Millimeter-Wave Spectrum of CF(2)Cl(2), Taking into Account the Hyperfine Structure

A new investigation of the CF(2)(35)Cl(2) ground state rotational spectrum in the 50-100 GHz frequency range gave an opportunity to improve the accuracy of rotational and quartic distortion parameters by an order of magnitude and to determine values of six sextic centrifugal distortion parameters. A special technique was used to process line profiles of unresolved or partially resolved hyperfine structures of rotational transitions. It allowed us to improve significantly values for the diagonal parameters of quadrupole coupling chi(aa), (chi(bb)-chi(cc)) and to determine the off-diagonal parameter chi(ab). Copyright 2000 Academic Press.     

Hyperfine measurement of magnetic compensation in ferrimagnetic (GdCe)Fe2 and (GdY)Fe2 compounds

Magnetic compensation in the ferrimagnetic series of compounds (Gd_XY_1?X)Fe₂ and (Gd_XCe_1?X)Fe₂ has been observed by Mössbauer measurements of the hyperfine field at Gd and Fe nuclei in external fields (B_app) up to 6 T. The hyperfine field shows a sharp change of 2B_app at the compensation composition x_C due to the alignment of the magnetization of the compound with the external field. Strong compositional dependence of this change allows an accurate determination of x_C in the two systems.     

First High-Resolution Infrared Observation of the Symmetry-Forbidden nu(5) Band of (10)B(2)H(6)

Spectra of (10)B monoisotopic diborane, B(2)H(6), have been recorded at high resolution (2-3 x 10(-3) cm(-1)) by means of Fourier transform spectroscopy in the region 700-1300 cm(-1). A thorough analysis of the nu(18) a-type, nu(14) c-type, and nu(5) symmetry-forbidden band has been performed. Of particular interest are the results concerning the nu(5) symmetry-forbidden band, which is observed only because it borrows intensity through an a-type Coriolis interaction with the very strong nu(18) infrared band located approximately 350 cm(-1) higher in wavenumber. The nu(5) band has been observed around 833 cm(-1) and consists of a well-resolved Q branch accompanied by weaker P- and R-branch lines. Very anomalous line intensities are seen, with the low K(a) transitions being vanishingly weak, and Raman-like selection rules observed. The determination of the upper state Hamiltonian constants proved to be difficult since the corresponding energy levels of each of the bands are strongly perturbed by nearby dark states. To account for these strong localized resonances, it was necessary to introduce the relevant interacting terms in the Hamiltonian. As a result the upper state energy levels were calculated satisfactorily, and precise vibrational energies and rotational and coupling constants were determined. In particular the following band centers were derived: nu(0) (nu(5)) = 832.8496(70) cm(-1), nu(0) (nu(14)) = 977.57843(70) cm(-1), and nu(0) (nu(18)) = 1178.6346(40) cm(-1). (Type A standard uncertainties (1varsigma) are given in parentheses.) Copyright 2000 Academic Press.     

Hyperfine Structure of the Configuration lll

The matrix elements for the hyperfine structure of the configuration lll in SL-Kopplung are expressed as linear combinations of the electron coupling constants α_li(10), α_li(01), α_li(12).     

{[K(18-C-6)][K(H2O)2]}[Cd(CN)4]的合成与结构分析

合成了配合物 { [K(18- C- 6 ) ][K(H2 O) 2 ]} [Cd(CN) 4 ](1) ,并通过元素分析、红外光谱、单晶 X-射线衍射进行了结构分析。配合物属单斜晶系 ,空间群 P2 (1) / n。晶体学数据 :a=0 .936 5 3(18) nm,b=1.6 178(3) nm,c=1.74 81(3) nm,β=91.332 (3)°,V=2 .6 479(9) nm3 ,Z=4 ,Dcalcd=1.4 5 3g/ cm3 ,F(0 0 0 ) =12 0 8,R1=0 .0 317,w R2 =0 .0 5 6 7。配合物中 [K(18- C- 6 ) ],[K(H2 O) 2 ]和 [Cd(CN) 4 ]基团通过 K N键和 K —π相互作用形成三维网状结构     

First Principles Determination of Hyperfine Parameters on fcc-Fe8X (X = C, N) Arrangements

In order to investigate some of the fundamental physical properties of the fcc-FeX (X = C, N) austenite solid solutions, we compare the hyperfine parameters obtained by Mössbauer ⁵⁷Fe spectrometry and those obtained by the full-potential linear augmented-plane wave (FLAPW) method. We have focused the study on isomer shifts and quadrupole splittings at Fe sites obtained by FLAPW assuming an Fe₈X structure to sketch the austenite. In the present work, we will discuss this point and compare the results of the calculations with experimental data.     

Hyperfine interactions of12B in BN (hexagonal)

Hyperfine interactions of¹²B(I =1⁺,T _1/2=21 ms) implanted in the substitutional site of B in BN (hexagonal) was studied by detecting -NMR. In order to measure the quadrupole coupling constant efficiently, we employed a newly developed quadrupole resonance technique (NNQR). The quadrupole moment of¹²B was determined to be |Q(¹²B)|=13.21±0.26 mb.     

Observation of the decay psi(2S)-->K0SK0L

The decay psi(2S)-->K(0)(S)K(0)(L) is observed using psi(2S) data collected with the Beijing Spectrometer at the Beijing Electron-Positron Collider; the branching fraction is determined to be B(psi(2S)-->K(0)(S)K(0)(L))=(5.24+/-0.47+/-0.48)x10(-5). Compared with J/psi-->K(0)(S)K(0)(L), the psi(2S) branching fraction is enhanced relative to the prediction of the perturbative QCD "12%" rule. The result, together with the branching fractions of psi(2S) decays to other pseudoscalar meson pairs (pi(+)pi(-) and K+K-), is used to investigate the relative phase between the three-gluon and the one-photon annihilation amplitudes of psi(2S) decays.     

First Observation of the nu(17)-nu(4) Difference Bands of Diborane (10)B(2)H(6) and (11)B(2)H(6)

An analysis of the nu(17)-nu(4) difference bands near 800 cm(-1) of two isotopic species, (10)B(2)H(6) and (11)B(2)H(6), of diborane has been carried out using infrared spectra recorded with a resolution of ca. 0.003 cm(-1). In addition, the nu(17) band of (10)B(2)H(6) has been recorded and assigned. Since this band in (11)B(2)H(6) had already been studied (R. L. Sams, T. A. Blake, S. W. Sharpe, J.-M. Flaud, and W. J. Lafferty, J. Mol. Spectrosc. 191, 331-342 (1998)), it was possible to derive precise energy levels and Hamiltonian constants for the 4(1) vibrational states of both isotopic species. Copyright 2000 Academic Press.     

First Observation of the Forbidden k-X Transition of (13)C(16)O

A weak rotationally resolved absorption band of (13)C(16)O has been identified from photographic spectra at 1078 ? and assigned to the forbidden transition from the X(1)Sigma(+) (v = 0) ground state to the k(3)Pi (v = 3) valence state. It is similar in structure to the corresponding band of (12)C(16)O but due to the fact it was photographed at a relatively low pressure only the two strongest rotational branches could be positively identified. It is the first time that the forbidden k-X transition has been observed for (13)C(16)O. The measured isotopic shift in the band origin provides independent confirmation of the new vibrational assignment of the k state by G. Berden, R. T. Jongma, D. Van der Zande, and G. Meijer (J. Chem. Phys. 107, 8303-8310 (1997)). Copyright 2000 Academic Press.     

Observation of a spin-parity 4+ K1(2090)

High statistics data for the reaction K^?p → K^?π⁺n at $\text{11}\text{GeV}\text{c}$ have been obtained in the LASS spectrometer at SLAC. A spherical harmonic moment analysis of the Kπ angular distribution displays evidence for a new K¹ state at $\text{2086}\text{MeV}\text{c}{}^2$ with the spin-parity assignment, J^P = 4⁺.     

{[K(18-C-6)][K(H_2O)_2]}[Cd(CN)_4]的合成与结构分析

合成了配合物 { [K(18- C- 6 ) ][K(H2 O) 2 ]} [Cd(CN) 4 ](1) ,并通过元素分析、红外光谱、单晶 X-射线衍射进行了结构分析。配合物属单斜晶系 ,空间群 P2 (1) / n。晶体学数据 :a=0 .936 5 3(18) nm,b=1.6 178(3) nm,c=1.74 81(3) nm,β=91.332 (3)°,V=2 .6 479(9) nm3 ,Z=4 ,Dcalcd=1.4 5 3g/ cm3 ,F(0 0 0 ) =12 0 8,R1=0 .0 317,w R2 =0 .0 5 6 7。配合物中 [K(18- C- 6 ) ],[K(H2 O) 2 ]和 [Cd(CN) 4 ]基团通过 K N键和 K —π相互作用形成三维网状结构     

Hyperfine interactions of 111Cd in TiO2 (Rutile) studied by perturbed angular correlations

The time-differential perturbed angular correlation for ¹¹¹Cd nuclei has been measured after ¹¹¹In implantation into polycrystalline TiO₂. The observed perturbation functions are characterized by a well-defined electric field gradient with the quadrupole coupling constant ν_Q = 105(1) MHz and the asymmetry parameter η = 0.18(1). We attribute these hyperfine parameters to ¹¹¹Cd on the (distorted) substitutional cation site in rutile. The PAC results are compared with those in SnO₂ rutile as well as with X-ray diffraction, RBS channeling experiments and point charge model calculations including relaxation of the probe atom surrounding.     

Observation of B+-->psi(3770)K+

We report the first observation of the decay B+-->psi(3770)K+ where the psi(3770) is reconstructed in the D0(-)D(0) and D+D- decay channels. The obtained branching fraction is B(B+-->psi(3770)K+)=(0.48+/-0.11+/-0.07)x10(-3). We have measured the branching fraction for the decay B+-->D0(-)D0K+ to be (1.17+/-0.21+/-0.15)x10(-3) and set a 90% confidence level upper limit of 0.90 x 10(-3) for the decay B+-->D+D-K+. We also present the results of a search for possible decays to D(-)D and D0(-)D(0)pi(0) of the recently observed X(3872) particle. The analysis is based on 88 fb(-1) of data collected at the Upsilon(4S) resonance by the Belle detector at the KEKB asymmetric-energy e(+)e(-) collider.     

~(159)TbII超精细结构光谱测量

利用具有光谱高分辨和选择性激发等特点的共线快离子束激光光谱学方法研究了159Tb II亚稳态 4 f95 d7H08和激发态 4 f96 p3 / 2 ( 1 5 /2 ,3/2 )的超精细结构光谱 ,所有光谱线可以很好地分辨 ;并由实验测量到的高分辨超精细结构光谱 ,给出了相应能级的超精细结构常数     

First (fuzzy) Hopf map from irreps of SU(2)

Using the spherical basis of the spin-ν operator, together with an appropriate normalized complex (2ν +1)-spinor on S ³ we obtain spin-ν representation of the U(1) Hopf fibration S ³ → S ² as well as its associated fuzzy version. Also, to realize the first Hopf map via the spherical basis of the spin-1 operator with even winding numbers, we present an appropriate normalized complex three-spinor. We put the winding numbers in one-to-one correspondence with the monopole charges corresponding to different associated complex vector bundles.