An efficient synthesis of acetylide/trimetal/acetylide molecular wires

Efficient syntheses are reported for incorporating trimetal units of the type M(3)(dpa)(4)(2+) (M = Cr, Co, Ni, and dpa = 2,2'-dipyridylamide) into polyalkynyl assemblies to give the prototypical bis-phenylacetylide complexes M(3)(dpa)(4)(CCPh)(2). Reactions of M(3)(dpa)(4)Cl(2) with LiCCPh have led only to mixtures of products which cocrystallize forming materials of the composition M(3)(dpa)(4)(CCPh)(x)()Cl(2)(-)(x)(). Here we report that acetonitrile complexes [M(3)(dpa)(4)(NCCH(3))(2)](PF(6))(2) react cleanly with LiCCPh in MeCN to afford the desired target molecules in 40-60% yield and in excellent purity. Isolation of the mixed ligand complex [Co(3)(dpa)(4)(NCCH(3))(CCPh)]PF(6) has been accomplished, which suggests that these reactions are stepwise and that it will be possible to synthesize mixed acetylide complexes (i.e., M(3)(dpa)(4)(CCR)(CCR')) via this method.     

Extensions of automorphisms and gauge symmetries

We characterize the automorphisms of aC ^*-algebra which extend to automorphisms of the crossed product by a compact group dual. The case where the inclusion is equipped with a group of automorphisms commuting with the dual action is also treated. These results are applied to the analysis of broken gauge symmetries in Quantum Field Theory to draw conclusions on the structure of the degenerate vacua on the field algebra.Dedicated to Huzihiro ArakiResearch supported by MURST and CNR, GNAFA     

Generation of 250 mW narrowband pulsed ultraviolet light by frequency quadrupling of an amplified erbium-doped fiber laser

We demonstrate a high-power, narrowband pulsed source at 390 nm by two stages of frequency doubling in periodically poled MgO:LiNbO(3) and periodically poled KTiOPO(4) of an amplified, passively mode-locked fiber laser. With a frequency quadrupling efficiency of 5.5% and a 0.1 nm bandwidth, the 250 mW ultraviolet source is a suitable compact pump source for many entanglement-based quantum information processing tasks.     

On the photoelectron spectrum of sulphur trioxide

He(I), He(II) and variable temperature Ne(I) photoelectron spectra of sulphur trioxide are reported. All six of the expected ionic states have been detected and assigned; the assignment differs from a previous one. Ab initio calculations in a medium basis set have been carried out and spectral intensities have been calculated; agreement between the calculations and the spectra is good. The calculations show a substantial S(3d) character in the S-O bond, and the spectra are consistent with this.