Efficient synthesis of diborylalkenes from alkenes and diboron by a new PSiP-pincer palladium-catalyzed dehydrogenative borylation

The efficient synthesis of various diborylalkenes such as 1,1-, trans-1,2-, and cyclic 1,2-diborylalkenes from alkenes and diboron was achieved for the first time. Selective preparation of di- and monoborylalkenes was also realized by the appropriate choice of reaction conditions. The reaction was found to proceed via a new mechanism of dehydrogenative borylation through a monoborylpalladium complex bearing an anionic PSiP-pincer ligand as a key intermediate, which realized the efficient borylation without sacrificial hydroboration or hydrogenation of the alkene.     

Platinum(II)-catalyzed generation and [3+2] cycloaddition reaction of α,β-unsaturated carbene complex intermediates for the preparation of polycyclic compounds

Pt(II)-catalyzed generation of unsaturated carbene complex intermediates from various propargyl ether derivatives based on electrophilic activation of alkynes was realized. These in situ generated unsaturated carbene complexes undergo [3+2] cycloaddition reaction with various vinyl ethers, leading to efficient formation of indoles, naphthols, and benzofuran fused with a five-membered ring in high yields.     

Photochemically promoted transition metal-free cross-coupling of acylsilanes with organoboronic esters

Intermolecular carbon-carbon bond formation between acylsilanes and organoboronic esters was achieved by photoirradiation under almost neutral, transition metal-free conditions. In this reaction, siloxycarbenes generated by photoisomerization of acylsilanes reacted with boronic esters to give the formal B-C bond insertion intermediates, which underwent unique rearrangement to afford the cyclic α-alkoxyboronic esters. Acidic treatment of the resulting crude products under air furnished the cross-coupled ketones in good yields.     

Surfactant-promoted novel reductive synthesis of supported metallic Cu nanoclusters and their catalytic performances for selective dehydrogenation of methanol

We have found a surfactant-promoted novel reductive synthesis of metallic Cu nanoclusters on metal oxides under hydrothermal synthesis conditions, which are active for the selective dehydrogenation of methanol.     

Oxygen isotope effect in optimally doped Bi2Sr2CaCu2O8+δ studied by low-energy ARPES

Using angle-resolved photoemission spectroscopy (ARPES) with low-energy tunable photons, we studied the oxygen isotope effect in optimally doped Bi₂Sr₂CaCu₂O_8+δ (Bi2212). We found the oxygen isotope shift in the real part of the electron self-energies [ReΣ(ω)s] along the nodal direction derived not only from the momentum distribution curves (MDCs) but also from the energy distribution curves (EDCs). Present results indicate straightforwardly the coupling between the nodal electrons and the phonons.     

Interplay among Coulomb interaction, spin-orbit interaction, and multiple electron-boson interactions in Sr2RuO4

Using polarization- and hν-dependent angle-resolved photoemission spectroscopy, we uncovered the fine details of a quasiparticle's dynamics of a typical multiband superconductor, Sr2RuO4. We found strong hybridization between the in-plane and out-of-plane quasiparticles via the Coulomb and spin-orbit interactions. This effect enhances the quasiparticle mass due to the inflow of out-of-plane quasiparticles into the two-dimensional Fermi surface sheet, where the quasiparticles are further subjected to the multiple electron-boson interactions. We suggest that the spin-triplet p-wave superconductivity of Sr2RuO4 is phonon mediated.     

Certified reference material for the determination of perfluorooctane sulfonate in acrylonitrile-butadiene-styrene resin (NMIJ CRM 8155-a)

A certified reference material (CRM) for the determination of perfluorooctane sulfonate (PFOS) in acrylonitrile-butadiene-styrene (ABS) resin (NMIJ CRM 8155-a) has been issued by the National Metrology Institute of Japan (NMIJ). The bulk material was prepared by mixing commercial ABS resin powder and potassium PFOS and cut into square plates (20 × 20 mm, 2 mm thick) as the CRM. Analytical processes combined with isotope-dilution mass spectrometry and liquid chromatography/mass spectrometry were optimised and applied for characterisation. One of the approaches adopted by NMIJ for certification is that results from two or more primary methods of measurement should be used; thus, two optimised isotope-dilution mass spectrometric methods (Methods 1 and 2 with reprecipitation and with reprecipitation/solid phase extraction, respectively, were validated mutually and employed) were used to determine the certified value. Homogeneity and stability of the square plates were evaluated and their uncertainty contributions (as relative standard uncertainties) were 1.43% for inhomogeneity and 6.96% for approximately two years’ instability. The certified mass fraction of linear PFOS (heptadecafluoro-1-octanesulfonic acid) in the CRM with expanded uncertainty (coverage factor k = 2, approximately 95% confidence interval) was (33.1 ± 5.0) mg kg^?1 as free acid of PFOS.