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排序方式: 共有229条查询结果,搜索用时 15 毫秒
1.
2.
Fumie Takei Daisuke Kodama Sugiko Nakamura Kiyotaka Onitsuka Shigetoshi Takahashi 《Journal of polymer science. Part A, Polymer chemistry》2006,44(1):585-595
Aryl isocyanides bearing free‐base and metallo‐porphyrins were prepared and polymerized with a Pd–Pt μ‐ethynediyl complex as the initiator to give polymers with narrow polydispersity indices. The molecular weights of the resulting polymers were precisely controlled by the initial feed ratio of the porphyrin monomer to the initiator. The UV–VIS spectra suggested that the porphyrin pendants are regularly arranged to form stacked columns. Metallo‐porphyrin polymers were also prepared by reacting free‐base porphyrin polymers with metal salts. The successive reactions of free‐base and zinc‐porphyrin monomers resulted in the formation of diblock polymers. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 585–595, 2006 相似文献
3.
Zusammenfassung Es wird eine Korrekturformel zur 8. Potenzformel von Philippoff-Heß vorgeschlagen, die auch die Fälle gut wiedergibt, wo die einfache 8. Potenzformel ebenso wie andere Viskositätsgleichungen bisher versagten. Im einzelnen wird die Gleichung geprüft an folgenden bisherigen Ausnahmen: Cellit in Eisessig (Philippoff-Heß), polymere-Hydroxydekansäuren in sym-Tetrachloräthan(Kraemer-von Natta), polymere Polystyrole in Benzol (Dane). In jedem Falle stellen diek-Werte gute Konstanten dar.Die charakteristische Viskositätskonstantek zeigt eine lineare Zunahme mit dem Molekulargewicht der Polymerhomologen.Die Temperaturabhängigkeit vonk unda wird geprüft. 相似文献
4.
Highly dispersed molybdena-titania catalyst can be prepared by an equilibrium adsorption method. In this method, molybdate
anions adsorb onto the positively charged titania surfaces via electrostatic attraction by controlling the pH of the impregnating
solution and they increase as an inverse function of the pH. 95Mo-NMR and UV spectroscopic studies of impregnating solution show that the polymeric species like Mo7O24
6-ions are adsorbed on titania in the acidic impregnating solution. XRD, Raman, and XPS data of the calcined samples show that
mono-layer coverage of molybdenum oxide over-layer possesses a highly distorted MoO6 group with a molecular geometry resembling the distorted square pyramid.
The catalytic oxidation of methanol over the surface molybdate species on titania possesses higher turnover numbers and higher
selectivities of partial oxidation products than the catalysts supported on alumina, silica, zirconia, or magnesia. Changes
of the surface properties either after reduction and sulfiding treatment over monolayer catalyst on titania have also been
investigated. The NO chemisorption and XPS studies show that two types of active sites appeared after reduction treatment:
one site is active for hydrogenation of 1,3-butadiene and the other site is active for metathesis of propene. A higher degree
coordinative unsaturations of MO is required for hydrogenation than metathesis. After sulfiding treatments of the catalyst,
hydrogenation of 1,3-butadiene also requires triply coordinative unsaturation, and hydrogenolysis of thiophene requires the
ensemble of doubly or triply coordinative unsaturations. 相似文献
5.
Diethyl bromodifluoromethyl phosphonate reacts readily with cadmium metal to form a stable cadmium complex. Depending on solvent, this functionalized organocadmium reagent exhibits stability for days to months. It reacts with a variety of electrophiles and serves as a synthetically useful source for the introduction of the difluoromethylene phosphonate group into organic compounds.The synthetic utility of a wide variety of fluoromethylene phosphonium ylides has been a major effort in our laboratory over the past several years [1]. The generation and capture of difluoromethylene ylides () as a general route to difluoromethylene olefins has been of especial interest to us [2]. In an effort to increase the nucleophilicity of the ylide, we have attempted to prepare the analogous phosphonate ylide (). Although we have achieved modest success [3] by capture of () in the reaction of sodium dialkyl phosphites with diethyl bromodifluoromethylphosphonate (), attempts to pregenerate (), either from diethyl difluoromethylphosphonate () or (), have met with little success. () appears to have minimal stability even at low temperatures, and scale up processes of synthetic value would seem to be difficult. 相似文献
6.
Summary Alumina may be considerably modified by impregnating at 100°C in the alkali metal phosphate solution. The available solution for modification was the KOH–K2HPO4–AlPO4 (11.51M) solution or the NaOH–Na2 HPO4 (0.81.1 M or 11.5M) solution. The appreciable improvement on chromatograms was obtained by preheating of the alumina, especially above 800°C prior to impregnating A further modification may be made by ignition of the alumina impregnated. The x-ray diffraction studies revealed the phase transformation of the alumina inducing the modification, and the essential factor of the present modification method being the thermal treatment of the alumina at temperatures forming -alumina. 相似文献
7.
Hirata K Suzuki T Noya A Takei I Hidai M 《Chemical communications (Cambridge, England)》2005,(29):3718-3720
The reactions of [Cp*MCl2]2(Cp*=eta5-C5Me5, M = Rh, Ir) with thiacalix[4]arene (TC4A(OH)4) and tetramercaptothiacalix[4]arene (TC4A(SH)4) gave the mononuclear complexes [(Cp*M){eta3-TC4A(OH)2(O)2}] and the dinuclear complexes [(Cp*M)2{eta3eta3-TC4A(S)4}] respectively, while the analogous reactions with dimercaptothiacalix[4]arene (TC4A(OH)2(SH)2) produced the tetranuclear complexes [(Cp*M)2(Cp*MCl2)2-{eta3eta3eta1eta1-TC4A(O)2(S)2}]. 相似文献
8.
Alkenyl, aryl or allylic selenides smoothly couple with Grignard reagents in the presence of Ni(II)-phosphine complexes as catalysts to afford the corresponding unsaturated compounds in good yields. The reactivity order of coupling reaction with BuMgBr catalyzed by NiCl2 [Ph2PCH2CH2CH2PPh2] was found to be PhSeMe « PhCl > PhSMe by the competitive reactions. 相似文献
9.
Mori M Oyama Y Suzuki A Takahashi K Yamada M Miyano K Miyata H Takei H Hirata KS Kajita T Kihara K Nakahata M Nakamura K Ohara S Sato N Suzuki Y Totsuka Y Yaginuma Y Koshiba M Suda T Tajima T Fukuda Y Nagashima Y Takita M Kaneyuki K Tanimori T Beier EW Frank ED Frati W Kim SB Mann AK Newcomer FM Van Berg R Zhang W 《Physical review D: Particles and fields》1991,43(9):2843-2846
10.
Toru Oba Yubi TatenoMisaki Ihara Takanori FukusumiNatsuki Takei Satoshi Ito 《Tetrahedron letters》2014
Radical reactions of a C3-vinylated chlorophyll derivative, methyl pyropheophorbide-a, which were induced by thiols and the conventional initiator azobisisobutyronitrile (AIBN) were examined in vitro for the first time. Thiyl radicals attacked regioselectively at the sole C3-vinyl group, and the anti-Markovnikov sulfanyl adducts were obtained as major products. The other peripheral substituents, as well as the chlorin macrocycle, remained intact. The AIBN-induced radical reaction competed with co-oxidation that afforded the C3-formyl chlorin. This method can open new routes to derivatization of vinyl chlorins. 相似文献