宽波段多步激发K_2-系统产生的钾原子高位态辐射

本文首次报道以690.0～715.0nm宽波段范围内任何波长的脉冲染料激光激发K_2—K系统,由高位钾分子与钾原子碰撞以及分子-原子的混合激发等过程而产生钾原子404.4,404.7和470.05～590.0nm波段内高位态辐射的实验结果,并对激发机制进行了探讨.     

Invariants de Maslov équivariants

We construct two cohomological invariants associated to pairs of Lagrangian sub-bundles of a symplectic bundle on a compact manifold upon which a compact Lie group is acting. The first invariant, which we call the classical equivariant Maslov H-invariant, provides an obstruction to Lagrangian transversality and lives in the Borel cohomology. The second invariant, which we call the equivariant Maslov U-invariant, generalises the author's results in K-Theory 13 (1998), 347–361 to the equivariant context and provides a necessary and sufficient condition for equivariant Lagrangian transversality, up to homotopic stability, and lives in the U-theory (intermediate between the real complex K-theories). As an application, we show that two Lagrangian sub-bundles of a symplectic bundle on a homogeneous space are always stably transverse.     

Factorization of a convolution operator and inverse problems for difference equations

Translated from Matematicheskie Zametki, Vol. 48, No. 5, pp. 97–108, November, 1990.     

A Hyland-Bernstein approach to the digital control of Pritchard-Salamon systems

In this paper we consider the fixed finite-order digital linear-quadraticcontrol of Pritchard-Salamon infinite-dimensional systems withunbounded input and output operators under gaussian disturbances.A set of necessary conditions is given in terms of the solvabilityof a discrete-time Hyland-Bernstein system of equations (twomodified Riccati equations and two modified Lyapunov equationscoupled by an projection operator).     

The 5v 3 bands of 18O enriched ozone: line positions of 16O16O18O, 16O18O16O, 16O18O18O and 18O16O18O

The four 5v ₃ bands of ¹⁸O enriched ozone have been observed and analysed for the first time. Two species (¹⁶O¹⁸O¹⁶O and ¹⁸O¹⁶O¹⁸O) belong to the C_2v symmetry group and two other (¹⁸O¹⁸O¹⁶O and ¹⁶O¹⁶O¹⁸O) to the C_s symmetry group. They have been recorded at a resolution of 0.008 cm^?1 with a pathlength of 32.16 m. Despite the very weak absorptions observed, almost 250 energy levels have been derived for each of the 4 species, with J ? 35 and K _a ? 13, and suitable sets of Hamiltonian parameters have been determined. For 3 species it has been necessary to account for the resonance between the (005) and (311) states to correctly reproduce the spectra observed. These resonances, anharmonic for C_2v, and hybrid (both anhar-monic and Coriolis) for C_s symmetry confirm the accidentally extremely strong coupling between the (005) and (311) states for ¹⁶O₃, due in that case to the very close distance between unperturbed energy levels. This work also confirms the excellent prediction of band centres of these four species derived from the recently determined isotopically invariant molecular potential function.     

The vertical spectrum of H2CO revisited: (SC)2-CI and CC calculations

The vertical electronic spectrum of formaldehyde has been studied by means of (SC)²-MR-SDCI and CCLR methods. Two basis sets of atomic natural orbitals (ANOs) complemented with a one-centre series of Rydberg orbitals were used. The first was taken from the CASPT2 study by Merchán, M., and Roos, B. O., 1995, Theoret. Chim. Acta, 92, 221, and may be described as C,O[4s3pld]/H[2slp] with a lslpld Rydberg series centred in the charge centroid of the ²B₂ state of the cation. The second was a larger basis set that may be described as C,O[6s5p3d2f]/H[4s3p2d] + 3s3p3d in the same centre. The (SC)² dressing may be applied efficiently to an MR-SDCI method and comparison with the dressed CAS-SDCI is satisfactory, in spite of the remarkable reduction in the CI space dimension. The consistency of the (SC)²-MR-SDCI results was tested also against the CCLR and CASPT2 results using the same basis sets and against the CCLR results using Dunning's aug- and daug-cc-pVQZ basis sets. The ³A₁(π → π *) state is correctly placed as the second excited triplet while the highly multi-configurational nature of the ¹A₁(π → π *) state is confirmed as well as its greatly mixed valence-Rydberg nature. This state is predicted as lying under the 10 eV level, on top of the (n_y → 3d) Rydberg states that are predicted in the 8.9–9.5eV region. The 5 ¹B₂(n^y → 4s) Rydberg state and the ¹B₂(σ_y → π*) also are predicted in this region. The triplet states also were calculated with the (SC)²-MR-SDCI method. The vertical ordering of the 2 ¹A₁(n_y → 3p_y) and 2 ¹B₂(n_y → 3p_z) states is discussed, as well as that of the ¹B₁(σ → π*) and the Rydberg ¹B₁(n_y → 3d_xy) states. This work shows the highly reliable values that may be reached applying the dressing method along with a large basis set. Such a procedure is made possible using an MR-SDCI selection of spaces instead of the CAS-SDCI that was used up to now in most (SC)² dressing applications.     

Virial coefficients and equations of state for mixtures of hard discs,hard spheres and hard hyperspheres

The composition-independent virial coefficients of a d-dimensional binary mixture of (additive) hard hyperspheres following from a recent proposal for the equation of state of the mixture (Santos, A., Yuste, S. B., and López de Haro, M., 1999, Molec. Phys., 96, 1) are examined. Good agreement between theoretical estimates and available exact or numerical results is found for d = 2, 3, 4 and 5, except for mixtures whose components are very disparate in size. A slight modification that remedies this deficiency is introduced and the resummation of the associated virial series is carried out, leading to a new proposal for the equation of state. The case of binary hard sphere mixtures (d = 3) is analysed in some detail.     

Ferrimagnetic coupling in oxamido-bridged Mn(II)Cu(II) compounds: a combined CASPT2 and DDCI study

Multiconfigurational perturbation theory (CASPT2) and difference dedicated configuration interaction (DDCI) are applied to study the ferrimagnetic coupling in an oxamido-bridged Mn(II)Cu(II) molecular species. CASPT2 reproduces the experimental coupling very well. From the partition of the CASPT2 energy, the most important contributions to the coupling are established. Spin populations are calculated with DDCI. The successive improvement of the N-electron wave function allows us to analyse the contributions to the spin delocalization.     

A Popov-theory-based survey on digital control of infinite-dimensional systems with unboundedness

This paper represents a Popov-theory-based assessment of thecurrent status of the digital control of infinite–dimensionalsystems with certain unboundedness in control and/or observation,summarizing some results and indicating which, in the authors'opinion, would be the promising directions for future research.