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  • 1
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 33 (1998), S. 4633-4641 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Soluble C60–N-vinylcarbazole copolymers with different C60 contents were synthesized in lithium naphthalene-initiated anionic polymerization reactions. 13C nuclear magnetic resonance (NMR) results provided strong evidence for the covalent attachment of poly(N-vinylcarbazole; PVK) units to the C60 cores. The chemical shifts located at 142.16, 143.21, 144.70, 145.61, 146.65, 147.09, 149.08 and 170.28 p.p.m. in the 13C NMR spectrum of the copolymer are assigned to the unsaturated carbon signals of the substituted C60 cage. Its ultraviolet–visible absorption spectrum tends to move to the longer wavelength compared with those of the N-vinylcarbazole (NVC) monomer and PVK, and the peak range also extended from about 350 to 640 nm due to “charge-transfer” interaction between C60 and N-ethylcarbazole units. X-ray diffraction evidence suggests that the structure of the resultant copolymer might be a layered structure. Like the C60 chemically modified PVK, this material also exhibits good photoconductivity and temperature sensitivity. An unusual temperature dependence of the ESR spectrum is observed. In addition, it is also found that both [60] fullerene polyanion salts [(Cn-60) M+n, M=Li, Na, K] and fullerene itself are unable to initiate the polymerization of such monomers as N-vinylcarbazole, styrene and acrylonitrile, etc. © 1998 Kluwer Academic Publishers
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  • 4
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract C60 chemically modified poly(N-vinyl-chloromethylcarbazole) was synthesized by the reaction of C60 with living poly(N-vinyl-chloromethylcarbazole) (PVCC) carbanions, which were prepared by α-position proton abstraction with NaH. The structural characterization techniques used were ultraviolet–visible, Fourier transform-infrared spectroscopy, X-ray diffraction, scanning electron microscopy, nuclear magnetic resonance and electron spin resonance, etc. All experimental results proved that C60 was covalently attached on the backbone chain of PVCC and consequently causes a remarkable enhancement of the photoconductivity of the parent polymer. Also, it was found that fullerenation of PVCC modified both the electronic structures of the carbazole pendant group and the interchain structure. © 1998 Chapman and Hall
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 3297-3302 
    ISSN: 0887-624X
    Keywords: C60 ; poly(p-bromostyrene) ; chemical modification ; fullerenes ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Addition of bulky C60 moiety, a powerful electron acceptor (EA = 2.6-2.8 eV), to the poly(p-bromostyrene)(PBS) by a novel organometallic reaction considerably changes the chemical and physical properties of this polymer. The product obtained is a “charm-bracelet” non-crosslinked brownish yellow polymer which is easily soluble in many common organic solvents, and has a single glass transition temperature [134.0°C vs. 83.2°C for poly(p-bromostyrene)], this being congruent with its chemical structure. Covalent attachment of C60 to the brominated polystyrene backbone is confirmed by a variety of techniques such as UV-VIS, FT-IR, TGA, DSC, SEM, ESR, GPC, and 13C-NMR. The results show that both the stereo-electronic effect and the steric hindrance of C60 have an important influence on the structure and physical properties of polymer. © 1996 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 573-577 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Lithium batteries are attractive for energy storage because of their high theoretical energy densities. A mechanism of an electrochemical intercalation reaction is suggested for the discharge of the first Li-fullerenated poly(N-vinylcarbazole) battery on the basis of experimental data obtained from cyclic voltammetry, FTIR, XRD, and ESR. The above battery has a higher open-circuit voltage (ca. 3.2 V), and its discharge may be ascribed to the electrochemical interacalation process of lithium in fullerenated poly(N-vinylcarbazole) for positive electrode materials. The effect of the discharge of the electric cell on the structure and paramagnetic property of fullerenated poly(N-vinylcarbazole) is discussed. © 1996 John Wiley Sons, Inc.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 2185-2190 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Addition of the C60 moiety, a powerful electron acceptor, to iodinated poly(N-vinylcarbazole) (PVKI) by chemical reaction modifies considerably the photoconductive property of PVKI. The photoinduced discharge rates for pure PVK, PVKI, C60-chemically modified PVKI (C60-PVKI copolymer), and C60-doped PVKI (a simple mixture of the component) under the same experimental conditions are found in the following order: C60-PVKI copolymer 〉 C60-doped PVKI 〉 PVKI 〉 PVK. The fullerenated PVKI has a visibly brownish yellow cast when compared with the unreacted polymer. The UV-vis absorption spectrum in which the main bands occur at 220, 230, 252, 268, 300, 332, and 346 nm extends the active range from about 300 to 860 nm. Also, its apparent temperature sensitivity is very intriguing, and an unusual temperature dependence for the ESR spectrum is observed. The photoconductive performance of the fullerenated polymer is closely related to its paramagnetism. A considerable difference of electronic structure between pure PVKI and the C60-PVKI copolymer is indicated. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 35 (1995), S. 705-710 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary A new route for the preparation of soluble fullerenated polymer through the reaction of carbanion intermediates of polymers with fullerenes, particularly C60, is demonstrated. Confirmation of the covalent attachment of C60 to the polystyrene backbone is by a variety of techniques such as UV-Vis, FT-IR, TGA, SEM and 13C NMR etc. The product, which has a visibly brownish yellow cast when compared with the unreacted polymer, is soluble in some common organic solvents. The thermal stability of pure polystyrene is enhanced by C60-chemical modification, and no bonds within the carbon sphere are broken.
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  • 9
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Addition of C60 moiety, a powerful electron acceptor to poly(N-vinylcarbazole) by chemical reaction results in the marked enhancement in photoconductivity relative to pure PVK and C60 /PVK mixtures (C60-doped PVK). The photoinduced discharge rates for pure PVK, C60-chemically modified PVK(C60-PVK copolymer) and C60-doped PVK under the same experimental conditions are found in the following order: C60-PVK copolymer〉C60-doped PVK〉pure PVK. The photoconductive performance in C60-PVK copolymer is closely related to fullerene level. The C60-PVK copolymer, which has a visibly earthy yellow cast when compared with the unreacted polymer, has a new structure in the UV-Vis absorption spectrum with the active range extending from about 280 to 870 nm. A qualitative comparison of the submicro-morphological structures for PVK, C60, C60-PVK and C60-doped PVK is given.
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  • 10
    ISSN: 0887-6266
    Keywords: fullerenes ; PVK ; UV-laser ablation ; aggregation and coalescence ; photoinduced electron transfer ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The phenomena of aggregation and coalescence of fullerenes in the UV-laser ablation time-of-flight mass spectrometric investigation of C60-modified poly(N-vinylcarbazole) both in the positive and in the negative ion channels have been observed. The results indicate that in C60 chemically modified PVK (C60-PVK) copolymer the nascent fullerene fragments ruptured from main chain can easily coalesce into large fullerenes through collisions, whereas in the C60-doped PVK the aggregation and coalescence of C60 were relative weak due to nonbounding action and incomplete charge transfer behavior between C60 and PVK. Furthermore, the photoinduced electron transfer behavior between C60 and carbazole units in the C60 chemically modified poly(N-vinylcarbazole) in benzonitrile by laser flash photolysis at 355 nm has also been investigated. Efficiency of the anion radical of C60 in copolymer at 1080 nm is higher than that of the C60-doped poly(N-vinylcarbazole) polymers. The formation of a C60 radical anion may be ascribed to photoinduced electron transfer between C60 pendanted on the main chain backbone and the inter-, and intrachain carbazole units in the copolymer. © 1997 John Wiley & Sons, Inc. 35: 1185-1190, 1997
    Additional Material: 6 Ill.
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