A cluster calculation for 6He spectrum

The ⁶He nucleus is considered as the cluster α + n + n system. The excitation energies of the low-lying levels are calculated using the configuration-space Faddeev equations. The analytical continuation method in a coupling constant is applied for calculation of resonance parameters. The αn interaction is constructed to reproduce the results of R-matrix analysis for αn-scattering data. A realistic AV14 potential describes the nn interaction. Additional three-body potential adjusted by the ground state energy of ⁶He is used. The energies of the low-lying resonances of ⁶He (0 ₁ ⁺ , 0 ₂ ⁺ , 2 ₁ ⁺ ) are reasonably reproduced by the calculations.     

Resonant parameters of <Superscript>5</Superscript>He and <Superscript>5</Superscript>Li states and nucleon-α scattering

A new method of analysis of resonant parameters in the framework of the J-matrix inverse scattering formalism is proposed. The method is applied to analysis of Nα scattering in various partial waves. The obtained 1/2^? and 3/2^? resonance energies and widths in ⁵He and ⁵Li nuclei are in good agreement with the results of other approaches. The eigenenergies entering the J-matrix phase shift parameterization are shown to correlate well with the respective results of no-core shell model calculations, in particular, in the case of non-resonant s-wave scattering.     

Tests of the discretized-continuum method in three-body dipole strengths

We investigate the ⁶He dipole distribution in a three-body α+n+n model. Two approaches are used to describe the three-body ¹⁻ continuum: the discretized-continuum method, where the scattering wave functions are approximated by square-integrable functions, and the R-matrix formalism, where their asymptotic behaviour is taken into account. We show that some ambiguity exists in the pseudostate method, owing to the smoothing technique, necessary to derive continuous distributions. We show evidence for the important role of the halo structure in the E1 dipole strength. We also address the treatment of Pauli forbidden states in the three-body wave functions.     

The v6 = 1 and v6 = 2 vibrational states of DCF3

The high-resolution infrared spectra of DCF₃ were reinvestigated in the ν₆ fundamental band region near 500 cm⁻¹ and around 1000 cm⁻¹ with the aim to assign and analyze the overtone level of the asymmetric CF₃ bending vibration v₆ = 2.The present paper reports on the first study of both its sublevels (A₁ and E corresponding to l = 0 and ±2, respectively) through the high-resolution analysis of the overtone band and the hot and bands.The well-known “loop method”, applied to and , yielded ground state energy differences Δ(K, J) = E₀(K, J) − E₀(K − 3,J) for the range of K = 6 to 30.In the final fitting of molecular parameters, we used the strategy of fitting all upper state data together with the ground state rotational transitions.This is equivalent to that calculating separately the and coefficients of the K-dependent part of the ground state energy terms from the combination loops.All rotational constants of the ground state up to sextic order could be refined in the calculation.This led to a very accurate determination of C₀ = 0.18924413(25) cm⁻¹, , and also .In the course of analyzing simultaneously the overtone band together with the and ν₆ bands, the original assignment of the fundamental ν₆ band [Bürger et al., J. Mol. Spectrosc. 182 (1997) 34-49] was found to be incompatible with the present one. Assignments of the (k + 1, l₆ = +1)/(k − 1,l₆ = −1) levels had to be interchanged, which changed the value of Cζ₆ = −0.14198768(26) cm⁻¹ and the sign of the combination of constants C − B − Cζ in the v₆ = 1 level to a negative value.     

π-He interactions at T=106 MeV

interactions at have been studied by means of a self-shunted streamer chamber filled with helium at atmospheric pressure. This technique allowed reconstruction of the complete kinematics of the nuclear events under analysis, since tracks of slow p, α, tritium and ³He are readily measurable. The study revealed that the ⁴He nucleus behaves as a Planck radiator, emitting a Planck-like spectrum of high energy γs, when hit by a π beam of . A resonant behaviour in the π⁻n invariant mass spectrum has been observed, with and in the neutron knockout reaction: we consider this to be the first experimental evidence for the existence of the Δ⁻. The observed mass shift and width narrowing are compatible with the activation of an isobaric collective resonance in the ⁴He nucleus. The collaboration has also observed a resonant behaviour in the π⁻pp invariant mass spectrum in the pp double-charge-exchange reaction, on nuclear photoemulsion, compatible with the activation of the J^P=0⁻d^′ dibaryonic resonance with a strong p-p final state interaction. A new direct measured upper limit for the ν_μ mass has been derived by measuring a complete decay π-μ-e event recorded at the CERN PS179 experiment (Ne scattering): at a 90% confidence level, .     

Search for the rare decays , , and

Rare decay modes , J/ψ→D⁻π⁺+c.c., and are searched for using events collected with the BESII detector at the BEPC. No signal above background is observed. We present upper limits on the branching fractions of , B(J/ψ→D⁻π⁺)<7.5×10⁻⁵, and at the 90% confidence level.     

Diode laser overtone spectroscopy of CO2 at 780 nm

Overtone absorption lines of ¹²C¹⁶O₂ have been examined by using a tunable diode laser (TDL) spectrometer in the region around . The spectrometer sources are commercially available double heterostructure InGaAlAs TDLs operating in the “free-running” mode, which allowed the detection of the line positions within . The observed carbon dioxide absorption lines belong to the ν₁+5ν₃ ro-vibrational band with rotational quantum number J up to 48. The minimum absorbance detected by the spectrometer (?5×10^-6) permitted to observe the weakest lines having the absorption cross section of the order of .     

Resonant enhancement of the formation of hydrogen-helium muonic molecules

Formation of muonic molecules and , where J is rotational quantum number, in electron conversion process is investigated at collision energies between 0.004 eV and 50 eV. Corresponding reaction rates are calculated in adiabatic approximation for the three-body Coulomb problem. Significant enhancement of the rates for and is found near 7 eV and 30 eV, respectively. It is shown that the enhancement is due to resonances present in elastic and scattering at these energies. Acceleration of dμ atoms up to the resonant energy could be realized in triple H-D-³He mixture due to the muon transfer from protium to deuterium. Experimental investigation of nuclear synthesis from molecular state directly formed in the mixture is suggested.     

Three-particle correlations from208Pb+6Li

Three-particle correlations in the reaction²⁰⁸Pb+⁶Li were studied near the Coulomb threshold between \(E_{6_{Li} } = 24\) and 30 MeV. Three reaction mechanisms contribute predominantly to the observed coincidences of the charged particles: 1. Coulomb excitation of the 2.184 MeV,J=3⁺ state of⁶Li, followed by the decay intoα+d, 2. Deuteron pick-up of the⁶Li to the ground state of⁸Be and sequential decay into twoα-particles and 3. Neutron-transfer to the ground state and the first excited states of²⁰⁹Pb:²⁰⁸Pb(⁶Li,αp). The last two reaction mechanisms explain the previously measured large contributions to theα-channel relative to thed-channel.     

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.     

Spectroscopic investigations on cometary molecules CO, CH and CH

The experimental potential energy curves for the electronic ground states of molecules like CO⁺, CH and CH⁺ observed in comets are constructed by using the Rydberg-Klein-Rees method as modified by Vanderslice et al. The ground state dissociation energies are determined by curve fitting technique using the five parameter Hulburt-Hirschfelder (H-H) function. The estimated dissociation energies are 8.33±0.19, 3.48±0.903 and for CO⁺, CH and CH⁺, respectively. These values are in good agreement with the literature values. Estimated dissociation energies of CO⁺, CH and CH⁺ are used in the relation given by Gaydon and ionization potentials are evaluated for CO and CH molecules. The estimated ionization potentials are 14.03 and , respectively for CO and CH. The Franck-Condon factors and r-centroids for the band system of - of CO⁺ molecule have been calculated employing an approximate analytical methods of Jarmain and Fraser. The absence of the bands in this system is explained.     

Laser spectroscopy of the A9-X8 transition of holmium monochloride

Using laser excitation spectroscopy, 18 red-degraded bands belonging to a single electronic transition of holmium monochloride have been observed in the 615-670 nm region. Thirteen of the bands, with vibrational levels 0?v^′?3 and 0?v″?4 have been obtained at high resolution and rotationally analyzed. Observation of the first lines in some of the bands has shown that Ω=8 in the ground state and Ω=9 in the upper state. By analogy with HoF, this transition has been labeled as A9-X8. The Ω=8 assignment for the X state establishes the ground state configuration of HoCl as Ho⁺(4f¹⁰6s²)Cl⁻, in accord with predictions of Ligand Field Theory. From the rotational analysis, the main equilibrium molecular constants of , for the upper state and , for the ground state have been obtained.     

Theory of antiferromagnetic exchange interaction for mixed-valent FeFe spin cluster in model complex of semimethemerythrin

The antiferromagnetic phenomena of both mixed valent Fe^IIIFe^II spin clusters and homodinuclear Fe^IIIFe^III clusters in complexes have been studied by means of our covalent magnetic exchange theoretical method. The sensitive relations between the exchange parameter J and the covalent factors N_A (for Fe^III) and N_B (for Fe^II) and the Fe?Fe separation R have been derived by use of our double-Slater function calculation procedure, the corresponding theoretical curve of J vs. N_A,N_B and R has been obtained. By taking the typical covalent factors of Fe^III and Fe^II, and using the observed Fe-O bond lengths: for Fe^III-O-Fe^II cluster in model complex {[Fe(acacen)]₂ONa}₂; for Fe^III-O-Fe^III cluster in oxyhemerythrin, we obtained the theoretical values: for Fe^III-O-Fe^II cluster and for Fe^III-O-Fe^III cluster. These are in good agreement with the corresponding experimental findings in {[Fe(acacen)]₂ONa}₂ and in oxyhemerythrin, respectively.     

Measurement of ultraweak transitions in the visible region of molecular oxygen

A highly sensitive cavity-enhanced frequency modulation spectroscopy technique has been used to measure ultraweak transitions in molecular oxygen that had not previously been characterized. The self-broadened half-width and line intensity of the measured transitions are reported. We include 12 high J transitions in the band of ¹⁶O₂ (the so-called A band), 59 transitions in the hot band of ¹⁶O₂, and 17 high J transitions in the band of ¹⁶O¹⁸O. Our measurements of line positions of the ¹⁶O¹⁸O transitions are used to determine improved molecular constants for the excited state of ¹⁶O¹⁸O.     

Nuclear reactions and the double beta decay

Charge-exchange reactions of (n,p) and (p,n) types at intermediate energies are introduced as a tool for the study of nuclear matrix element in ββ decay. Here, the (n,p) type reactions are realized through , where ²He refers to two protons in a singlet ¹S₀ state and where both of these are momentum analyzed and detected by the same spectrometer and detector. These reactions have been developed and performed exclusively at KVI, Groningen (NL), using an incident deuteron energy of 183 MeV. The  reaction is of (p,n) type and was developed at the RCNP facility in Osaka (JP) at incident energies of 420 MeV. Using both reaction types one can extract the Gamow-Teller transition strengths B(GT⁺) and , which define the two “legs” of the ββ decay matrix elements for the 2νββ decay. The high resolution available in both reactions allows a detailed insight into the excitations of the intermediate odd-odd nuclei and, as will be shown, some unexpected features are being unveiled.