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141.
Dinuclear iron(II)-cyanocarbonyl complex [PPN](2)[Fe(CN)(2)(CO)(2)(mu-SEt)](2) (1) was prepared by the reaction of [PPN][FeBr(CN)(2)(CO)(3)] and [Na][SEt] in THF at ambient temperature. Reaction of complex 1 with [PPN][SEt] produced the triply thiolate-bridged dinuclear Fe(II) complex [PPN][(CN)(CO)(2)Fe(mu-SEt)(3)Fe(CO)(2)(CN)] (2) with the torsion angle of two CN(-) groups (C(5)N(2) and C(3)N(1)) being 126.9 degrees. The extrusion of two sigma-donor CN(-) ligands from Fe(II)Fe(II) centers of complex 1 as a result of the reaction of complex 1 and [PPN][SEt] reflects the electron-rich character of the dinuclear iron(II) when ligated by the third bridging ethylthiolate. The Fe-S distances (2.338(2) and 2.320(3) A for complexes 1 and 2, respectively) do not change significantly, but the Fe(II)-Fe(II) distance contracts from 3.505 A in complex 1 to 3.073 A in complex 2. The considerably longer Fe(II)-Fe(II) distance of 3.073 A in complex 2, compared to the reported Fe-Fe distances of 2.6/2.62 A in DdHase and CpHase, was attributed to the presence of the third bridging ethylthiolate, instead of pi-accepting CO-bridged ligand as observed in [Fe] hydrogenases. Additionally, in a compound of unusual composition ([Na.(5)/(2)H(2)O][(CN)(CO)(2)Fe(mu-SEt)(3)Fe(CO)(2)(CN)])(n)((1)/(2)O(Et)(2))(n) (3), the Na(+) cations and H(2)O molecules combining with dinuclear [(CN)(CO)(2)Fe(mu-SEt)(3)Fe(CO)(2)(CN)](-) anions create a polymeric framework wherein two CN(-) ligands are coordinated via CN(-)-Na(+)/CN(-)-(Na(+))(2) linkages, respectively.  相似文献   
142.
Nanostructures of self-assembled monolayers (SAMs) are designed and produced using coadsorption and nanografting techniques. Because the structures of these artificially engineered domains are predesigned and well-characterized, a systematic investigation is possible to study the mechanical responses to force modulation under atomic force microscope tips. Force modulation imaging reveals characteristic contrast sensitivity to changes in molecular-level packing, molecule chain lengths, domain boundaries, and surface chemical functionalities in SAMs. By means of actively tuning the driving frequency, the resonances at the tip-surface contact are selectively activated. Therefore, specific surface features, such as the edges of the domains and nanostructures or desired chemical functionalities, can be selectively enhanced in the amplitude images. These observations provide a new and active approach in materials characterization and the study of nanotribology using atomic force microscopy.  相似文献   
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A macro-azoinitiator containing polyarylate segment and azo group was prepared by the solution polycondensation of azobiscyanopentanoyl chloride and hydroxy-terminated polyarylates having viscosity-average molecular weights of 6200, 8100, and 12 400. These macro-azoinitiators were used in the radical polymerization of styrene to synthesize polyarylate-polystyrene block copolymers. Thermal properties measured by the differential scanning calorimetry indicated the phase separated morphology of the block copolymers except at low molecular weight of the block constituents. © 1993 John Wiley & Sons, Inc.  相似文献   
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It is conceivable that the high-T c superconducting perovskites are conventional electronphonon superconductors. In this case one expects significant strong-coupling effects because of the unusually high ratiok B T c / of the order 0.1 and greater. We use a set of reasonable models for the Eliashberg function 2 F() (which takes into account available information on the phonon spectra and which fit the measuredT c 's) and calculate strong-coupling effects in the specific heatc s (T)/T c , the ratio 0/k B T c , the critical fieldsH c (T) andH c2 (T) including Pauli limiting, and other measurable quantities. Strongcoupling corrections turn out to be in the range of 0 to about 100%, depending on the quantity of interest. We discuss the perspectives of using strong-coupling effects as indicators for conventional electron-phonon superconductivity in the new materials.  相似文献   
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The formulation and use of a mixed integer mathematical programming location-allocation model, the Coal Logistics System (COLS), is presented in this study. COLS is used to evaluate the potential for reducing water-borne coal transportation costs, and concomitantly the costs of delivering coal to European markets. This cost reduction is accomplished through the use of supercolliers which would require the dredging of channels at selected ports or the use of offshore loading sites at East and Gulf Coast ports or both. The model developed and the analysis presented in this paper are intended to aid in the determination of the location and extent of these activities, and to indicate the size of the potential reduction in the costs of U.S. export coal. In order to be able to accommodate these deeper draft vessels at East and Gulf Coast ports, expensive improvements would need to be undertaken which may include the deepening of harbor channels to the depths required for 120 000 dead weight ton (dwt) or larger supercolliers. Since dredging requires large initial investments and has significant long-term maintenance costs, excess capacity could represent an inefficient use of both U.S. revenues and the ports' own funds. The use of offshore loading moorings to permit the topping off of supercolliers by self-unloading colliers at the deepwater sections of harbor channels has been proposed as a way of reducing trans-ocean transportation costs and avoiding the large investments and time delays associated with dredging activities. The Coal Logistics System was modified and extended to enable the evaluation of these two port improvement options to be undertaken in a consistent and realistic manner.  相似文献   
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