Estimation of secondary electron effect in the J-PARC rapid cycling synchrotron after first study

The J-PARC 3 GeV rapid-cycling synchrotron (RCS) is required to provide 1 MW pulsed protons to the spallation neutron target and the 50 GeV main ring. Since the RCS finally accelerates very high intensity beam such as 8.3 × 10¹³ ppp, the secondary electron cloud may affect the accelerator performance. We measured the secondary electron emission from the TiN coating surface and the ferrite sample. By using these measurement results, we estimated the effect of the electron cloud made by the emitted secondary electron at present beam parameters.     

Liquid crystalline phase transitions in hexakis(4-(4'-heptyloxy)biphenoxy)cyclotriphosphazene

Hexakis(4-(4'-heptyloxy)biphenoxy)cyclotriphosphazene (HHCP) was synthesized from hexachlorocyclotriphosphazene and 4-heptyloxy-4'-hydroxybiphenyl. The mesogenicity of HHCP was studied by DSC, FTIR spectroscopy and polarizing microscopy. Enantiotropic smectic C and nematic phases were observed between 450 and 455 K and 455 and 456 K, respectively, on heating, and between 456 and 455 K (nematic) and 455 and 440 K (smectic C) on cooling from the isotropic liquid phase. The introduction of the heptyloxybiphenoxy groups as side chains into cyclotriphosphazene has generated the liquid crystalline phase. FTIR spectroscopy showed that the P=N and P-O-(C) stretching vibrations converted to lower frequencies from 1224 to 1210 cm^-1 and from 920 to 910cm^-1, respectively, at the crystalline (C)-S_c phase transition. This result suggests that the state of the cyclotriphosphazene ring dramatically changes near the C-S_c phase transition.     

Pinning of texture and vortices of the rotating B-like phase of superfluid 3He confined in a 98% aerogel

We have investigated pinning effects on texture and vortices of the B-like phase of superfluid (3)He in a rotating aerogel up to +/-2pi rad/s by cw-NMR. We observed deformation of the NMR spectra in rotation, due to counterflow between the superflow and the normal flow. The average intensity of the counterflow was calculated from the change of NMR spectra. The rotation dependence of the counterflow intensity is similar to the magnetization curve of hard type II superconductors or the counterflow response of (4)He-II in packed powders. This counterflow behavior is in qualitative agreement with a model that vortices are pinned unless the counterflow exceeds a critical velocity v(c). The temperature independence of v(c) suggests that v(c) is associated with the expansion of primordial vortices.     

A study of 3He-4He tunneling motion in solid 3He-4He mixtures by means of T1ϱ measurements

³He spin relaxation time in the rotating frame (T_1?) has been measured for 2% ³He in ⁴He solid samples of different molar volume at exchange plateau region (0.5 K). From the data, the characteristic frequency by which a ³He atom exchanges its position with a neighboring ⁴He atom is determined.     

Laser-induced above-band-gap transparency in GaAs

We report the observation of large (approximately 40%) laser-induced above-band-gap transparency in GaAs at room temperature. The induced transparency is present only during the pulse width of the driving midinfrared laser pulses and its spectral shape is consistent with a laser-induced blueshift of the band edge. Our simulations based on the dynamic Franz-Keldysh effect reproduce the salient features of the experimental results, demonstrating, in particular, that the amount of the band edge shift is approximately given by the ponderomotive potential.     

Selective N-alkylation of amines using nitriles under hydrogenation conditions: facile synthesis of secondary and tertiary amines

Nitriles were found to be highly effective alkylating reagents for the selective N-alkylation of amines under catalytic hydrogenation conditions. For the aromatic primary amines, the corresponding secondary amines were selectively obtained under Pd/C-catalyzed hydrogenation conditions. Although the use of electron poor aromatic amines or bulky nitriles showed a lower reactivity toward the reductive alkylation, the addition of NH(4)OAc enhanced the reactivity to give secondary aromatic amines in good to excellent yields. Under the same reaction conditions, aromatic nitro compounds instead of the aromatic primary amines could be directly transformed into secondary amines via a domino reaction involving the one-pot hydrogenation of the nitro group and the reductive alkylation of the amines. While aliphatic amines were effectively converted to the corresponding tertiary amines under Pd/C-catalyzed conditions, Rh/C was a highly effective catalyst for the N-monoalkylation of aliphatic primary amines without over-alkylation to the tertiary amines. Furthermore, the combination of the Rh/C-catalyzed N-monoalkylation of the aliphatic primary amines and additional Pd/C-catalyzed alkylation of the resulting secondary aliphatic amines could selectively prepare aliphatic tertiary amines possessing three different alkyl groups. According to the mechanistic studies, it seems reasonable to conclude that nitriles were reduced to aldimines before the nucleophilic attack of the amine during the first step of the reaction.     

Unique origin of colors of armchair carbon nanotubes

The colors of suspended metallic colloidal particles are determined by their size-dependent plasma resonance, while those of semiconducting colloidal particles are determined by their size-dependent band gap. Here, we present a novel case for armchair carbon nanotubes, suspended in aqueous medium, for which the color depends on their size-dependent excitonic resonance, even though the individual particles are metallic. We observe distinct colors of a series of armchair-enriched nanotube suspensions, highlighting the unique coloration mechanism of these one-dimensional metals.     

Decarbonylative C-h coupling of azoles and aryl esters: unprecedented nickel catalysis and application to the synthesis of muscoride a

A nickel-catalyzed decarbonylative C-H biaryl coupling of azoles and aryl esters is described. The newly developed catalytic system does not require the use of expensive metal catalysts or silver- or copper-based stoichiometric oxidants. We have successfully applied this new C-H arylation reaction to a convergent formal synthesis of muscoride A.