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纳米洋葱状富勒烯的研究进展及动向 总被引:2,自引:0,他引:2
评述了纳米洋葱状富勒烯的研究发展过程和动向,论述了该物质的各种制备方法及其工艺,并对各种制备工艺进行了分析和探讨性研究,在此基础上比较论述了每种方法的优缺点,展望了纳米洋葱状富勒烯基础研究,宏量制备和应用研究的发展趋向。 相似文献
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《化工新型材料》2016,(8)
富勒烯C60的缺电子多烯结构,容易与自由基发生加成反应,被称为"自由基的海绵",可保护细胞免受自由基伤害。它的笼形结构还可以用作药物载体,实现靶向释放,因此在生物和医学领域中应用受到广泛的关注。但是,富勒烯本身具有强烈的疏水性,难以在生物介质中直接使用,因此,制备水溶性富勒烯衍生物及提高富勒烯在生物体内的有效摄入量,成为目前研究热点。针对这些问题,设计并制备了水溶性富勒烯羟基氨基多官能度的衍生物,通过氨基的引入,增加了富勒烯在水中溶解度,提高细胞对富勒烯衍生物摄入量。用有机元素分析仪、红外光谱、光电子能谱、热失重等手段对其元素组成和结构进行了表征,其结构式为:C60O~10(OH)~16(NH2)~6(NO2)~6·24H_2O。用激光粒度仪测定其粒径分布和Zeta电势,粒径分布在170nm,Zeta电势为-3.54mV(pH=7.0水溶液)。并探究其对细胞的抗氧化应激的保护作用,结果表明所制备的水溶性富勒烯具有较强的清除超氧阴离子自由基的能力,可使细胞免于氧化应激伤害,提高细胞成活率,并具有浓度依赖性。与富勒醇对比,证明氨基引入确实提高了细胞对富勒烯衍生物的摄入量,为富勒烯在生物医药中应用提供了基础数据。 相似文献
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重油残渣基新型碳功能材料的研究进展 总被引:1,自引:0,他引:1
综述了以重油残渣为原料,采用化学气相沉积法、共炭化法和微波等离子体法可控制备气相生长碳纤维、碳微球、内包铁洋葱状富勒烯、纳米碳管、内包金属碳微米颗粒及定向碳纳米薄膜等各种高附加值碳材料;采用等离子体氧化法、酸处理法、化学还原法等方法对气相生长碳纤维和碳微球进行表面修饰,在产物表面引入含氧官能团,解决了可溶性碳材料的制备问题;在碳微球表面引入Pt纳米颗粒,使重油残渣基新型碳材料在表面修饰和功能化后可望成为性能优异的吸附和催化材料. 相似文献
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The experimental conditions necessary for the preparation of polymeric composite films (membranes) containing an ordered structure of single-wall carbon nanotubes and higher fullerenes are determined. The films are obtained by ordering a homogeneous suspension of carbon nanotubes and fullerenes in the initial liquid prepolymer or monomer, followed by curing of the matrix. The parameters of ordering (duration, field strength) are estimated, which make possible realization of the proposed process for the preparation of carbon-containing composite films based on polymer matrices of the polycyanurate type. 相似文献
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AbstractFullerenes are made by the intersection of twelve pentagonal nanocones. This note deals with an innovative isomeric mechanism, based on a sequence of Stone-Wales rotations, for moving the pentagonal face on the cusp of the nanocone. The modified nanocone is the seed for creating new fullerenes with different symmetry and size. Present results may help to model fullerene formation and, on the pure algorithmic side, may contribute to evolve the computer tools that generate fullerenes. This mechanism may also find application in mimicking the behaviors of biological systems that, like many viruses, are also describable in terms of spherical cages tiled by polygons. 相似文献
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Yong‐Tao Shen Ke Deng Qing‐Dao Zeng Chen Wang 《Small (Weinheim an der Bergstrasse, Germany)》2010,6(1):76-80
A new hierarchical self‐assembling molecular template, which can size‐selectively immobilize fullerene molecules, is reported. The molecular template is fabricated from 1,3,5‐tris(10‐carboxydecyloxy)benzene (TCDB) and triangle‐shaped macrocycles. It is observed that the two‐dimensional hydrogen‐bonded achiral TCDB network affected by the 3NN‐Macrocycle becomes a chiral network. Host and guest molecules both form chiral arrangements with hexagonal empty pores. In addition, fullerenes and other molecules such as coronene can be entrapped in the empty pores or on the 3NN‐Macrocycle molecules. The adsorption constant (K) is estimated, from which it is concluded that the different filling behaviors of the fullerenes are associated with the different sizes of the guest species. This method provides a facile approach to molecularly designed surfaces and the study of fullerene molecular arrays on the single‐molecule level. 相似文献
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Francesco Giacalone Nazario Martín 《Advanced materials (Deerfield Beach, Fla.)》2010,22(38):4220-4248
A new classification on the different types of fullerene‐containing polymers is presented according to their different properties and applications they exhibit in a variety of fields. Because of their interest and novelty, water‐soluble and biodegradable C60‐polymers are discussed first, followed by polyfullerene‐based membranes where unprecedented supramolecular structures are presented. Next are compounds that involve hybrid materials formed from fullerenes and other components such as silica, DNA, and carbon nanotubes (CNTs) where the most recent advances have been achieved. A most relevant topic is still that of C60‐based donor‐acceptor (D–A) polymers. Since their application in photovoltaics D–A polymers are among the most realistic applications of fullerenes in the so‐called molecular electronics. The most relevant aspects in these covalently connected fullerene/polymer hybrids as well as new concepts to improve energy conversion efficiencies are presented. The last topics disccused relate to supramolecular aspects that are in involved in C60‐polymer systems and in the self‐assembly of C60‐macromolecular structures, which open a new scenario for organizing, by means of non‐covalent interactions, new supramolecular structures at the nano‐ and micrometric scale, in which the combination of the hydrofobicity of fullerenes with the versatility of the noncovalent chemistry afford new and spectacular superstructures. 相似文献
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Tae Min Choi Gun Ho Lee Young‐Seok Kim Jin‐Gyu Park Hyerim Hwang Shin‐Hyun Kim 《Advanced materials (Deerfield Beach, Fla.)》2019,31(18)
Colloidal particles with a repulsive interparticle potential spontaneously form crystalline lattices, which are used as a motif for photonic materials. It is difficult to predict the crystal arrangement in spherical volume as lattices are incompatible with a spherical surface. Here, the optimum arrangement of charged colloids is experimentally investigated by encapsulating them in double‐emulsion drops. Under conditions of strong interparticle repulsion, the colloidal crystal rapidly grows from the surface toward the center of the microcapsule, forming an onion‐like arrangement. By contrast, for weak repulsion, crystallites slowly grow and fuse through rearrangement to form a single‐crystal phase. Single‐crystal structure is energetically favorable even for strong repulsion. Nevertheless, a high energy barrier to colloidal rearrangement kinetically arrests the onion‐like structure formed by heterogeneous nucleation. Unlike the isotropic onion‐shaped product, the anisotropic single‐crystal‐containing microcapsules selectively display—at certain orientations but not others—one of the distinct colors from the various crystal planes. 相似文献
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H. Zorc Lj. Pa a Toli S. Martinovi D. Srzi 《Fullerenes, Nanotubes and Carbon Nanostructures》1994,2(4):471-480
Synthesis of buckminsterfullerene (C60) is highly simple and the mechanism of the molecule formation is quite well understood. It makes easier the search for the optimum conditions necessary for formation of massive fullerenes (more than 100 carbon atoms). The most popular graphite arc method has been used for fullerene synthesis in our laboratories. Other available methods, like laser ablation and E-gun evaporation, were not suitable for achieving of the convenient conditions. Results of the synthesis have been analyzed by laser desorption Fourier transform ion cyclotron resonance mass spectrometry (LD FT/ICR-MS).
The conditions for massive fullerenes synthesis are discussed in the paper. The special care has been given to the LD FT/ICR-MS analysis. The importance of cooling gas during fullerene nucleation and growth in the very specific vacuum conditions is analyzed. The necessity for a thorough dynamic plasma diagnostic during the giant fullerenes growth is suggested. 相似文献
The conditions for massive fullerenes synthesis are discussed in the paper. The special care has been given to the LD FT/ICR-MS analysis. The importance of cooling gas during fullerene nucleation and growth in the very specific vacuum conditions is analyzed. The necessity for a thorough dynamic plasma diagnostic during the giant fullerenes growth is suggested. 相似文献
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Fullerenes which were thought to be ‘superaromatics’ are actually ‘superalkenes’. Reactions in fullerenes are varied, ranging
from the addition of simple molecules like H2 to large molecules like dendrimers. The synthesis, structure, characterization, along with simple reactions like halogenation,
oxygenation, metalation, cycloaddition, polymerization and dendrimer addition are discussed. 相似文献