UV‐laser‐induced photolysis of trimethyl(vinyloxy)silane for chemical vapour deposition of polysiloxane films

The UV‐induced photolysis of trimethyl(vinyloxy)silane (TMVSi) induced by ArF laser, affording a multitude of unsaturated hydrocarbons and a solid polydimethylsiloxane, represents a convenient process of chemical vapour deposition in which the silicon of the parent is almost completely utilized for the formation of the solid phase and in which the morphology and composition of the films is affected by the configuration of the substrate and laser beam. Copyright © 1999 John Wiley & Sons, Ltd.     

Temperature-responsive,polymer-modified surfaces for green chromatography

Thermoresponsive poly(N-isopropylacrylamide) (PIPAAm) and its derivatives were utilized as chromatography column matrix modifiers to develop novel supports for thermoresponsive hydrophobic chromatography with aqueous mobile phase. In the column, matrix surfaces show thermoresponsive hydrophilic/hydrophobic property alterations, which alter interaction with and retention of solutes to be separated. We have also demonstrated that the electrostatic interaction of ionic solutes and charged, thermoresponsive polymer-modified surfaces can be modulated temperature changes in the aqueous mobile phase alone.     

Double Naphthalene‐Tagged Cyclodextrin‐Peptide Capable of Exhibiting Guest‐Induced Naphthalene Excimer Fluorescence

A cyclodextrin‐peptide hybrid (17NNβ) bearing two naphthalene units in the peptide side chain has been designed and synthesized as a novel chemosensor molecule. Circular dichroism study of the compound revealed that the peptide has α‐helix structure with a helix content of 41%. The peptide revealed both monomer and excimer emission and the intensity of the excimer emission increased while that of the monomer emission decreased upon addition of the guest compound. This behavior was observed for various guest molecules, suggesting that the system can be used for detecting molecules in aqueous solution.     

Cell sheet engineering: intelligent polymer patterned surfaces for tissue engineered liver

We describe a new culture system utilizing the temperature-responsive polymer grafted surface for designing of cell position and layered tissue reconstruction. Organizing of the hepatic tissue structure by controlling the culture system, that is patterned co-culture and layered cell sheet co-culture achieved by moving the cultured cells from the culture surface, resulted in regulation of the hepatocyte function. The technique for cell sheet manipulation would promote the liver tissue engineering in quality.     

Reversible 1,3‐dipolar cycloaddition of dimethyl 2‐thiono‐1,3‐dithiole‐4,5‐dicarboxylate with dimethyl acetylenedicarboxylate

It was shown that dimethyl 2‐thiono‐1,3‐dithiole‐4,5‐dicarboxylate ( 2 ) and dimethyl acetylenedicarboxylate (DMAD) undergo a 1,3‐dipolar cycloaddition to produce a short‐lived ylide intermediate ( 3 ). The 1,3‐dipolar cycloaddition took place even at room temperature, although sluggishly, but took place much more rapidly under application of a high pressure of 500 MPa. The 1,3‐dipolar cycloaddition is reversible and the ylide 3 immediately splits into 2 and DMAD. When the reaction of 2 with DMAD was carried out at room temperature without solvent, a spiro‐1,3‐dithiole ( 11 ) was formed in 11% yield, whereas the reaction at 150°C provided a thiophene derivative ( 13 ) in 41% yield. It was found that 11 undergoes a thermal rearrangement to 13 . Results of attempted chemical trapping of the ylide 3 are also reported. © 2000 John Wiley & Sons, Inc. Heteroatom Chem 11:434–440, 2000