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The complex [(N-benzyloxycarbonylprolyl)cyclopentadienyl]-Mo(CO)3Me was prepared by the reaction of the amino acid-functionalized cyclopentadienyl-lithium reagent with Mo(CO)6, and subsequent methylation with CH3I. The complex was characterized by FTIR, 1H and 13C NMR, and elemental analysis. A single-crystal X-ray diffraction study showed that the complex is chiral, crystallizing in the orthorhombic P212121 space group with the Flack parameter refining to –0.007(16), which unequivocally confirms the presence of an enantiomerically pure compound. The complex was examined as a catalyst precursor in the liquid-phase epoxidation of trans-β-methylstyrene at 280–330 K, using either tert-butylhydroperoxide (tert-BuOOH), cumylhydroperoxide or urea-hydrogen peroxide adduct as oxidant, and, optionally, a co-solvent. With chloroform and tert-BuOOH, the catalytic activity surpasses that previously reported for chiral complexes of the type CpMo(CO)3X, giving the epoxide isomers ((R,R)-(+) and (S,S)-(?)-1-phenylpropylene oxide) in excellent selectivity, albeit with negligible enantiomeric excess. FTIR spectroscopy showed that the oxidative decarbonylation of the tricarbonyl complex with tert-BuOOH is fast under the reaction conditions used, and that the structural integrity of the amino acid-functionalized cyclopentadienyl group is retained during this process. The use of the ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate as a solvent for the catalyst generates a biphasic liquid–liquid reaction system that enables, at the end of a catalytic cycle, the separation and reutilization of the catalyst.  相似文献   
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Using the framework of the grand canonical ensemble the effects of a two (or three) dimensional confinement (harmonic) potential on the magnetic properties of an ideal electron gas are investigated. The high temperature results for the magnetic moment obtained by Felderhof and Raval are generalized to take into account the spin. At low temperature the confinement potential introduces a new oscillatory phenomena besides a modification or even a destruction of the de Haas-van Alphen effect. The changes in Landau diamagnetism are also analysed.  相似文献   
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A novel V-shaped polyoxotungstate is formed when Ce(IV) metal centres bridge monolacunary [PW(11)O(39)](7-) anions to an unusual 1,4-bilacunary [PW(10)O(38)](11-) anion which appears with an unprecedented bridging structural motif.  相似文献   
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The development of smart solutions based on optical fiber technology for any kind of structure such as buildings, aircrafts, or even for human body kinematics, is becoming more and more common. The ability to provide coverings for different structures that can enable monitoring functions beside the esthetic purpose of the covering is an important add‐value characteristic. Nevertheless, an open issue is to find an effective solution for the fabrication and application procedure, preferably that scales at a production level. This article explores the insertion of optical fibers into polymeric PVC foils based on the spread‐coating fabrication process. The success of this integration approach allows the use of photonic technology in different fields with minor application issues. The material choice for the substrate is a crucial step when choosing integrated solution. Three PVC paste formulations were explored in order to guarantee the optimal integration of optical fiber. A high‐viscosity and not monolithic paste formulation emerged as the best choice. This formulation provided the best adhesion, reducing in great scale the surface undulation and paste displacement that the optical fiber tends to do and, its 362% stretch capability is sufficient for special applications, as strain sensitive one. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   
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