PubMed Health⌕ Search

Biomedical subjects

Weiqiang Gu

Publications and source records attributed to Weiqiang Gu.

2 recordsLinked to original sources

Heterogeneous catalysis using a nanostructured solid acid resin based on lyotropic liquid crystals.

The catalytic reactivity and selectivity of the first example of a nanostructured solid acid resin (1) are described. This new type of solid acid catalyst is formed by the self-assembly and copolymerization of two acidic lyotropic liquid crystals (LLCs), affording a columnar hexagonal polymer network with monodisperse nanochannels lined with sulfonic acid groups. The performance of this material as a heterogeneous catalyst was compared against that of two commercially available, amorphous sulfonic acid resins: Amberlyst-15 and Nafion NR50. Using the acid-catalyzed esterification of benzyl alcohol with 1-hexanoic acid in dry toluene as a test reaction, it was found that resin 1 displayed only slightly lower overall reactivity as compared to Amberlyst-15 and Nafion NR50 but more than an order of magnitude higher selectivity for the desired ester product over dibenzyl ether side-product. Control experiments revealed that the higher product selectivity is not due to differences in relative acidity between the nanostructured acid resin and the two amorphous resins. Instead, it appears that a large component of the enhanced selectivity is due to the regular nanostructure present in the LLC resin, which affords a much more uniform local acid microenvironment for reactions to occur. Resin 1 can also be recycled with almost complete recovery of catalytic activity and selectivity, and with essentially no leaching of reactive groups into the solution phase.

Journal Article↗

Photo-fries rearrangements of 1-naphthyl esters in the glassy and melted states of poly(vinyl acetate). Comparisons with reactions in less polar polymers and low-viscosity solvents.

The photo-Fries and associated photoreactions of four 1-naphthyl acylates have been examined in two types of poly(vinyl acetate) (PVAc) films above and below their glass transition temperatures, Tg. Because of the 'templating' effect of the esters on their reaction cavities, especially below Tg, the distributions of photo-Fries products, as mandated by the intermediate acyl/1-naphthyloxyl singlet radical pairs, are determined largely by the initial conformations of the guest molecules. Even above Tg, at 50 degrees C, where segmental chain motions of PVAc are relatively rapid, the influence of the cages in directing product formation is apparent. The radical-pair recombination rates for formation of the keto precursor of 2-(2-phenylpropanoyl)-1-naphthol upon irradiation of 1-naphthyl 2-phenylpropanoate in PVAc are reduced drastically as the temperature is lowered from above to below Tg. Comparison of results in PVAc with those in low-viscosity solvents (ethyl acetate and hexane) and low-polarity polymer films (polyethylene and polypropylene) indicate that interactions between the radicals produced from irradiation of 1 and the acetate pendant groups of PVAc, as well as the nature of its chain motions above and below Tg, influence enormously the course of the photo-Fries rearrangements.

Journal Article↗