Synthesis of polydihydropyridazinones from bis(3-benzoylpropionic acids) and aromatic dihydrazines

A new class of polydihydropyridazinones has been synthesized by the solution cyclopolycondensation in m-cresol of 4,4′-oxy- and 4,4′-ethylenebis(3-benzoylpropionic acids) with aromatic dihydrazines such as bis(4-hydrazinophenyl) sulfone and bis(4-hydrazinophenyl)methane. The polymers having inherent viscosities of 0.2–0.4 were highly soluble in a wide range of solvents including m-cresol, N,N-dimethylacetamide, and pyridine. Thermogravimetric analysis of the polydihydropyridazinones showed initial weight losses commencing at 290–350°C in both air and nitrogen.     

Observations of the collision-induced dipole transitions and of a quadrupole transition for barium in krypton

For Ba perturbed by Kr, collision-induced dipole transitions 6s²¹S₀ – 6snd¹D₂ (8?n?10) have been observed. The effective oscillator strength per unit Kr density was found to be 1.8–1.0 x 10^-23 cm³. For the electric-quadrupole transition 6s²¹S₀ -6s6d¹D₂, the oscillator strength is (2.0±0.4) x 10^-6.     

Multiphoton transitions in a macroscopic quantum two-state system

We have observed multiphoton transitions between two macroscopic quantum-mechanical superposition states formed by two opposite circulating currents in a superconducting loop with three Josephson junctions. Resonant peaks and dips of up to three-photon transitions were observed in spectroscopic measurements when the system was irradiated with a strong rf-photon field. The widths of the multiphoton absorption dips are shown to scale with the Bessel functions in agreement with theoretical predictions derived from the Bloch equation or from a spin-boson model.     

Vortex molecules in coherently coupled two-component Bose-Einstein condensates

A vortex molecule is predicted in rotating two-component Bose-Einstein condensates whose internal hyperfine states are coupled coherently by an external field. A vortex in one component and one in the other are connected by a domain wall of the relative phase, constituting a "vortex molecule," which features a nonaxisymmetric (pseudo)spin texture with a pair of merons. The binding mechanism of the vortex molecule is discussed based on a generalized nonlinear sigma model and a variational ansatz. The anisotropy of vortex molecules is caused by the difference in the scattering lengths, yielding a distorted vortex-molecule lattice in fast rotating condensates.     

Diode-end-pumped 4.2-W continuous-wave Yb:Y2O3 ceramic laser

We report on an efficient diode-end-pumped polycrystalline Yb:Y2O3 ceramic laser. Continuous-wave output power of 4.2 W at 1078 nm was obtained under pump power of 19.5 W. The corresponding slope efficiency was 29%. The beam quality factor (M2) at full pump power was measured to be 1.63. The threshold wavelengths of the laser at various output couplings were also investigated. It was found that the threshold wavelengths shifted approximately 5 nm when the reflectivity of the output coupler changed from 90% to 99.9%, as caused by the strong reabsorption effect in the ceramic sample.     

Sequence of phase transitions in a quasi-one-dimensional β-Na<Subscript>0.33</Subscript>V<Subscript>2</Subscript>O<Subscript>5</Subscript> compound with variable valence

The thermal properties—specific heat, thermal conductivity, and thermal expansion coefficients—of a single crystal of quasi-one-dimensional variable-valence β-Na_0.33V₂O₅ compound were studied. With lowering temperature, it sequentially undergoes the structural (T _S ～ 230 K), charge (T _C ～ 136 K), and magnetic (T _N ～ 22 K) phase transitions. The structural transition at T _S , resulting in the ordering of the Na ions, and the charge ordering at T _C , resulting in the charge redistribution over the positions of V ions, are accompanied by the anomalies in the temperature dependences of all the studied properties. The magnetic ordering at T _N results in the appearance of the canted antiferromagnetic structure and manifests itself only in the anomaly in the temperature dependences of the thermal expansion coefficients.     

EPR imaging to estimate the in vivo intracerebral reducing ability of mature rats after neonatal hypoxic-ischemic brain injury

A rat model of neonatal hypoxic-ischemic encephalopathy (Rice's model) was obtained by unilateral ligation of the common carotid artery of 7-day-old rats with hypoxia (exposure to 8% oxygen). To estimate the in vivo intracerebral reducing ability of the mature rats (8 weeks old) of Rice's model, temporal electron paramagnetic resonance (EPR) imaging of the brain of a rat receiving a blood-brain barrier-permeable nitroxide radical, 3-hydroxymethyl-2,2,5,5-tetramethylpyrrolidine-1-oxyl, was performed. In this imaging technique, the decay rate of the EPR signal intensity in a selected region of the brain is indicative of region-specific reducing ability. The effect of neonatal treatment of an antioxidant agent, 3-methyl-1-phenyl-2-pyrazolin-5-one (MCI-186), after a hypoxic-ischemic insult was also tested. It was found that the reducing ability had been depleted in the contralateral hemisphere of Rice's model rats; this depletion was suppressed by administering MCI-186.     

Spectral characteristics of a Yb-doped Y<Subscript>2</Subscript>O<Subscript>3</Subscript> ceramic laser

We report the experimental observation of random wavelength emission and intensity-dependent central-wavelength shift in a diode-pumped Yb³⁺-doped Y₂O₃ ceramic laser. We show experimentally that, like conventional lasers, the emission of the laser has fixed well-defined transverse modes; however, its instantaneous emission wavelengths change randomly with time. The central wavelength of the laser emission also shifts with the intracavity light intensity. A model was developed to describe the spectral behavior of Yb³⁺-doped lasers. We show that the observed random wavelength emission and central lasing wavelength shift of the laser could be well explained based on the strong reabsorption of light in the gain medium. PACS 42.55.Rz; 42.60.Mi; 42.55.Xi     

Michael addition of amines and thiols to dehydroalanine amides: a remarkable rate acceleration in water

In water, the rate of Michael addition of amines and thiols to dehydroalanine amides was greatly accelerated, leading to shorter reaction times and higher yields. The scope of the new conditions was tested with a range of amines, thiols, and dehydroalanine amides. The ease and efficiency of this method provides an attractive route to the synthesis of natural and unnatural amino acid derivatives.