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1.
Ibragimov A. G. Khafizova L. O. Zagrebel"naya I. V. Parfenova L. V. Sultanov R. M. Khalilov L. M. Dzhemilev U. M. 《Russian Chemical Bulletin》2001,50(2):292-296
A new method for the synthesis of dialkyl(ethyl)alanes by the reaction of EtAlCl2 with -olefins in the presence of Mg and a catalytic amount of Cp2TiCl2 (Ti(OPri)4, Ti(OBun)4) in THF was developed. 相似文献
2.
Dzhemilev U. M. Ibragimov A. G. Khafizova L. O. Khalilov L. M. Vasil"ev Yu. V. Tomilov Yu. V. 《Russian Chemical Bulletin》2001,50(2):297-299
1-Ethyl-2,3-fullerenoaluminacyclopropanes (EtAl)n(2-C60) were synthesized by the reaction of fullerene C60 with an excess of EtAlCl2 in the presence of Mg and using Cp2TiCl2 as the catalyst in a THF--toluene solution at 20 °C. Deuterolysis of fullerenoaluminacyclopropanes afforded a mixture of deuteriofullerenes C60Dm, where m = 6--12. 相似文献
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L. V. Parfenova S. V. Pechatkina L. M. Khalilov U. M. Dzhemilev 《Russian Chemical Bulletin》2005,54(2):316-327
The composition of intermediates of the Cp2ZrCl2-catalyzed hydroalumination of α-olefins by isobutylalanes (HAlBui
2, AlBui
3, ClAlBui
2) was studied by dynamic 1H and 13C NMR pectroscopy. The reaction of Cp2ZrCl2 with isobutylalanes affords the complex (Cp2ZrHCl·HAlBui
2)2 responsible for α-olefin hydroalumination.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 311–322, February, 2005. 相似文献
5.
V. A. D’yakonov R. K. Timerkhanov A. G. Ibragimov U. M. Dzhemilev 《Russian Chemical Bulletin》2007,56(11):2232-2235
Catalytic cycloalumination of cyclonona-1,2-diene upon treatment with Et3Al and EtAlCl2 in the presence of Cp2ZrCl2, leading to 10-ethyl-10-aluminabicyclo[7.3.01,9]dodec-8-ene (1) and 11-ethyl-11-aluminatricyclo[10.7.01,12.02,10]nonadeca-9,12-diene, respectively, was accomplished in high yields. A possibility for the selective transformation of compound
1 to 1-allyl-9-(pent-4-enyl)cyclonon-1-ene and 10-hydroxybicyclo[7.3.01,9]dodec-8-ene in one preparative step was demonstrated.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2156–2159, November, 2007. 相似文献
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Sm(II)-modified periodic mesoporous silica (PMS), Sm[N(SiHMe2)2]2(THF)x@MCM-41, was used for the synthesis of Sm(II) alkyl, alkoxide, and indenyl surface species via secondary ligand exchange. The performance of the novel Sm(II)-based organometallic–inorganic hybrid materials as initiators for the graft polymerization of methyl methacrylate (MMA) is reported. All of the Sm(II) hybrid materials including the new PMMA–PMS composites were characterized via N2 physisorption, elemental analysis, FTIR spectroscopy, and scanning electron microscopy (SEM). The organic–inorganic composites revealed complete pore blockage as well as enrichment and strong adhesion of the polymer at the exterior of the porous silica material. 相似文献
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Interface Engineering of a CoOx/Ta3N5 Photocatalyst for Unprecedented Water Oxidation Performance under Visible‐Light‐Irradiation
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Shanshan Chen Dr. Shuai Shen Guiji Liu Yu Qi Prof. Fuxiang Zhang Prof. Can Li 《Angewandte Chemie (International ed. in English)》2015,54(10):3047-3051
Cocatalysts have been extensively used to promote water oxidation efficiency in solar‐to‐chemical energy conversion, but the influence of interface compatibility between semiconductor and cocatalyst has been rarely addressed. Here we demonstrate a feasible strategy of interface wettability modification to enhance water oxidation efficiency of the state‐of‐the‐art CoOx/Ta3N5 system. When the hydrophobic feature of a Ta3N5 semiconductor was modulated to a hydrophilic one by in situ or ex situ surface coating with a magnesia nanolayer (2–5 nm), the interfacial contact between the hydrophilic CoOx cocatalyst and the modified hydrophilic Ta3N5 semiconductor was greatly improved. Consequently, the visible‐light‐driven photocatalytic oxygen evolution rate of the resulting CoOx/MgO(in)–Ta3N5 photocatalyst is ca. 23 times that of the pristine Ta3N5 sample, with a new record (11.3 %) of apparent quantum efficiency (AQE) under 500–600 nm illumination. 相似文献
9.
Tatiana B. Mikenas Vladimir A. Zakharov Lyudmila G. Echevskaya Michail A. Matsko 《Journal of polymer science. Part A, Polymer chemistry》2005,43(10):2128-2133
Data on ethylene polymerization over supported LFeCl2/MgCl2 catalysts {L = 2,6‐bis[1‐(2,6‐dimethylphenylimino)ethyl]pyridyl} containing AlR3 (R = Me, Et, i‐Bu, or n‐Oct) as an activator are presented. These catalysts are highly active (100–300 kg of polyethylene/g of Fe h bar of C2H4) and stable in ethylene polymerization at 70–80 °C. Data on the effects of the iron content, AlR3 type, Al(i‐Bu)3 concentration, and hydrogen presence on the catalyst activity are presented. The molecular structure of polyethylene produced with these catalysts (including the molecular masses, molecular mass distribution, branching, and number of C?C bonds) has been studied; data on the effects of AlR3 and hydrogen on the molecular structure are presented. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2128–2133, 2005 相似文献
10.
Xinghuo Xiao Wenyan Wang Jiali Wang Prof. Can Yang Prof. Guigang Zhang Prof. Xianjun Lang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(52):e202201244
Conjugated polymers feature promising structure and properties for photocatalytic water splitting. Herein, a hydrolysis strategy was demonstrated to rationally modulate the surface hydrophilicity and band structures of conjugated poly-benzothiadiazoles. High hydrophilicity not only enhances the dispersions of polymeric solids in an aqueous solution but also reduces the absorption energy of water molecules. Besides, both theoretical and experimental results reveal that a more positive valence band potential is generated, which contributes to enhancing the photocatalytic water oxidation performance. Accordingly, the surface-modified conjugated polymers show largely promoted photocatalytic water oxidation activities by deposition of cobalt oxides as cocatalysts. 相似文献