Hydrothermally stable mesoporous aluminosilicates with moderate acidity via degradation-assembly process and improved catalytic properties

Mesoporous aluminosilicates with hydrothermal stability and moderate acidity are synthesized via assembly of microporous zeolite precursors obtained by the degradation of zeolite NaY, denoted as “degradation-assembly” (DA) technique. By controlling the degradation degree of matrix NaY, precursors with larger spatial volume and stronger rigidity will be obtained. The characterization results showed that the walls of the mesophase in MDA (mesoporous aluminosilicate obtained by “DA” method) composed of the preformed zeolite Y building units and the moderate acidity was inherited from the introduced precursors. It was suggested that the more mature assembly units accounted for the increased acidity of MDA with more Al species retained in the framework of mesophases. The resulting aluminosilicates with simultaneously moderate acidity and hydrothermal stability showed superior catalytic properties when used in heavy oil catalytic cracking catalysts.     

Performance evaluation of asphalt containing layered double hydroxides with different zinc ratio in the host layer

The effects of five layered double hydroxides (LDHs) with different zinc ratio on the physical and rheological properties, chemical components, and anti-UV aging performance of asphalt were evaluated. Results show that LDHs improve the deformation resistance of asphalt at high temperature. After UV aging, LDH-modified asphalts show the smaller changes of physical and rheological properties and chemical components in comparison with asphalt, indicating the improved UV aging resistance. By comparison, the LDHs with higher ratio of zinc in the layers have the more outstanding UV reflection ability, leading to a beneficial effect in improving UV aging resistance of asphalt.     

Palladium and Copper Cocatalyzed Intermolecular Cyclization Reaction: Synthesis of 5‐Aminopyrazole Derivatives

A novel and efficient palladium and copper co‐catalyzed intermolecular cyclization of acetonitriles with hydrazones has been developed for the synthesis of 5‐aminopyrazoles through C C and C N bond formation. The reaction has the advantages of easily available starting materials, simple manipulation and mild reaction conditions. The reaction involving various substituted acetonitriles and hydrazones proceeds smoothly and 5‐aminopyrazoles are synthesized in good yields. In contrast to the aliphatic and heteroaromatic substrates, the aromatic substrates tend to have a higher degree of reactivity.

     

Dearomatization of Indole Derivatives via Palladium‐Catalyzed C?H Bond Functionalization of Pyrroles: Convenient Construction of Spiroindolenines

An intramolecular palladium(II)‐catalyzed dearomative arylation reaction of indoles via C H bond functionalization was developed, providing access to structurally novel spiroindolenines with moderate to good yields. A one‐pot process for the synthesis of spiroindoline derivatives was also realized.

     

Cobalt‐Catalyzed,Imine‐Directed Olefin Hydroarylation under Grignard‐Free Conditions

We report here that a cobalt catalyst generated from a cobalt(II) salt and a ligand using magnesium metal is capable of promoting hydroarylation reactions through chelation‐assisted C−H activation. With the appropriate choice of the ligand and other reaction conditions, ketimine‐ or aldimine‐directed branched selective hydroarylations of styrenes and ketimine‐directed hydroarylations of vinylsilane have been achieved. The reported catalytic systems may serve as more convenient alternatives to previously developed catalytic systems employing Grignard reagents as reducing agents.

     

Enantioselective One‐Pot Reaction: Organocatalyzed Synthesis of Fully Functionalized Oxabicyclo[2.2.2]octanes with Seven Contiguous Stereocenters

An enantioselective one‐pot Michael/Michael/Henry/hemiacetalization reaction between α,β‐unsaturated aldehydes, α‐ketoamides, and nitroalkenes under mild conditions catalyzed by a diarylprolinol silyl ether has been developed. The sequential methodology provides a direct approach to a wide range of fully substituted chiral oxabicyclo[2.2.2]octanes with seven contiguous stereocenters in moderate to excellent yields (up to 99%), high to excellent diastereoselectivities (up to >25:1 dr), and high to excellent enantioselectivities (up to 99% ee).

     

Catalyst-Controlled Selectivity in Oxidation of Olefins: Highly Facile Success to Functionalized Aldehydes and Ketones

Catalysis Letters - The attractive challenge in green chemistry is exploring novel heterogeneous catalyst system for catalyst-controlled product selectivity for oxidation of olefins. Hence, we...     

Preparation of antimicrobial activated carbon fiber for adsorption

Journal of Porous Materials - Activated carbon fiber (ACF) is often used as efficient adsorption material for removal of contaminants from water. However, the propagation of microorganism on ACF...     

Numerical Modeling and Experimental Study of Laser Assisted Machining of Fused Silica

Silicon - Fused silica is a kind of high-strength optical material, which is widely used in industry. It is slow and inefficient to process hard and brittle materials by conventional machining (CM)...     

Genomic and metabolomic analysis of Bacillus licheniformis with enhanced poly-γ-glutamic acid production through atmospheric and room temperature plasma mutagenesis

Poly-γ-glutamic acid is an extracellular polymeric substance with various applications owing to its valuable properties of biodegradability, flocculating activity, water solubility, and nontoxicity. However, the ability of natural strains to produce poly-γ-glutamic acid is low. Atmospheric and room temperature plasma was applied in this study to conduct mutation breeding of Bacillus licheniformis CGMCC 2876, and a mutant strain M32 with an 11% increase in poly-γ-glutamic acid was obtained. Genome resequencing analysis identified 7 nonsynonymous mutations of ppsC encoding lipopeptide synthetase associated with poly-γ-glutamic acid metabolic pathways. From molecular docking, more binding sites and higher binding energy were speculated between the mutated plipastatin synthase subunit C and glutamate, which might contribute to the higher poly-γ-glutamic acid production. Moreover, the metabolic mechanism analysis revealed that the upregulated amino acids of M32 provided substrates for glutamate and promoted the conversion between L- and D-glutamate acids. In addition, the glycolytic pathway is enhanced, leading to a better capacity for using glucose. The maximum poly-γ-glutamic acid yield of 14.08 g·L^–1 was finally reached with 30 g·L^–1 glutamate.