Optical properties of transparent barium titanate nanoparticle/polymer hybrid synthesized from metal alkoxides

A transparent BaTiO₃ particle/polymer hybrid was synthesized from a Ba–Ti double alkoxide modified with an organic ligand and its refractive index and second harmonic generation were studied. BaTiO₃ particles modified with 2-vinyloxyethanol (ethylene glycol monovinyl ether, EGMVE) were polymerized with methyl methacrylate (MMA) yielding the transparent BaTiO₃ particle/poly MMA hybrid. X-ray photoelectron spectra indicated that the formation of chemical bonds between BaTiO₃ nanoparticles and the organic matrix. The refractive indexes of the hybrid films depended on the crystallite size of BaTiO₃ nanoparticles and the volume fractions of BaTiO₃ and polymer phases. The hybrid film synthesized at BaTiO₃/8EGMVE/30H₂O/PMMA revealed a refractive index of 1.65 at 589 nm with an Abbe number of 54. The hybrid film exhibited a second harmonic wave of 532 nm on irradiation with a fundamental wave of 1,064 nm.     

One-pot synthesis of magnetic nanoparticles assembled on polysiloxane rod and their response to magnetic field

Rod-like assembled magnetite (Fe₃O₄) nanoparticles (NPs) were successfully synthesized in a one-pot process using a polysiloxane template derived from a dialkoxysilane. The assembly was constructed using the thiol-ene click reaction between thiol groups on the polysiloxane chain and allyl groups on Fe₃O₄ NPs. The thiol-containing polysiloxane chain and the allyl-containing Fe₃O₄ NPs were synthesized by the hydrolysis–condensation of 3-mercaptopropyl(dimethoxy)methylsilane and iron (III) allylacetylacetonate, respectively. Fe₃O₄ NPs of around 5 nm were uniformly dispersed on the siloxane rods and exhibited neither remanent magnetization nor coercivity. A fluid containing a dispersion of rod-like assembled Fe₃O₄ NPs showed yield stress even without the application of an external magnetic field, whereas spherical Fe₃O₄ NPs exhibited no yield stress. The rod-like assembled Fe₃O₄ NPs on anisotropic siloxane clearly exhibited typical magnetorheological behavior.     

Pyrimidines. 65. Synthesis of 6-substituted thieno[2,3-d]pyrimidine-2,4(1H,3H)-diones

Several 6-substituted thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione derivatives were synthesized. 6-Ethoxycarbonyl derivatives 3 and 7 were prepared by treatment of 6-chloro-5-formyluracil 1 and 6-chloro-5-cyanouracil 6 with ethyl 2-mercaptoacetate in the presence of a base. Electrophilic substitution reactions (Vilsmeier-Haack reaction, bromination, and nitration) of 5,6-unsubstituted thieno[2,3-d]pyrimidine 9 , prepared by condensation of 6-mercaptouracil 8 with chloroacetaldehyde, afforded the corresponding 6-formyl-, 6-bromo-, and 6-nitrothieno[2,3-d]pyrimidines 10, 15 and 16 , respectively.     

Nanomagnetism in nanocrystalline multiferroic bismuth ferrite lead titanate films

Multiferroics conventionally refer to the materials exhibiting co-existing electric, magnetic, and structure order parameters. Interplay between ferroelectricity, magnetism, and ferroelasticity in a single phase makes multiferroics truly multifunctional providing control over magnetic and electric ordering by applying electric and magnetic fields, respectively. Incorporation of multiferroic-based components into nanoscale applications will enable additional degrees of freedom in manipulating with spin and charge not easily attainable otherwise. Multiferroic bismuth ferrite lead titanate has been chemically synthesized in form of nanocrystalline films. The morphology of the films revealed a single perovskite phase confined within crystalline grains of few tens of nm in size. The films were found to exhibit ferroelectricity and ferromagnetism with characteristic electric polarization and magnetization hysteresis loops, transformations associated with spin reorientation in an external magnetic field and the spin-glassy behavior well above the room temperature. High degree of magnetic frustration and disorder in the spin system spatially confined in the nanograins, distribution of the grains anisotropy axis, inter-grain interactions, and the effects of uncompensated spins on the large effective surface/interface favored by the nanocrystalline morphology were assumed to be responsible for the anomalous magnetic properties and glassy dynamics in the films.     

Preparation of 1-Alkynyl (Trimethyl) Silanes from Trimethylsilylpropargyl Phenyl Ether and Organoboranes

Organoboranes have been recently demonstrated to be highly versatile reagents and intermediates for organic synthesis.¹ Several papers have been reported dealing with allenic or propargylic boranes for such purposes.² On the other hand, organosilicon compounds have become increasingly important in synthetic chemistry.³ In search of finding novel synthetic applications by combination of organoboranes and organosilanes, we examined a synthesis of 1-alkynyl (trimethyl) silanes from trimethylsilylpropargyl phenyl ether and trialkylboranes.     

Quenching of neutron E2 effective charge in neutron-rich nuclei and the ground-state spin-parity of 17C

The electric quadrupole moment of ¹⁷B and the g-factor of ¹⁷C were measured by using the fragmentation-induced nuclear polarization technique combined with the β-NMR method. The experimental quadrupole moment of ¹⁷B is found strikingly close to that of the neutron closed-shell isotope ¹³B, indicating a strong quenching of the neutron E2 core-polarization charge. From the result obtained for the ¹⁷C g-factor, we can conclude that the ground-state spin-parity of ¹⁷C is 3/2⁺. Received: 1 May 2001 / Accepted: 4 December 2001     

Modification of intracellular Ca2+ dynamics by laser inactivation of inositol 1,4,5-trisphosphate receptor using membrane-permeant probes

A membrane-permeant malachite green-conjugated IP3 analog (MGIP3/PM) was synthesized as a probe for small molecule-based CALI (smCALI), and its effect on the Ca2+ signaling in intact DT40 chicken B cells was examined. In DT40 B cells treated with the smCALI probe, laser irradiation inhibited IP3-induced Ca2+ oscillations in response to B cell receptor stimulation, demonstrating that IP3R was acutely inactivated. We then applied smCALI to clarify the mechanism of capacitative Ca2+ entry (CCE), in which involvement of IP3R has been suggested. Despite the inactivation of IP3R by smCALI, thapsigargin-induced CCE remained unaffected, providing evidence that functional IP3R is not required for CCE in DT40 cells. These results demonstrate the potency of the smCALI technique for the study of the roles of IP3R in complex intracellular Ca2+ dynamics.     

Chemical Processing of Potassium Substituted (Pb0.6Ba0.4)Nb2O6 Powders and Thin Films Through Metallo-Organics

Highly oriented tungsten bronze K_0.4(Pb_0.6Ba_0.4)_0.8Nb₂O₆ ferroelectric thin films have been prepared from metal alkoxides and metal acetate by chemical process. The formation of solid solution with potassium was found to be very effective to form the tungsten bronze phase at lower temperatures compared with (Pb_0.6Ba_0.4)Nb₂O₆. The amount of potassium in the composition of K_x(Pb_0.6Ba_0.4)_{1 – x/2}Nb₂O₆ [0 x 0.4] is also important to crystallize in the tungsten bronze phase. K_0.4(Pb_0.6Ba_0.4)_0.8Nb₂O₆ films with c-axis preferred orientation were successfully synthesized on MgO(1 0 0) and Pt(1 0 0)/MgO(1 0 0) substrates above 700°C. KPBN60 thin film on Pt(1 0 0)/MgO(1 0 0) showed a remnant polarization of 20 C/cm² and a coercive field of 140 kV/cm at –150°C.