THE ROLES OF REACTION INHOMOGENEITY IN PHASE SEPARATION KINETICS AND MORPHOLOGY OF REACTIVE POLYMER BLENDS

The roles of reaction inhomogeneity in phase separation of polymer mixtures were described and summarized via two examples:photocross-link of polymer mixtures in the bulk state and photopolymerization of monomer in the liquid state. The reaction kinetics,the reaction-induced elastic strain and the phase separation kinetics were monitored respectively by UV-Vis spectroscopy,Mach-Zehnder interferometry and laser-scanning confocal microscopy.It was found that phase separation in the bulk state was strongly ...     

UHV transmission electron microscopy on the reconstructed surface of (111) gold: I. General features

The reconstructed surface structure of (111) gold was studied by ultra-high vacuum transmission electron microscopy and diffraction and the results are described in this series of papers. In part I the observed fringes spaced about 6.3 nm in the images of (111) gold platelets grown on molybdenite, magnesium oxide and graphite are shown to be due to a reconstructed surface structure of unidirectional shrinkage of the surface layer by about 4% along one of the 〈1$\text{1}$0〉 directions on the (111) surface. The shrinkage of the surface layer of the same amount from the bulk lattice was found to take place on gold crystals of different lattice parameters, which were formed by pseudomorphic overgrowth of gold on gold containing various amounts of palladium and indium. Evidence is given for the fact that the shrinkage is not uniform and the observed fringes are not simple interference fringes between the shrunk surface layer and the underlying bulk lattice. At high temperatures the structure first transforms gradually and reversibly to an isotropically shrunk one, and finally the reconstruction disappears above about 900°C.     

Tumor affinity and DNA interactions of 57Co-bleomycin (author's transl)

Cobalt-57-bleomycin (BLM) has been proven to be the most stable and useful tumor-diagnostic agent among several radiolabelled BLMs. However, the considerably long half life of 57Co causes troubles in handling and preclude its extensive uses. In our previous work, BLM was proved to form two geometrical isomers, in chelating with Co. In this paper, we compared the tumor affinity of two isomers, to make an improvement of this drug's merit. We investigated biodistribution in tumor-bearing mice and DNA binding properties by fluorescence quenching technique and DNA melting study. A comparison of the data obtained suggests that isomerism affects the tumor affinity of the drug. Both tumor accumulation in tumor-bearing mice and stability of DNA binding of type I isomer were higher than those of type II. If a certain suitable radionuclide is inserted into cold Co-BLM type I isomer, this agent will be a greatly useful tumor-imaging radiopharmaceutical.     

Ultra-high-vacuum in situ electron microscopy of growth processes of epitaxial thin films

Extracts from recent results of ultra-high-vacuum in-situ electron microscopy of growth processes of epitaxial thin films are given. As a modified monolayer-by-monolayer mode, the growth process in Fe/(111)Au of the initial Frank-van der Merwe type, followed by the intrinsic γ → α transformation of Fe is mentioned. For the nucleation and growth mode, a systematic selection of epitaxial orientation according to interfacial lattice fitting, nucleation and coalescence features, the validity of Cabrera's suggestion extending Frank and van der Merwe's idea, the cluster mobility and effects of grown-in dislocations in substrate crystals are discussed on the basis of the observations.     

Single-walled carbon nanotubes acquire a specific lectin-affinity through supramolecular wrapping with lactose-appended schizophyllan

Single-walled carbon nanotubes can be entrapped within a helical superstructure composed of schizophyllan bearing lactoside-appendages to show an excellent water-solubility as well as a specific lectin-affinity.     

Rhodium-Catalyzed [2+1+2+1] Cycloaddition of Benzoic Acids with Diynes through Decarboxylation and C≡C Triple Bond Cleavage

It has been established that an electron-deficient cyclopentadienyl rhodium(III) (Cp^ERh^III) complex catalyzes the oxidative and decarboxylative [2+1+2+1] cycloaddition of benzoic acids with diynes through C≡C triple bond cleavage, leading to fused naphthalenes. This cyclotrimerization is initiated by directed ortho C−H bond cleavage of a benzoic acid, and the subsequent regioselective alkyne insertion and decarboxylation produce a five-membered rhodacycle. The electron-deficient nature of the Cp^ERh^III complex promotes reductive elimination giving a cyclobutadiene–rhodium(I) complex rather than the second intermolecular alkyne insertion. The oxidative addition of the thus generated cyclobutadiene to rhodium(I) (formal C≡C triple bond cleavage) followed by the second intramolecular alkyne insertion and reductive elimination give the corresponding [2+1+2+1] cycloaddition product. The synthetic utility of the present [2+1+2+1] cycloaddition was demonstrated in the facile synthesis of a donor–acceptor [5]helicene and a hemi-hexabenzocoronene by a combination with the chemoselective Scholl reaction.