Magnetic moment of short lived β-emitter 24mAl

The magnetic moment of short lived β-emitter ^24mAl (426 keV, I ^π ?=?1^?+?, T _1/2?=?131 ms) has been measured by means of β-NMR technique, for the first time. From the β-NMR spectrum, the magnetic moment was determined as $\left| {\upmu}\left( ^{\rm 24m}{\rm Al} \right) \right|=\left( {2.99\pm 0.09} \right){\upmu}_{\rm N}$ . Combined with the known magnetic moment of the mirror partner ^24mNa, the expectation value of <?S _z?> is obtained to be (0.08 ± 0.12). These values are reproduced well by the shell model calculation.     

Heteroareno-annelated estranes by triene cyclization

17-Thienyl-and 17-benzo[b]thienyl-3-hydroxyestra-1,3,5(10),16-tetraenes were synthesized by either sequential or one-pot Suzuki cross-coupling and Wittig olefination reactions. At 160 °C, heteroaryl substituted steroids were observed to undergo thermal intramolecular cyclization to produce E-ring heteroareno-annelated estranes.     

Suppression mechanism of the self-discharge reaction in nickel-metal hydride batteries using a sulfonated polyolefin separator

The suppression mechanism of the self-discharge reaction in nickel-metal hydride batteries using a sulfonated polyolefin separator was investigated with sealed-type AA size cells. The experimental results indicate that a sulfonated polyolefin separator effectively suppresses the self-discharge reaction in nickel-metal hydride batteries by trapping nitrogen-containing redox shuttle substances. It is also found that a sulfonated polyolefin separator traps the shuttle substances as gaseous ammonia. In the experiment examining the influence of the amount of the shuttle substances on the self-discharge, the starting point of the self-discharge agreed well with the point at which the nitrogen adsorption capacity of a sulfonated polyolefin separator reached its maximum.     

2′‐Amino‐3‐methoxy­pyrimidino­[5′,4′:16,17]­estra‐1,3,5(10),16‐tetraene

In the title compound, C₂₁H₂₅N₃O, the six‐membered ring that is fused to two other six‐membered rings in the estrane moiety adopts an envelope conformation. The compound shows intermolecular hydrogen bonding of the amine group to an N atom of the pyrimidine moiety, as well as weak intermolecular interactions involving H atoms in the hydro­phobic residue of the mol­ecule.     

Effects of the carrier-envelope phase in the multiphoton ionization regime

We theoretically investigate the effects of the carrier-envelope phase of few-cycle laser pulses in the multiphoton ionization regime. For atoms with low ionization potential, total ionization yield barely exhibits phase dependence, as expected. However, population of some bound states clearly shows phase dependence. This implies that the measurement of the carrier-envelope phase would be possible through the photoemission between bound states without energy-and-angle-resolved photoelectron detection. The considered scheme could be particularly useful to measure the carrier-envelope phase for a light source without an amplifier, such as a laser oscillator, which cannot provide sufficient pulse energy to induce tunneling ionization.     

Quadrupole Moments of Na Isotopes

The electric quadrupole coupling constants eqQ/h of ²⁰Na (I ^π = 2⁺, T _1/2 = 449.7 ms), ²¹Na (I ^π = 3/2, T _1/2 = 22.49 s) and ²⁵Na (I ^π = 5/2, T _1/2 = 59.6 s) in single crystal ZnO and TiO₂ were precisely measured by applying the β-NMR technique. The ratio of the quadrupole moments between ²⁰Na (²⁵Na) and ²¹Na was determined to be 0.728 ± 0.023 (0.011 ± 0.002).     

An enantiomeric nanoscale architecture obtained from a pseudoenantiomeric aggregate: covalent fixation of helical chirality formed in self-assembled discotic triazine triamides by chiral amplification

Covalent fixation of a chiral helical structure which is created in a self-assembling system by a chiral-amplification method based on the sergeants/soldiers principle is reported. Disk-shaped triazine triamides self-assembled to form columnar-type helical aggregates through pi-stacking interactions among the central triphenyltriazine moieties, hydrogen-bonding interactions among the amide groups, and van der Waals interactions among the alkyl groups in nonpolar solvents such as hexane, octane, toluene, and p-xylene. When the achiral triazine triamide soldier component is mixed with a tiny amount of the chiral triazine triamide sergeant component, control of the intrinsic supramolecular helicity of the self-assembled soldier component by the sergeant component leads to chiral amplification and formation of a pseudoenantiomeric aggregate with only one handedness of the helix. The helicity can be preserved by ring-closing olefin metathesis polymerization mediated by Grubbs catalyst when an achiral component with terminal olefinic groups forms the pseudoenantiomeric aggregate in the presence of a tiny amount of the chiral component without olefinic groups. After polymerization and removal of the chiral component, the polymeric architecture obtained from the achiral soldier component is optically active and thus can be regarded as an enantiomeric object in which the chiral information transferred from the chiral sergeant component is preserved. The nanoscale chiral structure is fixed perfectly, as indicated by CD spectroscopic evidence obtained in a polar THF medium at high temperature and low concentration. AFM and TEM observations show a nanoscale fibrous structure with a diameter of 2-4 nm, which corresponds to the molecular size of the triazine triamide monomer.     

Magnetic moment of23Mg

The magnetic moment of the²³Mg (I =3/2⁺, T_1/2=11.3 s), has been determined as |(²³Mg)|=0.5364±0.003 µ_N by use of -NMR detection with the recoil polarization obtained through a low energy nuclear reaction.     

Temperature dependence of Knight shifts for 12 B in Pt

The Knight shift of a short lived β-emitting nucleus ¹²B (I = 1, T _1/2 = 20 ms) implanted into Pt has been measured as a function of temperature (140?600 K) by means of the β-NMR method. The relation between the Knight shift and the susceptibility for Pt was deduced, which shows the similar tendency to that for the case of ¹²B in Pd.