DB(P-Ph) molecule on the values of F _VSO ^s is investigated. The radiative deactivation rate constants of the k _rad ^s triplet sublevels T ^s are estimated. It is found that the vibrations of the A′(B₁) symmetry in the fine-structure phosphorescence spectrum of DB(P-Ph) occur due to both the SO coupling exclusively in the P atom and the T ^x → S₀ transition (the x axis is perpendicular to the planar dibenzene framework of the molecule) with a high (preferential) population of this triplet sublevel.     

Probabilities of forbidden magnetic-dipole transitions in the hydrogen atom and hydrogen-like ions

Explicit formulasfor strongly forbidden magnetic-dipole transitiions between states njl and n′jl in the hydrogen atom and light hydrogen-like ions are derived. The expressions for transition probabilities are presented in the form W _{n′jl; njl} ^(M1) = D _n′n ^lj αm _e (αZ)¹⁰ (in relativistic units), where m _e is the electron mass, α is the fine-structure constant, and Z is the nuclear charge; the constants D _n′n ^lj are presented in an analytical form. Before now, only the D ₂₁ ^01/2 coefficient corresponding to the 1s _1/2–2s _1/2 transition was known in explicit form. The results obtained can be used in designing an experiment on parity violation in the hydrogen atom.     

Ds+ → π+ π+ π− decay: The $$1^3 P_0 s\bar s$$ component in scalar-isoscalar mesons

We calculate the processes \(D_s^ + \to \pi ^ + s\bar s\) and D _s ⁺ → π⁺resonance, respectively, in the spectator and W-annihilation mechanisms. The data on the reaction D _s ⁺ → π⁺ρ⁰, which is due to the W-annihilation mechanism only, point to a negligibly small contribution of the W annihilation to the production of scalar-isoscalar resonances D _s ⁺ ?π⁺f₀. As to spectator mechanism, we evaluate the \(1^3 P_0 s\bar s\) component in the resonances f₀(980), f₀(1300), and f₀(1500) and broad state f₀(1200–1600) on the basis of data on the decay ratios D _s ⁺ ?π⁺f₀/(D _s ⁺ ?π⁺_θ). The data point to a large \(s\bar s\) component in the \(f_0 (980):40 \lesssim s\bar s \lesssim 70\% \). Nearly 30% of the \(1^3 P_0 s\bar s\) component flows to the mass region 1300–1500 MeV, being shared by f₀(1300), f₀(1500), and broad state f₀(1200–1600): the interference of these states results in a peak near 1400 MeV with the width around 200 MeV. Our calculations show that the yield of the radial-excitation state\(2^3 P_0 s\bar s\)is relatively suppressed, \({{\Gamma (D_s^ + \to \pi ^ + (2^3 P_0 s\bar s))} \mathord{\left/ {\vphantom {{\Gamma (D_s^ + \to \pi ^ + (2^3 P_0 s\bar s))} {\Gamma (D_s^ + \to \pi ^ + (1^3 P_0 s\bar s))}}} \right. \kern-\nulldelimiterspace} {\Gamma (D_s^ + \to \pi ^ + (1^3 P_0 s\bar s))}} \lesssim 0.05\).     

High-frequency EPR of Cr<Superscript>2+</Superscript> ions in CdGa<Subscript>2</Subscript>S<Subscript>4</Subscript>

High-frequency broad-band (65–240 GHz) EPR is used to study impurity centers of bivalent chromium in a CdGa₂S₄ crystal. It is found that the EPR spectra correspond to tetragonal symmetry. The spin Hamiltonian H = βB · g · S + B ₂ ⁰ O ₂ ⁰ + B ₄ ⁰ O ₄ ⁰ + B ₄ ⁴ O ₄ ⁴ with the parameters B ₂ ⁰ =23659±2 MHz, B ₄ ⁰ =1.9±1 MHz, |B ₄ ⁴ |=54.2±2 MHz, g_‖=1.93±0.02, and g_⊥=1.99±0.02 is used to describe the observed spectra. It is concluded that chromium ions occupy one of the tetrahedrally coordinated cation positions.     

37 Years with the light scalar mesons. The learned lessons

Attention is paid to the production mechanisms of light scalars that reveal their nature. We reveal the chiral shielding of the σ(600) meson. We show that the kaon loop mechanism of the ? radiative decays, ratified by experiment, is four-quark transition and points to the four-quark nature of light scalars. We show also that the light scalars are produced in the two photon collisions via four-quark transitions in contrast to the classic P wave tensor qq? mesons that are produced via two-quark transitions γγ → qq?. We study the mechanism of production of the light scalar mesons in the D _s ⁺ → π⁺π^? e ⁺ν decays: D _s ⁺ → ss?e ⁺ν → [σ(600) + f ₀(980)]e ⁺ν → π⁺π^? e ⁺ν, and compare it with the mechanism of production of the light pseudoscalar mesons in the D _s ⁺ → (η/η′)e ⁺ν decays: D _s ⁺ → ss?e ⁺ν → (η/η′)e ⁺ν. As a result we find support to four-quark nature of light scalars. In the end, we outline the future research program.     

Fluorescence quenching of vaporous polycyclic aromatic hydrocarbons by oxygen

The fluorescence quenching by oxygen of vapors of nine polycyclic aromatic hydrocarbons with strongly different oxidation potentials 0.44 eV < E _ox < 1.61 eV (anthracene, 9-methylanthracene, 2-aminoanthracene, 9,10-dibromanthracene, pyrene, chrysene, phenanthrene, fluoranthene, and carbazole) is studied. From the dependences of the fluorescence decay rates and intensities on the oxygen pressure P _O2, the quenching rate constants k _S ^O2 for the excited singlet states S ₁ and the fraction f _S ^O2 of the S ₁ states quenched by oxygen are estimated. At P _O2 = 5 Torr, the k _S ^O2 constants vary from 1.2 × 10⁷ to 3.0 × 10⁵ s^?1 Torr^?1, while the fraction of the quenched excited singlet states changes from 0.1 (fluoranthene) to 0.7 (chrysene) and 0.8 (pyrene). The dependences of k _S ^O2 on the photophysical and electron-donor characteristics of the fluorescing compounds are analyzed. It is shown that, in the gas phase of anthracene and its derivatives, the magnitudes of k _S ^O2 are limited by the rate constants of gas-kinetic collisions k _gk and do not depend on the electron-donor characteristics of fluorophores, while the fraction of quenched states f _S ^O2 changes with the oxidation potential. For compounds with k _S ^O2 < k gk, both the rate constants k _S ^O2 and the fraction of quenched states f _S ^O2 depend on the E _ox of sensitizers, which demonstrates an important role played by the charge-transfer interactions in quenching of the S ₁ states. The dependence of the rate constants k _S ^O2 on the free energy of electron transfer ΔG _et is considered.     

Bound-exciton cathodoluminescence in ZnSe crystals and two-phonon resonance

A study has been made of the cathodoluminescence of ZnSe crystals annealed in vacuum [ZnSe(Vac)], in vacuum and, subsequently, in antimony melt [(ZnSe(Vac)(Sb)], or in a zinc melt with subsequent annealing in antimony [ZnSe(Zn)(Sb)]. The emission of all samples contained the I ₁ ^s,d -nLO series. The LO-phonon replicas of the emission line I ₁ ^s observed in ZnSe(Vac) samples are accompanied by single-plasmon satellites. The plasmon energy determining the replica separation is ?ω_p?10 meV. The emission lines of ZnSe(Zn)(Sb) samples have the smallest half-width. We report the first observation of anomalous broadening of the zero-phonon line I ₁ ^s in ZnSe(Vac) samples caused by a high zinc vacancy content. A theory on the shape of the emission spectrum under two-phonon resonance is developed including bound-exciton interaction with mixed plasmon-phonon vibrational modes. It is shown that the splitting of the I ₁ ^d line at T?2 K may originate from resonance exciton-phonon interaction between exciton-impurity complexes.     

Searching for Exotic States with b and c Quarks in D0 Experiment

The latest results of searching for exotic multiquark states with heavy quarks obtained in the D0 experiment (Fermi National Accelerator Laboratory, USA) are presented. In particular, the evidence of existence of a possible four-quark state X(5568) → B _s ⁰ π^±in the cases with hadronic and semileptonic decay channels of B _s ⁰ meson is considered, as well as the results of searching for the five-quark states in the J/ψΛ system.     

The Structure of Radiative Tunnel Recombination Sites in Emulsion Microcrystals of AgBr(I)

To identify the structure of emissive tunnel recombination sites in the emulsion microcrystals of silver bromide AgBr(I) with iodine contaminations and to determine the role of an emulsion medium in their formation, the temperature dependence of the luminescence spectra in the range from 77 to 120 K, the kinetics of the growth of the maximum luminescence intensity value at λ ≈ 560 nm, and the luminescence flash spectrum stimulated by the infrared light are investigated. Two types of the AgBr_{1 – x}(I _x ) (x = 0.03) microcrystals—namely, obtained in an aqueous solution and on a gelatin substrate—are used in the studies. It is established that the emissive tunnel recombination sites with a luminescence maximum at λ ≈ 560 nm in AgBr_{1 – x}(I _x ) (x = 0.03) are the {(I _a ^- I _a ^- )Ag _i ⁺ } donor–acceptor complexes with the I _a ^- iodine ions located in neighbor anionic sites of the AgBr(I) crystal lattice, next to which the Ag _i ⁺ interstitial silver ion is positioned. With an increase in the temperature, the {(I _a ^- I _a ^- )Ag _i ⁺ } sites undergo structural transformation into the {(I _a ^- I _a ^- )Ag_in⁺} sites, where n = 2, 3, …. Moreover, the {(I _a ^- I _a ^- )Ag _in ⁺ } sites (n = 2) after the capture of an electron and hole also provide the tunnel recombination with a luminescence maximum at λ ≈ 720 nm. The influence of an emulsion medium consists in that gelatin interacts with the surface electron-localization sites, i.e., the interstitial silver ions Ag _in ⁺ , n = 1, 2, and forms the complexes {Ag _in ⁰ G⁺} (n = 1, 2) with them. The latter are deeper electron traps with a small capture cross section as compared to the Ag _in ⁺ sites (n = 1, 2) and that manifest themselves in that the kinetics of the luminescence growth in AgBr(I) to a stationary level at λ ≈ 560 nm is characterized by the presence of “flash firing.” At the same time, the luminescence flash stimulated by IR light, for which the Ag _in ⁺ (n = 1, 2) electron-localization sites are responsible, is absent. It is supposed that the electrons localized on the {Ag _in ⁺ G⁺} complexes (n = 2) retain the capability for emissive tunnel recombination with holes localized on paired iodine sites with a luminescence maximum at λ ≈ 750 nm.     

Electronic structure of α-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>: Ab initio simulations and comparison with experiment

Al₂O₃ films 150 Å thick are deposited on silicon by the ALD technique, and their x-ray (XPS) and ultraviolet (UPS) photoelectron spectra of the valence band are investigated. The electronic band structure of corundum (α-Al₂O₃) is calculated by the ab initio density functional method and compared with experimental results. The α-Al₂O₃ valence band consists of two subbands separated with an ionic gap. The lower band is mainly formed by oxygen 2s states. The upper band is formed by oxygen 2p states with a contribution of aluminum 3s and 3p states. A strong anisotropy of the effective mass is observed for holes: m _h⊥ ^* ≈ 6.3m ₀ and m _h‖ ^* ≈ 0.36m ₀. The effective electron mass is independent of the direction m _e‖ ^* ≈ m _e⊥ ^* ≈ 0.4m ₀.     

Nuclear magnetic relaxation of spin<Emphasis Type="Italic">I</Emphasis>=1/2 scalar coupled to a quadrupolar nucleus in the presence of cross-correlation effects

The rigorous treatment of relaxation for the dipolar-multipolarAX spin system (I=1/2,S>1/2) in the presence of the dipolarI-S coupling, anisotropy chemical shift and quadrupolar interaction ofS spin is proposed. The calculations of the spin evolution under the relaxation Hamiltonian are based on the second-order time-dependent perturbation theory and are carried out in the operator representation. For this task the double commutator identities of the type [[I _±S _z ⁿ ,A _q ^μp ]A _?q ^μp ] and [[I _zS _z ⁿ ,A _q ^μp ]A _?q ^μp. ] are derived. The fist-order differential equations for the evolution of longitudinal two-spin orderI _zS _z ⁿ , z=magnetization ofS spinS _z ⁿ and coherences <I _±S _z ⁿ > in the spin systemIS with scalar coupling between spin 1/2 and quadrupolar spinS>1/2 were obtained. These equations are used to get equations for the evolutions of each component of the multiplet structure of spinI. The imaginary part of the cross-correlation spectral density function and indirect spin-spin coupling Hamiltonian are taken into account. Equations for the longitudinal components of theI spin spectrum in the presence of cross-correlation effects were obtained also. Longitudinal and transverse relaxation times and cross-relaxation times in the presence of cross-correlation D-CSA, Q-CSA, Q-D were analyzed.     

Spectroscopy of the <Stack><Subscript>Λ</Subscript><Superscript>7</Superscript></Stack>He nucleus in a three-cluster model

The _Λ ⁷ He hypernucleus is considered within the _Λ ⁵ He + n + n cluster model. The hyperon—nucleon interaction is described by a one-boson-exchange potential that is constructed on the basis of the NSC97f model. Phenomenological potentials are used to describe the αΛ and αN interactions. For the _Λ ⁵ Hen interaction, use is made of the folding-model potential. The calculations of the hyperon binding energy in the ground state of the _Λ ⁷ He hypernucleus on the basis of Faddeev equations in configuration space yield a result (5.35 MeV) that agrees well with preliminary experimental data (5.4 MeV). The problem of calculating the hyperon binding energy within the three-body approach is discussed. In calculating the energy spectrum of _Λ ⁷ He, use is made of a version of the method of analytic continuation in the coupling constant. Low-lying excited states of this nucleus can be classified as an analog of the corresponding states of the ⁶He nucleus with allowance for the clustering of the _Λ ⁵ He+n+n system in the ⁶He(J ^π)+Λ(s) form.     

Dominant decays of scalar leptoquarks and scalar gluons in the minimal four-color symmetry model

Fermionic and weak decays of the scalar leptoquarks S = S ₁ ⁽⁺⁾ , S ₁ ^(?) , and S _m and the scalar gluons F = F ₁ and F ₂ predicted by the minimal model involving four-color symmetry and the Higgs mechanism of quark-and lepton-mass splitting are considered. The widths and the branching ratios are calculated for these decays, and the results are analyzed versus the couplings and masses of decaying particles. It is shown that, at relatively small mass splittings Δm within scalar doublets (Δm < m _W), the fermionic decays S ₁ ⁽⁺⁾ → tl _j ⁺ , S ₁ ^(?) → v _i \(\tilde b\), S _m → t \(\tilde \nu \) _j, F ₁ → t \(\tilde b\), and F ₂ → t \(\tilde t\), which are characterized by few-GeV widths for m _S, m _F < 1 TeV and decay branching ratios close to unity, are dominant, but that, for Δm > m _W, the weak decays S → S′W and F → F’W compete with the above fermionic decays. In the case of m _S < m _t, the processes S ₁ ⁽⁺⁾ → cl _j ⁺ , S ₁ ^(?) → v _i \(\tilde b\), S _m → bl _j ⁺ , and S _m → c \(\tilde \nu \) _j, whose total branching ratios are Br(S ₁ ⁽⁺⁾ → cl ⁺) ≈ Br(S ₁ ^(?) → v \(\tilde b\)) ≈ 1, Br(S _m → bl ⁺) ≈ 0.9, and Br(S _m → c \(\tilde \nu \)) ≈ 0.1, appear to be dominant decays of scalar leptoquarks. Searches for these decays at LHC and the Tevatron are of interest.