Synchronization of mode-locked femtosecond lasers through a fiber link

Two mode-locked femtosecond fiber lasers, connected via a 7 km fiber link, are synchronized to an rms timing jitter of 19 fs, observed over the entire Nyquist bandwidth (half of the 93 MHz repetition frequency). This result is achieved in two steps. First, active cancellation of the fiber-transmission noise reduces timing jitter caused by path length fluctuations to a record level of 16 fs. Second, using a wide bandwidth interactivity actuator, the slave laser is synchronized to the incoming stable pulse train from the reference laser to within 10 fs. These results are confirmed by an optical cross-correlation measurement performed independently of the feedback loop operated in the microwave domain.     

Flexible and rapidly configurable femtosecond pulse generation in the mid-IR

We demonstrate a new experimental approach for flexible femtosecond pulse generation in the mid-IR by use of difference-frequency generation from two tightly synchronized Ti:sapphire lasers. The resultant mid-IR pulse train can be easily tuned, with an adjustable repetition frequency up to 100 MHz, a pulse energy of approximately 1.5 x 10(-13) J, and an intensity noise similar to that of the Ti:sapphire. Rapid switching of the mid-IR wavelength and programmable amplitude modulation are achieved by precision setting of the time delay between two original pulses.     

Crystal structures of two one-dimensional coordination polymers constructed from Mn<Superscript>2+</Superscript> ions,chelating hexafluoro-acetylacetonate anions,and flexible bipyridyl bridging ligands

The syntheses and crystal structures of two one-dimensional coordination polymers, [Mn(C₅HO₂F₆)₂(C₁₆H₂₀N₂)] _n (1) and [Mn(C₅HO₂F₆)₂(C₂₀H₂₀N₂)] _n (2), are described, where C₅HO₂F₆ ^? is the hexafluoro acetylacetonate anion, C₁₆H₂₀N₂ is 1,6-bis(4-pyridyl)-hexane, and C₂₀H₂₀N₂ is 1,4-bis[2-(3-pyridyl)ethyl]-benzene. In both phases, the metal ion lies on a crystallographic twofold axis and is coordinated by two chelating C₅HO₂F₆ ^? anions and two bridging bipyridyl ligands to generate a cis-MnN₂O₄ octahedron. The bridging ligands, which are completed by crystallographic inversion symmetry in both compounds, connect the metal nodes into zigzag [20 1 ] chains in 1 and contorted [001] chains in 2. Intrachain C–H???O interactions occur in 1 but not in 2, which may be correlated with the relative orientations of the ligands. Crystal data: 1, C₂₆H₂₂F₁₂MnN₂O₄, M _r = 709.40, monoclinic, C2/c (No. 15), a = 9.3475(2) Å, b = 16.6547(3) Å, c = 18.3649(4) Å, β = 91.1135(8)°, V = 2858.50(10) ų, Z = 4, R(F) = 0.030, w R(F ²) = 0.075. 2, C₃₀H₂₂F₁₂MnN₂O₄, M _r = 757.44, monoclinic, C2/c (No. 15), a = 19.9198(2) Å, b = 10.6459(2) Å, c = 16.8185(3) Å, β = 119.8344(8)°, V = 3093.91(9) Å3, Z = 4, R(F) = 0.032, w R(F ²) = 0.078.     

Synthesis and crystal structure of [Mn(NCS)2L2] (L = 3,6-bis-(2-methylpyridyl)-1,2-pyridazine)

The synthesis and molecular structure of the title compound are reported. The metal ion has a distorted octahedral geometry and is coordinated by two cis thiocyanate nitrogens, two trans pyridine nitrogens and two cis pyridazine nitrogens. The structure has an orthorhombic space group Pbcn with a = 12.9376(6) Å, b = 13.4312(7) Å, c = 18.8992(9) Å, V = 3284.1(3) ų, and Z = 8.     

Mechanism of aerobic decomposition of Angeli's salt (sodium trioxodinitrate) at physiological pH

The recent determination that Angeli's salt may have clinical application as a nitrogen oxide donor for treatment of cardiovascular diseases such as heart failure has led to renewed interest in the mechanism and products of thermal decomposition of Angeli's salt under physiological conditions. In this report, several mechanisms are evaluated experimentally and by quantum mechanical calculations to determine whether HNO is in fact released from Angeli's salt in neutral, aerobic solution. The mechanism of product autoxidation is also considered.