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151.
A titanocene-ferrocenyl complex, (5-ferrocenyl-2-hydroxybenzenecarboxylato- O,O′)-bis(methylcyclopentadienyl)titanium(IV) 4, and an unexpected ionic complex, [C7H8NO3]- [(C5H5)Fe(C5H4)SO3]·H2O3 were synthesized and characterized by IR, ^1H NMR and elemental analysis. Compound 3 is of triclinic, space group P1 with a = 5.954(2), b = 13.208(5), c = 13.252(5) A, α = 60.993(7),β = 84.342(8),γ = 86.933(8)°, Z = 2, V = 906.8(6)A^3, Dc = 1.601 g/cm^3, μ(MoKα) = 0.987 mm^-1, F(000) = 452, the final R = 0.0647 and wR = 0.1333 for 2311 observed reflections (I 〉 2σ(I)). Compound 4 belongs to the monoclinic system, space group P2 1/c with α = 14.3310(9), b = 12.5065(8), c = 12.9406(10) A, β = 95.101(4)°, Z = 4, V = 2310.2(3) A^3, Dc = 1.513 g/cm^3, μ(MoKα) = 1.004 mm^-1, F(000) = 1088, the final R = 0.0461 and wR = 0.1048 for 2112 observed reflections (1 〉 2σ(I)). 相似文献
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153.
Yoshihiko Nishimori Katsuhiko Kanaizuka Dr. Tomochika Kurita Toshiaki Nagatsu Yu Segawa Fumiyuki Toshimitsu Satoshi Muratsugu Dr. Mitsuya Utsuno Dr. Shoko Kume Dr. Masaki Murata Dr. Hiroshi Nishihara Prof. 《化学:亚洲杂志》2009,4(8):1361-1367
Electronic conductivity of molecular wires is a critical fundamental issue in molecular electronics. π‐Conjugated redox molecular wires with the superior long‐range electron‐transport ability could be constructed on a gold surface through the stepwise ligand–metal coordination method. The βd value, indicating the degree of decrease in the electron‐transfer rate constant with distance along the molecular wire between the electrode and the redox active species at the terminal of the wire, were 0.008–0.07 Å?1 and 0.002–0.004 Å?1 for molecular wires of bis(terpyridine)iron and bis(terpyridine)cobalt complex oligomers, respectively. The influences on βd by the chemical structure of molecular wires and the terminal redox units, temperature, electric field, and electrolyte concentration were clarified. The results indicate that facile sequential electron hopping between neighboring metal–complex units within the wire is responsible for the high electron‐transport ability. 相似文献
154.
咪唑类离子液体中二茂铁的电化学行为 总被引:1,自引:1,他引:0
用自制的铂超微电极研究了二茂铁(Fc)在咪唑类离子液体中的电化学行为,计算了Fc在离子液体中的扩散系数和粘度系数.结果表明,二茂铁在这些离子液体中均呈现较好的可逆性,测得的扩散系数比用常规电极测得的大,说明超微电极比常规电极有更大的扩散传质速率. 相似文献
155.
设计合成了2-[(2′-二茂铁基)-乙烯基]-8-羟基喹啉(1)、2-[(2′-BINOL基)-乙烯基]-8-羟基喹啉(2)及其金属铝配合物3和4.通过红外光谱(IR)和核磁共振谱(1 H NMR)等波谱测试技术对其结构进行了表征,结果表明成功实现了目标化合物的合成;通过电子吸收光谱(UV-Vis-NIR)及荧光光谱(EP)对配体1、2以及配合物3、4进行了光物理性质研究.结果显示配体2对Al 3+离子具有强的选择识别功能,有望成为优良的离子识别添加剂;而配合物3在480nm处发出强蓝光,有望成为一种优良的蓝色电致发光材料. 相似文献
156.
合成了2, 3, 4-三-(11-二茂铁基)十一烷氧基苯甲酸, 用元素分析、核磁共振谱, 红外及紫外光谱等对产物进行了表征. 利用循环伏安法(CV), 线性扫描伏安法(LSV), 常规脉冲伏安法(NPV), 计时电流法(CA)和计时电量法(CC)研究了该物质的电化学行为, 测定了其电化学参数. 结果表明该二茂铁基两亲性分子在溶液中具有良好的氧化还原可逆性, 是由扩散控制的可逆过程, 且三个二茂铁基团之间没有强相互作用而显示等同的氧化还原性. 相似文献
157.
H. W. I. Peerlings R. A. T. M. Van Benthem E. W. Meijer 《Journal of polymer science. Part A, Polymer chemistry》2001,39(18):3112-3120
A novel, fast, and simple synthetic procedure for polycarbamate/urea dendrimers, based on an AB–CD2 coupling strategy, is presented. The reactivity difference of the two isocyanate functionalities of the AB building block allows the construction of these dendrimers without the necessity of activation or deprotection steps. This makes it possible to construct dendrimers within 2–3 days, even the largest dendrimers. The resulting dendrimers could be fully characterized by 13C NMR, IR spectroscopy, and mass spectrometry. The synthetic strategy necessitates only techniques such as stirring, heating, and accurate dosing, and there is no workup required for the purification of the compounds. On account of a wide variety of polyols, amines, and aminoalcohols, this new procedure is not limited to the synthetic strategy followed but allows the incorporation of a large variety of functional molecules in the core, in the branching units, or at the end groups. The method is even applicable when organometallic species are incorporated into the dendritic structure, thereby showing its versatility. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3112–3120, 2001 相似文献
158.
159.
A series of neutral and oxidized π-bridged biferrocenes (Fc—x—Fc) and biferrocenylenes (FC(—x—)2Fc) (x= —CH=CH—, —CH3,C=CCH3—) were prepared and their physical properties have been studied by means of Mössbauuer and cyclic voltammetry. The electrode reaction of these bridged ferrocene derivatives appears to involve a consecutive two-step oxidation process. The results also show that the voltage difference between the first and second oxidaton potentials of the bridged biferrocenes was found to be largely exceeded that founded for the corresponding the bridged biferrocenylenes. The Mössbauer data show that the oxidation of doubly bridged Fc(—x—)2Fc with iodine, DDQ, and TCNQ given the corresponding dioxidized salts only and no stable mixed-valence compounds were found. 相似文献
160.
Christopher T. Chantler Nicholas A. Rae M. Tauhidul Islam Stephen P. Best Joey Yeo Lucas F. Smale James Hester Narges Mohammadi Feng Wang 《Journal of synchrotron radiation》2012,19(2):145-158
Methods for the quantification of statistically valid measures of the uncertainties associated with X‐ray absorption fine structure (XAFS) data obtained from dilute solutions using fluorescence measurements are developed. Experimental data obtained from 10 mM solutions of the organometallic compound ferrocene, Fe(C5H5)2, are analysed within this framework and, following correction for various electronic and geometrical factors, give robust estimates of the standard errors of the individual measurements. The reliability of the refinement statistics of standard current XAFS structure approaches that do not include propagation of experimental uncertainties to assess subtle structural distortions is assessed in terms of refinements obtained for the staggered and eclipsed conformations of the C5H5 rings of ferrocene. Standard approaches (XFIT, IFEFFIT) give refinement statistics that appear to show strong, but opposite, preferences for the different conformations. Incorporation of experimental uncertainties into an IFEFFIT‐like analysis yield refinement statistics for the staggered and eclipsed forms of ferrocene which show a far more realistic preference for the eclipsed form which accurately reflects the reliability of the analysis. Moreover, the more strongly founded estimates of the refined parameter uncertainties allow more direct comparison with those obtained by other techniques. These XAFS‐based estimates of the bond distances have accuracies comparable with those obtained using single‐crystal diffraction techniques and are superior in terms of their use in comparisons of experimental and computed structures. 相似文献