Reductive Rearrangement of Tetraphenyldiphosphine Disulfide To Trigger the Bisthiophosphinylation of Alkenes and Alkynes

The facile synthesis of organophosphorus compounds is of great importance for the development of new synthetic methods by using air-stable sources of phosphorus. In this respect, a synthetic method that is based on a reductive rearrangement and is capable of converting air-stable pentavalent phosphorus compounds into reactive trivalent phosphorus compounds is a powerful tool. Tetraphenyldiphosphine disulfide, which is a shelf-stable solid, was the focus of this study, and it was shown to undergo reductive rearrangement to trigger the bisthiophosphinylation of a variety of alkenes, such as terminal, cyclic, internal, and branched alkenes, 1,3-dienes, and terminal alkynes when exposed to light without any catalyst, base, or additive.     

Star polymer with crosslinked core and water‐soluble poly(N‐hydroxyethylacrylamide)‐arms: Synthesis by arm‐first method using ATRP and characterizations by SEC‐MALS and SAXS measurement in water

Core crosslinked star (CCS)‐polymers with water‐soluble arms composed of poly(N‐hydroxyethylacrylamide) (PHEAA) are described. N‐Hydroxyethylacrylamide was polymerized by the atom transfer radical polymerization consisting of ethyl 2‐chloropropionate, copper(I) chloride (CuCl), and tris[2‐(dimethylamino)ethyl]amine in an ethanol/water mixed solvent at 20 °C. The obtained PHEAA‐arms were subsequently coupled using N,N′‐methylenebisacrylamide as the crosslinking agent and sodium L ‐ascorbic acid (AscNa) as the reaction activator. A total of 17 representative coupling reactions with diverse conditions are discussed together with the characterizations of the products mainly by size exclusion chromatograph equipped with the multiangle laser light scattering detector (SEC‐MALS). Consequently, the coupling reactions provided CCS‐polymers with PHEAA‐arms (CCS‐PHEAAs) having weight averaged‐molecular weights determined by SEC‐MALS (M_w,MALS) ranging from 63.8 kg mol^?1 to 832 kg mol^?1, which corresponded to the average arm‐number (N_arm) ranging from 4.1 to 42, respectively. CCS‐PHEAA with the M_w,MALS of 250 kg mol^?1 was isolated and characterized by small angle X‐ray scattering measurements in 0.05 M NaNO₃ aq. at 25 °C, which was shown to possess a star‐shaped structure and exist as single molecules with a radius of gyration at the infinite dilution condition (<R_g²>_z,0^1/2) of 74 ± 4 Å. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

Alternative Synthesis of Dibenzo-and Dipyrido-[1,3]Diazepines from Thioamides and o,o′-Diaminobiaryls

Thioamides were treated with iodomethane, and then o,o′-diaminobiphenyl or bipyridyl to afford 6-substituted-5H-dibenzo- or dipyrido [1,3]diazepines in good yields.     

Crystal growth and dopant segregation of Ce:LiSrAlF6 and Eu:LiSrAlF6 crystals with high dopant concentrations

Ce:LiSrAlF₆ and Eu:LiSrAlF₆ crystals with different dopant concentrations were grown by the micro-pulling-down method. The crystals with high dopant crystal included the secondary phase as clusters with the plate shape in BSE images. The secondary phases were identified CeF₃ and EuF₂, respectively, by the EDS analysis and powder-XRD measurement. Eu concentration against the Sr sites in the Eu 2% doped LiSAF crystal were most uniform in the range 0.9–1.6 atm% using the EPMA.     

Observation of single-spin transport in an island-shaped CoFeB double magnetic tunnel junction prepared by magnetron sputtering

The Co₄₀Fe₄₀B₂₀(CFB)/MgO/CFB/MgO/CFB-based multilayer was prepared by conventional magnetron sputtering and utilised in the fabrication of double magnetic tunnel junctions (DMTJs) for which the middle CFB layers were island-shaped. By analysing the magnetic property of the CFB islands with Langevin’s equation, it was possible to identify their diameters of 7.6, 8.9 and 11.0 nm; accordingly submicron-scaled DMTJs were fabricated to investigate single-spin transport phenomena. The coulomb staircase and the oscillatory tunnel magnetoresistive (TMR) were able to be observed at 6 K, where the TMR ratio was enhanced up to 60%, which is the highest value ever achieved in this structure.