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Preparation of 1,3-Diketones and of Nitro-diketones by (1:1)-Acylation of Lithium Enolates with Acyl Chlorides Slow addition of precooled solutions of lithium enolates in THF (Fig. 1) to solutions of equimolar amounts of acyl chlorides in the same solvent at temperatures between ? 80 and ? 100° furnishes 1, 3-diketones in acceptable to good yields (Tables 1?3). Even 3-nitropropionyl and 4-nitrobutyryl chloride can be employed for the (1:1)-acylation of enolates to give the synthetically useful 5- and 6-nitro-1, 3-diketones 13 and 25 , respectively. The scope and the limitations of this method of preparing 1, 3-diketones are given and are compared with alternative methods.  相似文献   
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We report experimental observations of the negative-group-velocity (v(g)) phenomenon in an integrated-optical two-port ring-resonator circuit. We demonstrate that when the v(g) is negative, the (main) peak of output pulse appears earlier than the peak of a reference pulse, while for a positive v(g), the situation is the other way around. We observed that a pulse splitting phenomenon occurs in the neighborhood of the critical-coupling point. This pulse splitting limits the maximum achievable delay and advancement of a single device as well as facilitating a smooth transition from highly advanced to highly delayed pulse, and vice versa, across the critical-coupling point.  相似文献   
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Recent experiments suggest that gold single-atom contacts and atomic chains break at applied voltages of 1 to 2 V. In order to understand why current flow affects these defect-free conductors, we have calculated the current-induced forces on atoms in a Au chain between two Au electrodes. These forces are not by themselves sufficient to rupture the chain. However, the current reduces the work to break the chain, which results in a dramatic increase in the probability of thermally activated spontaneous fracture of the chain. This current-induced embrittlement poses a fundamental limit to the current-carrying capacity of atomic wires.  相似文献   
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Here we report on the accumulation of ground-state NH molecules in a static magnetic trap. A pulsed supersonic beam of NH (a1Δ) radicals is produced and brought to a near standstill at the center of a quadrupole magnetic trap using a Stark decelerator. There, optical pumping of the metastable NH radicals to the X3Σ? ground state is performed by driving the spin-forbidden A3Π ← a1Δ transition, followed by spontaneous A → X emission. The resulting population in the various rotational levels of the ground state is monitored via laser induced fluorescence detection. A substantial fraction of the ground-state NH molecules stays confined in the several milliKelvin deep magnetic trap. The loading scheme allows one to increase the phase-space density of trapped molecules by accumulating packets from consecutive deceleration cycles in the trap. In the present experiment, accumulation of six packets is demonstrated to result in an overall increase of only slightly over a factor of two, limited by the trap-loss and reloading rates.  相似文献   
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A simple high-order Galerkin finite element scheme is formulated to compute both the guided and leaky modes of anisotropic planar waveguides with a diagonal permittivity tensor. Transparent boundary conditions derived from the Sommerfield radiation conditions are used to model the fields at the computational boundaries that allow the radiation into the high index cladding/substrate and decay into the low index cladding/substrate, hence work for both guided and leaky modes. Richardson's extrapolation is employed to achieve high-order accuracy by only using simple first-order-polynomial basis functions. Schemes up to sixth-order of accuracy in the effective index are demonstrated. The resulted non-linear sparse matrix eigenvalue equation is solved using an iterative procedure. The ability of the scheme to compute leaky and guided modes of various structures with isotropic and anisotropic materials, step and graded index profiles is demonstrated; including its applications to investigate the properties of ARROW structures.  相似文献   
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The first state selective electron capture cross section measurements at eV energies are reported for collisions between C4+ ions and H2 molecules. The cross sections are measured in a crossed beam experiment by means of Photon Emission Spectroscopy. The ion beams are decelerated in an octopole ion trap where the trap is used to guide the ion beam through the collision region. The experimental results are in excellent agreement with previous measurements at higher energies. The 3-state atomic orbital calculations of Gargaud and McCarroll generally agree with our measurements although there are some discrepancies at lower energies. However, the results for C4+ are still on a relative scale. To put our measurements on an absolute scale the N4++ H system is investigated at keV energies. These results are in good agreement with the data of previous experiments. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   
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