Optical properties of extreme tellurium nanowires formed in subnanometer-diameter channels.

Single tellurium (Te) chains attract much attention as extreme nanowires with unique electronic and spintronic properties. Here, we encapsulate Te from a melt into channels of zeolites AFI (∼0.73 nm-channel diameter) and mordenite (MOR, ∼0.

4-methylumbelliferone Prevents Liver Fibrosis by Affecting Hyaluronan Deposition, FSTL1 Expression and Cell Localization.

4-methylumbelliferone (4MU) is an inhibitor of hyaluronan deposition and an active substance of hymecromone, a choleretic and antispasmodic drug. 4MU reported to be anti-fibrotic in mouse models; however, precise mechanism of action still requires further investigation. Here we describe the cellular and molecular mechanisms of 4MU action on CCl-induced liver fibrosis in mice using NGS transcriptome, Q-PCR and immunohistochemical analysis.

Calorimetric and dielectric studies of ferroelectric sodium nitrite confined in a nanoscale porous glass matrix.

Heat-capacity measurements of the sodium nitrite confined in a nanoscale porous glass matrix show that the intermediate incommensurate phase, present in the bulk, has disappeared and that the first-order ferroelectric transition becomes suppressed and gradual. The ferroelectric transition temperature is shifted considerably to lower temperatures. Two noncritical dielectric modes were observed; however, the observed giant growth of the dielectric constant on heating through the transition temperature TC is shown to be mainly due to the electrode polarization effect.

A New Strategy for the Synthesis of alpha-Difluoromethyl-Substituted alpha-Hydroxy and alpha-Amino Acids.

A new method for the preparation of alpha-chlorodifluoromethyl-, alpha-bromodifluoromethyl-, and alpha-difluoromethyl-substituted alpha-hydroxy and alpha-amino acid esters 11, 19-21 is described. The key step of the synthesis is the regioselective alkylation of ketones 5, 7-9 and imines 16-18 with C-nucleophiles. The ketones 7-9 are readily available from 3,3,3-trifluorolactate 1 by a five-step procedure.