基于层层自组装碳纳米管的应变检测仪

通过对微小应变检测意义的分析,提出了本检测仪在实际应用方面的价值和前景。基于对碳纳米管导电机理的分析、制备薄膜电阻,利用其电阻随形变变化较为灵敏的特性,将电阻的变化转换为电压值的变化,经过数据采集、放大和数字处理设计了应变传感器。     

Supramolecular Polymer Based on Poly (Ethylene-co-Vinyl Alcohol)-g-Ureidopyrimidinone: Self-Assembly and Thermo-Reversibility

The synthesis of a poly (ethylene-co-vinyl alcohol) (EVOH)-based supramolecular polymer by graft functionalization of EVOH with ureidopyrimidinone groups (UPy) has been studied. The resulting polymer, designated as EVOH-U, has been studied from a thermo-reversibility point of view. Generally, UPy, itself, can be self-assembled through fourfold hydrogen bonding, but in dimethyl sulfoxide solvent, it favors a tautomeric form that is incapable of self-assembly. Thermal treatment was applied as a means of manipulating the tautomerism. With applying consecutive heating and annealing procedures, the disruption and reversible regeneration of UPy hydrogen bonds were investigated by differential scanning calorimetry. The results showed about 91% and 86% of the hydrogen bonds regenerated after first and second adequate thermal treatments. Dynamic mechanical-thermal analysis (DMTA) confirmed the thermo-reversibility of EVOH-U as well. Moreover, DMTA showed that, after disruption and regeneration of hydrogen bonds, the EVOH-U specimen retained its structural integrity.     

A Voltage-Responsive Synthetic Cl−-Channel Regulated by pH

Transmembrane protein channels are an important inspiration for the design of artificial ion channels. Their dipolar structure helps overcome the high energy barrier to selectively translocate water and ions sharing one pathway, across the cell membrane. Herein, we report that the amino-imidazole (Imu) amphiphiles self-assemble via multiple H-bonding to form stable artificial Cl⁻-channels within lipid bilayers. The alignment of water/Cl⁻ wires influences the conduction of ions, envisioned to diffuse along the hydrophilic pathways; at acidic pH, Cl⁻/H⁺ symport conducts along a partly protonated channel, while at basic pH, higher Cl⁻/OH⁻ antiport translocate through a neutral channel configuration, which can be greatly activated by applying strong electric field. This voltage/pH regulated channel system represents an unexplored alternative for ion-pumping along artificial ion-channels, parallel to that of biology.     

Supramolecular Catalysis of the oxa-Pictet–Spengler Reaction with an Endohedrally Functionalized Self-Assembled Cage Complex

An endohedrally functionalized self-assembled Fe₄L₆ cage complex can catalyze oxa-Pictet—Spengler cyclizations of tryptophols and various aldehyde derivatives, showing strong rate accelerations and size-selectivity. Selective molecular recognition of substrates controls the reactivity, and the cage is capable of binding and activating multiple different species along the multistep reaction pathway. The combination of a functionalized active site, size-selective reactivity, and multistep activation, all from a single host molecule, illustrates the biomimetic nature of the catalysis.     

Effect of Butyl α-Hydroxymethyl Acrylate Monomer Structure on the Morphology Produced via Aqueous Emulsion Polymerization-induced Self-assembly

Polymerization-induced self-assembly(PISA) is an efficient and versatile method to afford polymeric nano-objects with polymorphic morphologies. Compared to dispersion PISA syntheses based on soluble monomers, the vast majority of emulsion PISA formulations using insoluble monomers leads to kinetically-trapped spheres. Herein, we present aqueous emulsion PISA formulations generating worms and vesicles besides spheres. Two monomers with different butyl groups, n-butyl(n BHMA) and tert-butyl(t BHMA) α-hydroxymethyl acrylate, and thus possessing different water solubilities were synthesized via Baylis-Hillman reaction. Photoinitiated aqueous emulsion polymerizations of n BHMA and t BHMA employing poly(ethylene glycol) macromolecular chain transfer agents(macro-CTAs, PEG45-CTA, and PEG113-CTA) at 40 °C were systematically investigated to evaluate the effect of monomer structure and solubility on the morphology of the generated block copolymer nano-objects. Higher order morphologies including worms and vesicles were readily accessed for t BHMA, which has a higher water solubility than that of n BHMA. This study proves that plasticization of the core-forming block by water plays a key role in enhancing chain mobility required for morphological transition in emulsion PISA.