Measurement of the Magnetic Moment of the First Excited State in 93Sr Using on-line TDPAC technique

The g-factor of the first excited state of ⁹³Sr (E = 213 keV, T _1/2 = 4.6 ns) was measured by an on-line TDPAC technique with use of the strong hyperfine field in Fe metal. The Larmor frequency ω _L = (2.60 ± 0.15) × 10⁸ rad/s was obtained. The g-factor is derived as g = −0.227 ± 0.013 from g = −ℏω _L/B _hf μ _N. If the spin of the first excited state of ⁹³Sr is assumed to be 3/2, the g-factor is predicted by a simple core-excitation model as g = −0.22, which is in good agreement with the present experimental result.     

Precise Nuclear Quadrupole Moments of 8B and 13B

The electric quadrupole coupling constants eqQ/h of ⁸B (, T _1/2 = 769 ms) and ¹³B (, T _1/2 = 17.4 ms) in single crystal TiO₂ have been precisely measured by the β-NQR technique. The ratios of these Q moments to Q(¹²B) were determined as ∣Q(⁸B)/Q(¹²B)∣ = 4.882(32) and ∣Q(¹³B)/Q(¹²B)∣ = 2.768(24).     

Precise measurement of magnetic moment of short-lived β-emitting nuclei12B ( I π=1+, T 1/2=20.18 ms)

The spin polarized β-emitting nuclei¹²B (I ^π=1⁺,T _1/2=20.18 ms) were produced by the nuclear reaction¹¹B(d, p)¹²B and by the selection technique of the incident deuteron energy and the¹²B recoil angle following the nuclear reaction. The nuclear magnetic moment of the short-lived nuclei¹²B was measured by β-NMR with the β-NMR and β-NQR setup established for the first time in China. The nuclear magnetic moment of¹²B was determined to be μ=0.99993±0.00048 nm org=0.99993±0.00048 after the precise correction of the Knight shift.     

Four quasi-particle level at 2256 keV in182Re

In-beam nuclear spectroscopic studies of¹⁸²Re, following the reaction¹⁸¹Ta(α, 3n)¹⁸²Re have been made using gamma-ray and internal conversion electron techniques.K-conversion coefficients for several transitions have been measured and the multi-polarities of the various transitions assigned. In particular, the spin and parity of the four-quasi-particle isomeric level at 2256 keV were determined to be 16⁻. Theg-factor of this level has been measured to beg = 0·32 ± 0·05. On the basis of theg-factor and the decay pattern of this level, a configuration {v9/2⁺ [624↑]v7/2⁻ [514↓]v7/2⁻ [503↑]π9/2⁻ [514↑]} _k ^x = 16⁻ has been assigned to this level. The nature of the retardation of the gamma transitions deexciting this level is discussed. It is argued that the measured retardation factors can be explained if the nucleus has a triaxial shape.     

Quadrupole moment measurement of the highly deformed πg 9/2⊗νh 11/2 band in 130Pr

The quadrupole moment for the πg _9/2⊗νh _11/2 band in the ^130>Pr nucleus has been measured using the Doppler-shift attenuation method. A centroid shift analysis was carried out and a value of Q₀=6.1±0.4 eb, corresponding to an axial prolate deformation of β₂=0.35(3), has been determined. This is the first direct experimental confirmation of the deformation-driving character of the πg _9/2 orbital in an odd-odd nucleus in the A≃135 superdeformed region. Received: 23 April 1998     

The estimates of periodic potentials in terms of effective masses

LetG _n=(A _n ⁻ , A _n ⁺ ),n≧1, denote the gaps,M _n ^± be the effective masses and Σn=[A _n−1 ⁺ ,A _n ^- ],A ₀ ⁺ =0, be the spectral bands of the Hill operatorT=−d ²/dx ²+V(x) inL ² (R), whereV is a 1-periodic real potential fromL ²(0,1). Let the length gapL _n=|G_n|, h_n be the height of the corresponding slit on the quasimomentum domain and Δ_n=π²(2n−1)−∣Σ_n∣>0 be the band reduction. Let ,n≧1, denote the gap length for the operator . Introduce the sequencesL={L_n}, h={h_n}, l={l_n}, Δ={Δ_n},M ^±={M _n ^± } and the norms ,m≧0. The following results are obtained: i) The estimates of‖V‖, ‖L‖, ‖h‖ ₁, ‖l‖₁, ‖δ‖ in terms of ‖M^±‖₂, ii) identities for the Dirichlet integral of quasimomentum and integral of potentials and so on, iii) the generation of i), ii) for more general potentials. The research described in this publication was made possible in part by grant from the Russian Fund of Fundamental Research and INTAS.     

Hyperfine Interaction of 140Ce(←140La) in CaB6

A ¹⁴⁰La(I ^π=3⁻, T _1/2=40.3 h)-doped layer has been produced in CaB₆ by means of radioactive isotope (RI) beam technique: ¹⁴⁰Cs(I ^π=1⁻, T _1/2=63.7 s) was implanted into CaB₆ and the radioactive equilibrium of ¹⁴⁰Ba–¹⁴⁰La was achieved. The concentration of La in CaB₆ was La/Ca ∼0.001. Obtained TDPAC spectra of the 2083 keV level of ¹⁴⁰Ce (I ^π=4⁺, T _1/2=3.4 ns, μ=+4.35±0.10 μ _N ) followed by the β decay of ¹⁴⁰La showed the existence of hyperfine magnetic fields: B _hyp=−15.0±0.5 T and −1.00±0.15 T. This revised version was published online in September 2006 with corrections to the Cover Date.     

ESR studies of sepiolites

The electron spin resonance (ESR) spectra for each beige and brown sepiolites from Polatli-Ankara, Turkey, a clay mineral of Mg₈Si₁₂O₃₀(OH)₄(OH₂)₄(H₂O)₈, at 77 K have their own single characteristic peak atg ≈ 1.99, which begins to anneal from 437 and 536°C, respectively. The sextet lines of Mn²⁺ were also observed in addition to two peaks (g = 4.4 and 5.0) associated with Fe³⁺. A high-quality sepiolite called “meerschaum” from Sepetci-Eskisehir, Turkey, has two characteristic peaks atg ≈ 1.99, which begins to anneal from 419°C, and atg ≈ 2.03. ESR intensities of the signal atg ≈ 1.99 for beige, brown sepiolites and meerschaum are enhanced by γ-ray irradiation to give equivalent dosesD _E = 11.8 ± 3.4, 4.7 ± 2.3 and 4.6 ± 1.2 kGy, respectively. The ESR ages obtained by assessing the annual dose rate from the content of²³⁸U,²³²Th and⁴⁰K determined by γ-ray spectroscopy are 1.8 ± 0.8, 0.7 ± 0.5 and 0.9 ± 0.2 Ma, respectively, falling into the Pliocene Epoch in geological time scale in agreement with the stratigraphy.     

The β-decay of 22Al

In an experiment performed at the LISE3 facility of GANIL, we studied the decay of ²²Al produced by the fragmentation of a ³⁶Ar primary beam. A β-decay half-life of T_1/2 = 91.1±0.5ms was measured. The β-delayed one- and two-proton emission as well as β-α and β-delayed γ-decays were measured and allowed us to establish a partial decay scheme for this nucleus. New levels were determined in the daughter nucleus ²²Mg. The comparison with model calculations strongly favours a spin-parity of I^π = 4⁺ for the ground state of ²²Al.     

Rotational analysis of the 0–9, 0–10 and 0–11 bands of theA 2II u -X 2II g band system of (16O18O)+

High-resolution spectra of the 0–9, 0–10 and 0–11 bands of theA ²II _u —X ²II _g system of (¹⁶O¹⁸O)⁺ ion have been studied for their rotational structure. This study enables a direct determination of the Λ-doubling parameters of theA ²II _u andX ²II _g states. The model of ‘pure precession’ explains, though not entirely, the Λ-doubling of theX ²II _a state as arising out of its interaction with theB ² Σ _g ⁻ state. The Λ-doubling in theA ²II _u state was found insignificant.     

Stabilization of Ion-Radicals in the Structure of Calcium Sulfite

Using the EPR- and IR-spectroscopy methods, we studied the conditions of formation of stable ion-radicals in the structure of calcium sulfite and determined the limits of their stability. We detected and identified the ion-radicals SO ₂ ⁻ with g(iso) = 2.0055 in the initial substances, two types of thermally induced SO ₂ ⁻ (with g₁ = 2.0093, g₂ = 2.0045, and g₃ = 2.0020, and g₁ = 2.0104, g₂ = 2.0049, and g₃ = 2.0018) when the substance was heated, and three types of mechanically induced SO ₃ ⁻ (with g_⊥ = 2.0036 and g_‖ = 2.0022, with g(iso) = 2.0033 and ΔH = 0.1 mT and with g(iso) = 2.0031 and ΔH = 0.33 mT) when the substance was ground up. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 72, No. 3, pp. 391–396, May–June, 2005.     

Radical formation in lithium trifluoromethane-sulfonate for ESR dosimetry

Lithium trifluoromethane-sulfonate (Li-TFMS:CF₃SO₃Li) irradiated by γ-rays showed an electron spin resonance (ESR) powder spectrum having the rhombicg-factor ofg _xx = 2.0259 ± 0.0005,g _yy = 2.0112 ± 0.0005 andg _zz = 2.0025 ± 0.0005 and a triplet hyperfine coupling constant ofA _xx/gβ= 0.8 ± 0.15 mT.A _yy andA _zz are not obtained because of the broadened spectrum. The energy levels,g-factor,A _xx/gβ and optical absorption spectrum of several conceivable radicals such as C^⋅F₂SO₃Li, CF₃-S-O^⋅ and CF₃-S-O-O^⋅ have been calculated by softwares MOPAC-V2 and Gaussian-98 based on ROHF (Restricted Hatree-Fock for open shell molecule). The most probable radical was ascribed to CF₃-SO^⋅ from both calculated and experimental results. The response to γ-ray dose and the thermal stability have been studied in addition to the effect of UV illumination for possible use of the signal intensity in ESR dosimetry. The obtained number of free radicals per 100 eV (G-value) was 1.23 ± 0.40.     

Electromagnetic moments of short lived β emitters 21F, 23Mg, 27Si and 39Ca

The β-NMR spectra of ²¹F, ²³Mg, ²⁷Si and ³⁹Ca which were produced in heavy ion collisions and implanted in various crystals have been observed. The magnetic moments of ²¹F and ²⁷Si were determined to be |μ(²¹F)| = 3.9194 ± 0.0012 μ_N and |μ(²⁷Si)| = 0.8653 ± 0.0003 μ_N, respectively. The electric quadrupole coupling constants were determined for the first time to be |eqQ(²¹F in MgF₂)/h|= 9.94 ± 0.09 MHz, |eqQ(²³Mg in MgF₂)/h|= 1.96 ± 0.06 MHz, |eqQ(²⁷Si in Al₂O₃)/h|= 1.90 ± 0.12 MHz, |eqQ(³⁹Ca in CaCO₃)/h|= 0.60 ± 0.04 MHz. From the present eqQ/h, the Q moments were deduced as |Q(²¹F)|= 110 ± 22 mb, |Q(²³Mg)|= 114 ± 3 mb, |Q(²⁷Si)|= 60 ± 13 mb and |Q(³⁹Ca)|= 36± 7 mb. The present data were compared with the theoretical values obtained by the OXBASH shell model code. This revised version was published online in August 2006 with corrections to the Cover Date.     

Isomeric states in 214Th and 213Th

Isomeric states in ²¹⁴Th and ²¹³Th were identified by means of γ -rays measured in delayed coincidence with the implanted evaporation residues. These were produced in irradiations of ¹⁶⁴Dy with ⁵⁴Cr projectiles and separated in-flight by the velocity filter SHIP. An isomeric state of I ^π = 8⁺ with a half-life of (1.24±0.12) μs was identified in ²¹⁴Th . The configuration π[1h _9/2 ⊗ 2f _7/2] was assigned to this state. An isomeric state with a half-life of (1.4±0.4) μs was observed in ²¹³Th . Tentatively it was assigned to an I ^π = 13/2⁺ state.     

Optical parameters measurement for diagnostic and photodynamic therapy of human cervical adenocarcinoma (HeLa) cell line

The purpose of this study was to investigate the optical properties, absorption coefficient (μ _a ) scattering coefficient (μ _s ) and refractive indices, (n) of HeLa cell line in a suspension of 2% minimum essential medium (MEM) at two different (632.8 and 532.0 nm) wave lengths of laser light. Optical properties were determined with Kubelka Munk Model (KMM) and refractive index measurement was made through minimum angle of deviation method (MAD). We reported μ _a = 8.643 ± 0.187 and 2.348 ± 0.249 cm⁻¹ and μ _s = 5.609 ± 0.287 and 88.166 ± 2.833 cm⁻¹ at 632.8 and 532.0 nm, respectively. Refractive index was found to be 1.332 and 1.312 at 632.8 nm and 532.0 nm, respectively. The discussed results provide a route of information for clinical diagnosis, therapeutic application and dosimetry studies in HeLa and other cell lines.     

Determination of Trace Mercury by Solid Substrate-Room Temperature Phosphorimetry Quenching Method Based on Catalytic Effect of Hg2+on Formation of the Ion Association Complex [Sn(XO)6]4+·[(Fin)4]

A new method for the determination of trace mercury by solid substrate-room temperature phosphorimetry (SS-RTP) quenching method has been established. In glycine-HCl buffer solution, xylenol orange (XO) can react with Sn⁴⁺ to form the complex [Sn(XO)₆]⁴⁺. [Sn(XO)₆]⁴⁺ can interact with Fin⁻ (fluorescein anion) to form the ion associate [Sn(XO)₆]⁴⁺·[(Fin)₄]⁻, which can emit strong and stable room temperature phosphorescence (RTP) on polyamide membrane (PAM). Hg²⁺ can catalyze H₂O₂ oxidizing the ion association complex [Sn(XO)₆]⁴⁺·[(Fin)₄]⁻, which causes the RTP to quench. The ΔIp value is directly proportional to the concentration of Hg²⁺ in the range of 0.016–1.6 fg spot⁻¹ (corresponding concentration: 0.040–4.0 pg ml⁻¹, 0.40 μl spot⁻¹), and the regression equation of working cure is ΔIp=10.03+83.15 m Hg²⁺ (fg spot⁻¹), (r=0.9987, n=6) and the detection limit (LD) is 3.6 ag spot⁻¹(corresponding concentration: 9.0×10^–15 g ml⁻¹, the sample volume: 0.4 μl). This simple, rapid, accurate method is of high selectivity and good repeatability, and it has been successfully applied to the determination of trace mercury in real samples. The reaction mechanism for catalyzing H₂O₂ oxidizing the ion association complex ([Sn(XO)₆]⁴⁺·[(Fin)₄]⁻) SS-RTP quenching method to determine trace mercury is also discussed.     

Precise measurement of the magnetic moment of17F(I x =5/2+,T 1/2=64.5 s) and its hyperfine interactions in ionic crystals

Hyperfine interactions of β-emitting¹⁷F implanted in single crystals of NaF and CaF₂ were studied. The nuclear magnetic moment of theT ^π=5/2⁺ state was determined with an improved precision to be |μ(¹⁷F;π=5/2⁺,T _1/2=64.5s|=4.72130±0.00025. nm. Isoscalar magnetic moments of the doubly closed shell ±1 nucleon nuclei around mass number 16 were derived and the effective nucleon mass in the nucleus was discussed.     

High spin states in 63Cu

Excited states of ⁶³Cu were populated via the ⁵²Cr+¹⁰O (65 MeV) reaction using the gamma detector array equipped with charged particle detector array for reaction channel separation. On the basis of γ-γ coincidence relations and angular distribution ratios, a level scheme was constructed up to E _n=7 MeV and J ^π=23/2⁽⁺⁾. The decay scheme deduced was interpreted in terms of shell model calculations, with a restricted basis of the f _5/2, p _3/2, p _1/2, g _9/2 orbitals outside a ⁵⁶ ₂₈Ni core.     

Molecular Stark effect spectroscopy of diflavonol and inhomogeneous broadening of its electronic spectra in erythrocyte membranes

Using spectroscopy of the molecular Stark effect and fluorescence spectroscopy, we study the characteristics of diflavonol 3,7-dihydroxy-2,8-di(4-dimethylaminophenyl)-4H,6H-pyrano[3,2-g]chromene-4,6-dione (DFME), which demonstrates intramolecular charge and proton phototransfer. In the ground state, this dye has only one form and, in the excited state, it has two forms, i.e., normal and phototautomeric. We found that, for the normal form of DFME, the transition dipole moment that is responsible for the absorption (m _a ), the dipole moment in the equilibrium ground state (μ _g ), and the change of the dipole moment upon transition of the molecule in the excited Franck-Condon state (Δ ^a μ) are parallel. In the ground equilibrium state, the dipole moments in 1,4-dioxane and cyclohexane are equal to μg = 12.2 × 10⁻³⁰ C m and μ _g = 11.0 × 10⁻³⁰ C m, respectively. Upon excitation, they increase by Δ ^a μ = 61 × 10⁻³⁰ C m and Δ ^a μ = 50.2 × 10⁻³⁰ C m in these solvents. We study the spectral characteristics of DFME in organic solvents and erythrocyte membranes. A spectral inhomogeneity of DFME in erythrocyte ghosts is found. The inhomogeneous broadening of fluorescence spectra is manifested as a long-wavelength shift of the band of the normal form of DFME by 1640 cm⁻¹ upon excitation at the red edge of the absorption spectrum.     

Weak correlation between isomer excitation probabilities and the ground state deformation parameters of nuclei

The photoexcitation of isomer ^157m Gd (11/2-, 426 keV, T _1/2 = 18.5 μs) in reaction (γ, γ′) was studied on the pulsed nonferromagnetic betatron at St. Peterburg State University. Only two strong intermediate structures (IntS) with E ₁ = 4.0 ± 0.1 MeV, (σΓ)₁^iso = 5 eV b and E ₂ = 5.3 ± 0.1 MeV, (σΓ)₂^iso = 40 eV b, respectively, were found. Comparison of the spectra IntS of isomers ^157m Gd and ^181m Ta demonstrates the weak correlation between isomer excitation probabilities and ground states deformation parameters.