Preparation of crosslinked epoxy microparticles via phase inversion

Differential scanning calorimetry (DSC) and scanning electron microscopy (SEM) studies have been performed to reveal a crosslinked epoxy nature of the spherical particles formed in cured epoxy/DDS/PMMA blends. An interesting phase inversion phenomenon was observed in cured DGEBA/DDS/PMMA blends, which occurred at a relatively low thermoplastic composition of 20 phr PMMA in blends. A unique method of preparing crosslinked epoxy spheres of controlled sizes based on cure-induced phase inversion is described in this report. Several factors have been found to affect the geometry of the formed epoxy spheres. The volume fraction of PMMA in the blends strongly dominates the influence. With the increase of PMMA volume fraction in the blends, the spheres not only become smaller in sizes, but also more regular in the spherical geometry due to less impingement. The crosslinking density (DDS phr in the blends) has been found to influence the average sizes of the spheres. The cure temperature has relatively limited effects only when the PMMA loadings in the blends are relatively small. Various potential applications for the epoxy microspheres may be investigated in future studies. © 1996 John Wiley & Sons, Inc.     

两个包含醚氧桥联三羧酸配体的锌(Ⅱ)配位聚合物的合成、晶体结构及荧光性质

选用2种醚氧桥联三羧酸配体(H_3cpta和H_3dbba)和4,4′-联吡啶(4,4′-bipy)或菲咯啉(phen)与ZnCl_2进行水热合成反应,构筑了2个一维链状配位聚合物[Zn(μ-Hcpta)(4,4′-bipy)(H_2O)]_n(1)和{[Zn_3(μ_3-dbba)_2(phen)_3]·6H_2O}_n(2),并对其结构和荧光性质进行了研究。结构分析结果表明2个配合物分别属于单斜晶系,P2_1和I2空间群。配合物1和2具有两种不同的一维链结构。     

强激光等离子体中光子的运动

通过严格求解广义协变的光子运动的测地线方程,讨论了准静态时一线等温膨胀的自洽激光等离子体中光子的运动.用数值方法得到了光子速度的空间分布曲线. 关键词：     

High-light induced superoxide radical formation in cytochrome b₆f complex from Bryopsis corticulans as detected by EPR spectroscopy

The generation of superoxide radical (O?·?) in Cyt b?f of Bryopsis corticulans under high light illumination was studied using electron paramagnetic resonance (EPR) spectroscopy. This could be evidenced by the addition of SOD which specifically reacted with O?·?. The generation of O?·? was lost in the absence of oxygen and was found to be suppressed in the presence of NaN? and be scavenged by extraneous antioxidants such as ascorbate, β-carotene and glutathione which could also scavenged 1O?*. These results indicated that O?·? which produced under high light illumination in Cyt b?f of B. corticulans might rise from a reaction which 1O?* could participated in. Also the photo-protection mechanism to Cyt b?f complex by antioxidants which might contain in thylakoid was speculated.     

嵌入式三色光变器

为了提升现有导模共振防伪光变器件的性能,设计了一种基于ZnS覆盖膜的一维单周期矩形结构三色光变器.当自然光入射角为45°时,可在0°,58°,90°方位角分别获得相应的蓝、绿、红三色反射峰,对研究结果进行了物理解释.分析并提出了该器件周期、槽深、膜厚以及入射角变化对反射峰的影响规律,对器件的设计、制作和测试有重要指导作用.三色光变器基于简单结构实现方位角调节的自然光三色光变效果,可运用传统激光全息产业的模压和蒸镀工艺进行制作,在光变图像防伪领域有重要应用.     

A Conformational Restriction Strategy for the Control of CRISPR/Cas Gene Editing with Photoactivatable Guide RNAs**

The CRISPR/Cas system is one of the most powerful tools for gene editing. However, approaches for precise control of genome editing and regulatory events are still desirable. Here, we report the spatiotemporal and efficient control of CRISPR/Cas9- and Cas12a-mediated editing with conformationally restricted guide RNAs (gRNAs). This approach relied on only two or three pre-installed photo-labile substituents followed by an intramolecular cyclization, representing a robust synthetic method in comparison to the heavily modified linear gRNAs that often require extensive screening and time-consuming optimization. This tactic could direct the precise cleavage of the genes encoding green fluorescent protein (GFP) and the vascular endothelial growth factor A (VEGFA) protein within a predefined cutting region without notable editing leakage in live cells. We also achieved light-mediated myostatin (MSTN) gene editing in embryos, wherein a new bow-knot-type gRNA was constructed with excellent OFF/ON switch efficiency. Overall, our work provides a significant new strategy in CRISPR/Cas editing with modified circular gRNAs to precisely manipulate where and when genes are edited.     

Combination of electrochemistry and the concurrent reduction and substitution chemistry to provide a facile and versatile tool for preparing functional polyanilines

Polyaniline as the first commercially available conducting polymer has recently received great attention from both academic and industrial communities. Although there have been quite a few reports on substituted polyanilines, none of them are concerning about the amino- and alkylthio-substituted polyanilines. Unlike other substituted polyanilines, the attempts in synthesizing poly(alkylthioaniline) directly from the alkylthioaniline monomer via chemical and electrochemical oxidative-coupling chemistry were all fail. On the other hand,we have recently discovered that the amino and alkylthio functional groups can be easily introduced to the backbone of emeraldine polyaniline via the concurrent reduction and substitution chemistry. Further combination of electrochemistry and the concurrent reduction and substitution chemistry can provide us a facile and versatile tool for preparing functional polyanilines. Different functional groups can be introduced sequentially to the same polymer backbone. The concentrations of each substituents can be easily controlled. This new process provides us a useful utility for tailoring the molecular and the electronic structures of polyanilines to render them with appropriate and possibly new material properties suitable for many different potential applications.     

Dual-Atom Catalysts Derived from a Preorganized Covalent Organic Framework for Enhanced Electrochemical Oxygen Reduction

Dual-atom catalysts (DAC) are deemed as promising electrocatalysts due to the abundant active sites and adjustable electronic structure, but the fabrication of well-defined DAC is still full of challenges. Herein, bonded Fe dual-atom catalysts (Fe₂DAC) with Fe₂N₆C₈O₂ configuration were developed through one-step carbonization of a preorganized covalent organic framework with bimetallic Fe chelation sites (Fe₂COF). The transition from Fe₂COF to Fe₂DAC involved the dissociation of the nanoparticles and the capture of atoms by carbon defects. Benefitting from the optimized d-band center and enhanced adsorption of OOH* intermediates, Fe₂DAC exhibited outstanding oxygen reduction activity with a half-wave potential of 0.898 V vs. RHE. This work will guide more fabrication of dual-atom and even cluster catalysts from preorganized COF in the future.     

Gravitational Perturbation Induced by an Intense Laser Pulse

The energy-level shifts of the hydrogen spectrumin curved spacetime induced by intense short laserpulses are studied. With present high-power laser pulsesthe magnitude of the energy-level shifts of highly excited hydrogen atom should bedetectable.     

强激光等离子体中自由电子的经典行为

通过严格求解广义协变的电子运动方程,讨论了强激光等离子体中自由电子的经典行为.利用数值模拟,得到了自洽激光等离子体电磁场中自由电子运动的轨迹,并与平面波电磁场中自由电子的运动进行了比级. 关键词：