28 research outputs found

    Geomorphic Response of the Sandy River, Oregon, Following Removal of Marmot Dam

    No full text
    The October 2007 breaching of a temporary cofferdam constructed during removal of the 15-meter (m)-tall Marmot Dam on the Sandy River, Oregon, triggered a rapid sequence of fluvial responses as ~730,000 cubic meters (m3) of sand and gravel filling the former reservoir became available to a high-gradient river. Using direct measurements of sediment transport, photogrammetry, airborne light detection and ranging (lidar) surveys, and, between transport events, repeat ground surveys of the reservoir reach and channel downstream, we monitored the erosion, transport, and deposition of this sediment in the hours, days, and months following breaching of the cofferdam

    Ground- and Excited-State Structure and Spin State of a Nickel-Bipyridine Photocatalyst Revealed by X-ray Absorption Spectroscopy

    No full text
    Photo-assisted catalysis using Ni complexes is an emerging field for cross-coupling reactions in organic synthesis. However, the mechanism by which light enables and enhances reactivity of these complexes often remains elusive. Although optical techniques have been widely used to study the ground and excited states of photocatalysts, they lack the specificity to interrogate the electronic and structural changes at specific atoms. Herein we report metal-specific studies using static and transient Ni L- and K-edge X-ray absorption spectroscopy of a prototypical Ni photocatalyst, (dtbbpy)Ni(o-tol)Cl (dtb = 4,4-di-tert-butyl, o-tol = ortho-tolyl). We discovered that the ground state of this complex has a mixed-spin character of ~70/30% singlet/triplet. Furthermore, we confirm that the long-lived (~5 ns) excited state is a tetrahedral metal-centered triplet state. These results pave the way for the future design of Ni-bipyridine based photocatalysts by, for example, judiciously tuning the electronic and geometric properties of the ligands with the goal of increasing excited-state lifetimes and quantum yields of reactive species
    corecore