共查询到20条相似文献,搜索用时 14 毫秒
1.
Romanova I. P. Yusupova G. G. Fattakhov S. G. Nafikova A. A. Kovalenko V. I. Yanilkin V. V. Kataev V. E. Azancheev N. M. Reznik V. S. Sinyashin O. G. 《Russian Chemical Bulletin》2001,50(3):445-452
N-Isocyanurato-substituted aziridino[1,2][60]fullerenes were synthesized for the first time as the main products by the reaction of isocyanurato-substituted azides with C60. The thermal stability and the electrochemical behavior of the compounds synthesized were studied. 相似文献
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Shengqiang Xiao Yongjun Li Yuliang Li Huibiao Liu Junpeng Zhuang Fushen Lu Deqing Zhang 《Tetrahedron letters》2004,45(20):3975-3978
[60]Fulleropyrrolidines were used as secondary amines to react with aldehydes through reductive aminations to afford N-alkylated derivatives. In spite of the very weak base activity of the nitrogen atom of N-unsubstituted [60]fulleropyrrolidines, this method was found to be efficient at the aid of sodium triacetoxyborohydride. Several N-alkylated derivatives were synthesized and fully characterized. 相似文献
4.
Masaru Kawaguchi Atsushi Ikeda Seiji Shinkai Ion Neda 《Journal of inclusion phenomena and macrocyclic chemistry》2000,37(1-4):253-258
[60]Fullerene (C60)-calix[n]areneinteractions were studied in toluene:MeCN = 10:1 (v/v)using an electrochemical method. In the presence ofhomooxacalix[3]arenes and calix[5]arenes, bothEpc and pa shifted to the negativepotential, whereas they were scarcely affected by theaddition of calix[4]arenes. The2values electrochemically determined forthe association with C60
- are generallysmaller than the 1 valuesspectroscopically determined for the association withC60. The tendency indicates that thecharge-transfer-type interaction is one of thedriving forces for C60 inclusion.thanks|Author for correspondence 相似文献
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Romanova I. P. Yusupova G. G. Nafikova A. A. Kovalenko V. I. Sinyashin O. G. 《Russian Chemical Bulletin》2002,51(8):1491-1496
A single di(azahomo)[60]fullerene isomer was prepared for the first time by the reaction between [60]fullerene and isocyanurato-substituted azide. The structure of the product was established by 1H and 13C NMR, UV, and IR spectroscopy. 相似文献
6.
QianRongLI LiQunLI ShaYANG 《中国化学快报》2005,16(6):729-732
Photochemical [2 2] cycloaddition of C60 with podophyllotoxin derivative containing a cyclohexadienone group in o-dichlorobenzene afforded an isomeric mixture of adducts and a pure adduct of C60-fused podophyllotoxin derivatives. The structures of the products were characterized by MS, NMR and IR spectra. 相似文献
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Masaki Ozawa Jing Li Kentaro Nakahara Lixin Xiao Hiroharu Sugawara Koichi Kitazawa Kazushi Kinbara Kazuhiko Saigo 《Journal of polymer science. Part A, Polymer chemistry》1998,36(17):3139-3146
A novel series of polyamides having [60]fullerene moieties in the main chain were synthesized by a direct polycondensation of [60]fullerenobis(acetic acid) or [60]fullerenobis(acetic acid)/isophthalic acid mixture with a diamine in the presence of triphenyl phosphite and pyridine. Various properties of the polyamides were characterized by means of IR, GPC, TGA, DSC, UV–visible, and photoluminescence. The molecular weight Mw of the [60]fullerene-containing polyamides was observed in the range from about 300,000 to 3,000; upon the changing of the ratio of [60]fullerenobis(acetic acid)/isophthalic acid in the starting mixture, the resulting Mw decreased with increasing the ratio. Most of the thermal and optical properties gradually changed as the ratio changed; the major optical absorption band in visible range exhibited a significant tailing, which shifted toward a longer wavelength, while the photoluminescence spectrum red-shifted with increasing [60]fullerene content. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 3139–3146, 1998 相似文献
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Romanova I. P. Kalinin V. V. Nafikova A. A. Yakhvarov D. G. Zverev V. V. Kovalenko V. I. Rusinov G. L. Plekhanov P. V. Charushin V. N. Sinyashin O. G. 《Russian Chemical Bulletin》2003,52(1):173-178
The reaction of [60]fullerene with 2-azidopyrimidines affords fullerenoimidazopyrimidines, whose electron affinity is higher than that of nonmodified C60. 相似文献
9.
The homodinuclear bismetallacyclopropa[60]fullerene complexes (η2-C60)M(μ-η1,η1-trans-Ph2PCHCH PPh2)2M(η2-C60) (1, M = Pt; 2, M = Pd) were prepared by reaction of C60 with M(dba)2 (dba = dibenzylideneacetone) and trans-1,1′-bis(diphenylphosphino)ethylene in 82% and 92% yield, whereas reaction of C60 with Pd(dba)2 and trans-dppet followed by treatment with C60 and Pt2(dba)3 gave rise to the heterodinuclear complex (η2-C60) Pd(μ-η1,η1-trans-Ph2PCHCH PPh2)2Pt(η2-C60) (3) in 65% yield. Mechanistic study showed that these reactions involve the intermediates of monometallacyclopropa[60]fullerene diphosphine ligands (η2-C60)M(η1-trans-Ph2PCHCHPPh2)2 (4, M = Pt; 5, M = Pd). All the mono- and bismetallacyclopropa[60]fullerene complexes 1-5 have been fully characterized by elemental analysis and spectroscopy, as well as for 2 by X-ray crystallography. 相似文献
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Study of the factors determining the outcome of cycloaddition of isocyanurato-substituted azides to [60]fullerene 总被引:2,自引:0,他引:2
Sinyashin O. G. Romanova I. P. Yusupova G. G. Nafikova A. A. Kovalenko V. I. Azancheev N. M. Fattakhov S. G. Reznik V. S. 《Russian Chemical Bulletin》2001,50(11):2162-2171
The final outcome of cycloaddition of isocyanuratoalkyl azides to C60 depends on the temperature, the thermal stability of azides, the substituents in the isocyanurate ring, and the number of methylene groups in the alkyl radical. The thermal transformations of the monoadducts obtained were studied. 相似文献
11.
Romanova I. P. Yusupova G. G. Nafikova A. A. Yakhvarov D. G. Larionova O. A. Sinyashin O. G. 《Russian Chemical Bulletin》2004,53(1):144-147
A reaction of [60]fullerene with O,O-dibutyl azidophosphate affords a first representative of phosphorylated azahomo[60]fullerenes, which is easier to reduce electrochemically than the starting C60. 相似文献
12.
采用AM1的方法优化了翡翠绿[60]富勒烯C60[C(CH3)(CO2-t-Bu)2]6的结构.利用CI-ZINDO方法计算了基于晶体结构参数和优化结构的化合物及其衍生物的吸收光谱.计算结果与实验值吻合得很好. 相似文献
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I. P. Romanova O. G. Sinyashin G. G. Yusupova V. I. Kovalenko Yu. Ya. Efremov Yu. V. Badeev I. I. Vandyukova I. A. Arakelyan 《Russian Chemical Bulletin》1999,48(11):2144-2148
The reaction of [60]fullerene with diphenylphosphinoyl azide in toluene or ino-dichlorobenzene in the presence of traces of water affords 2-[N-(diphenylphosphoryl)amino]-1-hydroxy[60]fullerene This reaction in THF gives a mixture of (N-diphenylphosphoryl)[60]fullerenol[1,2-b]aziridine and a product of partial hydrolysis of the bisadduct of phosphorylated azide and fullerene.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2168–2172, November, 1999. 相似文献
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《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):1263-1273
Abstract A new synthetic approach for the fabrication of core‐shell like conducting elastomers was described. The approach utilized the facile intermolecular self‐assembly of poly(dimethylsiloxane) (PDMS) in DMSO leading to formation of a core particle, while soluble oligoaniline (A x ) segments dispersed in the solution phase resembling a shell overlayer for building the morphology. This morphology was demonstrated by bis[penta(tetraanilinofullereno)] bis(aminopropyl)poly(dimethylsiloxane) [PDMS‐(F5A4)2] triblock co‐oligomers synthesized using a functionalized C60 derivative as a linker. Observation of 1H NMR spectroscopic responses on the PDMS particle formation in DMSO‐d 6 is consistent with the proposed core‐shell geometry with oligoaniline moieties located at the shell overlayer. 相似文献
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The reaction between 2 equiv of [60]fullerene and 6,8,15,17-tetraphenylheptacene-7,16-quinone leads to both cis and trans-bis[60]fullerene adducts. This result contrasts sharply with the highly diastereoselective syn additions of [60]fullerenes across 6,13-diphenylpentacene and 6,8,15,17-tetraphenylheptacene. The importance of spatially dependent [60]fullerene-[60]fullerene π-stacking interactions in promoting a syn addition of [60]fullerenes is discussed. 相似文献
16.
单加成环丙烷富勒烯膦酸酯衍生物的合成与电化学性能 总被引:1,自引:0,他引:1
在Mn(OAc)3•2H2O催化下, C60分别和亚甲基二膦酸四乙酯、氰基亚甲基膦酸二乙酯或乙氧羰基亚甲基膦酸二乙酯在氯苯中回流, 生成3个单加成环丙烷富勒烯膦酸衍生物C60C(R)PO(OEt)2 [1, R=PO(OEt)2; 2, R=COOEt; 3, R=CN]. 与以前报道的Bingel反应法相比, 该方法副产物少并且缩短了反应时间. 采用循环伏安法发现1, 2的还原电位相对于C60发生负移, 而3的还原电位相对于C60却正移40 mV, 表明引入象氰基一样具有很强吸电子能力的取代基团, 可以改善富勒烯球的电化学性能, 合成电子接受能力较强的富勒烯衍生物. 相似文献
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自由基清除是富勒烯及其衍生物的一种重要特性. 首次制备了1种二加成亚甲基富勒烯[60]膦酸酯衍生物(bis-methanophosphonate [60]fullerene, BMPF)的纳米颗粒水悬液(n-BMPF), 并采用邻苯三酚自氧化法结合分光光度法, 测定了n-BMPF对超氧阴离子自由基的清除作用. 结果显示, 制备的n-BMPF溶液较稳定, 适合生物学实验. 同时, 它表现出很强的清除超氧阴离子自由基的能力, 并具有浓度依赖性. 当n-BMPF的终浓度为12 μmol/L时, 其对超氧阴离子自由基的清除率达到91.96%. n-BMPF的活性远大于已报道具有自由基清除作用的水溶性富勒烯衍生物富勒醇. 这些数据表明n-BMPF可能作为一种新型高效的自由基清除剂, 在生物医学领域具有潜在的应用价值. 相似文献
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[2+2] click chemistry followed by Prato reaction is reported the first time for energy level tunable functionalization of C60. The novel kind of D–A–A C60 charge-transfer complexes exhibits strikingly enhanced optoelectronic properties and significant third-order nonlinear optical potentials. Meanwhile, structures of the ‘click’ C60 products were fully characterized by NMR, IR, and MS. By introducing TCNE, TCNQ, F4-TCNQ click monomers, we obtained energy level tunable fullerene derivatives in high solubility, which was beneficial for processing. Furthermore, UV–vis spectra were enlarged with end-absorptions into the near infrared region, indicating excellent nonlinear optical properties. The electrochemical properties have been studied by cyclic voltammograms, which were in good correlation with the optical spectroscopic and DFT data. 相似文献
20.
Yu Chen Yun Zhao Ruifang Cai Zu-En Huang Lixiang Xiao 《Journal of Polymer Science.Polymer Physics》1998,36(14):2653-2663
The novel C60–styrene copolymers with different C60 contents were prepared in sodium naphthalene-initiated anionic polymerization reactions. Like the pure polystyrene, these copolymers exhibited the high solvency in many common organic solvents, even for the copolymer with high C60 content. In the polymerization process of C60 with styrene an important side reaction, i.e., reaction of C60 with sodium naphthalene, would occur simultaneously, whereas crosslinking reaction may be negligible. 13C-NMR results provided an evidence that C60 was incorporated covalently into the polystyrene backbone. In contrast to pure polystyrene, the TGA spectrum of copolymer containing ∼ 13% of C60 shows two plateaus. The polystyrene chain segment in copolymer decomposed first at 300–400°C. Then the fullerene units reptured from the corresponding polystyrene fragments attached directly to the C60 cores at 500–638°C. XRD evidence indicates that the degree of order of polymers increases with the fullerene content increased in terms of crystallography. Incorporation of C60 into polystyrene results in the formation of new crystal gratings or crystallization phases. In addition, it was also found that [60]fullerene and its polyanion salts [C60n−(M+)n, M = Li, Na] cannot be used to initiate the anionic polymerization of some monomers such as acrylonitrile and styrene, etc.© 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2653–2663, 1998 相似文献