Unified theory of bound and scattering molecular Rydberg states as quantum maps

Using a representation of multichannel quantum defect theory in terms of a quantum Poincaré map for bound Rydberg molecules, we apply Jung's scattering map to derive a generalized quantum map, that includes the continuum. We show that this representation not only simplifies the understanding of the method, but moreover produces considerable numerical advantages. Finally we show under what circumstances the usual semi-classical approximations yield satisfactory results. In particular we see that singularities that cause problems in semi-classics are irrelevant to the quantum map.     

SENSITIZED PHOTOOXYGENATION ACCORDING TO TYPE I MECHANISM (RADICAL MECHANISM) — PART III. EXPERIMENTS WITH CONTINUOUS ILLUMINATION

Abstract— The photochemical reaction in the system thionine (sensitizer), allylthiourea (ATU, acceptor), and oxygen was studied with continuous illumination. In oxygen-free aqueous solution thionine is photoreduced to leucothionine. With oxygen, however, a photooxygenation of the acceptor takes place. At the same time the quantum yield of the bleaching reaction of thionine decreases markedly in comparison with that of the oxygen-free solution. At about 100 sec after the beginning of illumination, the overall quantum yield of the bleaching reaction diminishes further because the leucothionine formed during the reaction now becomes transformed into thionine. The quantum yields do not change significantly over the range of oxygen concentrations studied (initial concentration 1 × 10^-5 to 5 × 10^-5 M ). In addition they are independent of the light intensity. The influence of the pH and the acceptor concentration were also investigated.
The sensitizer is not only bleached reductively, but is also partly destroyed by oxidation. The results are in agreement with the reaction scheme elucidated by flash photolysis measurements.
In accordance with this reaction scheme, the primary reaction (a) of the reductive bleaching of the sensitizer, (b) of the photooxygenation of the acceptor and (c) of the oxidative destruction of the sensitizer, is identical in all cases. This process is the redox reaction between the sensitizer triplet and the acceptor, where a semithionine and an ATU-radical are formed. The reaction represents an example of a Type I photooxygenation according to the notation of Gollnick.     

CORTICOSTEROID (METHYLPREDNISOLONE) MODULATION OF PHOTOPEROXIDATION BY ULTRAVIOLET LIGHT IN LIPOSOMES

Abstract— UV irradiation of ovolecithin liposomes produced a dose dependent wave of peroxidation which reached a peak and then fell again coincident with substrate exhaustion. This correlated well with subsequent increases in membrane permeability. There was a progressive loss of unsaturated fatty acids, and when cholesterol was incorporated into liposomes, the UV produced a progressive loss of this steroid.
Methylprednisolone sodium succinate, a synthetic corticosteroid, was found to inhibit this peroxidation in a dose dependent manner, also ameliorating membrane permeability increases when present during irradiation, but not able to compensate for pre-existing damage. When cholesterol was present in the liposomes, methylprednisolone sodium succinate was also able to protect this steroid from UV peroxidative damage.
The rates of reaction in this system suggested that polyunsaturated fatty acids, even when present in extremely small concentrations, underwent an initial rapid wave of peroxidation, which served to initiate the slower rate of lipoperoxidation within the bulk of mono- and di-"unsaturates". At low concentrations, the corticosteroid preferentially blocked damage to mono- and di-unsaturated fatty acids, affecting the polyunsaturated fatty acids as well, at higher concentrations.
This study suggests that the corticosteroid, methylprednisolone sodium succinate, possesses antioxidant properties in lipid systems subjected to free radical peroxidation.     

Recherches dans la série des cyclitols XXXVII Etude par spectrométrie de masse

Low resolution mass spectra of cyclohexane-triols, -tetrols, -pentols and -hexols and of some of their deuterium labelled derivatives have been measured. The results indicate that for some geometrical isomers quantitative differences between ion intensities are significant, allowing to deduce the stereochemistry of the molecule from its mass spectrum. In all these compounds the electron impact induced elimination of water occurs mainly by interaction between OH groups. There is a correlation between the relative abundance of (M – H₂O)⁺ and (M ?2 H₂O)⁺ ions and the number of axial hydroxyls in the more stable conformation of the molecule. Difficulties encountered in deducing fragmentation patterns, and determination of number and position of deuterium atoms in the molecule of ms-inositol are discussed.     

聚焦形貌恢复方法模型设计

采用基于拉普拉斯算符聚焦形貌恢复方法,提出了模拟目标深度测量的数值模型。数值模拟的核心是基于通过几何光学预测的理想图像的卷积与透镜广义孔径函数的多色点扩散函数,即用聚焦误差替代抛物线圆柱形貌或高斯函数。该模型可以使用基于聚焦形貌恢复方法的传感器真实组件参数、光源光谱、光学系统离差、相机的光谱灵敏度。提出了光学系统离差（消球差、消色差、色差）对确定目标表面形貌的精确度和可靠性的影响。结果表明,该模型可以有效提高实验效率,缩短时滞,降低成本。     

Origin of regge symmetry for wigner coefficients ofLU(2)

Using general properties of the representations of unitary groups and their relations to representations of symmetric groups, the 3j symbol of the unitary unimodular group ?U(2) is written in terms of a 9j symbol of the unitary unimodular group ?U(J) withJ being the sum of the threej's. The result yields the Regge symmetry of the 3j symbol as a consequence of new relations between Wigner coefficients and special invariants of unitary groups on one hand and the association symmetry of the symmetric group on the other.