Nuclear magnetic moment of the 9.7 h 12− isomer 196mAu

The magnetic hyperfine splitting v_M=|gμ_NB_HF/h| of ^196mAu (j^π=12^?; configuration ¦(π$\text{11}\text{2}$($\text{v}\text{13}\text{2}{}^{\mathrm{+}}\text{)〉}{}_{12}{}^{\mathrm{?}}$; $\text{T}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 9.7}\text{h}\text{)}$ as dilute impurity in Ni has been determined with nuclear magnetic resonance on oriented nuclei as 96.0(2) MHz. With the known hyperfine field B_HF = ?264.4(3.9) kG corrected for hyperfine anomalies the g-factor and magnetic moment of ^196mAu are deduced to be |g| = 0.476(7) and |μ| = 5.72(8) μ_N. Taking into account the known magnetic properties of $\text{π}\text{1}\text{2}{}^{\mathrm{?}}$ and $\text{v}\text{13}\text{2}{}^{\mathrm{+}}$ isomeric states in the neighbouring odd Pt, Au and Hg nuclei the structure of the 12^? state is discussed.     

Nuclear moments of the low abundant natural isotope 176Lu and hyperfine anomalies in the lutetium isotopes

The atomic beam magnetic resonance method combined with laser-induced state- and isotopeselective detection of metastable atoms has been used to investigate the hyperfine structure of the ²D ground multiplet in ¹⁷⁵Lu and ¹⁷⁶Lu. The analysis of the data yields not only accurate values for the hyperfine interaction constants, the nuclear magnetic dipole moment of ¹⁷⁵Lu, and the electronic g_J, factors, but also the first directly measured value of the nuclear magnetic dipole moment of the low abundant isotope ${}^{176}\text{Lu}\text{: μ}{}_{\mathrm{I}}\text{(}{}^{176}\text{Lu) = 3.1692 (45)μ}{}_{\mathrm{<mtext>N</mtext>}}$ (corrected for diamagnetic shielding). The spectroscopic quadrupole moment of ¹⁷⁶Lu was calculated from the ratio of the B-factors and the quadrupole moment of ${}^{175}\text{Lu}\text{: Q}{}_{\mathrm{<mtext>s</mtext>}}\text{(}{}^{176}\text{Lu}\text{) = 4.92 (3)}\text{b}$. Moreover, the magnetic hyperfine anomalies for the isotopic chain ^{175,176,176m,177}Lu were determined. A quadrupole hyperfine anomaly between ¹⁷⁵Lu and ¹⁷⁶Lu was not found when comparing the ratio of the B-factors in the states ${}^2\text{D}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}\text{and}{}^2\text{D}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}$. From a comparison of the quadrupole moment of ¹⁷⁵Lu obtained from the hyperfine structure data and the quadrupole moment measured in muonic lutetium atoms semi-empirical Sternheimer shielding factors could be estimated.     

Negative magnetoresistance in (SN)x single crystal

The magnetoresistance in (SN)x single crystals is composed of the normal positive and negative components. The former increases in proportion to the square of the magnetic field B². The latter is remarkable at temperatures below 4.2 K and saturates at relatively low magnetic field (? 30 kG). The coefficient $\text{S(=}\text{lim}\text{B→0}\text{{??}\text{(}\text{δρ}\text{ρ}{}_0\text{)}\text{?B}{}^2\text{})}$ of this negative magnetoresitance shows features similar to those of semiconductors with Toyozawa's theory. These results of negative magnetoresistance are explained in terms of carrier scattering by localized magnetic moments.     

Magnetic moment of the 72+[404] ground state of 10.5 h 175Ta

The magnetic hyperfine splitting ν_M = |gμ_NB_HF/h| of ${}^{175}\text{Ta}\text{(J}{}^{\mathrm{\pi }}\text{=}\text{7}\text{2}{}^{\mathrm{+}}$; $\text{T}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 10.5}\text{h}\text{)}$ in Fe has been measured with the technique of nuclear magnetic resonance on oriented nuclei as 320.4(1) MHz. With the known hyperfine field $\text{B}{}_{\mathrm{<mtext>HF</mtext>}}\text{(}\text{Ta}\text{Fe}\text{) = ?648(13)}\text{kG}$ the magnetic moment of the $\text{7}\text{2}{}^{\mathrm{+}}\text{[404]}$ ground state of ¹⁷⁵Ta is deduced to be $\text{¦μ¦ = 2.27(5)μ}{}_{\mathrm{<mtext>N</mtext>}}$.     

Nuclear magnetic moment of the 3.9 s112− isomer 193mAu

The magnetic hyperfine splitting ν_M = |gμ_NB_HF/h| of ${}^{\mathrm{<mtext>193</mtext><mtext>m</mtext>}}\text{Au}\text{(j}{}^{\mathrm{\pi }}\text{=}\text{11}\text{2}{}^{\mathrm{?}}\text{, E = 290}\text{keV}$; $\text{T}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 3.9}\text{s}\text{)}$ as a dilute impurity in Ni has been measured with nuclear magnetic resonance on oriented nuclei as 226.4(2) MHz. With the known hyperfine field B_HF = ?264.4(3.9) kG corrected for hyperfine anomalies the g-factor and magnetic moment of ^193mAu are deduced to be |g| = 1.123(17) and |μ| = 6.18(9) μ_N.     

Theory of negative magnetoresistance in three-dimensional systems

Theory of negative magnetoresistance in two-dimensional systems due to delocalization of electrons by magnetic field by Hikami, Larkin, and Nagoaka is extended to the case of three-dimension. The increase in conductivity by magnetic field is independent of the direction of the current relative to that of the magnetic field, and is proportional to $\text{H}{}^2\text{τ}{}_{\mathrm{?}}{}^{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}$, τ_? being energy relaxation time of electrons, when the magnetic field H is small. If τ_? is large enough at low temperature and H is not too small, it is independent of the parameter characterizing the system, and is of the form $\text{0.918?H mho cm}{}^{\mathrm{?1}}$ (H in kOe).     

The decay process 11ΛB → π− + 11C

The branching ratios are calculated for ¹¹_ΛB decay to the ¹¹C ground and excited states below 8 MeV for two possible spin values of ¹¹_ΛB. It is found that the decay rate to the ¹¹C^★ state at E^★ = 6.48 MeV is comparable in magnitude to that leading to the ¹¹C ground state if $\text{J(}{}^{11}{}_{\mathrm{\Lambda }}\text{B}\text{) =}\text{5}\text{2}$ is assumed. This result, unlike the branching ratios calculated for the $\text{J(}{}^{11}{}_{\mathrm{\Lambda }}\text{B}\text{) =}\text{7}\text{2}$ case, is in accord with experiment and lends support to the assumption that $\text{J =}\text{5}\text{2}$ holds for ¹¹_ΛB. The necessity of the reinterpretation of some of the so-called ¹³_ΛC events in terms of ${}^{11}{}_{\mathrm{\Lambda }}\text{B}\text{→ π}{}^{\mathrm{?}}\text{+}{}^{11}\text{C}{}^1$ is indicated.     

Beta-decay asymmetry and nuclear magnetic moment of 24Nam(T12 = 20 ms)

Polarized isomeric ${}^{24}\text{Na}{}^{\mathrm{m}}\text{(T}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 20}\text{ms}\text{, I}{}^{\mathrm{\pi }}\text{= 1}{}^{\mathrm{+}}\text{)}$ nuclei were produced by capture of polarized thermal neutrons in a NaF single crystal at room temperature. The asymmetric β-decay radition of ²⁴Na^m was used to detect nuclear magnetic resonance signals yielding the magnetic moment $\text{|μ(}{}^{24}\text{Na}{}^{\mathrm{m}}\text{)| = 1.930 (3)}\text{n.m.}$ (uncorrected).     

Energy levels of low lying triplet states of N2 from infrared emission studies

A theoretical model used to describe the $\text{B′}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{?}}$ and B³Π_g states of N₂ is presented. Using recently acquired high resolution spectra of the $\text{B′}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{?}}\text{→ B}{}^3\text{Π}{}_{\mathrm{g}}$ (0-0) band, rotational energy levels of the v = 0 vibrational levels of these two states are generated with this model. These levels are in excellent agreement with those obtained using a combination differences technique. The precision of the model generated levels is 0.01 cm^?1. The previously unpublished rotational levels of Dieke and Heath for the $\text{A}{}^3\text{Σ}{}_{\mathrm{u}}{}^{\mathrm{+}}$, B³Π_g and C³Π_u states are referenced to the $\text{N}{}_2\text{X}{}^1\text{Σ}{}_{\mathrm{g}}{}^{\mathrm{+}}$ (v = 0, J = 0) ground level and tabulated here. Estimates of the precision of their work are made.     

The g-factor of the 132+ state in 207Po and the mesonic contribution to the moment of the i132-neutron

The magnetic moment of the $\text{13}\text{2}{}^{\mathrm{+}}$ state in ²⁰⁷Po was determined to be μ = ?0.910 ± 0.014 n.m. An analysis of this value and other known moments of $\text{i}{}_{\mathrm{<mtext>13</mtext><mtext>2</mtext>}}$ neutron states around ²⁰⁸Pb supports the existence of a mesonic contribution of at least ?0.3 n.m. to the moment.     

Binding energies of λλ hypernuclei and the λλ interaction

The binding energies of the ΛΛ hypernuclei ¹⁰_ΛΛBe and ⁶_ΛΛHe are calculated variationally with a 2α + 2Λ and with an α + 2Λ model, respectively. For ¹⁰_ΛΛBe the integrations were made with Monte Carlo techniques while for ⁶_ΛΛHe direct numerical methods were used. A wide range of phenomenological ΛΛ potentials based on meson-exchange models was considered. An approximately universal linear relation between the calculated values of $\text{B}{}_{\mathrm{\Lambda \Lambda }}\text{(}{}^{10}{}_{\mathrm{\Lambda \Lambda }}\text{Be}\text{)}$ and of $\text{B}{}_{\mathrm{\Lambda \Lambda }}\text{(}{}^6{}_{\mathrm{\Lambda \Lambda }}\text{He}\text{)}$ is obtained. For the experimental value of $\text{B}{}_{\mathrm{\Lambda \Lambda }}\text{(}{}^{10}{}_{\mathrm{\Lambda \Lambda }}\text{Be}\text{) = 17.7 ± 0.1}\text{MeV}$ this relation predicts a much too small value of $\text{B}{}_{\mathrm{\Lambda \Lambda }}\text{(}{}^6{}_{\mathrm{\Lambda \Lambda }}\text{He}\text{)}$, well below the lower limit of the quoted experimental value of 10.9 ± 0.6 MeV. For ΛΛ potentials with repulsive cores the relations, for a given $\text{B}{}_{\mathrm{\Lambda \Lambda }}\text{(}{}^{10}{}_{\mathrm{\Lambda \Lambda }}\text{Be}\text{)}$, between the low-energy ΛΛ scattering parameters a, r₀ and the intrinsic range b are both approximately universal and independent of the detailed potential shape. For the experimental value of $\text{B}{}_{\mathrm{\Lambda \Lambda }}\text{(}{}^{10}{}_{\mathrm{\Lambda \Lambda }}\text{Be}\text{)}$ the preferred values are 2.5 ? ?a ? 3.5 fm, 2.6 ? r₀ ? 3.1 fm. The large and negative values of a correspond to conditions not too far from a bound ¹S₀ ΛΛ state and could indicate a 6-quark dibaryon state with the same quantum numbers and above the ΛΛ threshold.     

Determination of molecular constants of nitric oxide from (1-0), (2-0), (3-0) bands of the 15N16O and 15N18O isotopic species

The (1-0), (2-0), and (3-0) transitions of ¹⁵N¹⁶O and ¹⁵N¹⁸O are investigated. The wavenumbers of the rotation-vibration lines are reported for the overtone bands and the ${}^2\text{Π}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}\text{-}{}^2\text{Π}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$ (1-0) subband. It is shown that in the data reduction it is advantageous to calculate first merged spectroscopic constants ignoring the Λ-type doubling. The vibrational constants ω_e, ω_ex_e, ω_ey_e and the vibrational dependence of the rotational constants are determined. The study of ¹⁵N¹⁸O allows the determination of the equilibrium values of the centrifugal distortion correction A_De to the spin-orbit constant and of the spin-rotation constant γ_e from the isotopic invariance of the ratios $\text{A}{}_{\mathrm{<mtext>De</mtext>}}\text{B}{}_{\mathrm{<mtext>e</mtext>}}$ and $\text{γ}{}_{\mathrm{<mtext>e</mtext>}}\text{B}{}_{\mathrm{<mtext>e</mtext>}}$. It is found that $\text{A}{}_{\mathrm{<mtext>De</mtext>}}\text{B}{}_{\mathrm{<mtext>e</mtext>}}\text{= (?3.9 ± 1.3) × 10}{}^{\mathrm{?6}}$ and $\text{γ}{}_{\mathrm{<mtext>e</mtext>}}\text{B}{}_{\mathrm{<mtext>e</mtext>}}\text{= (?4.00 ± 0.05) × 10}{}^{\mathrm{?3}}$.     

The microwave spectrum of MnO3F

The microwave spectrum of MnO₃F has been remeasured and several corrections and new results have been obtained: B₀ = 4129.141 MHz, D_J = 1.12 kHz, D_JK = 1.87 kHz; $\text{α}{}_3{}^{\mathrm{B}}\text{= 8.622}$, $\text{α}{}_5{}^{\mathrm{B}}\text{= ? 11.994}$, $\text{α}{}_6{}^{\mathrm{B}}\text{= 6.042}$, |q₅| = 16.005, and |q₆| = 8.456 MHz.     

Band contour analysis of compounds with pure isotopes: The E fundamentals of HC35Cl3

The vibration-rotation transitions for v = 1 ← 0 of NO (${}^2\text{Π}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$) have been studied by using the technique of laser magnetic resonance spectroscopy. Five magnetic resonance lines are observed with three CO laser lines in the range from 1859 to 1886 cm^?1. From these, three zero-field transition frequencies, v = 1 ← 0; $\text{R(}\text{3}\text{2}\text{)}$, $\text{P(}\text{7}\text{2}\text{)}$, and $\text{P(}\text{9}\text{2}\text{)}$ are obtained with an accuracy of ±0.0007 cm^?1. The molecular constants which have been determined by borrowing centrifugal constants from a previous infrared work are $\text{B}{}_{02}{}^1\text{= 1.72004 ± 0.00006}\text{cm}{}^{\mathrm{?1}}$, $\text{B}{}_{12}{}^1\text{= 1.70212 ± 0.00010}\text{cm}{}^{\mathrm{?1}}$, and $\text{G(v = 1) ? G(v = 0) (}\text{for}{}^2\text{Π}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{) = 1875.8470 ± 0.0007}\text{cm}{}^{\mathrm{?1}}$.     

Microwave optical double resonance and continuous wave dye laser excitation spectroscopy of NO2: Rotational assignment of the K = 0−4 subbands of the 593 nm band

A rotational assignment of approximately 80 lines with K_a′ = 0, 1, 2, 3, and 4 has been made of the 593 nm ${}^2\text{A}{}_1\text{→}{}^2\text{B}{}_2$ band of NO₂ using cw dye laser excitation and microwave optical double-resonance spectroscopy. Rotational constants for the ²B₂ state were obtained as A = 8.52 cm^?1, B = 0.458 cm^?1, and C = 0.388 cm^?1. Spin splittings for the K_a′ = 0 excited state levels fit a simple symmetric top formula and give $\text{(?}{}_{\mathrm{bb}}\text{+ ?}{}_{\mathrm{cc}}\text{)}\text{2}\text{= ?0.0483}\text{cm}{}^{\mathrm{?1}}$. Spin splittings for K_a′ = 1 (N′ even) are irregular and are shown to change sign between N′ = 6 and 8. Assuming that the large inertial defect of 4.66 amu Ų arises solely from A, a structure for the ²B₂ state is obtained which gives $\text{r}\text{(NO) = 1.35}\text{A}\text{?}$ and an ONO angle of 105°. Alternatively, weighting the three rotational constants equally gives $\text{r = 1.29}\text{A}\text{?}$ and θ = 118°.     

Core polarization and magnetic moment of some odd-mass nuclei around N = 50

The effect of core polarization on the magnetic moment is studied for odd-mass nuclei around $\text{N = 50:}{}^{\mathrm{85,\; 87}}\text{Kr}\text{,}{}^{\mathrm{87,\; 89}}\text{Sr}\text{,}{}^{91}\text{Zr and}{}^{89}\text{Y}$. The calculation is done in the framework of the modified Tamm-Dancoff approximation (MTDA). The ground-state wave function is calculated using the configuration space of p?f$\text{\$}\text{?}$and ?dg$\text{\$}\text{?}$shells. The core polarization correction to the magnetic moment is considerable for all the nuclei, except ⁸⁹Y, and it depends upon the particular form of the interaction. For ⁸⁹Y the last odd proton is in the $\text{p}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$ level and the smallness of the correction is supported by the observed value of the magnetic moment.     

On a least upper bound Tc of superconductors with paramagnetic impurities

We have obtained a least upper bound, $\text{k}{}_{\mathrm{B}}\text{T}{}_{\mathrm{c}}\text{? c(μ}{}^1\text{, t)A}$, on the critical temperature T_c of an isotropic superconductor with paramagnetic impurities described by the scattering matrix t for fixed values of μ¹. We have also obtained the corresponding optimal spectrum $\text{α}{}^2\text{F(m) = Aδ[ω?d(μ}{}^1\text{, A]}$. The numerical results for the functions $\text{c(μ}{}^1\text{, t)}\text{and}\text{d(μ}{}^1\text{, t)}$ are presented for $\text{α}{}^1\text{= 0.1}$ and 0.16 in the form of universal curves representing $\text{c(μ}{}^1\text{, t)}\text{and}\text{d(μ}{}^1\text{, t)}$ as functions of the reduced impurity concentration $\text{t}\text{= t/A}$. We have also established an upper limit to the reduced critical concentration $\text{t}{}_{\mathrm{crit}}$ for an arbitrary shape of α²F(ω)1.     

Absolute vacuum ultraviolet absorption spectra of some gaseous azabenzenes

Absolute extinction coefficient and oscillator strength of pyridine, pyrimidine, pyrazine, and s-triazine were recorded with moderate resolution in the region of 3.5–9.5 eV. Analogous to ${}^1\text{A}{}_{\mathrm{<mtext>1</mtext><mtext>g</mtext>}}\text{→}{}^1\text{B}{}_{\mathrm{<mtext>2</mtext><mtext>u</mtext>}}$, ¹B_1u, ${}^1\text{E}{}_{\mathrm{<mtext>1</mtext><mtext>u</mtext>}}\text{π → π}{}^1$ transitions of benzene, several $\text{n → π}{}^1$ and Rydberg transitions are presented and discussed.     

Magnetic moment and half-life of the isomeric 112− state in 107Cd

An isomeric level in ¹⁰⁷Cd at 845 keV populated by the reactions ¹⁰⁷Ag(p, n), ¹⁰⁶Cd(d, p) and ¹⁰⁴Pd(α, n) has been observed. The half-life of this state is $\text{T}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 77(7)}\text{ns}$, and the spin and parity are $\text{I}{}^{\mathrm{\pi }}\text{=}\text{11}\text{2}{}^{\mathrm{?}}$. The magnetic moment has been determined by the pulsed beam time-differential perturbed angular distribution method (DPAD) to be μ = ?1.012(12) n.m.