Meso-tetraaryl cofacial bisporphyrins delivered by Suzuki cross-coupling

The Suzuki cross-coupling methodology provides a facile synthetic approach for the modular preparation of meso-tetraaryl cofacial bisporphyrins anchored by xanthene and dibenzofuran. This synthetic method furnishes cofacial bisporphyrin templates with enhanced steric and electronic protection from mu-oxo formation and oxidative degradation. The ability of these platforms to support multielectron oxidation chemistry mediated by proton-coupled electron transfer (PCET) is demonstrated by their reactivity for the catalytic disproportionation of hydrogen peroxide to oxygen and water.     

Aerobic catalytic photooxidation of olefins by an electron-deficient Pacman bisiron(III) mu-oxo porphyrin

The synthesis and oxygen atom transfer (OAT) photoreactivity of a diiron(III) mu-oxo meso-tripentafluorophenyl bisporphyrin appended to a dibenzofuran spacer are presented. Reaction of 4,6-diformyldibenzofuran under standard Lindsey conditions furnishes the parent cofacial porphyrin architecture in a single step. These cofacial porphyrins photocatalyze the oxidation of sulfides and olefins using visible light and molecular oxygen as the terminal oxidant. High turnover numbers reflect the enhanced stability of the electron-deficient diiron(III) mu-oxo bisporphyrin core appended to a dibenzofuran spacer under aerobic conditions.     

Surface characterization, modification chemistry, and separation performance of polyimide and polyamidoamine dendrimer composite films

6FDA-polyimide films modified by polyamidoamine (PAMAM) dendrimers with generations of 0, 1, and 2 are reported in this article. The actual molecular conformation and bulk size of these three generation dendrimers immobilized on polyimide surface were characterized by atomic force microscopy. After comparing with the results of dynamic simulation, we believe that the disk-shape cluster structure of dendrimers has been developed on the polymer surfaces. The amidation and cross-linking reaction between dendrimers and polyimide were examined and quantified by X-ray photoelectron spectroscopy, attenuated total reflection Fourier transform infrared spectroscopy, and gel content measurements. Modification time and the generations of PAMAM dendrimer have been verified as two important factors in determining the properties of modified polyimide films. These modified polyimide films exhibit excellent gas separation performance. The ideal selectivity of He/N(2) increases tremendously to about 200% as compared to that of the original polyimide film. Particularly, the separation performance of CO(2)/CH(4) gas pair can be improved beyond the upper bond limit possibly due to the strong interactions of dendrimer molecules with CO(2), which was verified by sorption tests.     

Compact 21-W 2-mum intracavity optical parametric oscillator

We report on an intracavity optical parametric oscillator (OPO) placed within a compact diode-pumped Nd:YALO laser cavity. This OPO utilizes a pair of KTP crystals, which are diffusion bonded together in a walk-off-compensated configuration. We have generated up to 21.4 W of 2-mum radiation, operating in a few-kilohertz range.     

A Comparison of Two Variational Methods

A discussion is given of the relation between the maximum functionaltheorem and Schwinger's variational principle, and it is shownthat the bound given by Schwinger's principle is better thanor the same as that given by the maximum functional theorem.     

Nanographite impurities in carbon nanotubes: their influence on the oxidation of insulin, nitric oxide, and extracellular thiols

There has been growing interest in the use of modified-carbon-nanotube electrodes in applications such as the electrochemical detection of biologically significant compounds, owing to their apparent "electrocatalytic" properties and ability to enhance oxidative signals. In spite of their salient properties, little work has been done to further examine the reasons for these reported characteristics. In this report, we present clear evidence that the presence of nanographite impurities within carbon nanotubes (CNTs) is responsible for providing the previously reported enhanced electrochemical response. We have demonstrated this effect on homocysteine, N-acetyl-L-cysteine, nitric oxide, and insulin, which are important biological agents in the body. Moreover, we also showed that the influence of nanographite impurities on the electrochemistry of carbon nanotubes is prevalent among a variety of CNTs, such as single-walled CNTs, double-walled CNTs, and few-walled CNTs. Our findings will have a profound influence upon the biomedical applications of CNTs.     

Gas‐transport properties of indan‐containing polyimides

A series of indan‐containing polyimides were synthesized, and their gas‐permeation behavior was characterized. The four polyimides used in this study were synthesized from an indan‐containing diamine [5,7‐diamino‐1,1,4,6‐tetramethylindan (DAI)] with four dianhydrides [3,3′4,4′‐benzophenone tetracarboxylic dianhydride (BTDA), 3,3′4,4′‐oxydiphthalic dianhydride (ODPA), (3,3′4,4′‐biphenyl tetracarboxylic dianhydride (BPDA), and 2,2′‐bis(3,4′‐dicarboxyphenyl) hexafluoropropane dianhydride (6FDA)]. The gas‐permeability coefficients of these four polyimides changed in the following order: DAI–BTDA < DAI–ODPA < DAI–BPDA < DAI–6FDA. This was consistent with the increasing order of the fraction of free volume (FFV). Moreover, the gas‐permeability coefficients were almost doubled from DAI–ODPA to DAI–BPDA and from DAI–BPDA to DAI–6FDA, although the FFV differences between the two polyimides were very small. The gas permeability and diffusivity of these indan‐containing polyimides increased with temperature, whereas the permselectivity and diffusion selectivity decreased. The activation energies for the permeation and diffusion of O₂, N₂, CH₄, and CO₂ were estimated. In comparison with the gas‐permeation behavior of other indan‐containing polymers, for these polyimides, very good gas‐permeation performance was found, that is, high gas‐permeability coefficients and reasonably high permselectivity. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 2769–2779, 2004