A convenient method for the preparation of α-vinylfurans by phosphine-initiated reactions of various substituted enynes bearing a carbonyl group with aldehydes

α-Vinylfurans were obtained by phosphine-initiated cyclization of various enynes bearing a carbonyl group at the ene end in the presence of various aldehydes, in moderate to high yields. The reaction may consist of 1,6-addition of phosphine to the enynes, ring closure, and Wittig reaction between the ylid resulting from cyclization and an aldehyde. Thus, various aldehydes were able to be used in the reaction. The reaction was influenced greatly by the substituents at the acetylene position (R¹) and the α-position of the carbonyl group (R³).     

Snowballs of radioactive ions — nuclear spin polarization of core ions

Short-lived ions¹²B (beta-radioactive, T_1/2=20.3 ms) sustaining nuclear spin polarization were introduced into superfluid helium at 1.7 K. It was found that the¹²B ions were transported as charged entities under a static electric field and that the nuclear polarization was maintained throughout the lifetime of¹²B nuclei. Polarization of¹²B was determined through beta-NMR method. Snowball, a singly charged microcluster of helium atoms formed around an impurity ion, is responsible for the behaviour and thus constitutes a suitable environment for preserving nuclear polarization of the core ions¹²B. In a separate experiment snowballs were produced by implanting⁸Li (T_1/2=830 ms) into liquid helium and detected by means of alpha particles from the core ions to guarantee that the snowballs survive longer than the lifetime of¹²B.     

Estimation of monomer reactivity ratios by nonlinear least-squares procedure with consideration of the weight of experimental data

To obtain the optimum values of the monomer reactivity ratios for the copolymerization systems with largely different reactivities between both monomers, a nonlinear least-squares procedure which took into account the weights of experimental data, was proposed and discussed. The weights of the data were treated for the errors arisen from the amounts of monomers charged, the densities of monomers, the weights of copolymer formed, and the composition of copolymer. The least-squares procedure with the consideration of the weights was applicable to both differentiated equation and integrated equation derived by Lewis and Mayo. This procedure was applied to radical copolymerizations of α-substituted crotonic esters with styrene, and reasonable monomer reactivity ratios were obtained. It was noted that errors from the copolymer composition were more important than those from the other factors and that the use of the integrated equation was recommended even when the copolymers were isolated at low conversions.     

Coherent storage of photoexcited triplet states using 29Si nuclear spins in silicon

Pulsed electron paramagnetic resonance spectroscopy of the photoexcited, metastable triplet state of the oxygen-vacancy center in silicon reveals that the lifetime of the m(s)=±1 sublevels differs significantly from that of the m(s)=0 state. We exploit this significant difference in decay rates to the ground singlet state to achieve nearly ~100% electron-spin polarization within the triplet. We further demonstrate the transfer of a coherent state of the triplet electron spin to, and from, a hyperfine-coupled, nearest-neighbor (29)Si nuclear spin. We measure the coherence time of the (29)Si nuclear spin employed in this operation and find it to be unaffected by the presence of the triplet electron spin and equal to the bulk value measured by nuclear magnetic resonance.     

Discovery of deeply bound π− states in the208Pb(d,3He) reaction

Narrow lines were observed around 133 MeV excitation energy in the²⁰⁸Pb(d,³He) reaction atT _d=300 MeV/u using the Fragment Separator System at GSI. They are assigned to the deeply boundπ ^??²⁰⁷Pb states with configurations of $\left( {2p} \right)_{\pi ^ - } $ (3p_1/2, 3p_3/2) _n ^?1 .     

Catalyzed intramolecular olefin insertion into a carbon-carbon single bond

Intramolecular insertion of a C-C double bond into a C-C single bond was achieved by treatment of cyclobutanone bearing an o-styryl group at the 3-position with a catalytic amount of a cationic rhodium(I)-dppp complex. Initially, rhodium is inserted between the carbonyl carbon and the alpha-carbon of the cyclobutanone. Intramolecular coordination of the vinyl group results in its migratory insertion into the C-Rh linkage. Reductive elimination affords benzobicyclo[3.2.1]octan-3-one. Notably, a ring-opened alpha,beta-unsaturated ketone was obtained when dppe was used instead of dppp. In this reaction, rhodium cleaved the bond between the alpha sp3 carbon and the beta sp3 carbon of the cyclobutanone. The coordinating vinyl group directs this new regioselectivity of cleavage observed with the dppe ligand.     

Deeply bound 1s and 2p pionic states in 205Pb and determination of the s-wave part of the pion-nucleus interaction

We observed well-separated 1s and 2p pi(-) states in 205Pb in the 206Pb(d,3He) reaction at T(d) = 604.3 MeV. The binding energies and the widths determined are B(1s) = 6.762+/-0.061 MeV, Gamma(1s) = 0.764(+0.154)(-0.171) MeV, B(2p) = 5.110+/-0.045 MeV, and Gamma(2p) = 0.321(-0.062)(+0.060) MeV. They are used to deduce the real and imaginary strengths of the s-wave part of the pion-nucleus interaction, which translates into a positive mass shift of pi(-) in 205Pb.     

Determination of hydrogen concentration in amorphous silicon films by nuclear elastic scattering (NES) of 100 MeV 3He2+

Nuclear elastic scattering (NES) of 100 MeV ³He²⁺ ions was used to determine the amount of hydrogen atoms in hydrogenated amorphous silicon film fabricated by reactive sputtering. The total amount of hydrogen in this film was determined to be (1.12 ± 0.1) x 10²² cm^-3 within the accuracy of ～ 10%.