Reaction-diffusion phenomena in a PDMS matrix can modify its topography

Various reagents and solvents can be absorbed into polydimethylsiloxane (PDMS), which may be a concern for many applications. We hypothesize that these absorbed reagents can also react with each other within the elastomer matrix. Here we demonstrate this phenomenon and use it as a means to physically modify the surface topography of the PDMS by generating wrinkles or pores.     

Adsorption behavior of metal ions onto a bovine serum albumin (BSA) membrane monitored by means of an electrode-separated piezoelectric quartz crystal.

The interaction between metal ions and bovine serum albumin (BSA) was studied by using a piezoelectric quartz crystal (PQC) arranged in the electrode-separated configuration. A silanized surface of the PQC was coated with a BSA membrane via a coupling reaction with glutaraldehyde. The frequency shifts obtained from PQC coated with a BSA membrane suggested that various kinds of metal ions could be adsorbed onto the BSA membrane from aqueous solutions containing a low concentration of metal ions (2 or 10 micromol dm(-3)), only when the BSA was denatured with an alkaline solution. Anionic species of Pt(IV) and Au(III) were adsorbed onto the denatured BSA membrane from an acetic acid solution at pH 2.2, and cationic species of Cd(II), Zn(II), Co(II), Ni(II), Cu(II), and Ag(I), and cations, such as Ca2+, Ba2+, and Mg2+, were adsorbed from ammonia buffer at pH 9.5, whereas Al(III), Cr(III), Fe(III), Hg(II), and Pb(II) were hardly adsorbed. The adsorption mechanisms of these metal ions are discussed, based on the electrostatic interaction between the metal ions and the denatured BSA membrane, and complex formation between the metal ions and amino acid residues of the denatured BSA. Further, the PQC coated with a denatured BSA membrane was applied to the determination of Pt and Cd, using large frequency shifts for Pt(IV) and Cd(II).     

Oxygenation of substituted 2′-hydroxyacetophenone 4-bromophenylhydrazones promoted by cobalt(II) schiff base complex

Substituted 2′-hydroxyacetophenone 4-bromophenylhydrazones are oxygenated readily in the presence of Co(Salpr) in ethanol to give 2-(4-bromophenylazo)-1,3-benzodioxoles in good yield. The results are rationalized in terms of the decomposition of a peroxy cobalt(III) complex intermediate by a mechanism similar to the Darkin oxidation.     

A facile photochemical route to C-5 and C-6 allyl-substituted uracil nucleosides

Irradiation of 5-iodouridine or 6-iodo-1,3-dimethyluracil in aq. acetonitrile in the presence of allyltrimethylsilane provided the corresponding 5- or 6-allylated product.     

Regio-controlled hydrogen-deuterium exchange of biologically important indoles under uv irradiation

Photochemical hydrogen-deuterium exchange reaction of biologically important indoles is reported. The regioselectivity of the photodeuteration was found to be controlled by the ammonium group of the side chain.