Temperature effect on the vapor-phase exciplexes of cyano-substituted anthracenes

The emission spectra and lifetimes of the vapor-phase exciplexes of four cyano-substituted anthracenes with N,N-dimethylaniline (DMA) as a donor are examined over a wide temperature range. The activation energies associated with the exciplex dissociation are calculated to be of the order of 10 kcal/mol. The entropy change in forming the exciplexes is discussed in relation to the efficiency of the exciplex formation. For various donors other than DMA, preliminary results on how they interact with excited 9,10-dicyanoanthracene are also given.     

Highly Selective Separation of Rhodopsin from Bovine Rod Outer Segment Membranes Using Combination of Divalent Cation and Alkyl(thio)glucoside

The micellization process of bovine rod outer segment (ROS) membranes is investigated utilizing a series of neutral detergents. It is found that when alkyl(thio)glucosides with an appropriate hydrophilic–lipophilic balance (e.g. octylthioglucoside) are used in combination with a divalent cation, rhodopsin is selectively extracted from ROS membranes at a specific detergent-to-membrane ratio. This allows remarkable purification of rhodopsin by a single-step solubilization, because the residual membranes are heavily aggregated in the presence of divalent cation and are therefore easily sedimented by low-speed centrifugation. The absorption spectrum of the supernatant reproducibly exhibits an A₂₈₀/A₅₀₀ value of 1.6, an excellent value that could rarely be obtained by chromatographic purification. The degree of purification also depends on the type of divalent cation included in the solubilization solution; specific binding of IIB-series cations (Zn²⁺ and Cd²⁺) to ROS membranes is suggested to play an important role in the solubilization process. The present result represents a unique example of selective solubilization of a specific membrane protein from highly aggregated membranes.     

Cascade Rearrangement of 5-Cyclopentylidenecyclooctanones

Acid-catalyzed rearrangement of 5-cyclopentylidenecyclooctanone derivatives 9a-c was examined to obtain polyspiropolyquinanes 11a-c, considered to have a unique helical structure, through cascade rearrangement pathways consisting of continuous transannular cyclization followed by successive 1,2-alkyl shifts. The substrates were prepared easily by use of the Wittig or McMurry reaction. Reaction of the 5-cyclopentylidenecyclooctanone (9a) with acid gave the expected dispirotriquinane ketone 11a in high yield. The precise mechanism was elucidated by a deuterium-labeling experiment. In the case of the ketone 9b, having another spiroannulated cyclopentane ring attached on 9a, the trispirotetraquiane 11b was not obtained but the bis-propellane-type tetrahydrofuran 25 was produced exclusively. The 5-(5'-cyclopentylidenecyclooctylidene)cyclooctanone (9c) afforded the polycyclic compounds 27-31, depending on the acid used, instead of the desired tetraspiropentaquinane 11c. The structures of the products were determined by NMR spectral data including 2D (13)C INADEQUATE spectra and X-ray crystallographic analyses. The unexpected rearrangement pathways are also discussed.     

Spatial distribution of YO molecules ejected from laser-ablated YBa2 Cu3 O7−x

One-dimensional imaging laser-induced fluorescence spectroscopy has been used for in-situ measurements of spatial distributions of YO molecules produced during the ArF-laser ablation of YBa₂ Cu₃ O _7–x in vacuum and oxygen gas environment. The time-integrated angular distribution of particles ejected in vacuum has a cos ⁿ form, where 11 <n < 13. When oxygen gas was introduced, YO molecules were confined in a smaller volume, and temporal changes of their spatial distribution were interpreted in terms of blast-wave formation.     

Prolonged release of drug from triacetyl-β-CyD complex for oral and rectal administration

Triacetyl--cyclodextrin (TA--CyD), a hydrophobic cyclodextrin derivative, that is insoluble in water, was used to form a complex with flufenamic acid (FA). FA-TA--CyD complex formation was demonstrated by differential scanning calorimetry and powder X-ray diffractometry. The release rate of FA from the FA-TA--CyD complexes in phosphate buffer pH 6.8 was significantly retarded compared to that of FA from the FA and glucose mixture. When the FA-TA--CyD complexes were administered directly into the intraduodenal lumen, the plasma concentration of FA remained at a plateau level (10-18 g/ml) for 6–8 h. An increased mean residence time of FA following FA-TA--CyD complexes administration was observed. These results indicate that TA--CyD may serve as a hydrophobic carrier in prolonged-release preparations of FA.     

Alternating Sign Matrices and Some Deformations of Weyl's Denominator Formulas

An alternating sign matrix is a square matrix whose entries are 1, 0, or –1, and which satisfies certain conditions. Permutation matrices are alternating sign matrices. In this paper, we use the (generalized) Littlewood's formulas to expand the products and 2 as sums indexed by sets of alternating sign matrices invariant under a 180° rotation. If we put t = 1, these expansion formulas reduce to the Weyl's denominator formulas for the root systems of type B _n and C _n. A similar deformation of the denominator formula for type D _n is also given.