Adaptive H∞ Chaos Anti-synchronization

A new adaptive H∞ anti-synchronization （AHAS） method is proposed for chaotic systems in the presence of unknown parameters and external disturbances. Based on the Lyapunov theory and linear matrix inequality formulation, the AHAS controller with adaptive laws of unknown parameters is derived to not only guarantee adaptive anti-synchronization but also reduce the effect of external disturbances to an H∞ norm constraint. As an application of the proposed AHAS method, the H∞anti-synchronization problem for Genesio-Tesi chaotic systems is investigated.     

Nano-sized patterns derived from a SiCN preceramic polymer: Fabrication and their characterization

A microfabrication of ceramic materials with a low shrinkage has created inevitable demands in the fields of micro total analysis systems (μ-TAS) and microfluidic devices with thermal, chemical, and mechanical stability. In this study, nano-sized patterns were prepared using a soft lithographic technique, followed by the UV and thermal curation of a non-oxide SiCN preceramic polymer. The characterization of the thermal and mechanical properties of the cured preceramic polymer revealed that it becomes ceramic-like after the heat treatment at higher temperature than 600 °C. The heat-treated nano-sized patterns showed a low linear shrinkage as well as good chemical stability and optical properties. The results showed the feasibility of enormous potentials of the cured preceramic polymer because of the low shrinkage, the high optical transparency, and the thermal and chemical stability.     

Effect of stereosequences on crystallinity and properties of zone‐drawn poly(vinyl alcohol) microfibrils

To effectively orient the molecular chains of novel syndiotactic poly(vinyl alcohol) (PVA) microfibrillar fiber (PVA fibril), a high‐temperature zone‐drawing method was adopted. The PVA fibrils were directly prepared from the saponification and in situ fibrillation without a spinning procedure. The maximum draw ratio of the PVA fibril increased with a decrease in the syndiotactic diad (r‐diad) content, indicating that the deformability of PVA molecules was lowered in higher syndiotactic PVA. Degree of crystal orientations up to 0.990 were achieved by stretching the PVA fibril with the r‐diad content of 65.1% and the original degree of crystal orientation of 0.902 at 250 °C close to its crystal melting temperature (T_m). When the same draw ratio was applied to the fibrils, a higher crystal orientation was achieved for the fibrils having higher syndiotacticity. Wide‐angle X‐ray data show that the longitudinal crystal sizes of drawn PVA fibrils were larger in higher syndiotacticities. The degree of crystal orientation, crystallinity, T_m, longitudinal crystal size, and tensile strength of the maximum drawn PVA fibril with a r‐diad content of 65.1% were 0.99, 0.97, 279 °C, 187 Å, and 4.66 N/tex, respectively. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 1263–1271, 2001     

An Efficient Synthesis of 2,8-Diazabicyclo[4.3.0]-nonane Derivatives via Intramolecular Cyclization Reaction

Novel 5-functionalized-2,8-diazabicyclo[4.3.0]nonane derivatives 5 were synthesized from epoxide 1 through 4 steps in 46.7～52.6% yield.     

New synthetic technology for the synthesis of hindered alpha-diazoketones via acyl mesylates

[formula: see text] A mild and reliable one-pot protocol for the elaboration of sterically demanding carboxylic acids into alpha-diazoketones via acyl mesylates has been developed. Aside from delineating the reaction parameters which render this strategy quite general for hindered carboxylic acids, we have directly proven the existence of the fleeting acyl mesylate group as the reactive species in these reactions and shed light onto the differing mechanisms which are operative in the activation of hindered and simple carboxylic acids with methanesulfonyl chloride.     

Catalytic transfer hydrogenation of conjugated nitroalkenes using decaborane: synthesis of oximes

alpha,beta-Unsaturated nitroalkenes are readily reduced to the corresponding aldoximes and ketoximes in good yields, using a system of decaborane (B10H14) and DMSO in methanol in the presence of 10% Pd/C at room temperature under nitrogen.     

Oxygen-promoted Pd(II) catalysis for the coupling of organoboron compounds and olefins

Reported herein is a mild and efficient Pd(II) catalysis, leading to the formation of carbon-carbon bonds between a broad spectrum of organoboron compounds and alkenes. Molecular oxygen was employed to reoxidize the resultant Pd(0) species back to Pd(II) during catalytic cycles. This oxygen protocol promoted the desired Pd(II) catalysis, whereas it retarded competing Pd(0) catalytic pathways such as Heck or Suzuki couplings. [reaction: see text]