A Pd-catalyzed asymmetric synthesis of Si-stereogenic dibenzosiloles is developed through enantioselective C-H bond functionalization of prochiral 2-(arylsilyl)aryl triflates. High chemo- and enantioselectivities are achieved by employing a Josiphos-type ligand under mild conditions.

FeCl3-mediated oxidative fusion of meso-linked dibenzo[a,g]corannulene-porphyrin dyads 6M afforded fused porphyrins 7M bearing a five-membered ring connection, but similar oxidation of β-linked dyads 9M provided fused porphyrins 10M bearing a six-membered ring connection, both in a regiospecific manner. While fused dyads 10M exhibit modestly red-shifted absorption and fluorescence profiles, fused dyads 7M display characteristically red-shifted absorption bands reflecting antiaromatic dehydropurpurin electronic networks.

Enantioselective direct aldol reaction of α-substituted nitroacetates with aqueous formaldehyde for the synthesis of α-alkyl serines has been achieved under base-free neutral phase-transfer conditions with a bifunctional chiral phase-transfer catalyst.

FeCl3 in combination with t-BuOOt-Bu as an oxidant was found to catalyze oxidative coupling of alkylamines with arenes, nitroalkanes, and 1,3-dicarbonyl compounds to give arylmethylamines, β-nitroalkylamines, and 2-(aminomethyl)-1,3-dicarbonyl compounds, respectively.

Poly(vinyl alcohol) (PVA) gels can be easily prepared by either the freeze‐thawing (FT gel) method or by the cast‐drying (CD gel) method. Although the resulting nanostructured networks of the FT and CD gels are similar, their physical properties are quite different; while CD gels are transparent and elastic, FT gels are opaque and less elastic. Moreover, the tear energy of the FT gels is much greater than that of the CD gels, which is a direct result of micrometer‐scale differences in their network structures. In order to control the distribution of microcrystallites on nano‐ and micrometer scales, FT gels were prepared from PVA solutions with different water contents. As a result, the gel gradually became more transparent as the initial water content was decreased; and accordingly, the tear energy decreased. Tear resistance was improved in the case of FT gels by repeating the number of FT cycles, whereas with CD gels, this was achieved by increasing the gelation temperature. These results indicate that the microscopic network structures are characterized by a micrometer‐scale bundled‐polymer (fibril), which determines the tear energy of FT gels. Simple methods to control the fibril network structure of FT gels using a unidirectional freezing method are presented herein, with the swelling and mechanical properties of modified FT gels discussed in terms of their multiple‐scale network structures. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41356.