All‐Metal Antiaromaticity in Sb4‐Type Lanthanocene Anions

Antiaromaticity, as introduced in 1965, usually refers to monocyclic systems with 4n π electrons. This concept was extended to all‐metal molecules after the observation of Li₃Al₄^? in the gas phase. However, the solid‐phase counterparts have not been documented to date. Herein, we describe a series of all‐metal antiaromatic anions, [Ln(η⁴‐Sb₄)₃]^3?(Ln=La, Y, Ho, Er, Lu), which were isolated as the K([2.2.2]crypt) salts and identified by single‐crystal X‐ray diffraction. Based on the results obtained from the chemical bonding analysis, multicenter indices, and the electron‐counting rule, we conclude that the core [Ln(η⁴‐Sb₄)₃]^3? fragment of the crystal has three locally π‐antiaromatic Sb₄ fragments. This complex represents the first locally π‐antiaromatic all‐metal system in the solid state, which is stabilized by interactions of the three π‐antiaromatic units with the central metal atom.     

Metabolic Labeling and Imaging of N‐Linked Glycans in Arabidopsis Thaliana

Molecular imaging of glycans has been actively pursued in animal systems for the past decades. However, visualization of plant glycans remains underdeveloped, despite that glycosylation is essential for the life cycle of plants. Metabolic glycan labeling in Arabidopsis thaliana by using N‐azidoacetylglucosamine (GlcNAz) as the chemical reporter is reported. GlcNAz is metabolized through the salvage pathway of N‐acetylglucosamine (GlcNAc) and incorporated into N‐linked glycans, and possibly intracellular O‐GlcNAc. Click‐labeling with fluorescent probes enables visualization of newly synthesized N‐linked glycans. N‐glycosylation in the root tissue was discovered to possess distinct distribution patterns in different developmental zones, suggesting that N‐glycosylation is regulated in a developmental stage‐dependent manner. This work shows the utility of metabolic glycan labeling in elucidating the function of N‐linked glycosylation in plants.     

Water‐in‐Supercritical CO2 Microemulsion Stabilized by a Metal Complex

Herein we propose for the first time the utilization of a metal complex for forming water‐in‐supercritical CO₂ (scCO₂) microemulsions. The water solubility in the metal‐complex‐stabilized microemulsion is significantly improved compared with the conventional water‐in‐scCO₂ microemulsions stabilized by hydrocarbons. Such a microemulsion provides a promising route for the in situ CO₂ reduction catalyzed by a metal complex at the water/scCO₂ interface.     

Peculiar All‐Metal σ‐Aromaticity of the [Au2Sb16]4− Anion in the Solid State

Gas‐phase clusters are deemed to be σ‐aromatic when they satisfy the 4n+2 rule of aromaticity for delocalized σ electrons and fulfill other requirements known for aromatic systems. While the range of n values was shown to be quite broad when applied to short‐lived clusters found in molecular‐beam experiments, stability of all‐metal cluster‐like fragments isolated in condensed phase was previously shown to be mainly ascribed to two electrons (n=0). In this work, the applicability of this concept is extended towards solid‐state compounds by demonstrating a unique example of a storable compound, which was isolated as a stable [K([2.2.2]crypt)]⁺ salt, featuring a [Au₂Sb₁₆]^4? cluster core possessing two all‐metal aromatic AuSb₄ fragments with six delocalized σ electrons each (n=1). This discovery pushes the boundaries of the original idea of Kekulé and firmly establishes the usefulness of the σ‐aromaticity concept as a general idea for both small clusters and solid‐state compounds.     

Low frequency acoustic signals associated with rock falls,thunderstorms, and wind turbulences in field environment

This paper characterized the observed low frequency acoustic signals generated by rock falls, thunderstorm, and wind turbulence in large rocky landslide. A digital infrasonic recording system was deployed on site to capture real-time low frequency acoustic signals associated with rock falls. An advanced non-stationary signal analysis method, i.e. Empirical Mode Decomposition (EMD), was applied to get insight to the characteristics of the low frequency acoustic signals induced by the hazards. Joint time–frequency distribution spectra technique was used to detect distinctive features of the events. The study shows that the low frequency acoustic signals can be excited by rock falls, thunderstorm and wind turbulence in the field environment, but the signal varies in both time domain and frequency domain with different patterns depending on the physical processes. The results demonstrated that the EMD-based signal processing technique is capable of extracting distinctive features to differentiate acoustic signals in real environment.     

Design of Enhanced Catalysts by Coupling of Noble Metals (Au,Ag) with Semiconductor SnO2 for Catalytic Reduction of 4‐Nitrophenol

The reduction of 4‐nitrophenol (Nip) into 4‐aminophenol (Amp) by NaBH₄, which is catalyzed by both binary and ternary yolk–shell noble‐metal/SnO₂ heterostructures, is reported. The binary heterostructures contain individual Au or Ag nanoparticles (NPs) and the ternary heterostructures contain both Au and Ag NPs. The Au@SnO₂ yolk–shell NPs are synthesized via a silica seeds‐mediated hydrothermal method. Subsequently, the Au@SnO₂@Ag and Au@SnO₂@Au yolk–shell–shell (YSS) NPs are synthesized, whereby SnO₂ is located between the Au and Ag NPs. The morphology, composition, and optical properties of the as‐prepared samples are analyzed. For the binary heterostructures, the rate of the reduction reaction increases with decreasing particle size. The catalytic results demonstrate the synergistic effect of Au and Ag in the ternary metal–semiconductor heterostructures, which is beneficial to the catalytic reduction of Nip into Amp. Both the binary and ternary heterostructures exhibit significantly better catalytic performances than the corresponding bare Au and Ag NPs. It is envisaged that the current synthesized strategy will promote further interest in the field of bimetal NP‐based catalysis.     

Analysis of the dynamics of laser induced plume propagation from liquid matrix using fast photography

Glycerol, a liquid matrix material for matrix-assisted laser desorption ionization mass spectrometry, was irradiated by a tunable pulsed infrared laser at wavelengths of 2.80 μ.m, 2.94 μ.m, 3.10 μ.m and 3.50 μ.m, covering the OH and CH stretch vibrations. A fast photography system was introduced to analyze the dynamic process of plume propagation induced by laser ablation up to 1000 μ.s of the delay time. Propagation distance of the plume front was measured and the corresponding velocities were calculated; they varied with the wavelength and decreased with the delay time. At the tunable wavelength of the peak of the OH absorption (3.0 μ.m), theoretical calculations indicate that energy deposition from the pulsed laser is in the regime of stress confinement. The mode of energy deposition depends on the wavelength of the OH vibration and its distance from the absorption maxima. However, stages after a 10 μ.s delay at various wavelengths show a certain similarity in the distance of plume propagation, which can be well fitted by a drag model.     

Effects of surface residual species in SBA-16 on encapsulated chiral (1S,2S)-DPEN-RuCl<Subscript>2</Subscript>(TPP)<Subscript>2</Subscript> in asymmetric hydrogenation of acetophenone

The SBA-16 obtained by different routes of elimination of organic templates were used as the hosts for encapsulation of chiral Ru complex (1S,2S)-DPEN-RuCl₂(TPP)₂ (1) (DPEN = 1,2-diphenylethylene-diamine, TPP = triphenyl phosphine). The methods for removing templates had distinct effects on the amount of residual template in SBA-16, which made the SBA-16 with different surface and structure properties. 1 encapsulated in SBA-16 extracted with the mixture of pyridine and ethanol showed higher activity and enantioselectivity for acetophenone asymmetric hydrogenation.