@article{37959,
  abstract     = {{<jats:p>Catalytic nucleophilic substitution of alcohols makes organic synthesis greener</jats:p>}},
  author       = {{Longwitz, Lars and Werner, Thomas}},
  issn         = {{0036-8075}},
  journal      = {{Science}},
  keywords     = {{T2, CSSD}},
  number       = {{6456}},
  pages        = {{866--867}},
  publisher    = {{American Association for the Advancement of Science (AAAS)}},
  title        = {{{The Mitsunobu reaction, reimagined}}},
  doi          = {{10.1126/science.aay6635}},
  volume       = {{365}},
  year         = {{2019}},
}

@article{10013,
  abstract     = {{<jats:p>Ultrafast nonequilibrium dynamics offer a route to study the microscopic interactions that govern macroscopic behavior. In particular, photoinduced phase transitions (PIPTs) in solids provide a test case for how forces, and the resulting atomic motion along a reaction coordinate, originate from a nonequilibrium population of excited electronic states. Using femtosecond photoemission, we obtain access to the transient electronic structure during an ultrafast PIPT in a model system: indium nanowires on a silicon(111) surface. We uncover a detailed reaction pathway, allowing a direct comparison with the dynamics predicted by ab initio simulations. This further reveals the crucial role played by localized photoholes in shaping the potential energy landscape and enables a combined momentum- and real-space description of PIPTs, including the ultrafast formation of chemical bonds.</jats:p>}},
  author       = {{Nicholson, C. W. and Lücke, A. and Schmidt, Wolf Gero and Puppin, M. and Rettig, L. and Ernstorfer, R. and Wolf, M.}},
  issn         = {{0036-8075}},
  journal      = {{Science}},
  pages        = {{821--825}},
  title        = {{{Beyond the molecular movie: Dynamics of bands and bonds during a photoinduced phase transition}}},
  doi          = {{10.1126/science.aar4183}},
  year         = {{2018}},
}

@article{40173,
  abstract     = {{<jats:title>Here, There, Everywhere</jats:title>
          <jats:p>
            Random walks are a powerful mathematical method that can be used to simulate certain processes in biology, chemistry, or even the stock market. They present a statistical method for mapping the possible routes that processes can take. Quantum walks are expected to be able to probe multiple paths simultaneously. Quantum walks have been demonstrated for one-dimensional, or straight-line, walks. Now,
            <jats:bold>
              Schreiber
              <jats:italic>et al.</jats:italic>
            </jats:bold>
            (p.
            <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" page="55" related-article-type="in-this-issue" vol="336" xlink:href="10.1126/science.1218448">55</jats:related-article>
            , published online 8 March) demonstrate an optical system that can simulate quantum walks over a two-dimensional system, thereby providing the capability of describing much more complex processes.
          </jats:p>}},
  author       = {{Schreiber, Andreas and Gábris, Aurél and Rohde, Peter P. and Laiho, Kaisa and Štefaňák, Martin and Potoček, Václav and Hamilton, Craig and Jex, Igor and Silberhorn, Christine}},
  issn         = {{0036-8075}},
  journal      = {{Science}},
  keywords     = {{Multidisciplinary}},
  number       = {{6077}},
  pages        = {{55--58}},
  publisher    = {{American Association for the Advancement of Science (AAAS)}},
  title        = {{{A 2D Quantum Walk Simulation of Two-Particle Dynamics}}},
  doi          = {{10.1126/science.1218448}},
  volume       = {{336}},
  year         = {{2012}},
}

@article{8633,
  author       = {{Greilich, A. and Shabaev, A. and Yakovlev, D. R. and Efros, Al. L. and Yugova, I. A. and Reuter, Dirk and Wieck, A. D. and Bayer, M.}},
  issn         = {{0036-8075}},
  journal      = {{Science}},
  pages        = {{1896--1899}},
  title        = {{{Nuclei-Induced Frequency Focusing of Electron Spin Coherence}}},
  doi          = {{10.1126/science.1146850}},
  year         = {{2007}},
}

@article{23488,
  abstract     = {{Studies of current dynamics in solids have been hindered by insufficiently brief trigger signals and electronic detection speeds. By combining a coherent control scheme with photoelectron spectroscopy, we generated and detected lateral electron currents at a metal surface on a femtosecond time scale with a contact-free experimental setup. We used coherent optical excitation at the light frequencies ωa and ωa/2 to induce the current, whose direction was controlled by the relative phase between the phase-locked laser excitation pulses. Time- and angle-resolved photoelectron spectroscopy afforded a direct image of the momentum distribution of the excited electrons as a function of time. For the first (n = 1) image-potential state of Cu(100), we found a decay time of 10 femtoseconds, attributable to electron scattering with steps and surface defects.}},
  author       = {{Gudde, J. and Rohleder, M. and Meier, Torsten and Koch, S. W. and Hofer, U.}},
  issn         = {{0036-8075}},
  journal      = {{Science}},
  number       = {{5854}},
  pages        = {{1287--1291}},
  title        = {{{Time-Resolved Investigation of Coherently Controlled Electric Currents at a Metal Surface}}},
  doi          = {{10.1126/science.1146764}},
  volume       = {{318}},
  year         = {{2007}},
}

@article{48999,
  abstract     = {{<jats:p>The fast dephasing of electron spins in an ensemble of quantum dots is detrimental for applications in quantum information processing. We show here that dephasing can be overcome by using a periodic train of light pulses to synchronize the phases of the precessing spins, and we demonstrate this effect in an ensemble of singly charged (In,Ga)As/GaAs quantum dots. This mode locking leads to constructive interference of contributions to Faraday rotation and presents potential applications based on robust quantum coherence within an ensemble of dots.</jats:p>}},
  author       = {{Greilich, A. and Yakovlev, D. R. and Shabaev, A. and Efros, Al. L. and Yugova, I. A. and Oulton, R. and Stavarache, V. and Reuter, Dirk and Wieck, A. and Bayer, M.}},
  issn         = {{0036-8075}},
  journal      = {{Science}},
  keywords     = {{Multidisciplinary}},
  number       = {{5785}},
  pages        = {{341--345}},
  publisher    = {{American Association for the Advancement of Science (AAAS)}},
  title        = {{{Mode Locking of Electron Spin Coherences in Singly Charged Quantum Dots}}},
  doi          = {{10.1126/science.1128215}},
  volume       = {{313}},
  year         = {{2006}},
}

