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Synthesis and purification

9 Oligo- and Poly thiophene Field Effect Transistors Oligo- and poly thiophene field effect [Pg.472]

An additional way to obtain larger domains is by rapid thermal annealing of a polycrystalline film [53, 54]. With this procedure, grains with lateral dimensions of many fjm may be grown, as exemplified in Fig. 12. Unfortunately, these domains. [Pg.472]

The liquid-phase processability [34,55-57] and thin film ordering [55,57-60] of thiophene oligomers is greatly enhanced by appropriate substitution at the terminal a carbons. On the other hand, substitution at internal positions imparts considerable [Pg.473]

CN s of exceptionally high purity are required for optimum performance in applications but the synthetic products usually contain impurities such as amorphous carbon, carbon nanoparticles, and some metal catalyst. Different methods have been described for the purification of nanotubes [77] most involve oxidation by use of mineral acids and/or gas phase oxidation to remove catalytic metal particles [Pg.949]


Federica Bertoncin is gratefully acknowledged for the synthesis and purification of 2.4b-e and some equilibrium constant measurements with these compounds. [Pg.69]

J. C. T. Kwak at Dalhousie University, Halifax, Canada. We gratefully acknowledge the Dutch Organisation for Scientific Research (NWO) for a travel grant to S.O. Theo Rispens is most gratefully acknowledged for the synthesis and purification of 5.5a-c. [Pg.158]

Cost. It is necessary to produce the feedstock from which the monomer is generated, viz, the dimer, at a cost which can be supported by the commercial appHcation, and yet allow it to be economically competitive with all other alternative ways to achieve the same end result. This factor often, but not always, seriously limits the amount of effort that can be put iato dimer synthesis and purification. [Pg.429]

We next address selected Raman scattering data collected on nanotubes, both in our laboratory and elsewhere. The particular method of tubule synthesis may also produce other carbonceoiis matter that is both difficult to separate from the tubules and also exhibits potentially interfering spectral features. With this in mind, we first digress briefly to discuss synthesis and purification techniques used to prepare nanotube samples. [Pg.136]

Synthesis and Purification of Multi-Walled and Single-Walled Carbon Nanotubes... [Pg.2]

There have been a considerable efforts at synthesis and purification of MWCNT for the measurements of its physical properties. The time is, however, gradually maturing toward its industrial application. As to SWCNT, it could not be efficiently obtained at first and, furthermore, both of its purification and physical-properties measurement were difficult. In 1996, it became that SWCNT could be efficiently synthesized [14,16] and, since then, it has become widely studied mainly from the scientific viewpoints. In what follows, the synthesis and purification of MWCNT and SWCNT are to be summarised itemisingly. [Pg.2]

We have reviewed the electronic properties of CNTs probed by magnetic measurements. MW- and SWCNTs can individually be produced, however, the parameters of CNTs are uncontrollable, such as diameter, length, chirality and so on, at the present stage. Since the features of CNTs may depend on the synthesis and purification methods, some different experimental observation on CNT properties has been reported. It is important, however, that most of papers have clarified metallic CNTs are actually present in both MW- and SWCNTs. The characteristic of CESR of SWCNTs is different from that on non-annealed MWCNTs, but rather similar to that on annealed multi-walled ones. The relationship of the electronic properties between SW- and MWCNTs has not yet been fully understood. The accurate control in parameter of CNTs is necessary in order to discuss more details of CNTs in future. [Pg.86]

The synthesis and purification of cumyl alcohol (CumOH), p-dicumyl methyl ether (DCE)) and 2-chloro-2,4,4-trimethylpentane (TMPC1), and the sources and purification of methyl chloride (MeCl), methylcyclohexane (MCHx), isobutylene have been described [9, 10]. P-Pinene (P-PIN), (Aldrich), was chromatographed over alumina (activity I, Fisher), and freshly distilled over CaH2 under nitrogen according to 1H-NMR spectroscopy and GC analysis the purity was >99%. 2,6-Di-/er/-butylpyridine (DtBP), (Aldrich), anhydrous A,A-dimethylacetamid (DMA), (Aldrich), ethylaluminum dichloride (EtAlCl2), 1.0 M solution in hexanes (Aldrich), and methanol (Fisher) were used as received. [Pg.2]

A change of state is a physical change that does not alter chemical properties. It usually takes place by increasing or decreasing the temperature of a substance. The ability to change the state of substances is important in the synthesis and purification of chemicals. [Pg.9]

Flow-sheets of the plant are shown in Figs. 7.1-4 to 7.1-6. The plant consists of three units (I) DMFP synthesis and purification (Fig. 7.1-4), (2) synthesis of DMFAP (Fig. 7.1-5), and (3) separation and purification of DMFAP hydrochloride (Fig. 7.1-6). Steps (1) and (3) are performed in MPPs, while unit (2) is a dedicated plant, that would be difficult to adapt for other processes. [Pg.445]

At the point a compound is recognized and then considered for potential pharmaceutic or therapeutic usefulness, researchers will be both consumers of and contributors to the data-information-knowledge cycle that characterizes science. Initially, in the synthesis and purification phase of drug development, information about the compound s chemistry and physical properties may be both sought and created. Whether or not the compound has been of interest to other researchers may be determined by searching public records of grant and contract awards and also by searching resources that cover preliminary and early research results. The patent status of the compound may need to be established. [Pg.771]

Valko, K., Measurements of physical properties for drug design in industry, in Valko, K. (ed.), Separation Methods in Drug Synthesis and Purification, Elsevier, Amsterdam, 2001, Ch. 12. [Pg.267]

To facilitate parallel synthesis and purification of triazolyl derivatives of sugars, the products are tagged with an azulene chromophore. For this purpose, guajazulene, an inexpensive azulene, is converted to propargylic ester 1094 and reacted with mannose derivative 1095 to provide a mixture of regioisomers 1096 (44%) and 1097 (32%). Separation of the products can be easily achieved by chromatography because they are visible on the column (Scheme 181) <2006EJ01103>. [Pg.122]

This provides new options for synthesis and purification of sensitive oiganometallic complexes N. Spetse-ris, S. Hadida, D. P. Curran, T. Y. Meyer, "Organic/fluor-ous phase extraction A new tool for the isolation of organometallic complexes , OrganometaL 1998,171458. [Pg.37]

HL Ball, P Mascagni. Chemical synthesis and purification of proteins a methodology. Int J Pept Prot Res 48, 31, 1996. [Pg.258]

Stevenson S, Stephen RR, Amos TM, Cadorette VR, Reid JE, Phillips JP (2005) Synthesis and purification of a metallic nitride fullerene bisadduct exploring the reactivity of Gd(NZ ,C80. J. Am. Chem. Soc. 127 12776-12777. [Pg.179]

Explain selected reaction synthesis and purification steps for small molecule drugs. [Pg.356]

M. Lammerhofer, and W. Lindner, in K. Valko (ed.), SeparationMethods in Drug Synthesis and Purification (Book Series Handbook of Analytical Separations—Volume 1), Elsevier, Amsterdam, Netherlands, 2000, pp. 337. [Pg.107]

Stehle, P., and Rtirst, P. (1985). Isotachophoretic control of peptide-synthesis and purification - a novel-approach using ultraviolet detection at 206 nm.. Chromatogr. 346, 271—279. [Pg.304]

Stehle, P, Riirst, P, Ratz, R., and Rau, H. (1988). Isotachophoresis of quaternary 4,4 -bipyridyIium salts-analytical control of synthesis and purification procedures.. Chromatogr. 449, 299—305. [Pg.304]

In order to guarantee an efficient performance of the CNT-based electrochemical devices, attention has to be paid not only to CNT synthesis and purification but also to the way that the CNT electrode is built up. There have been many studies in the literature dealing with CNT dispersions either on conducting substrates or forming composites. In this subsection we will address the different carbon-nanotube deposition techniques and carbon-nanotube arrangements on different electrode surfaces. [Pg.135]


See other pages where Synthesis and purification is mentioned: [Pg.137]    [Pg.96]    [Pg.275]    [Pg.7]    [Pg.375]    [Pg.34]    [Pg.40]    [Pg.749]    [Pg.124]    [Pg.222]    [Pg.313]    [Pg.286]    [Pg.37]    [Pg.12]    [Pg.419]    [Pg.134]    [Pg.1246]    [Pg.78]    [Pg.578]    [Pg.91]    [Pg.233]    [Pg.271]    [Pg.16]   
See also in sourсe #XX -- [ Pg.337 , Pg.338 , Pg.339 , Pg.340 , Pg.341 , Pg.342 ]




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Experiment 22 Synthesis, Purification and Analysis of an Organic Compound

Purification and the Chemical Yield of Synthesis

Synthesis and Purification of Arc-Grown SWCNTs

Synthesis and Purification of Carbon Nanotubes

Synthesis and Purification of Lactides

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