非对称性Janus粒子的制备与可控组装

古罗马的双面神(Janus)常被用来描述具有两种不同化学结构或性质的不对称粒子, Janus粒子由于自身的特殊性能在药物载体、电子器件和乳液稳定等方面表现出良好的发展势头, 其应用前景日益受到人们的重视. 目前, Janus 粒子作为基本的组装基元受到越来越多的关注, 相关组装方法也被广泛地研究, 包括本体组装、界面组装和外界驱动力调控等, 特别是Janus 粒子的双亲修饰与功能化. 本文综述了现今Janus 粒子制备方法及对其进行修饰组装的最新研究进展, 详细讨论比较了一步合成法、聚合物自组装法和晶种直接生长等方法的特点及差异, 并对一些新型功能Janus粒子的设计及潜在的应用前景进行了展望.     

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。     

Janus粒子的表面改性及其对共混聚合物的增容性能研究

本文以雪人状的SiO_2@PDVB Janus粒子为模板,通过表面改性获得具有不同表面性质的Janus粒子,包括在SiO_2半球分别引入聚丁二烯(PBd)与聚异戊二烯(PI),以增加SiO_2@PDVB Janus粒子中无机的SiO_2半球对聚合物基质的亲和性.随后将改性前后的Janus粒子分散到聚苯乙烯(PS)/顺丁橡胶(PBd)及聚苯乙烯(PS)/异戊橡胶(PI)的共混体系中,考察了不同Janus粒子对共混物相结构的影响.结果发现,与未改性的Janus粒子相比,引入聚合物刷的Janus粒子可更有效地提高其界面增容效果,抑制共混物相分离的动力学.     

聚合物Janus微粒材料的制备与应用

聚合物Janus微粒是指具有各向异性微观结构的微/纳米聚合物粒子。因在乳液稳定、聚合物混合、可控组装、生物医药、多相催化和功能涂层等领域有重要的应用价值,聚合物Janus微粒材料的可控制备和应用研究已成为新型多功能和智能高分子材料研究的前沿领域。本文首先归纳了聚合物Janus微粒在制备方法、环境响应类型和应用领域的最新进展,进而分析了不同制备方法的优缺点。表面选择性修饰、微流体合成技术、自组装和种子聚合等方法都可用于制备具有可控尺寸、微观结构和表面性质的聚合物Janus微粒,但纳米级微粒微观结构的精确控制和大量合成还存在一定的挑战。环境响应性多组分聚合物Janus微粒在自组装和药物控释方面有其特殊的优势,而简单高效的种子聚合法有望应用于工业生产聚合物Janus固体表面活性剂。预计天然和多功能型聚合物Janus微粒的制备和应用研究将会是未来发展的趋势。     

两亲性Janus粒子在蜂窝状多孔聚合物膜上的自组装性能

采用具有两亲性的两面体(Janus)粒子实现稳定的粒子界面组装与水滴模板法自组装过程相结合的方法获得了粒子在蜂窝状多孔聚合物薄膜内壁的高效定向修饰.通过与均质粒子组装形貌的对比,证明了Janus粒子因其特殊的界面自组装活性,可以获得高粒子加量条件下的规则多孔结构,解决了使用均质粒子时存在的结构有序性和粒子修饰密度之间的矛盾.而在较低粒子加量的条件下,Janus粒子也展示出与均质粒子极为不同的组装形貌.这一方法的建立,为新型表面功能化材料的制备提供了一个新的思路.     

含Janus粒子组装体的构筑、调控及功能的模拟与理论分析

Janus粒子由于其表面性质与形状特征的不对称性而展现出独特的力学、光学、电学、磁学和表面两亲性能,在构筑复杂组装结构及设计新型功能材料方面有着广阔的应用前景.本文主要从计算机模拟与理论分析的角度,结合相关实验体系,系统地总结了目前对含Janus粒子组装体的体系构筑、结构调控及材料功能等的相关研究进展.从Janus粒子自组装结构的精确构筑与动态响应性、界面结构的熵驱调控、非平衡组装动力学及含Janus粒子组装体功能的模拟与预报等4个方面,详细阐述了Janus粒子的复杂多级组装结构及其背后蕴含的热力学与动力学的机理,并介绍了一系列基于含Janus粒子组装体的聚合物基复合材料独特的功能及其潜在应用.在此基础上,指出合理设计Janus粒子的非对称性质以及巧妙调控组装体内的熵、焓平衡,是控制其多级组装结构,进而开发相应新型功能材料的关键,并对Janus粒子未来的理论和模拟研究趋势进行了展望.     

Janus粒子制备研究*

具有不对称双面结构的Janus粒子以其独特性能,在乳液稳定、光学、生物传感、药物输送、电子学等领域具有潜在的应用前景。本文就近年来Janus粒子制备技术的研究进展进行了总结,详细地介绍了Janus粒子主要制备方法,包括微流体合成、拓扑选择表面改性、模板导向自组装、可控相分离及可控表面成核,并指出了各种Janus粒子制备技术存在的问题及其发展方向,认为基于可控相分离及表面成核的合成方法成本较低,产率较大,有可能得到更为广泛的应用。     

含二氧化硅组份Janus纳米粒子的制备方法和应用研究进展

Janus纳米粒子的非对称结构赋予其在空间结构和物理化学性质的各向异性,在半导体、催化、分散介质、生物医药等领域表现出优于普通纳米材料特性,是近年来纳米材料的研究热点.近些年来的研究报道多集中在含二氧化硅组份的Janus纳米粒子上,按其化学组成主要分为无机物-二氧化硅和聚合物-二氧化硅两大类.按此分类分析比较了Janus纳米粒子的制备方法,并介绍了其在药物输送、表面活性剂和催化等领域的应用现状.     

Janus 粒子在环境检测领域中的应用

Janus 粒子,也称为阴阳结构粒子或两面性非对称粒子,是指表面上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 粒子因其独特的结构和功能已经逐渐成为生物医药、催化、材料以及防污等领域中的新型功能材料。在环境检测领域,Janus材料亦因其特殊的光学、磁学及电学性能,为提高检测灵敏度、选择性和稳定性等提供了新的研究方向。基于此,本文主要讨论了Janus材料在环境检测方面的特点、优势和相关应用。最后,本文基于本课题组的研究经验以及工作中所面临的问题,对本领域的发展和未来的研究方向提出了展望,以期对本领域的未来发展提供指导。     

配体链包覆纳米粒子的表面相分离及自组装的模拟研究

通过耗散粒子动力学方法,模拟了二元配体链包覆的纳米粒子表面的相分离行为,并与现有的模拟和实验体系进行对比.研究结果印证了相分离驱动力是配体链错位所导致的构象熵的结论.进一步以相分离得到的Janus和三嵌段Janus结构纳米粒子作为构筑单元,研究了其在选择性溶剂中的自组装行为.结果表明,Janus粒子易自组装成为双层囊泡结构,而三嵌段Janus粒子则更易形成单层囊泡结构.对于从配体链包覆的纳米粒子出发,设计具有特殊功能的囊泡提供了理论支持.     

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%.     

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.     

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.     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula.     

KMnO4-mediated oxidative CN bond cleavage of tertiary amines: Synthesis of amides and sulfonamides

KMnO₄-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.     

Chemistry of heterocyclic compounds at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, over 50 years (Review)

The review contains a concise historical account and information on the most significant researches undertaken by the staff at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences on the Chemistry of Heterocyclic Compounds. Dedicated to Academician of the Russian Academy of Sciences B. A. Trofimov on his 70th jubilee. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1443–1502, October, 2008.     

Highly regioselective Buchwald–Hartwig amination at C-2 of 2,4-dichloropyridine enabling a novel approach to 2,4-bisanilinopyridine (BAPyd) libraries

The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines.     

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.