100-Gb/s undersea transmission with high spectral efficiency using pre-filtered QPSK modulation format

We provide a review of our recent 100-Gb/s, high spectral efficiency (SE) experiment targeting transoceanic and regional undersea transmission distances. We demonstrated that simple pre-filtering at the transmitter together with a maximum a posteriori probability (MAP) detection algorithm can significantly improve SE. We transmitted 96×100-Gb/s pre-filtered polarization division multiplexed return-to-zero quadrature phase shift keyed (PDM-RZ-QPSK) channels with 300% SE over 10608 km using 52-km spans of 150-μm 2 fiber and simple single-stage erbium-doped fiber amplifiers (EDFAs). We also achieved 400% SE over 4368 km using similar techniques.     

Magnetism and superconductivity in ErNi2B2C

We have performed a series of neutron diffraction experiments from the magnetic order and the vortex lattice in single crystal ErNi₂B₂C. The incommensurate magnetic structure develops additional even harmonics below the ‘ferromagnetic’ ordering temperature, T _F of 2.3 K. This feature and the existence of rods of diffuse scattering suggest the development of ferromagnetic microdomain walls. The magnetic structure is very sensitive to the application of a magnetic field with changes in modulation vector and harmonic content. Studies of the vortex lattice show the presence of a 45° reorientation transition and a distorted hexagonal to square transition as a function of applied field. Further distortions of the vortex lattice occur at T _N, but no changes are seen at T _F.     

5]Pericyclynes Are Not Homoaromatic

[5]Pericyclynes were investigated at high ab initio and density functional levels. On the basis of the geometric, energetic, and magnetic criteria of aromaticity, [5]pericyclynes are not homoaromatic despite their intriguing structure. The strain energy of [5]pericyclynes is negligible.     

Structure and formation of gaseous [C4H5O]+ ions. IV—Ions derived from the cyclopropenium ion [C3H3]+

Characterization of [C₄H₅O]⁺ ions in the gas phase using their metastable ion and collisional activation spectra shows that the three isomeric ions HC?C? \documentclass{article}\pagestyle{empty}\begin{document}$ \mathop {\rm C}\limits^{\rm + } $\end{document}H? OCH₃, CH₃O? \documentclass{article}\pagestyle{empty}\begin{document}$ \mathop {\rm C}\limits^{\rm + } $\end{document}?C?CH₂ and ? OCH₃ related to the two stable [C₃H₃]⁺ cations [HC?C? CH₂]⁺ and are stable for ≥ 10^?5s. In contrast to the formation of cyclopropenium ions, it is found that the methoxy cyclopropenium ion is not generated from acyclic precursor molecules. The small but significant intensity differences found in the collisional activation spectra of [C₃H₃]⁺ ions generated from HC?C? CH₂I and HC?C? CH₂Cl possibly indicate the presence of [C₃H₃]⁺ ions of different structures.     

Evidence for associative ligand exchange processes on solvated lithium cations

The ligand exchange mechanism of solvated lithium cations has been studied using DFT calculations (RB3LYP/6-311+G**). The water exchange mechanism on [Li(H(2)O)(4)](+) was found to be limiting associative (A) involving a five-coordinate intermediate, whereas ammonia exchange on [Li(NH(3))(4)](+) was found to follow an associative interchange (I(a)) mechanism. The suggested mechanisms are discussed in reference to available experimental and theoretical data.