Performance of underwater adaptive array including mutual coupling effects

In this paper, the mutual coupling effects on the performance of underwater adaptive arrays are analyzed. This study manifests the discrepancies between cases of considering and ignoring the mutual coupling effects. The least mean square (LMS) based adaptive array is utilized to illustrate the mutual coupling effects. Numerical examples show that the performance of an underwater adaptive array can be improved as mutual coupling effects are considered. The consideration of mutual coupling effects is necessary in analyzing underwater adaptive arrays.     

Effect of SOCl2 treatment on electrical and mechanical properties of single-wall carbon nanotube networks

Chemical modification by SOCl2 of an entangled network of purified single-wall carbon nanotubes, also known as 'bucky paper', is reported to profoundly change the electrical and mechanical properties of this system. Four-probe measurements indicate a conductivity increase by up to a factor of 5 at room temperature and an even more pronounced increase at lower temperatures. This chemical modification also improves the mechanical properties of SWNT networks. Whereas the pristine sample shows an overall semiconducting character, the modified material behaves as a metal. The effect of SOCl2 is studied in terms of chemical doping of the nanotube network. We identified the microscopic origin of these changes using SEM, XPS, NEXAFS, EDX, and Raman spectroscopy measurements and ab initio calculations. We interpret the SOCl2-induced conductivity increase by p-type doping of the pristine material. This conclusion is reached by electronic structure calculations, which indicate a Fermi level shift into the valence band, and is consistent with the temperature dependence of the thermopower.     

Stabilization of interchange modes in mirror plasmas by a nonlinear rf-plasma wave coupling process

Experimental and theoretical studies are made of the consequences of a nonlinear coupling process between pump rf waves and interchange modes in mirror plasmas. It is demonstrated that the interchange-stable operation window exists depending on the applied rf power and gamma=omega(0)/Omega(i), where omega(0) (Omega(i)) is the angular frequency of the applied rf wave (ion cyclotron frequency). Results are shown that the nonlinear wave coupling process gives rise to the operation window near the resonance (gamma approximately equal to 1), which is elucidated by theoretical analyses combined with full rf wave simulations.     

Plan for nuclear symmetry energy experiments using the LAMPS system at the RIB facility RAON in Korea

We review the calculation of the equation of state of pure neutron matter using quantum Monte Carlo (QMC) methods. QMC algorithms permit the study of many-body nuclear systems using realistic two- and three-body forces in a non-perturbative framework. We present the results for the equation of state of neutron matter, and focus on the role of three-neutron forces at supranuclear density. We discuss the correlation between the symmetry energy, the neutron star radius and the symmetry energy. We also combine QMC and theoretical models of the three-nucleon interactions, and recent neutron star observations to constrain the value of the symmetry energy and its density dependence.     

Copper-catalyzed intramolecular C–N coupling reaction of aryl halide with amide

An efficient and concise method for the ligand-free copper-catalyzed intramolecular C–N bond coupling was developed, which afforded various (NH)-phenanthridinones in good to excellent yields with tolerance of various substrates.     

Electron-Transfer Protocol for the Hydroxyalkenylation of Alkenes Using 1,2-Bis(phenylsulfonyl)ethylene

We report a protocol for alkene hydroxyalkenylation. Using a persulfate anion as a one-electron-oxidation reagent and 1,2-bis(phenylsulfonyl)ethylene as a radical acceptor in the presence of water, alkenes were converted into the corresponding 1-phenylsulfonyl-4-hydroxyalkenes in good to high yields. The hydroxyalkenylation process involves the nucleophilic hydroxylation of alkene radical cations to give β-hydroxyalkyl radicals, which, after a radical addition/β-elimination sequence, provide the products. We also report a photocatalytic protocol for alkoxyalkenylation.     

Dioxygen Activation of a Trinuclear CuICuICuI Cluster Capable of Mediating Facile Oxidation of Organic Substrates: Competition between O‐Atom Transfer and Abortive Intercomplex Reduction

The dioxygen activation of a series of Cu^ICu^ICu^I complexes based on the ligands ( L ) 3,3′‐(1,4‐diazepane‐ 1,4‐diyl)bis(1‐{[2‐(dimethylamino)ethyl](methyl)amino}propan‐2‐ol) ( 7‐Me ) or 3,3′‐(1,4‐diazepane‐1,4‐diyl)bis(1‐{[2‐(diethylamino)ethyl](ethyl)amino}propan‐2‐ol) ( 7‐Et ) forms an intermediate capable of mediating facile O‐atom transfer to simple organic substrates at room temperature. To elucidate the dioxygen chemistry, we have examined the reactions of 7‐Me , 7‐Et , and 3,3′‐(1,4‐diazepane‐1,4‐diyl)bis[1‐(4‐methylpiperazin‐1‐yl)propan‐2‐ol] ( 7‐N‐Meppz ) with dioxygen at ?80, ?55, and ?35 °C in propionitrile (EtCN) by UV‐visible, 77 K EPR, and X‐ray absorption spectroscopy, and 7‐N‐Meppz and 7‐Me with dioxygen at room temperature in acetonitrile (MeCN) by diode array spectrophotometry. At both ?80 and ?55 °C, the mixing of the starting [Cu^ICu^ICu^I( L )]¹⁺ complex ( 1 ) with O₂‐saturated propionitrile (EtCN) led to a bright green solution consisting of two paramagnetic species: the green dioxygen adduct [Cu^IICu^II(μ‐η²:η²‐peroxo)Cu^II( L )]²⁺ ( 2 ) and the blue [Cu^IICu^II(μ‐O)Cu^II( L )]²⁺ species ( 3 ). These observations are consistent with the initial formation of [Cu^IICu^II(μ‐O)₂Cu^III( L )]¹⁺ ( 4 ), followed by rapid abortion of this highly reactive species by intercluster electron transfer from a second molecule of complex 1 to give the blue species 3 and subsequent oxygenation of the partially oxidized [Cu^IICu^ICu^I( L )]²⁺ ( 5 ) to form the green dioxygen adduct 2 . Assignment of 2 to [Cu^IICu^II(μ‐η²:η²‐peroxo)Cu^II( L )]²⁺ is consistent with its reactivity with water to give H₂O₂ and the blue species 3 , as well as its propensity to be photoreduced in the X‐ray beam during X‐ray absorption experiments at room temperature. In light of these observations, the development of an oxidation catalyst based on the tricopper system requires consideration of the following design criteria: 1) rapid dioxygen chemistry; 2) facile O‐atom transfer from the activated cluster to substrate; and 3) a suitable reductant to rapidly regenerate complex 1 to accomplish efficient catalytic turnover.     

Tandem three-component reactions of aldehyde, alkyl acrylate, and dialkylmalonate catalyzed by ethyl diphenylphosphine

A new highly efficient three-component reaction of alkyl acrylate, aldehyde and dialkyl malonate using ethyl diphenylphosphine as organocatalyst has been described. Various highly functional compounds bearing hydroxyl groups and the ester functions can be easily prepared in moderate to good yields according to our one-step procedure. The reactions are believed to proceed via Morita-Baylis-Hillman reactions of alkyl acrylate and aldehydes, followed by the Michael addition reactions of dialkyl malonates. Our reactions indicated that the intermediate species formed in the phosphine-catalyzed MBH reaction are an effective organic base to catalyze the Michael addition reactions of dialkyl malonates to the preformed MBH adducts.