Formation of one-dimensional C60 rows on TiO2(110)-1 x 2-cross-link structure and their local polymerization

Adsorption and growth of a C(60) monolayer on a TiO(2)(110)-1 x 2-cross-link structure were investigated by scanning tunneling microscopy (STM). Single C(60) molecules were preferentially anchored at the cross-link site due to interaction with undercoordinated Ti cations, and C(60) rows grew along the troughs between the 1 x 2-added rows. The C(60) monolayer structure is characterized by closely packed (r(C(60)-C(60)) = 1.0 nm) C(60) rows that are paired with every second added row (separation of paired rows is 1.1 nm). By applying a high negative bias voltage (-3.5 V) to an STM tip on the C(60) monolayer, C(60) oligomers were formed accompanied with the contraction of C(60)-C(60) distance along the C(60) row and bright contrast in the STM image.     

A self-adaptive moving mesh method for the Camassa-Holm equation

A self-adaptive moving mesh method is proposed for the numerical simulations of the Camassa-Holm equation. It is an integrable scheme in the sense that it possesses the exact N-soliton solution. It is named a self-adaptive moving mesh method, because the non-uniform mesh is driven and adapted automatically by the solution. Once the non-uniform mesh is evolved, the solution is determined by solving a tridiagonal linear system. Due to these two superior features of the method, several test problems give very satisfactory results even if by using a small number of grid points.     

Two-dimensional crystal growth and stacking of bis(phthalocyaninato) rare earth sandwich complexes at the 1-phenyloctane/graphite interface

Initial stages of two-dimensional crystal growth of the double-decker sandwich complex Lu(Pc*)2 [Pc* = 2,3,9,10,16,17,23,24-octakis(octyloxy)phthalocyaninato] have been studied by scanning tunneling microscopy at the liquid/solid interface between 1-phenyloctane and highly oriented pyrolytic graphite. High-resolution images strongly suggest alignment of the double-decker molecules into monolayers with the phthalocyanine rings parallel to the surface. Domains were observed with either hexagonal or quadrate packing motifs, and the growing interface of the layer was imaged. Molecular resolution was achieved, and the face of the phthalocyanine rings appeared as somewhat diffuse circular features. The alkyl chains are proposed to be interdigitating to maintain planar side-by-side packing.     

Sonochemical immobilization of noble metal nanoparticles on the surface of maghemite: mechanism and morphological control of the products

Aqueous sample solutions containing noble metal ions (HAuCl₄, Na₂PdCl₄, H₂PtCl₆), polyethyleneglycol monostearate, and magnetic maghemite nanoparticles were irradiated with high power ultrasound. Analyses of the products showed that noble metal ions were reduced by the effects of ultrasound, and the formed noble metal nanoparticles were uniformly immobilized on the surface of the maghemite. The present “one pot process” significantly simplifies the immobilization of noble metal nanoparticles on the surface of supports, compared with the conventional impregnation method. The average diameter of immobilized Au was 7–13 nm, and the diameters of Pd and Pt were several nm. The diameters depended upon the concentration of polyethyleneglycol monostearate and the concentration of noble metal ions, but not upon the maghemite concentration, indicating the possibility of the morphological controls of the products by adjusting these preparation conditions. The measurements of the average diameters and the numbers of immobilized Au nanoparticles obtained under various conditions suggest that the nucleation of Au does not occur on the surface of maghemite, but it might occur in the homogeneous bulk solution.     

Electronic absorption and emission spectra of Alq3 in solution with special attention to a delayed fluorescence

Tris(8-quinolinolato)aluminum(III) (Alq₃) shows electronic absorption bands at 378, 360 (in a 1:1 mixed solvent of methanol and ethanol (ME) at 77 K), 334, 316, 300, 263, 255.8, and 233 nm in ethanol at room temperature. According to the polarized fluorescence excitation spectrum together with MO calculations, for instance, the 360 nm band is assigned to an LL CT transition (an intramolecular charge transfer transition between two ligands), and the 378 nm band to an LM/ML CT one (an intramolecular charge transfer transition between ligand and metal). Alq₃ shows a broad fluorescence band peaking at around 478 nm in the ME matrix at 77 K. The emission spectrum measured with a phosphoroscope has two emission bands at 567 and 478 nm. The 567 nm band accompanies vibronic bands at 578 and 605 nm, being safely assigned to a phosphorescence of Alq₃. The lifetimes of the 478 and 567 nm bands are both 5.4 ms. The lifetime of the 478 nm band together with the band position and its band shape indicate that this band can be assigned to a delayed fluorescence.     

Diode-pumped 65 fs Kerr-lens mode-locked Yb(3+):Lu(2)O(3) and nondoped Y(2)O(3) combined ceramic laser

Diode-pumped Kerr-lens mode-locked laser operation of Yb(3+):Lu(2)O(3) and nondoped Y(2)O(3) combined ceramics has been achieved; 65 fs pulses with an average power of 320 mW under 5 W of pump power were obtained at the center wavelength of 1032 nm. The spectral bandwidth and the time bandwidth product were 18.9 and 0.345 nm, respectively. To our knowledge, this is the first demonstration of a Kerr-lens mode-locked laser operation based on Yb(3+):Lu(2)O(3) ceramic.     

Spectral coherent-state quantum cryptography

A novel implementation of quantum-noise optical cryptography is proposed, which is based on a simplified architecture that allows long-haul, high-speed transmission in a fiber optical network. By using a single multiport encoder/decoder and 16 phase shifters, this new approach can provide the same confidentiality as other implementations of Yuen's encryption protocol, which use a larger number of phase or polarization coherent states. Data confidentiality and error probability for authorized and unauthorized receivers are carefully analyzed.     

Albidosides H and I,two new triterpene saponins from the barks of Acacia albida Del. (Mimosaceae)

Two new triterpene saponins, albidosides H (1) and I (2), along with the three known saponins were isolated from the barks of Acacia albida. Their structures were elucidated on the basis of extensive 1D- and 2D-NMR studies and mass spectrometry. Albidosides H (1) and I (2) were assayed for their cytotoxicity against HeLa and HL60 cells using MTT method.     

Connectivity keeping edges in graphs with large minimum degree

The old well-known result of Chartrand, Kaugars and Lick says that every k-connected graph G with minimum degree at least 3k/2 has a vertex v such that G−v is still k-connected. In this paper, we consider a generalization of the above result [G. Chartrand, A. Kaigars, D.R. Lick, Critically n-connected graphs, Proc. Amer. Math. Soc. 32 (1972) 63–68]. We prove the following result:Suppose G is a k-connected graph with minimum degree at least 3k/2+2. Then G has an edge e such that G−V(e) is still k-connected.The bound on the minimum degree is essentially best possible.     

Structural changes of poly-L-lysine in solution and lyophilized form

Two structural changes of poly-l-lysine have been studied by various spectroscopic techniques; one is a structural change of a random coil sample in solution to a mixture of alpha-helix and beta-sheet during rapid freezing in the lyophilizing process, and the other is a pressure-induced structural change from an alpha-helix to a beta-sheet structure for a lyophilized sample.