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961.
The first dinuclear iron(II) complexes of any 4-substituted 3,5-di(2-pyridyl)-4H-1,2,4-triazole ligands, [Fe(II)2(adpt)2(H2O)1.5(CH3CN)2.5](BF4)4 and [Fe(II)2(pldpt)2(H2O)2(CH3CN)2](BF4)4, are presented [where adpt is 4-amino-3,5-di(2-pyridyl)-4H-1,2,4-triazole and pldpt is 4-pyrrolyl-3,5-di(2-pyridyl)-4H-1,2,4-triazole]. Both dinuclear complexes feature doubly triazole bridged iron(II) centers that are found to be [high spin-high spin] at all temperatures, 4-300 K, and to exhibit weak antiferromagnetic coupling. In the analogous monometallic complexes, [Fe(II)(Rdpt)2(X)2](n+), the spin state of the iron(II) center was controlled by appropriate selection of the axial ligands X. Specifically, both of the chloride complexes, [Fe(II)(adpt)2(Cl)2] x 2 MeOH and [Fe(II)(pldpt)2(Cl)2] x 2 MeOH x H2O, were found to be high spin whereas the pyridine adduct [Fe(II)(adpt)2(py)2](BF4)2 was low spin. Attempts to prepare [Fe(II)(pldpt)2(py)2](BF4)2 and the dinuclear analogues [Fe(II)2(Rdpt)2(py)4](BF4)4 failed, illustrating the significant challenges faced in attempts to develop control over the nature of the product obtained from reactions of iron(II) and these bis-bidentate ligands.  相似文献   
962.
Thin films of alternating maleic acid/anhydride copolymers (poly(octadecene-alt-maleic acid/anhydride), POMA; poly(propene-alt-maleic acid/anhydride), PPMA; poly(styrene-alt-maleic acid/anhydride), PSMA) were studied to unravel the influence of the comonomer characteristics in the backbone on the surface-energetic properties of the copolymer films in the dry state and in contact with aqueous solutions. Water contact angle measurements revealed a graduation of the wettability of the dry hydrolyzed and annealed copolymer films that was dependent on the comonomer unit. It ranged from moderately hydrophilic (PPMA, annealed gamma(sv) = 39.9 mJ/m2) to very hydrophobic (POMA, annealed, gamma(sv) = 18.4 mJ/m2) surfaces. Liquid-fluid contact angle measurements using captive air bubbles were performed in different aqueous media (pure water, phosphate-buffered saline, and 10(-)(3) M KCl of two different pH values (pH = 3 and pH = 10) to study the copolymer films in their hydrated states relevant for biointerfacial phenomena. It was found that the graduation of the wettability of the copolymer films in the dry state is overall maintained upon immersion in aqueous solutions. The dependence of the wettability on the pH value of the aqueous medium could be related to the (de)protonation of the carboxylic groups.  相似文献   
963.
The development of C1-symmetric aminosulfoximines, their highly modular synthesis, and their application in enantioselective copper-catalyzed Mukaiyama-type aldol reactions between pyruvates and enolsilanes is described. In this context, the influence of the ligand architecture as well as the optimization of the reaction conditions are discussed. In detail, the dependence of the catalyst efficiency on the solvent, the metal source and the temperature are reported, and an interesting additive effect is highlighted. Furthermore, the substrate scope will be presented. With the optimized catalyst system, a number of aldol products with quaternary stereogenic centers have been obtained in high yields and with enantiomeric excesses up to 99 %.  相似文献   
964.
965.
The oxygen incorporation reaction in undoped SrTiO(3) was investigated by electrical measurements (pressure modulation technique) in the temperature range from 650-920 degrees C and by means of tracer exchange experiments in the temperature range from 458-600 degrees C. The surface of the undoped SrTiO(3) single crystals was modified by alkaline earth metal compounds leading to a tremendous enhancement of the effective surface exchange rate for oxygen incorporation as compared to the uncoated surface.  相似文献   
966.
967.
968.
In the framework of nonrelativistic quantum mechanics we derive a necessary condition for four Coulomb charges (m1(+), m2(-), m3(+), m4(-)), where all masses are assumed finite, to form the stable system. The obtained stability condition is physical and is expressed through the required minimal ratio of Jacobi masses. In particular, this provides the rigorous proof that hydrogen-antihydrogen and muonium-antimuonium molecules and hydrogen-positron-muon systems are unstable. It also proves that replacing hydrogen in the hydrogen-antihydrogen molecule with its heavier isotopes does not make the molecule stable. These are the first rigorous results on the instability of these systems.  相似文献   
969.
We report experimental evidence of transitions from limit cycle oscillations through a phase turbulent regime to space-time defect turbulence in a spatially (quasi-)one-dimensional electrochemical system with nonlocal coupling. The transitions are characterized in terms of the defect density, the Karhunen-Loève decomposition dimension, and a measure of the degree of spatial correlation in the data. Furthermore, these quantities give the first experimental confirmation that the spatial coupling range in electrochemical systems indeed depends on the distance between the working and the counterelectrode.  相似文献   
970.
Phase noise is a critical issue for the sensitivity of the interferometric gravitational-wave detector Laser Interferometer Space Antenna that requires laser sources with 1 W of output power. A low-power seed laser with a subsequent fiber amplifier is in discussion, and we report on spectrally resolved phase-noise measurements of an ytterbium-doped fiber amplifier emitting 1 W of output power from 10 mW of seed power. Phase-noise measurements for Fourier frequencies from 10(-4) Hz to 100 kHz show 60 rad/Hz0.5 at 10(-4) Hz and 0.2 mrad/Hz0.5 at 1 kHz. This measured excess phase noise is orders of magnitude below the free-running phase noise of nonplanar ring oscillators.  相似文献   
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