Generation of subterawatt sub-10-fs blue pulses at 1-5 kHz by broadband frequency doubling

Blue pulses with durations of 8.5 fs are generated by broadband frequency doubling of subterawatt Ti:sapphire laser systems at 1-5-kHz repetition rates. The average powers are 1.6 W at 5 kHz and 1.9 W at 1 kHz. The peak power is 0.16 TW with a duration of 12 fs at 1 kHz.     

Humidity-dependent reversible aggregation of rhodamine 6G dye immobilized within layered niobate K4Nb6O17

The spectroscopic behavior of rhodamine 6G (R6G) dye intercalated in layered hexaniobate K4Nb6O17 was investigated. R6G cations were intercalated into the niobate through displacement of preintercalated alkylammonium ions. Powder X-ray diffraction and elemental analysis indicated that the dye molecules were densely accommodated in the interlayer spaces of niobate. The spectroscopic behavior of intercalated R6G was characterized by humidity-dependent aggregation at room temperature. The dye molecules were present dominantly as monomers under humid conditions (93% relative humidity (RH)), while they formed dimers under relatively dry conditions (20% RH). The aggregation-deaggregation of dye occurred reversibly depending on the humidity. The reversible aggregation was not accompanied by a large alteration of the interlayer structure of the sample, because only a small amount of water was adsorbed/desorbed with a small change in the basal spacing of the intercalation compound during the humidity change.     

Copper‐Catalyzed Oxyboration of Unactivated Alkenes

The first regiodivergent oxyboration of unactivated terminal alkenes is reported, using copper alkoxide as a catalyst, bis(pinacolato)diboron [(Bpin)₂] as a boron source, and (2,2,6,6‐tetramethylpiperidin‐1‐yl)oxyl (TEMPO) as an oxygen source. The reaction is compatible with various functional groups. Two regioisomers are selectively produced by selecting the appropriate ligands on copper. The products may be used as a linchpin precursor for various other functionalizations, and net processes such as carbooxygenation, aminooxygenation, and dioxygenation of alkenes can be achieved after C?B bond transformations. Mechanistic studies indicate that the reaction involves the following steps: 1) Transmetalation between CuOtBu and (Bpin)₂ to generate a borylcopper species; 2) regiodivergent borylcupration of alkenes; 3) oxidation of the thus‐generated C?Cu bond to give an alkyl radical; 4) trapping of the resulting alkyl radical by TEMPO.     

Oryzamutaic acids H-J, new alkaloids from an Oryza sativa mutant with yellow endosperm

Three new nitrogen-containing heterocyclic alkaloids, oryzamutaic acids H-J (1-3), were isolated from the endosperm (polished rice) of an Oryza sativa mutant. The structures and relative stereochemistries of 1-3 were elucidated on the basis of spectroscopic analyses. The presence of three carbons, each bound to a carboxyl group and a nitrogen atom in the structure of 1, suggests that oryzamutaic acids H-J (1-3) are generated from three molecules of a single amino acid.     

Palladium‐Catalyzed C?H Fluorosilylation of 2‐Phenylpyridines: Synthesis of Silafluorene Equivalents

Treatment of 2‐phenylpyridines with amino(1,3,2‐dioxaborolan‐2‐yl)diphenylsilane produced fluorosilylated 2‐phenylpyridines in good to excellent yields under palladium catalysis. This reaction is the first example of C H fluorosilylation. Single‐crystal X‐ray structure analysis revealed a Lewis acid–base interaction between the silicon and nitrogen atoms, and the obtained fluorosilylated products are silafluorene equivalents. The fluorosilylated products showed stronger fluorescence than the corresponding silafluorene derivative.     

Coherent soft X-ray (λ=18.9 nm) generation in a transient gain scheme in molybdenum plasma

We investigate the threshold conditions for coherent soft x-ray generation using a compact hybrid (neodymium-doped glass-sapphire titanate) laser with an output energy of several hundred millijoules. Collisional excitation of molybdenum ions in a longitudinal-pumping scheme was used for x-ray (λ=18.9 nm) generation. The generated radiation exhibited a low divergence and a strong dependence on the delay between picosecond and femtosecond pumping radiations.     

Studies of advanced soft X-ray laser and coherent higher harmonic generation using intense subpicosecond laser produced high density plasma

Current activities on our research of soft X-ray lasers and higher harmonic generations using intense, subpicosecond lasers are reviewed. Especially for soft X-ray lasers we experimentally demonstrate that by longitudinally pumping 2-mm-long molybdenum preformed plasma with high-intensity 475 fs duration laser pulse, a highly directive soft-X-ray laser at 18.9 nm wavelength is generated. The divergence of the beam is evaluated to be of the submilliradian order, and only requires pump laser energy of 150 mJ. Simulations show that the pedestal in the main pump pulse can generate electron density and gain profiles with large spatial gradients, which result in the selective amplification of low-order transverse modes. The present result is the demonstration of an efficient and alternative method of improving the spatial coherence of X-ray lasers with amplified spontaneous emission medium, with possibilities of becoming an excellent tool to explore various application experiments. In higher harmonic generation, topics related to observation of blue shift due to collisionless absorption process is described.     

Distribution and fate of biologically formed organoarsenicals in coastal marine sediment

Marine organisms, including phyto‐ and zoo‐plankton, macroalgae, and animals, concentrate arsenic in various organic forms. However, the distribution and fate of these organoarsenicals in marine environments remains unclear. In this study, the distribution of organoarsenicals in coastal marine sediment in Otsuchi Bay, Japan, has been determined. Methylarsonic acid, dimethylarsinic acid, trimethylarsine oxide, arsenobetaine, arsenocholine and other unidentified arsenic species were detected in marine sediment by high‐performance liquid chromatography–inductively coupled plasma mass spectrometry analysis of methanol–water extracts. Arsenobetaine was the dominant organoarsenical at four of the seven stations where tests were carried out, and unidentified species or dimethylarsinic acid dominated at the other stations. Total organoarsenicals (as arsenic) in the surface sediment amounted to 10.6–47.5 µg kg^?1 dry sediment. Core analysis revealed that concentrations of organoarsenicals decreased with depth, and they are considered to be degraded within 60 years of deposition. These results show that organoarsenicals formed by marine organisms are delivered to the sediment and can be degraded within several decades. Copyright © 2005 John Wiley & Sons, Ltd.