The effect of methyl group on the mechanical properties of hydrophobic association hydrogel

Hydrophobic association hydrogels were fabricated via micellar copolymerization of acrylamide and hydrophobic monomers lauryl (meth)acrylate (LA or LMA) in an aqueous solution of sodium dodecyl sulfate. The effect of methyl groups of hydrophobic monomers on the crosslinking network structure and mechanical behavior of the gels was investigated on the basis of rubber elastic theory. It was found that the LMA-gel exhibited higher effective crosslink density and elastic modulus. The methyl groups of hydrophobic monomers limited the flexibility of the methacrylate backbone in the association domain, which resulted in the increment of chains constraints. With the increase of stretch rate, the dissipated energy of LMA-gel increased more highly than that of LA-gel. In addition, the methyl group hindered the movement of polymer chains, leading to the lower recovery efficiency of dissipated energy for LMA-gel. In contract, the LA-gel exhibited a rapid response to external force, and possessed better elasticity and self-recovery property. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56, 1505–1512     

Bimetallic Gold(I) Complexes with Ethynyl‐Helicene and Bis‐Phosphole Ligands: Understanding the Role of Aurophilic Interactions in their Chiroptical Properties

Monometallic gold(I)‐alkynyl‐helicene complexes ( 1 a , b ) and bimetallic gold(I)‐alkynyl‐helicene architectures featuring the presence ( 2 a , b ) or absence ( 3 a , b ) of aurophilic intramolecular interactions were prepared by using different types of phosphole ligands (mono‐phosphole L1 or bis‐phospholes L2 , 3 ). The influence of the Au^I d¹⁰ metal center(s) on the electronic, photophysical, and chiroptical properties of these unprecedented phosphole‐gold(I)‐alkynyl‐helicene complexes was examined. Experimental and theoretical results highlight the importance of ligand‐to‐ligand‐type charge transfers and the strong effect of the presence or absence of Au^I–Au^I interactions in 2 a , b .     

Experimental Study of Liquid Hydrocarbons Pyrolysis to Acetylene in H2/Ar Plasma

Liquid hydrocarbons including n-hexane, cyclohexane and toluene are pyrolyzed in H₂/Ar plasma to investigate the effects of feedstock properties and key operating conditions (e.g., the feedstock specific input power and residence time) on the reaction performance. The experiments verify that the non-aromatic hydrocarbons show better chemical reactivity than partially aromatic substances. Meanwhile, the straight-chain alkanes and cycloalkanes have better yields of ethylene during the pyrolysis. The results also demonstrate that the pyrolysis reactions are almost completed within the first 0.8?ms in Ar/H₂ plasma independent of the feed substances (i.e., liquid hydrocarbons), where the increased feedstock specific input power enhances the reactant conversions and correspondingly raises the yields of acetylene. At a feedstock specific input power of 4.7?×?10⁴?kJ/kg, the n-hexane conversion is over 90?% and the yield of acetylene reaches 70?%. In addition, when using n-hexane as the feedstock, very little coke is formed during the course of reaction. Comprehensive comparisons of the current experiments with the data reported in the literature are made to point out the key influencing factors, i.e., the effective mass ratio of C/H (R _C/H) in the gaseous phase and the quench temperature. Both two factors would need to be enhanced in order to get a better performance. Finally, the improvements on the specific energy requirement of this process are discussed.     

昆明长水国际机场鸟击防治管理信息平台系统架构

本文从昆明长水国际机场鸟击防治工作现状出发,提出人工管理、纸质台账存在的问题,由此引出构建鸟击防治管理信息平台的必要性。在需求及技术框架层面上,对系统功能进行了简洁明了的说明。     

Metal-free phthalocyanine single crystal: Solvothermal synthesis and near-infrared electroluminescence

A metal-free purple H₂Pc single crystal was synthesized by a facile solvothermal method, and its solubility and near-infrared (NIR) optical properties were also investigated due to its potential applications as a light-emitting layer for OLEDs. The H₂Pc single crystal is insoluble in 1-chlorine naphthalene and other organic solvents. It gives a wide absorption in the range from 620 nm to 679 nm and a wide emission in near 922 nm. As an active light-emitting layer, H₂Pc was employed to fabricate electroluminescent (EL) devices with a structure of ITO/NPB (30 nm)/Alq₃:H₂Pc (30 nm)/BCP (20 nm)/Alq₃ (20 nm)/Al. The emission center is at 936 nm when the H₂Pc doping concentration is 20 wt%. The doping concentration strongly governs the emission intensity. When doping concentration decreases from 10 wt% to 1 wt%, the emission intensity remarkably fades, and simultaneously the emission center undergoes a blue shift.     

Electrochemical Tri- and Difluoromethylation-Triggered Cyclization Accompanied by the Oxidative Cleavage of Indole Derivatives

Considering their unique roles in organic synthesis, and pharmaceutical and agrochemical applications, the development of fluoroalkylation, cyclization, and indole oxidative cleavage are important topics. Herein, an unprecedented electrochemical tri- and difluoromethylation/cyclization/indole oxidative cleavage process occurring in an undivided cell is presented. The protocol employs a readily prepared Langlois reagent as the fluoroalkyl source, affording a series of tri- or difluoromethylated 2-(2-acetylphenyl)isoquinoline-1,3-diones in good yields with excellent stereoselectivity. It is worth noting that this new methodology merges the fluoroalkylation/cyclization of N-substituted acrylamide alkenes with the oxidative cleavage of an indole C(2)=C(3) bond under external oxidant-free conditions.     

Rhodium-Catalyzed Dimerization of Diaryl Acetylenes in the Presence of Grignard Reagents: Synthesis of 1,2,3-Triphenyl Naphthalene Derivatives

An efficient Rh-catalyzed dimerization of diaryl acetylenes was achieved in the presence of Wilkinson catalyst, AgF₂, and 1.5 equivalent of PhMgBr in toluene, providing the 1,2,3-triaryl naphthalene derivatives in moderate to good yields.

Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file.     

DanHong Injection inhibits the development of primary abdominal aortic aneurysms in apoE knockout mice

Clinical observations indicate that DanHong Injection （DHI） can increase blood flow and reduce various syndromes in patients with cardiovascular disease. How- ever, it still needs to define the function of DHI and the involved mechanisms in details, such as the protective effect on the development of primary abdominal aortic aneurysms （AAAs）. In this study, we determined whether DHI is able to inhibit AAA in apoE knockout （apoE-/-） mice. Thirty apoE-/- male mice on high-fat diet （0.5 % cholesterol, 21% fat） were randomly divided into two groups and received i.p. injection of saline （100 μL/day） and DHI （100 μL/day）, respectively, for 16 weeks. At the end of experiment, we determined the development of atherosclerosis in en face aorta and aneurysms,pathological morphology of arterial wall, and serum lipid levels. We also determined the expression of monocyte chemoattractant protein-1 （MCP-1）, MMP-2, and MMP-9 mRNA in aortic wall using real-time RT-PCR. Our results indicated that high-fat diet induced the development of AAAs in apoE-/- mice, but the induction was totally blocked by DHI （P 〈 0.01）. The result of staining of abdominal aortic cross sections showed that DHI main- tained the collagen content in arterial wall, thereby pre- venting the animals from the development of AAA. Although DHI had little effect on serum total- and LDL- cholesterol levels, it reduced the expression of MCP-1, MMP-2, and MMP-9 mRNA in aortic wall （P 〈 0.01）. Taken together, our study suggests that DHI can inhibit the high-fat diet-induced AAA formation. The inhibitory effects may be related to the maintenance of the collagen content and inhibition of expression of AAA-related genes. Our study may suggest a new application of DHI in clinics.     

The effect of phosphate buffer solutions on uniconazole complexation with hydroxypropyl-β-cyclodextrin and methyl-β-cyclodextrin

The inclusion complexes of uniconazole [(E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-lyl)-1-penten-3-ol, UCZ] with two cyclodextrin derivatives, hydroxypropyl-β-cyclodextrin (HP-β-CD) and methylated-β-cyclodextrin (Me-β-CD), were prepared and characterized by ¹H NMR and FT-IR. The phase solubility of UCZ and HP-β-CD, UCZ and Me-β-CD, which displays the ability of CDs complexation and solubilization, was studied in aqueous solutions and phosphate buffer solutions (PBS) with different property pH values (6.2, 7.2, 8.0). The solubility results indicated that the pH of PBS showed more enhancement on the interaction of HP-β-CD and UCZ than Me-β-CD with the increasing pH value, and the optimal pH value for complexation of UCZ and HP-β-CD, UCZ and Me-β-CD was at 8.0 and at 7.2, respectively. These were also determined by UCZ release behavior and dissolution studies of the complexes in solid state.