Browsing by Author "Yang, F."

Versatile ruthenium(II) complexes allow for site-selective CH oxygenations with weakly-coordinating aldehydes. The challenging CH functionalizations proceed with high chemoselectivity by rate-determining CH metalation. The new method features an ample substrate scope, which sets the stage for the step-economical preparation of various bioactive heterocycles.

A ruthenium(II) complex derived from the electron-deficient aromatic carboxylic acid 3-(F3C)C6H4CO2H proved to be a highly efficient catalyst for dehydrative alkyne annulation by NH-free hydroxamic acids in water. The CH/NOH functionalization occurred with excellent positional selectivity as well as ample substrate scope, setting the stage for effective intermolecular alkenylations of hydroxamic acids. Detailed mechanistic studies were suggestive of a kinetically relevant CH metalation by carboxylate assistance along with subsequent migratory alkyne insertion, reductive elimination, and intramolecular oxidative addition.

While components of the pathway that establishes left-right asymmetry have been identified in diverse animals, from vertebrates to flies, it is striking that the genes involved in the first symmetry-breaking step remain wholly unknown in the most obviously chiral animals, the gastropod snails. Previously, research on snails was used to show that left-right signaling of Nodal, downstream of symmetry breaking, may be an ancestral feature of the Bilateria [1, 2]. Here, we report that a disabling mutation in one copy of a tandemly duplicated, diaphanous-related formin is perfectly associated with symmetry breaking in the pond snail. This is supported by the observation that an anti-formin drug treatment converts dextral snail embryos to a sinistral phenocopy, and in frogs, drug inhibition or overexpression by microinjection of formin has a chirality-randomizing effect in early (pre-cilia) embryos. Contrary to expectations based on existingmodels [3-5], we discovered asymmetric gene expression in 2- and 4-cell snail embryos, preceding morphological asymmetry. As the formin-actin filament has been shown to be part of an asymmetry-breaking switch in vitro [6, 7], together these results are consistent with the view that animals with diverse body plans may derive their asymmetries from the same intracellular chiral elements [8].

Soil particle-size distribution (PSD) is one of the most fundamental physical attributes of soil due to its strong influence on other soil properties related to water movement, productivity, and soil erosion. Characterizing variation of PSD in soils is an important issue in environmental research. Using ordination methods to characterize particle size distributions (PSDs) on a small-scale is very limited. In this paper, we selected the Cele River Basin on the north slope of the Middle Kunlun Mountains as a study area and investigated vegetation and soil conditions from 1960 to 4070 m a.s.l. Soil particle-size distributions obtained by laser diffractometry were used as a source data matrix. The Canonical Correspondence Analysis (CCA) ordination was applied to analyse the variation characteristics of PSDs and the relationships between PSDs and environmental factors. Moreover, single fractal dimensions were calculated to support the interpretation of the ordination results. Our results indicate that a differentiation of 16 particle fractions can sufficiently characterize the PSDs in CCA biplots. Elevation has the greatest effect on PSDs: the soil fine fractions increase gradually with increasing elevation. In addition, soil pH, water and total salt content are significantly correlated with PSDs. CCA ordination biplots show that soil and vegetation patterns correspond with one another, indicating a tight link between soil PSDs and plant communities on a small scale in arid regions. The results of fractal dimensions analysis were rather similar to CCA ordination results, but they yielded less detailed information about PSDs. Our study shows that ordination methods can be beneficially used in research into PSDs and, combined with fractal measures, can provide comprehensive information about PSDs. Crown Copyright (C) 2010 Published by Elsevier B.V. All rights reserved.

Room-temperature azole C-H arylations were accomplished with inexpensive copper(I) compounds by means of photoinduced catalysis. The expedient copper catalysis set the stage for site-selective C-H arylations of non-aromatic oxazolines under mild reaction conditions, and provides step-economical access to the alkaloid natural products balsoxin and texamine.

Versatile ruthenium catalysts enabled unprecedented C-H bond oxygenations of aryl Weinreb amides with ample scope under exceedingly mild reaction conditions, thereby also giving access to valuable ortho-hydroxylated aldehydes. Mechanistic studies provided strong support for a kinetically relevant C-H bond activation.

We present results of a time-resolved pump-probe experiment where a Si sample was exposed to an intense 15 keV beam and its surface monitored by measuring the wavefront deformation of a reflected optical laser probe beam. By reconstructing and back propagating the wavefront, the deformed surface can be retrieved for each time step. The dynamics of the heat bump, build-up and relaxation, is followed with a spatial resolution in the nanometer range. The results are interpreted taking into account results of finite element method simulations. Due to its robustness and simplicity this method should find further developments at new x-ray light sources (FEL) or be used to gain understanding on thermo-dynamical behavior of highly excited materials. (C) 2011 Optical Society of America