金属基仿生超滑表面制造及其应用

金属是人类社会赖以生存和发展的重要物质基础,是构成现代文明社会的支撑材料,增加金属材料的特殊性能,拓宽金属材料的应用范围,已经成为自然科学交叉研究的热点。受自然界启发,研究人员通过探究猪笼草口缘区的超滑行为,在微/纳米结构基底中注入低表面能润滑液,形成固液复合涂层,设计并制备出具有特殊润湿性的仿生超滑表面,显现出优异的自愈、防冰、防污、耐腐蚀、抗生物黏附、自清洁等性能。该方法为金属基体上设计构建仿生超滑表面,并实现其表面多功能性,进而为其在海洋防污、生物医疗、航空航天、制冷、工业生产等领域实现更广泛的应用提供了可能。本文从仿生超滑表面的设计原理、制备工艺、金属基体仿生超滑表面的应用以及未来发展趋势和挑战四个方面对金属基体仿生超滑表面的研究进展进行了综述。     

Janus粒子的制备及功能化应用

Janus粒子是指表面具有两种或两种以上不同化学组成或性质的不对称粒子,目前Janus粒子的制备方法仍在发展中,同时也逐渐形成了Janus粒子在生物医药、催化、材料以及防污等领域功能化应用的研究重点。本文从Janus粒子制备和应用两个方面方法来介绍Janus粒子的研究进展。制备方法主要包括表面选择性修饰法、晶种生长法、微流控法、嵌段共聚物自组装法和电化学沉积法等。应用方面则着重介绍了Janus粒子在生物医药、界面催化、表面活性剂、复合材料、微米马达和防污等方面的功能化应用,并对Janus粒子未来的发展趋势做了展望。     

防冰高分子材料

防冰高分子材料作为一种新型功能高分子材料,在电力、通讯及运输等领域有广泛应用.表面的覆冰现象往往开始于冰的成核,发展于冰的传递,危害于冰的积聚.针对材料表面冰晶形成的环节,揭示冰晶形成的分子机制是设计和开发防冰高分子材料的关键.本文简要介绍了本课题组在防冰高分子材料领域的研究进展,包括设计搭建的基本研究设备,以及具有调控冰成核、控制冰传递、降低冰黏附等不同功能的防冰高分子材料.     

多功能超润湿材料的设计制备与应用

仿生超润湿材料是指类似自然界中生命体具有的特殊浸润界面性质的一类材料。近20年来,研究人员通过模仿自然,揭示了一系列超润湿界面材料的构建机理,设计制备了多种仿生超润湿材料,并将这些具有特殊表面浸润性能的材料拓展应用到了国防、军工、航空航天、建筑、农业、医疗、海洋防污等众多领域。本文首先介绍表面润湿现象的基础理论,接着从仿生的角度出发,介绍了以仿荷叶、鱼鳞、沙漠甲虫、猪笼草为代表的几种拥有不同表面浸润性能的材料,并总结了这几种材料的仿生设计原理、结构与性能的关系以及所面临的问题。综述了近年来仿生超润湿材料在防污抗菌、防雾防霜防覆冰、油水分离等方面的应用进展,最后展望了仿生超润湿材料的发展方向。     

防冰材料研究进展及其在风电领域的应用展望

新型防冰材料在风力发电领域具有非常广泛的应用前景。风机叶片表面的覆冰现象通常与冰的成核和冰生长两个因素息息相关。本文总结了本课题组在防冰材料方面的研究进展，包括抑制冰成核、防止冰生长、降低冰粘附力以及在低温与高湿等极端环境下具有光热除冰性能的防冰涂层。防冰材料技术的进步势必极大促进风电行业的发展，对我国的经济转型和能源结构调整具有重要意义。     

SLIPS功能表面的制备及应用

仿猪笼草唇叶结构的滑移功能表面(SLIPS)是通过将全氟液体、硅油或离子液体等润滑油注入到提前构建好的含有多孔或分级粗糙结构基底制备得到.由于毛细作用力和范德华力,动态油膜能够稳定锁定在粗糙基底中.所得到SLIPS的化学均相表面和特殊的液-固结合界使其展现出优异的液体排斥性、自修复性和高压稳定性等,并在近十年内成为表界...     

防覆冰涂层构建机理及制备

航空、通信、电力和运输设备的覆冰现象给人们的生产、生活带来许多不便,甚至引起重大经济损失,防覆冰涂层主要通过材料表面特殊物理化学性能与微相形貌来实现抗冰目的,这类材料需要兼具防结冰性和疏冰性,从延长结冰时间和降低冰的附着力两方面来减轻甚至消除冰雪积聚,是目前研究的热点。本文从防覆冰机理入手,深入探讨了防结冰性和疏冰性的影响因素,阐述了防覆冰涂层材料的设计与制备方面的最新进展,并对防覆冰涂层目前存在的问题与发展方向进行了分析和展望。     

超疏水涂层防覆冰机理及制备

结构物表面严重覆冰有时会威胁人们的生命财产安全,影响经济社会的平稳运行。超疏水涂层具有超大接触角、低滚动角的特性,在防覆冰领域有很好的应用前景。本文重点总结了超疏水涂层防覆冰机理的相关研究结果,并简单综述了聚合物-微粒复合材料类、特殊表面结构类两种典型超疏水型防覆冰涂层的研究进展,指出了目前在超疏水型防覆冰涂层研究中存在的不足,并对其发展趋势进行了展望。     

超疏水性表面的制备及应用进展

近年来,受荷叶、水黾腿、壁虎脚等天然超疏水生物表面特性的启发,研究者们进行了大量仿生超疏水表面材料的制备及应用研究。超疏水性表面因其特殊的微纳分层结构,具有自清洁、防覆冰、防腐蚀、减阻等优异性能。本文阐述了表面润湿、疏水的基本机理,以及超疏水表面研究的理论基础,对超疏水表面制备的最新研究进展进行了综述,并揭示了研究中存在的问题。最后,介绍了超疏水表面在涂料、织物、防腐、抗菌及防雾等领域中的应用,展望了其未来的研究方向和前景。     

超疏水表面的制备方法

超疏水表面材料具有防水、防污、可减少流体的粘滞等优良特性,是目前功能材料研究的热点之一.其中超疏水表面的制备方法是研究的关键点.介绍和评述超疏水表面的制备方法,对该领域的发展方向进行了展望.     

二氧化碳和丙烯直接合成甲基丙烯酸的NiPMo/TiO2催化剂的研究

用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%.     

Synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives

Different approaches for the synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives from simple amino acids have been investigated. A library of 33 precursors for the preparation of N-hydroxy pyrazinones was obtained in moderate to good yields.     

α-Amino acid derived enaminones and their application in the synthesis of N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates and other heterocycles

A new and simple synthesis of novel N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates are enaminones, which can also be isolated, characterized, and used for the construction of other functionalized heterocycles, before they spontaneously decompose to pyrrole products. 4-Hydroxypyrroles are prone to partial aerial oxidation but can be efficiently alkylated or reduced to stable polysubstituted pyrrolidine derivatives.     

Specific intramolecular aromatic CH insertion of diazosulfonamides

The chemoselectivity in the intramolecular CH insertion of various diazosulfonamides has been experimentally studied. The results reveal that the aliphatic 1,4-, 1,5-, or 1,6-C(sp³)?H insertions of diazosulfonamides are not accessible, while the aromatic 1,5-C(sp²)?H insertion can be realized specifically by adjusting the diazo-adjacent group. In addition, the general chemoselectivities in the intramolecular CH insertions of diazosulfonyl compounds are summarized. Generally, diazosulfones undergo both aromatic 1,5-C(sp²)?H and aliphatic 1,5- and 1,6-C(sp³)?H insertions, while diazosulfonates undergo aliphatic 1,5- and 1,6-C(sp³)?H insertions. However, diazosulfonamides only undergo aromatic 1,5-C(sp²)?H insertion.     

A general and convenient synthesis of 4-(tosylmethyl)semicarbazones and their use in amidoalkylation of hydrogen,heteroatom, and carbon nucleophiles

A general synthesis of previously unknown semicarbazone-based α-amidoalkylating reagents, 4-(tosylmethyl)semicarbazones, has been developed. The synthesis involved three-component condensation of semicarbazones of aliphatic or aromatic aldehydes with the same or other aldehydes and p-toluenesulfinic acid. The scope and limitations of this reaction were investigated. The compounds obtained were demonstrated to be an efficient α-(4-semicarbazono)alkylating agents. They were reacted with H- (sodium borohydride), O- (sodium methylate), S- (sodium phenylthiolate), N- (pyrrolidine, sodium succinimide), P- (trialkyl phosphites), and C-nucleophiles (sodium diethyl malonate) to give the corresponding products of the tosyl group substitution, 4-substituted semicarbazones, including analogues of nitrofurazone. Among the prepared compounds tested in vitro for antibacterial and antifungal activity, three nitrofuryl-containing semicarbazones exhibited high biological activities with minimum inhibitory concentration (MIC) values of 8–32 μg/mL.     

Synthesis of novel chiral bidentate hydroxyalkyl-N-heterocyclic carbene ligands and their application in palladium-catalyzed Mizoroki–Heck couplings and asymmetric addition of diethylzinc to benzaldehyde

A small library of new chiral bidentate hydroxyalkyl-imidazolium salts 1 is conveniently synthesized on multi-gram scale from inexpensive and commercially available chiral pool amino acids. The corresponding carbenes, generated by deprotonation of imidazolium salts 1, in combination with palladium(II) chloride were tested in the Mizoroki–Heck coupling reaction. The most significant results in terms of yields and reactivities were achieved with low catalyst loading. The catalytic activities of these imidazolium salts were also investigated in the asymmetric addition of diethylzinc to benzaldehyde. The use of MgO nanoparticles as an additive in conjunction with these ligands played a crucial role in increasing the efficiency of these reactions.     

Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction

In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments.     

N-Heterocyclic carbene-palladacyclic complexes: synthesis,characterization and their applications in the C-N coupling and α-arylation of ketones using aryl chlorides

N-Heterocyclic carbene-palladacyclic complexes 3 were successfully achieved in a one-pot procedure under mild conditions. The structure of 3a was unambiguously confirmed by X-ray single crystal diffraction and it was an active catalyst in the Buchwald-Hartwig amination and α-arylation of ketones even at very low catalyst loadings (0.01?mol%).     

Iodine-mediated oxidative Pictet-Spengler reaction using terminal alkyne as the 2-oxoaldehyde surrogate for the synthesis of 1-aroyl-β-carbolines and fused-nitrogen heterocycles

An efficient iodine-mediated oxidative Pictet-Spengler reaction in dimethyl sulphoxide (DMSO) using terminal alkynes as the 2-oxoaldehyde surrogate for the synthesis of aryl (9H-pyrido[3,4-b]indol-1-yl)methanones is described. The scope of the protocol includes the total synthesis of Fascaplysin, Eudistomins Y₁ and Y₂. The methodology is extended for preparing pyrrolo[1,2-a]-quinoxaline and indolo[1,5-a]quinoxaline derivatives. The utility of 1-aroyl-β-carbolines was demonstrated by performing palladium-catalyzed β-carboline directed ortho-C(sp2)-H functionalization of the phenyl ring with thiomethyl (SMe) group using DMSO as source and for accessing 4-aryl-canthin-6-ones.     

Facile synthesis of bicyclic 1-arylpyrazol-5-ones

In this Letter, we described a facile method for constructing fused bicyclic 1-arylpyrazol-5-one ring system. We employed various methylene-containing carboxylic acids as the substrates and proved that the pyrazolone ring closure requires activated methylene group in intermediate II. Accordingly, a series of structurally diversified, fused bicyclic 1-arylpyrazol-5-ones was prepared in moderate to high yields using the requisite substrates.