Hyperfine interactions in isolated ions

Conclusion It has been demonstrated that the effect of a tilted multifoil array on an ensemble of nuclei approaches a regular precession in a field of magnitude pH in the direction of the tilt axis. The magnitude of the precession can, under certain circumstances, be considerably larger than in a transient field, the only other method available today for measurements in the picosecond range. The technology of multifoil arrays has not been fully mastered to date, the immediate objective being the construction of arrays which keep their shape and spacings for many hours in a particle beam.     

Nd:YAG laser pumped at 946 nm

A Nd:YAG laser crystal was pumped at 946 nm and lased at 1064 nm. This pump-lase format was investigated in order to reduce the quantum defect between the pump and laser photons as compared to other pump schemes of this material. To the best of our knowledge, this is the first realization of this scheme. A room temperature absorption coefficient and linewidth of approximately 0.075 cm(-1) and approximately 1 nm for 1% at. Nd(+3) concentrations were measured for the 946 nm absorption line. Those parameters impose both narrow-bandwidth pumping and a long absorption path. By increasing the laser crystal temperature above room temperature, the absorption cross sections at 946 and 938 nm increase due to enhanced thermal population of the upper energy level of the ground manifold. The possibility of exploiting this phenomenon to enhance the pump absorption is also discussed.     

Parity violation in the 17/2−–17/2+ doublet in93Tc

The parity-violating mixing of the 17/2^– and 17/2⁺ levels in⁹³Tc nuclei, polarized by the tilted multifoil interaction, was measured by the observation of the forward-backward-ray asymmetry. The nuclear polarization, induced by the tilted multifoils, was measured directly for the neighboring^88,90Zr isomers. The forward to backward asymmetry was determined to be A=(2.5±2.1) 10^–3 which implies a parity violating matrix element ¦H _PV )¦=(4.0±3.7)meV.     

Q-switching an all-fiber laser using acousto-optic null coupler

A new method for Q-switching an all-fiber laser is presented. It is based on induced acoustic long period grating operating on a null coupler, which acts as acoustically controlled tunable output coupler. Q-switching is achieved by switching on and off the acoustic wave in a burst mode, thereby generating laser pulses that are ~400 times shorter than the acoustically controlled coupler’s rise time. Output pulse energy of 22 μJ and temporal width of ~100 ns were measured at a wavelength of 1.54 μm.     

Tilted foil polarization of radioactive beam nuclei

Tilted foil polarization has up to now been mostly applied to nuclear reaction products recoiling out of a target traversed by a primary particle beam. Being a universal phenomenon it can be applied equally well to beams of particles, primary or secondary, radioactive or other. There are however some technical considerations arising from the nature of the beam particles. Radioactive beams are associated with ground state nuclei. They usually have low nuclear spin and as a consequence-as will be shown later-low polarization. Secondary beams are usually low in intensity and do not impose any constraints on the foils they traverse; unlike intense primary heavy ion beams which, if they traverse the foils, essentially limit the foil material to carbon. We review here briefly the tilted foil polarization process and then discuss an experiment with an isomer beam. Finally we review experiments with radioactive beams, past, present and planned for the future.     

Synthetic studies towards congeners of phomactin A. Re-examination of the structure of Sch 49028

The total syntheses of the epoxy cyclic hemiacetal structures 8 and 9, which are isomeric with the structure 6 proposed for the phomactin known as Sch 49028 isolated from the marine fungus Phoma sp. are described. Neither of these structures showed spectroscopic data consistent with those reported for the purported natural product, adding credibility to the proposal that the structure Sch 49028 does not exist in nature and that its NMR spectroscopic data should have been assigned as phomactin A (1).     

A total synthesis of (+/-)-phomactin A

A total synthesis of the PAF antagonist phomactin A (1), isolated from the marine fungus Phoma sp. is described. The synthesis is based on a Cr(II)/Ni(II) macrocyclisation from the aldehyde vinyl iodide 14, leading to the key phomactatrienol intermediate 16a, followed by elaboration of 16a to the epoxyketone 21, which undergoes spontaneous pyran and hemiacetal ring formation to 1 on deprotection with DDQ.     

A total synthesis of phomactin A

A total synthesis of phomactin A (1) based on a Cr(II)/Ni(II) macrocyclisation from the aldehyde vinyl iodide 11, leading to 12, followed by elaboration of the epoxyketone 16, which then undergoes spontaneous pyran-hemiacetal formation on deprotection, is described.     

Synthesis of a tetraoxy-bis-nortaxadiene, en route to taxol, using a cascade radical cyclisation sequence

Concise syntheses of the substituted enynediones 28a, 33b and 36 starting from the cyclohexenealdehyde 18, corresponding to ring A in the taxanes, and the vinylstannane 24, are described. Treatment of 36 with Bu₃SnH-AIBN did not lead to the oxy-substituted taxadiene 37 expected from a tandem radical macrocyclisation-radical transannulation sequence; instead, a mixture of unidentified products resulted. When the PMB ether 33b corresponding to the alcohol 36 was treated with Bu₃SnH-AIBN under similar conditions, p-anisaldehyde was isolated, as a major by-product, but no evidence for the formation of a taxadiene could be observed. In contrast, the iododienynedione 41, i.e., deoxy 36, underwent a tandem radical macrocyclisation-transannulation sequence, when treated with Bu₃SnH-AIBN, leading to the tetraoxy-bis-nortaxadiene 42 in 44% yield. Attempts to synthesise the alcohol 28b from the silyl ether 28a en route to the iodide 28c instead gave the substituted tetrahydrofuran 29 via an intramolecular oxy-Michael reaction.