Low-energy transition depopulating the isomeric 8+ level in 208Po

Conversion electron measurements of the low-energy transition depopulating the isomeric 8⁺ level in ²⁰⁸Po yielded E_γ = 4025 ± 20 eV and the conversion intensity ratios N₁/N₂ ? 0.2, N₂/N₃ = 0.75 ± 0.10, N_4.5/N₃ ? 0.2, O/N₃ = 0.35 ± 0.10, P/N₃ ? 0.1 and N₃/M₃ = 0.4 ± 0.2. These ratios are in accord with our calculations for the E2 multipolarity and exclude all other multipolarities with L ≦ 4. The total conversion coefficient was calculated to be 1.31 × 10⁷.     

Axially symmetric time-dependent Hartree-Fock study of the 208Pb + 208Pb reaction

A time-dependent Hartree-Fock calculation assuming axial and reflection symmetry constraints is performed for the head-on collision of ²⁰⁸Pb + ²⁰⁸Pb systems at E_lab≈1600 MeV. The calculation suggests the excitation of surface modes in the reaction and the energy loss characteristic of a deep inelastic process. An estimate of neck-radius and neck-formation time is given.     

The g-factor difference for the 61+ and 88+ states in 210Po

The difference in g-factors for the 6₁⁺ and 8₁⁺$\text{(πh}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}{}^2\text{)}$ states in ²¹⁰Po has been measured as $\text{(g}{}_6\text{? g}{}_8\text{)}\text{g}{}_8\text{= 2.0 ± 0.7\%}$. This result represents a small violation of additivity. A value of g₈ = 0.909 ± 0.011, independent of g₆, was also obtained.     

Molecular-orbital X-rays from 1 GeV 208Pb + 208Pb and 209Bi + 209Bi collisions

We have measured the spectra of continuum X-rays above the characteristic K lines for 4.5 to 4.8 MeV/N ²⁰⁸₈₂Pb → ²⁰⁸₈₂Pb, Pb → Bi, Bi → Pb and Bi → Bi collisions. Above ≈400 keV X-ray energy the spectral shape and intensity agree roughly with calculations of Kirsch et al. for the 1sσ molecular-orbital (MO) X-ray spectrum from Pb-Pb. Deviations from the theory below ≈400 keV suggest transitions to other MO's.     

Electroexcitation of high spin states in 208Pb

The formfactors for the electroexcitation of the collective states of ²⁰⁸Pb have been calculated within the Model of Separable Residual Interaction (MSI); the results for the even parity states up to J^π = 10⁺ agree nicely with recent measurements. It turns out, that the energies of the lowest collective states of positive parity follow rather closely a J(J + 1) law.     

Decay amplitudes of the 208Pb(0+) analogue resonance

Measurements were made of elastic and inelastic proton scattering on ²⁰⁷Pb targets in the energy range from 11.1 to 14.4 MeV. The scattering to the $\text{1}\text{2}{}^{\mathrm{?}}$ ground state and to the $\text{3}\text{2}{}^{\mathrm{?}}$ and $\text{5}\text{2}{}^{\mathrm{?}}$ exciced levels was analyzed in terms of a 0⁺ analogue resonance interfering with the non-resonant background and with the contribution from the 3^? resonance. The resonance parameters were determined together with the magnitude and relative sign of three background components.     

High multipolarity electroexcitations in 207Pb and 206Pb

We report the identification of new high multipolarity transitions in ²⁰⁷Pb and ²⁰⁶Pb by the measurement of their form factor. A comparison to the corresponding excitations in ²⁰⁸Pb is presented.     

12C1 and 8Be production in 12C + 208Pb collisions

The mechanisms involved in the production of fast α-particles in ¹²C-induced reactions have been studied for the ¹²C + ²⁰⁸Pb system at the bombarding energies of E_12c = 132, 187 and 230 MeV. Absolute cross sections for the reactions ²⁰⁸Pb(¹²C. ¹²C¹→α + ⁸Be), ²⁰⁸Pb(¹²C, ⁸Be(g.s.)) and ²⁰⁸Pb(¹²C, ⁸Be(2.94 MeV)) have been determined by coincidence measurement of two or three correlated α-particles. Inclusive α-particle production cross sections were also measured at E_12c = 187 MeV. It is found that the inelastic process (¹²C, ¹²C¹→α + ⁸Be) does not contribute significantly to fast α-particle production but that the production of ⁸Be by projectile fragmentation is an important source of α-particles. At the highest bombarding energy (230 MeV) it appears that the ¹²C → 3α fragmentation reaction becomes more prominent at the expense of the ¹²C→α + ⁸Be fragmentation channel.     

Vibrational intensity distributions for the various electronic states of O2+, N2+ and CO+ produced by photoionization

The vibrational intensity distributions produced by the process of photoionization are tabulated as a function of wavelength between 745 and 304 Å for all major electronic states of O₂⁺, N₂⁺ and CO⁺. The technique of photoelectron spectroscopy was used with an electron energy analyzer of known luminosity.     

Properties of single-particle states in the 208Pb region

The properties of single-particle states in the ²⁰⁸Pb region are obtained by subtracting from the empirical values the dressing effects of the multipole particle-hole and pairing phonons. Use is made of the particle-vibration formalism. Single-particle energies, one-body transfer spectroscopic factors and effective quadrupole charges are examined within this framework.     

Transition densities between the 01+, 21+, 41+, 02+, 22+, 11− and 31− states in 12C derived from the three-alpha resonating-group wave functions

All the multipole transition densities between the seven T = 0 states in ¹²C are calculated with the use of the microscopic 3α resonating-group wave functions which are obtained by dynamically solving the 3α relative motion with the total antisymmetrization taken into account exactly. The observed elastic and inelastic electron scattering form factors for the transition to the 2₁⁺, 4₁⁺, 0₂⁺, 1₁^?and 3₁^? states are well reproduced with no additional effective charge. The existence of a deformed intrinsic state for the 0₁⁺, 2₁⁺and 4₁⁺states is deduced by the analysis of the transition densities between them which are derived by the weak-coupling-type 3α wave functions; the intrinsic density distribution is illustrated. The monopole density distribution of the 0₂⁺, 2₂⁺ and 1₁^?, states is found to be much longer ranged than that of the 0₁⁺, 2₁⁺ and 4₁⁺ states; the 3₁^? state case is intermediate. On the basis of the transition densities between the 0₁⁺, 2₁⁺, 0₂⁺ and 2₂⁺ states, analysis is made of the transition between the shell-like states and the molecule-like states with a large spatial-structure change. Specific, effective nucleon-nucleon interactions are folded into the transition densities here obtained. The evident dependence of the radial shape of the folded nucleon-¹²C form factors on the choice of the interactions and the multi-step form factors for the excitation of the 0₂⁺, 1₁^? and 3₁^? states are discussed.     

A study of particle-vibration multiplets in 203Tl using the 205Tl(p,t)203Tl, 208Pb(p,t)206Pb and 206Pb(p,t)204Pb reactions

The ²⁰⁵Tl(p, t)²⁰³Tl reaction has been used at 26.2 MeV to obtain additional information on the particle-vibration multiplets in ²⁰³Tl. Enhancement factors for the L = 0 and L = 2 transitions to the lower excited states of ²⁰³Tl were well accounted for by using enhancement factors from the ²⁰⁶Pb(p, t)²⁰⁴Pb reaction and the wave functions from the intermediate coupling calculations of Covello and Sartoris. Additional data on the ²⁰⁸Pb(p, t)²⁰⁶Pb reaction at 26.2 MeV were used along with data at other energies to examine the energy dependence of the zero-range enhancement factors.     

Inelastic electron scattering form factors of low-lying states in 208Pb

Inelastic electron scattering form factors for some low-lying excited states of ²⁰⁸Pb are calculated within the Migdal theory of interacting quasiparticles. The fairly good agreement with experiment is discussed.     

Proton orbit sizes in 208Pb

The sub-Coulomb (t,α) reaction has been employed in the determination of the rms radii of the $\text{3s}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{, 2}\text{d}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}\text{, 1}\text{h}{}_{\mathrm{<mtext>11</mtext><mtext>2</mtext>}}$, and $\text{2}\text{d}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}$ proton orbits in ²⁰⁸Pb. The experimental values are compared to the results of Hartree-Fock calculations.     

Core polarization effects in the πh92 shell and g-factors of the 8+ states in 204Po and 206Po

The $\text{g-}\text{values of}\text{[(π}\text{h}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}\text{)}{}^2\text{, 8}{}^{\mathrm{+}}\text{]}$ isomeric levels in ²⁰⁴Po and ²⁰⁶Po have been measured with the stroboscopic method. The results obtained are: $\text{g(}{}^{204}\text{Po}\text{) = 0.923±0.013}\text{and}\text{g(}{}^{206}\text{Po}\text{) = 0.919±0.013}$. These and other known $\text{g-}\text{factors of}\text{(π}\text{h}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}\text{)}{}^{\mathrm{n}}$ states in the ²⁰⁸Pb region are compared with theoretical predictions in order to analyze the dependence of the $\text{h}{}_{\mathrm{<mtext>9</mtext><mtext>2</mtext>}}$ proton g-value on the core constitution. The variation of the g-values is systematically smaller than expected from first-order configuration mixing theory, if pure shell-model wave functions are assumed.     

Combined analysis of the PFOODR data on the a 3Σ u+ , 23Πg, 23Σ g+ , 33Πg, and 43Σ g+ states of the K2 molecule

The known and new heterogeneous spectral data on the triplet states a ³Σ _u ⁺ , 2³Π_g, 2³Σ _g ⁺ , 3³Π_g, and 4³Σ _g ⁺ of the K₂ dimer are simultaneously fitted. The data published in J. Mol. Spectrosc. 234, 41 (2005) are refined. The new information used in the analysis contains the data on the 2³Σ _g ⁺ state, which have not been considered previously. The range of internuclear distances where the potential function of the lowest triplet state a ³Σ _u ⁺ is defined is extended. Original Russian Text ? V.B. Sovkov, V.S. Ivanov, D. Li, F. Xie, Li Li, 2007, published in Optika i Spektroskopiya, 2007, Vol. 103, No. 5, pp. 747–751.     

Fully self-consistent description of high spin magnetic states in 208Pb

Magnetic transverse form factors of 12^? and 14^? states in ²⁰⁸Pb are calculated in a fully self-consistent manner utilizing the effective density dependent interaction D1. Reduction of the strength due to the RPA polarization and the ground state correlations is observed and found to be independent of the momentum transfer. Nuclear structure implications particular to two close lying 12^? states are discussed.     

Magnetic moments of the 12+ isomeric states in 194, 196, 198Pb

The g-factor of the 12⁺ isomeric state in lead isotopes with A = 194, 196, 198 was measured using the time-differential perturbed angular distribution method (TDPAD). The values obtained are respectively g(194) = ?0.158(6); g(196) = ?0.157(7); g(198) = ?0.144(11). A more precise determination of the 12⁺ level half-life is also made. The g-factprs of these nuclear states, which are described with v(i_{$\text{13}\text{2}$})^?2 as the main configuration, are surprisingly constant over a large mass range (between A = 206 and 194). A core polarization analysis explains this trend: the polarization induced on neutrons in i_{$\text{13}\text{2}$} orbit decreases with the mass number A (blocking effect), but a compensation is provided by the other spin-orbit partners f_{$\text{7}\text{2}$}-f_{$\text{5}\text{2}$} and P_{$\text{3}\text{2}$}-P_{$\text{1}\text{2}$}.     

Elastic and inelastic scattering of 120 MeV 18O from 208Pb and the spin alignment of the 2+ state of 18O

The elastic and inelastic scattering of ¹⁸O ions at 120 MeV from a target of ²⁰⁸Pb have been studied. Cross sections for excitation of the 2⁺ state at 1.982 MeV in ¹⁸O and of the 3^? state at 2.61 MeV in ²⁰⁸Pb were measured. In addition, the populations of the m-substates for the ¹⁸O excitation were deduced from the Doppler-broadened line shapes. The data were subjected to a coupled-channels analysis using either Woods-Saxon or folding-model potentials. In addition, the ¹⁸O excitation was found to be described very well by use of a semi-microscopic model. The analyses consistently indicated the presence of a positive static hexadecapole moment of several e · fm⁴ for the 2⁺ state of ¹⁸O. The m-substate population distributions were found to be better fitted if a vector spin-orbit coupling was introduced for the 2⁺ state of ¹⁸O with a sign opposite to that for the nucleon-nucleus case.     

Lifetime of electronic states of CO2+

The radiative lifetimes of the $\text{A}\text{?}{}^2\text{Π}{}_{\mathrm{u}}$ and $\text{B}\text{?}{}^2\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{+}}$ states of CO₂⁺ were measured by means of the delayed coincidence method. Excitation was performed by a pulsed electron beam incident on CO₂. The results of these measurements are 115 ± 5 nsec for the $\text{A}\text{?}{}^2\text{Π}{}_{\mathrm{u}}$ state and 126 ± 3 nsec for the $\text{B}\text{?}{}^2\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{+}}$ state.