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1.
Water solubilization of carbon nanoparticles (nanocarbons), single-walled nanotubes (SWCNTs), nano-onions (NOs) and nanodiamonds (NDs) has been achieved through their covalent functionalization by fluorination and subsequent derivatization with sucrose. The covalent bonding of sucrose to the surface of the fluorinated nanocarbons was attained by a one-step fluorine substitution reaction with sucrose-derived lithium monosucrate under sonication in DMF at room temperature. This chemical process provides a simple, inexpensive, and easily scalable method for hydrophilic chemical modification of SWCNT, NO, and ND surfaces to produce sucrose-functionalized nanocarbons that become soluble in water, DMF, ethanol, and other polar solvents. The sucrose-functionalized nanocarbon particles are expected to be biocompatible due to the abundance of hydroxyl groups available for hydrogen bonding and further chemical modification. Relevant examples have been given.  相似文献   

2.
We have investigated the exohedral functionalization of [60]fullerene, especially bisaddition; we have revealed the regioselectivity of bisaddition and the properties of obtained bisadducts. The bisaddition without any restriction generally shows low regioselectivity. The electronic and photophysical properties of bisadducts mainly depend on the addition patterns and are almost independent of the nature of addends. We have also attained the regioselective synthesis of bisadducts by controlling the distance and orientation between two reactive species with suitable covalent templates and their application into some functional materials. The synthesis of fullerene‐containing interlocked molecules, such as catenanes and rotaxanes, was accomplished by using a noncovalent interaction, mainly a donor‐acceptor interaction, in addition to the covalent functionalization. The bistable rotaxanes, which can serve as a molecular shuttle or switch, were also successfully prepared. DOI 10.1002/tcr.201000036  相似文献   

3.
Small multilayer fullerenes, also known as carbon nano-onions (CNOs; 5-6 nm in diameter, 6-8 shells), show higher reactivity than other larger carbon nanostructures. Here we report the first example of an in situ polymerization of aniline on phenyleneamine-terminated CNO surfaces. The green, protonated, conducting emeraldine polyaniline (PANI) was directly synthesized on the surface of the CNO. The functionalized and soluble CNO/PANI composites were characterized by TEM, SEM, DSC, Raman, and infrared spectroscopy. The electrochemical properties of the conducting CNO/PANI films were also investigated. In comparison with pristine CNOs, functionalized carbon nanostructures show dramatically improved solubility in protic solvents, thus enabling their easy processing for coatings, nanocomposites, and biomedical applications.  相似文献   

4.
Polyelectrolyte multilayer microcapsules were used as templates to prepare monodisperse poly(ethylene glycol) (PEG) hydrogel microspheres, which can react with amine-bearing molecules.  相似文献   

5.
碳笼化学(下)   总被引:2,自引:0,他引:2  
封继康 《有机化学》1993,13(1):25-34
本文介绍并评述了碳笼化学的最新进展, 指出这是一个前景十分诱人的现代化学新兴领域。  相似文献   

6.
Solvent-free functionalization of carbon nanotubes   总被引:12,自引:0,他引:12  
A fundamentally new single-walled and multiwalled carbon nanotube sidewall functionalization technique has been developed in which solvent is not required and the reaction times are greatly shortened (1 h at 60 degrees C). Exploiting the long linear dimension of the nanotube ropes by macroscopic mechanical deformation, reactive sites are generated merely by mechanically deforming the tubes using a stir bar. This approach eliminates the need for large volumes of solvent ( approximately 2 L/g), which were formerly considered essential due to the insolubility of carbon nanotubes. Using a series of 4-substituted anilines and a nitrite, the aryl diazonium intermediates were generated in situ and permitted to react with the tubes. Raman, IR, and UV spectroscopies, coupled with thermogravimetric analyses and solubility studies, support the assignments.  相似文献   

7.
The dependences of oxygen sorption on time, gas pressure (up to 760 torr), and sample temperature were determined experimentally for three adsorbents (fullerene, astralene, and activated carbon). The difference in their adsorption abilities was shown to be related to the special features of their structures, primarily to the differences in surface area and pore volume. This conclusion was substantiated by X-ray studies of the structure of the powders. The characteristic heats of adsorption, specific surface areas, pore volumes and sizes, and characteristic energies of adsorption, which are responsible for the sorption properties of the adsorbents studied, were determined.  相似文献   

8.
A. N. Nesmeyanov Institute of Heteroorganic Compounds, Russian Academy of Sciences, 117813 Moscow. Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 6, pp. 1457–1458, June, 1992.  相似文献   

9.
Multiwalled carbon nanotubes (MWNT) were functionalized with poly(L-lactic acid) (PLLA) with different molecular weights using a "grafting to" technique. The oxidized MWNT (MWNT-COOH) were converted to the acyl-chloride-functionalized MWNT (MWNT-COCl) by treating them with thionyl chloride (SOCl2) and reacting them with PLLA to prepare the MWNT-g-PLLA. FTIR and Raman spectroscopy revealed that the PLLA was covalently attached to the MWNT, and the weight gain due to the functionalization was determined by thermogravimetric analyses (TGA). The Raman signals of the MWNT were greatly weakened as a result of the PLLA grafting. The morphology of the grafted PLLA was examined by using SEM and TEM. The amount of grafted PLLA depended on the molecular weight of the PLLA. The PLLA coated on the MWNT became thicker and more uniform with increasing PLLA molecular weight from 1000 to 3000. However, the amount of grafted PLLA became lower when the molecular weight of PLLA was further increased to 11,000 and 15,000, and the PLLA attached to the MWNT showed a squid leglike morphology forming blobs and leaving much of the MWNT surface bare.  相似文献   

10.
Organic functionalization of carbon nanotubes   总被引:11,自引:0,他引:11  
A very general and versatile method for functionalizing different types of carbon nanotubes is described, using the 1,3-dipolar cycloaddition of azomethine ylides. Approximately one organic group per 100 carbon atoms of the nanotube is introduced, to yield remakably soluble bundles of nanotubes, as seen in transmission electron micrographs. The solubilization of the nanotubes generates a novel, interesting class of materials, which combines the properties of the nanotubes and the organic moiety, thus offering new opportunities for applications in materials science, including the preparation of nanocomposites.  相似文献   

11.
12.
The methods of preparing hydroxylated fullerenes in which hydroxyl groups are attached either directly to the fullerene framework or via various linkers are generalized and analyzed. The methods of synthesis of poly(urethanes) based on hydroxyfullerenes of both types are considered. The syntheses afford linear, network, and star-shaped polymers containing a covalently bonded fullerene. The physical, physicochemical, and mechanical properties of fullerene-containing poly(urethanes) are described.  相似文献   

13.
The structural and thermal properties of small carbon clusters (C N , N = 13, 20, and 32) are investigated by constant energy Molecular Dynamics simulations over a wide range of temperatures, i.e., from T = 0K to above the melting point of graphitic carbon. The Tersoff interatomic potential [6] is used to mimic the covalent bond between the carbon atoms in the cluster. We find that small carbon clusters start to fragment or to evaporate atoms or C2 or C3 units before fully developing a liquidlike phase. As a consequence, some relevant isomers (such as rings, bowls, hollow cages) are thermally isolated from each other i.e., there are no thermally activated isomerization transitions between them. Possible implications of our results on the growth mechanism of fullerenes are discussed.  相似文献   

14.
The use of carbon nanostructures in different modalities is a topic of growing interest. This article provides a systematic comparison of surfactant-coated single-wall carbon nanotubes, multi-wall carbon nanotubes and C(60) fullerenes as pseudostationary phases (PSPs) in electrokinetic chromatography. The differences on the electrophoretic behaviour as a function of the pseudostationary phase for phenolic compounds, triazines and nitroimidazole derivatives have been explored. Phenolic compounds, triazines and nitroimidazole derivatives has been selected as model compounds of aromatic compounds, pi-exceeding heteroaromatic compounds and pi-deficient heteroaromatic compounds, respectively. Resolution was also evaluated on the basis of the differences in the electrophoretic behaviour and in this sense the best PSP for each group of compounds can be proposed.  相似文献   

15.
16.
We describe a new synthetic strategy to produce multifunctionalized carbon nanotubes using a combination of two different addition reactions, the 1,3-dipolar cycloaddition of azomethine ylides and the addition of diazonium salts, both via a simple and fast microwave-induced method. The presence of multifunctionality on the SWNTs has been confirmed using the most useful techniques for the characterization of carbon nanotubes. The doubly functionalized SWNTs can be considered potentially useful for many interesting applications.  相似文献   

17.
Carbon nanotubes (CNTs) are very promising as carriers for the delivery of bioactive molecules. The multifunctionalization of CNTs is necessary to impart multimodalities for the development of future CNT-based multipotent therapeutic constructs. In this context, we report the first example of covalent trifunctionalization of different types of CNTs. Our strategy is a simple and efficient methodology based on the simultaneous functionalization of the nanotube surface with three different active groups. The reaction is performed in one step by arylation with diazonium salts generated in situ. The CNTs are functionalized with benzylamine moieties blocked with three different protecting groups that can be selectively removed under specific conditions. The trifunctionalized CNTs were characterized by TEM, thermogravimetric analysis, and Raman and UV/Vis/NIR spectroscopy, while the amine loading was determined by using the Kaiser test. The sequential removal of the protecting groups of the amine functions allows the grafting of the molecules of interest on the nanotube surface to be controlled.  相似文献   

18.
It was reported that carbon nanotube (CNT) was functionalized with the electroactive Nile blue (NB), which is a phenoxazine dye, by a method of adsorption to form a NB-CNT nanocomposite. The NB-CNT nanocomposite was characterized by several spectroscopic techniques, for example, Ultraviolet-visible spectroscopy (UV-VIS), Fourier transform infrared (FTIR), Raman spectroscopy and scanning electron microscopy (SEM) etc., and the results showed that NB could rapidly and effectively be adsorbed on the surface of CNT with a high stability without changing the native structure of NB and the structure properties of CNT. Moreover, it was shown that the dispersion ability of CNT in aqueous solution had a significantly improvement after CNT functionalized with NB even at a level of high concentration, for example, 5 mg of NB-CNT per 1 mL of H2O. The NB-CNT/ glasssy carbon (GC) electrode was fabricated by modifying NB-CNT nanocomposite on the GC electrode surface and its electrochemical properties were investigated by cyclic voltammetry. The cyclic voltammetric results indicate that CNT can improve the electrochemical behavior of NB and greatly enhance its redox peak currents. While the NB-CNT/GC electrode exhibited a pair of well-defined and nearly symmetrical redox peaks with the formal potential of (−0.422±0.002) V (versus SCE, 0.1 mol/L PBS, pH 7.0), which was almost independent on the scan rates, for electrochemical reaction of NB monomer; and the redox peak potential of NB polymer located at about −0.191 V. The experimental results also demonstrated that NB and CNT could synergistically catalyze the electrochemically oxidation of NADH (β-nicotinamide adenine dinucleotide, reduced form) and NB-CNT exhibited a high performance with lowing the overpotential of more than 560 mV. The NB-CNT/GC electrode could effectively sense the concentration of NADH, which was produced during the process of oxidation of substrate (e.g. ethanol) catalyzed by dehydrogenase (e.g. alcohol dehydrogenase). The presented method for functionalization of CNT had several advantages, such as rapid and facile CNT functionalization, easy electrode fabrication and high electrocatalytic activity, etc., and could be used for fabrication electrochemical biosensor on the basis of dehydrogenase. __________ Translated from Acta Chimica Sinica, 2007, 65(1): 1–9 [译自: 化学学报]  相似文献   

19.
20.
We report, for the first time, the organic functionalization of carbon onions. The functionalization was achieved via 1,3-dipolar cycloaddition of azomethine ylides to a mixture of amorphous carbon and concentric fullerenes. Once functionalized, the onions become soluble in organic solvents and it is possible to purify them from the rest of carbon. Their nonlinear optical properties have been studied in solution for application as broadband optical limiters. It was found that the functionalized onions are an example of soluble material that functions equally well in both the visible and the NIR regions.  相似文献   

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