Die Hyperfeinstrukturaufspaltung des Grundzustandes2 S 1/2 und das magnetische Kerndipolmoment von Au197

The hyperfine structure of the groundstate 6s ² S _1/2 and the nuclear magnetic dipole moment of gold 197 have been studied by the atomic beam magnetic resonance technique. A special high frequency arrangement is described. The hyperfine structure separationΔ v was determined fromΔF=1 transitions. The magnetic dipole momentμ _I was measured by a direct method. The experiments yield the following results:Δv (²S_1/2)=(6099,309±0,010) Mc/secμ _I (Au¹⁹⁷)=+(0,1445±0,0014)μ _K.     

Niederenergetische Gammalinien vom Neutroneneinfang in Lu 175 und Lu 176

The low energy gamma-rays from neutron-capture in Lu 175 and Lu 176 have been investigated by means of the bent crystal-spectrometer at the DR-3-reactor at Risø. From the transitions in Lu 177 3 rotational bands have been determined. The levels of the (404)K=7/2⁺ groundstate rotational band are: 121,62 keV (I=9/2), 268,79keV (I=11/2), 440,66 keV (I=13/2), 636,22 keV (I=15/2), 854,34 keV (I=17/2). The level-sequence of the (514)K=9/2^?-band is: 150,39 keV (I=9/2), 288,99 keV (I=11/2), 451,49 keV (I=13/2), 637,05 keV (I=15/2) and 844,88 keV (I=17/2). At 457,92 keV is the basis for the (402)K=5/2⁺-band the higher levels of which are 552,05 keV (I=7/2), 671,89 keV (I=9/2), 816,63 keV (I=11/2), 985,23 keV (I=13/2), 1176,73keV (I=15/2) and probably 1389,5 keV (I=17/2). The energies of the levels apart from the 1389 keV-level have an accuracy of 7×10^?5. The energy differences between the 3 bands agree very well with the values expected from the Bohr-Mottelson-formulaE=A·I(I+1)+B·I ²(I+1)². The calculated branching-ratios within the 3 bands are in fairly good agreement with the experimental values. Theg _K -factors have been determined for 2 bands: It was found that for the (514)-bandg _K =1,16±0,04 and for the (402)-bandg _K =1,33±0,07.     

Das Kernquadrupolmoment des Mn55

With a recording photoelectric Fabry-Perot spectrometer and an atomic-beam light source the hyperfine structure of the Mn I-resonance linesλ=4031 Å,λ=4033 Å,λ=4034 Å (3d ⁵4s ² a ⁶ S _5/2?3d ⁵4s4p z ⁶ P _7/2,5/2,3/2 ⁰)and of the inter-combination linesλ=5395 Å andλ=5433 Å (3d ⁵4s ² a ⁶ S _5/2?3d ⁵4s4p z ⁸ P _7/2,5/2 ⁰) was measured. Furthermore the resonance lines have been measured with a pulsed atomic-beam in absorption. In this case the quotient (I ₀(ν)?I(ν))/I ₀(ν) was recorded, whereI(ν)=I ₀(ν) exp(?α(ν)d) is the observed intensity with absorption andI ₀(ν) the intensity of the light source. From the hyperfine structure splitting the value of the electric quadrupole moment of Mn⁵⁵ was derived to be:Q(Mn⁵⁵)=+(0.35±0.05)·10^?24 cm².     

On <Emphasis Type="Italic">K</Emphasis>β radiation of Ar<Superscript>16+</Superscript> ions in coronal plasma

The measured and calculated data obtained in this and earlier works for the intensity ratio G₃= I[Kβ₂]/I[Kβ₁] of the intercombination and resonance Kβ lines corresponding to the 1s3p³P₁→1s₂₁S₀ (Kβ₂) and 1s3p¹P₁→1s²¹S₀ (Kβ₁) transitions in the coronal plasma spectrum of Ar¹⁶⁺ ions were compared with each other. In this work, the G₃ ratio was measured on the TEXTOR (Julich, Germany) tokamak equipped with high-resolution Bragg spectrometers and other diagnostic instruments. The calculations carried out within the framework of the radiative-collision model using the ATOM, MZ, and GKU programs developed in the Lebedev Physical Institute, Russian Academy of Sciences, are in agreement, to the experimental accuracy, with all the data obtained on the PLT (Princeton, USA), ALCATOR-C (Cambridge, USA), and TEXTOR tokamaks. It is shown that the previously observed factor of 1.3–2 discrepancies between the measured and G₃ values calculated using the HULLAC code and appreciably exceeding the experimental error are caused by the use of inaccurate atomic data and simplified atomic kinetics in those works. The results presented in this work are evidence for the high accuracy of our atomic data (transition rates) and for the possibility of effectively using, on their basis, the K_β lines of multicharged ions in X-ray spectrum diagnostics of electron temperature and density in laboratory and astrophysical coronal plasma sources.     

Nature of the pygmy resonance in continuous <Emphasis Type="Italic">γ</Emphasis> spectra

Two-step-cascade spectra of the ¹⁷¹Yb(n, γγ)¹⁷²Yb reaction have been measured using thermal neutrons. They are compared to calculations based on experimental values of the level density and radiative strength function obtained from the ¹⁷³Yb(³He, aγ)¹⁷²Yb reaction. The multipolarity of a 6.5(15) μ _N ² resonance at 3.3(1) MeV in the strength function is determined to be M1 by this comparison.     

Mössbauer effect and magnetic moment of the 75.9 keV level in Yb171

The Mössbauer effect of the second excited state of theK=1/2 rotational band in Yb¹⁷¹ at 75.9 keV withI=5/2 was studied to determine its magnetic moment μ=(1.01±0.01)nm. This value agrees well with the one predicted by the previously determined magnetic parameters of theK=1/2 rotational band, confirming the adiabatic separation of intrinsic and rotational wave functions.     

Die isomeren Atomkerne: Yb169m,Yb175m,Yb177m

Short lived isomers of Yb were produced by neutron irradiation of enriched isotopes and have been investigated with the aid of scintillation spectrometers. Yb^169m decays with a half-life ofT _1/2=(46±2) sec emitting only L-radiation. This decay is assumed to be the same as the E 3-transition of 24 keV following the electron capture of Lu¹⁶⁹. Yb^175m [T _1/2=(0,072±0,005) sec] emitsγ-rays of (495±15) keV. The measured K-conversion coefficientα _{K 495}=0,24±0,04 and the total conversion coefficientα _{4 5}=0,6±0,3 indicate the transition to be M3. Yb^177m [T _1/2=(6,4±0,1) sec] decays by a cascade of twoγ-rays. The isomeric (228±3) keV-transition is followed by a (104±1,5) keV-radiation. The measured conversion coefficients areα _{K 228}=4,1±0,4 andα _{K 228}=6,5±0,5 for the first transition andα _{K 104}=0,39±0,05 andα ₁₀₄=0,51±0,05 for the second, indicating a M3-E1-cascade. For the M 3-transition the measured coefficients agree well with those calculated for a nucleus of finite size, but they differ by a factor of 1,5 for the E1-transition.     

Depolarizing collision anisotropy and collision echo in ytterbium vapor

A photon echo induced exclusively by collisions of ytterbium atoms with buffer gas atoms has been observed at a 0 ? 1-type¹ S ₀(6s ²)-³ P ₁(6s6p) ¹⁷⁴Yb transition. The polarization properties of a collision echo and the buffer gas density dependence of its intensity agree with theoretical predictions of a model of depolarizing collisions that takes into account the dependence of a relaxation matrix on the velocity of active particles. Thus, direct experimental evidence of the relaxation anisotropy due to depolarizing collisions has been obtained.     

Effect of vibronically induced spin-orbit coupling of electronic ππ* states on nonradiative intersystem crossing: Naphthalene

The effect of (I) S ₁(¹ B _2u ) ? T ₁(³ B _1u ) and (II) S ₁ ? T ₂ (³ B _3g ) ? T ₁ transitions in naphthalene on the rate constant K _ST ^s of the S ₁ ? T ₁ nonradiative transitions to all triplet sublevels s = z, y, x of the T ₁ state has been investigated in the approximation of vibronically induced spin-orbit couplings, taking into account all out-of-plane vibrational modes. The shapes of the vibrational modes that are most active in these transitions are determined. The calculated values K _ST = (0.33–0.75) × 10⁷ s^?1, obtained with allowance for the I and I + II transitions, are consistent with the experimental values (K _ST)_exp found by different researchers. It is established in all calculation versions that K _ST > K _ST ^z > k _ST ^x . This relation is in qualitative agreement with the known magnetooptical data.     

Bestimmung des elektrischen Kernquadrupolmomentes des ungeraden stabilen Strontium-87-Kerns

In order to determine the electric quadrupole moment of Sr⁸⁷ (I= 9/2) the hyperfine structure-splitting of the 5s5p ³ P ₁-state of the SrI-spectra was investigated by optical double resonance. By detection of high frequency transitions (ΔF=±1,Δm _F=0,±1) in an external magnetic fieldH ₀≈0 one obtains the hyperfine structure separations asv _F=11/2?F=9/2=1463·149 (6) Mc/sec andv _F=9/2?F=7/2=1130·264 (6) Mc/sec. From these frequencies one calculates the magnetic hyperfine structure-splitting constantA=?260·084 (2) Mc/sec and the electric quadrupole interaction constantB=?35·658 (6) Mc/sec. B leads to an electric quadrupole moment ofQ(Sr⁸⁷)=+0·36 (3)·10^?24 cm².     

Chemical Shift of the <Emphasis Type="Italic">K</Emphasis><Subscript>α1</Subscript> and <Emphasis Type="Italic">K</Emphasis><Subscript>α2</Subscript> Lines of the X-ray Emission Spectrum of Yb(II)/Yb(III) Fluorides: a Quantum-Chemical Investigation

Chemical shifts of the K_α1 and K_α2 lines (the 2p_3/2 → 1s_1/2 and 2p_1/2 → 1s_1/2 transitions, respectively) of the X-ray emission spectrum of the Yb atom in fluorides have been calculated by ab initio modeling the electronic structure. The valence transition Yb(II) → Yb(III) has been analyzed by examples of YbF₂, YbF₃, and Yb₂F₄ molecules and YbF₂⁺ cation. The relativistic pseudopotential and basis sets corresponding to it have been constructed for the ytterbium atom. They were used in calculations by the two-component noncollinear version of the density functional theory (DFT) with the PBE0 exchange-correlation functional. Results for the three-coordinated Yb(II) in the FYbF₂YbF dimer demonstrated a very weak dependence of the chemical shift on the coordination number of the Yb atom and on the molecular association of ytterbium difluoride. Chemical shifts of the X-ray emission spectrum for the ytterbium compound are related mainly to the change in the occupation of the 4 f shell.     

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.     

Band interaction in <Superscript>162</Superscript>Dy, <Superscript>168</Superscript>Er,and <Superscript>172</Superscript>Yb

Coriolis interaction between levels of two rotational bands in ¹⁷²Yb with K ^π = 2⁺ and 3⁺ and in ¹⁶⁸Er between levels with K ^π = 0^?, 1^?, and 2^? is studied. The values of the interaction parameters are obtained. The mutual influence of two bands in ¹⁶²Dy with ΔK = 2, K _i ^π = 0 ₂ ⁺ and 2 ₁ ⁺ due to Coriolis interaction is demonstrated.     

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.     

Excitation of the Yb II transitions terminating on the low-lying odd levels

Excitation of the transitions from the even levels of a singly charged ytterbium ion that terminate on the low-lying odd levels 4f ¹³(² F°)6s ^{2 2} F°, 4f ¹⁴(¹ S)6p ² P°, and 4f ¹³(² F°_7/2)5d6p(³ D)³[3/2]° is experimentally studied by measuring 51 excitation cross sections at an electron energy of 50 eV, and 16 optical excitation functions are determined within the electron energy range 0–200 eV. The largest magnitudes of the measured cross sections exceed 3 × 10^?17 cm².     

Gammaübergänge und Energieniveaus in Dy 165

220 neutron capture Gamma rays of Dy 165 were measured with the Risø curved crystal spectrometer. The intense transitions permitted the construction of a level scheme for this oddN nucleus. The rotational bandsK=7/2⁺[633],K=1/2^?[521] andK=5/2^?[512] were precisely localized, including the spin 11/2 states. Gammavibrational bands built on these Nilsson orbits were observed with their band heads at 538.6, 573.5 and 570.2 keV. TheI=5/2 term at 533 keV can be considered as the 5/2^?[523] Nilsson state. The branching ratios allowed the determination of (g _K?g^R)²-factors for the [633], [521] and [512] bands and yieldedE 1-hindrance factors.     

Effect of the orbital structure and symmetry of electronic states on nonradiative <Emphasis Type="Italic">S-T</Emphasis> intersystem crossing: Dibenzofuran

The nonradiative S-T intersystem crossing S ₁(ππ*) ? T ₁(ππ*) in dibenzofuran (DB(O)) molecules has been theoretically investigated within the model of vibronically induced spin-orbit (VISO) coupling of electronic states, where the vibronic perturbation takes into account all out-of-plane vibrational modes of a molecule. It is established that the S-T intersystem crossing S ₁(¹ A ₁) ? T ₁(³ B ₂) involves also the intermediate (T _m )T ₂(³ A ₁) and T ₃(³ B ₂) triplet states. The calculated rate constant K _ST = (4.5–4.7) × 10⁷s^?1 of the nonradiative transition is in agreement with the known experimental data. The manifestation of approximate (belonging to the D _2h group) symmetry of singlet and triplet molecular states in VISO couplings has been studied. An effect of the heavy (oxygen) atom of a DB(O) molecule on K _ST is established.     

Hyperfeinstruktur-Untersuchungen im Rhenium-I-Spektrum

By optical means (i.e. hollow cathode, Fabry-Perot-interferometer and spectrograph) the hyperfine structure of 15 transitions in the Re-I spectrum was investigated. This permits to state the hfs coupling constantsA, B for 15 levels belonging to the configurations (5d ⁵) 6s ², (5d ⁵) 6s 6p, (5d ⁵) 6s 7s, (5d ⁶) 6s, (5d ⁶) 6p and (5d ⁴) 6s ² 6p. It was found that the (5d ⁵) 6s ^{2 6} S _5/2 ground state, too, shows a small hfs. Of its magnetic splitting both size and sign could be determined (A _0,185,187=?2,2±0,4 mK); for a possible quadrupole splitting upper limits were obtained. Estimates of the quadrupole moments resulted inQ _185,187?2,9b. — In the case of two levels (x ⁶ P _7/2 andy ⁶ F _11/2) the hfs analysis raises doubts as to their classification.     

Dasβ-Spektrum des Cs137

Theβ-ray spectrum of Cs¹³⁷ has been measured with an iron-free spectrometer. The energy of the soft component was found to beE ₀=514±2 keV. The parameterk of the hard-component shape factorC _2VA ⁽²⁾ (W)=q ²+kp ² was determined to bek=0.015±0.004. Theβ intensities amount to 6.5% (hard component) and 93.5% (soft component). TheK conversion coefficient of the isomeric transition was measured to beα _K=0.093±0.003, in excellent agreement withSliv's theoretical value.     

Analyse von Hyperfeinstrukturen des Eu151, Am241 und einiger 3 d-Elemente mittels „Exchange Polarization“

It is shown how several discrepancies in the optical hfs of the Eu can be understood as consequences of the exchange polarization of the inner and outers-electrons by the spin of the half filled (4f ⁷)-subshell, an effect which should produce additional magnetic fields at the nucleus. Thus from the two different values of the electronic splitting constanta _6s in the two Eu-II ground states the polarization field from the 6s-shell (Δ H _6s ) is determined to be ca. +260 KG, and the formal splitting constantσ (??3 mK) of the (4f ⁷)-subshell yields ca. ?350 KG for the fieldΔ H _(1?5) from the five innern s-shells (n=1?5) in good agreement with the strength of the inner field obtained from recent Mössbauer effect studies.Δ H _(1?5) is deduced to be approximately equal in all sufficiently analysed ground and excited configurations of the neutral and ionised Eu atom ((4f ⁷) 6s, 6p, 5d, 6s ² and 6s 6p). Other elements with half filled subshells (Am, Mn) show similar features in their optical hfs. For Am⁺ ((5f ⁷) 7s) ca. ?2200 KG are found for the inner field (Δ H _(1?6)). For several 3d-elements it was found that the agreement between the calculated polarization fields and those following from experimental results is better than assumed so far.