Towards the Description of Core-Excited States within the Framework of Many-Body Perturbation Theory

Gegenstand dieser Arbeit ist die Entwicklung effizienter und robuster Methoden zur Beschreibung von Ladungs- und ladungsneutralen Anregungen von kernnahen Zuständen in molekularen Systemen mittels Vielteilchen-Störungstheorie. Um auch die Anwendbarkeit auf Systeme, die schwere Elemente beinhalten, zu gewährleisten, wird der Formalismus in einem zwei-komponentigen Kramers-symmetrischen Rahmen präsentiert. Dies erlaubt neben skalarrelativistischen Effekten auch die explizite Beschreibung der Spin-Bahn-Wechselwirkung. Die erarbeiteten Ansätze bleiben jedoch auch im ein-komponentigen, nichtrelativistischen Grenzfall gültig. Es wird eine neue Methode zur Berechnung von Quasiteilchenenergien in der GW-Näherung vorgestellt und bewertet. Dabei wird die Beschreibung von Ladungsanregungen, den Ionisierungsenergien und Elektronenaffinitäten, gleichermaßen für Valenz- und Rumpfelektronen ermöglicht. Diese Technik verringert gerade für die letztere Anwendung den Aufwand drastisch im Vergleich zu etablierten Methoden und besitzt zudem auch Vorteile für Systeme mit einer hohen Zustandsdichte. Die so erhaltenen Quasiteilchenenergien werden im Weiteren als Ausgangspunkt zur Berechnung von ladungsneutralen Anregungen, wie sie zur Beschreibung von Experimenten aus der Röntgenabsorptionsspektroskopie benötigt werden, mittels der Bethe-Salpeter Gleichung verwendet. Es werden zwei Ansätze diskutiert, die bereits im Rahmen der Dichtefunktionaltheorie und post-Hartree–Fock Methoden bekannt sind. Erstere folgt der gedämpften linearen Antworttheorie und führt eine künstliche Lebenszeit für angeregte Zustände ein. Dies ermöglicht die Berechnung dynamischer Polarisierbarkeiten für beliebige Frequenzen. Die zweite Methode nutzt die schwache Kopplung zwischen den Anregungen rumpfnaher und Valenzelektronen in der elektronischen Hesse-Matrix. Das Problem wird in einem entsprechenden Unterraum der Einfachanregungen von Rumpfelektronen gelöst. Beide Methoden werden im Folgenden zusammen mit den entsprechenden Implementierungen vorgestellt und auf die Möglichkeit zur Beschreibung von Anregungen von kernnahen Elektronen bewertet. Die Ergebnisse werden mit weiteren Methoden, sowie experimentellen Daten verglichen, und auf reale Fragestellungen angewandt

Robust relativistic many-body Green’s function based approaches for assessing core ionized and excited states

A two-component contour deformation (CD) based GW method that employs frequency sampling to drastically reduce the computational effort when assessing quasiparticle states far away from the Fermi level is outlined. Compared to the canonical CD-GW method, computational scaling is reduced by an order of magnitude without sacrificing accuracy. This allows for an efficient calculation of core ionization energies. The improved computational efficiency is used to provide benchmarks for core ionized states, comparing the performance of 15 density functional approximations as Kohn–Sham starting points for GW calculations on a set of 65 core ionization energies of 32 small molecules. Contrary to valence states, GW calculations on core states prefer functionals with only a moderate amount of Hartree–Fock exchange. Moreover, modern ab initio local hybrid functionals are also shown to provide excellent generalized Kohn–Sham references for core GW calculations. Furthermore, the core–valence separated Bethe–Salpeter equation (CVS-BSE) is outlined. CVS-BSE is a convenient tool to probe core excited states. The latter is tested on a set of 40 core excitations of eight small inorganic molecules. Results from the CVS-BSE method for excitation energies and the corresponding absorption cross sections are found to be in excellent agreement with those of reference damped response BSE calculations

Bi- and trinuclear coinage metal complexes of a PNNP ligand featuring metallophilic interactions and an unusual charge separation

A selective synthesis of bi- and trinuclear complexes featuring a tetradentate monoanionic PNNP ligand is presented. The binuclear coinage metal complexes show a typical fourfold coordination for Cu and Ag, which changes to a bifold coordination for Au. The latter is accompanied by an unusual charge separation. Optical properties are investigated using photoluminescence spectroscopy and complemented by time-dependent density-functional-theory calculations. All compounds demonstrate clearly distinguished features dependent on the metals chosen and differences in the complex scaffold

Tissue factor pathway inhibitor-2 is a novel inhibitor of matrix metalloproteinases with implications for atherosclerosis

Degradation of ECM, particularly interstitial collagen, promotes plaque instability, rendering atheroma prone to rupture. Previous studies implicated matrix metalloproteinases (MMPs) in these processes, suggesting that dysregulated MMP activity, probably due to imbalance with endogenous inhibitors, promotes complications of atherosclerosis. We report here that the serine proteinase inhibitor tissue factor pathway inhibitor-2 (TFPI-2) can function as an MMP inhibitor. TFPI-2 diminished the ability of the interstitial collagenases MMP-1 and MMP-13 to degrade triple-helical collagen, the primary load-bearing molecule of the ECM within human atheroma. In addition, TFPI-2 also reduced the activity of the gelatinases MMP-2 and MMP-9. In contrast to the "classical" tissue inhibitors of MMPs (TIMPs), TFPI-2 expression in situ correlated inversely with MMP levels in human atheroma. TFPI-2 colocalized primarily with smooth muscle cells in the normal media as well as the plaque's fibrous cap. Conversely, the macrophage-enriched shoulder region, the prototypical site of matrix degradation and plaque rupture, stained only weakly for TFPI-2 but intensely for gelatinases and interstitial collagenases. Evidently, human mononuclear phagocytes, an abundant source of MMPs within human atheroma, lost their ability to express this inhibitor during differentiation in vitro. These findings establish a new, anti-inflammatory function of TFPI-2 of potential pathophysiological significance for human diseases, including atherosclerosis

Bright Luminescence in Three Phases—A Combined Synthetic, Spectroscopic and Theoretical Approach

Combining phase-dependent photoluminescence (PL) measurements and quantum chemical calculations is a powerful approach to help understand the influence of the molecular surroundings on the PL properties. Herein, a phosphine functionalized amidinate was used to synthesize a recently presented bimetallic gold complex, featuring an unusual charge separation. The latter was subsequently used as metalloligand to yield heterotetrametallic complexes with an Au-M-M-Au “molecular wire” arrangement (M=Cu, Ag, Au) featuring metallophilic interactions. All compounds show bright phosphorescence in the solid state, also at ambient temperature. The effect of the molecular environment on the PL was studied in detail for these tetrametallic complexes by comparative measurements in solution, in the solid state and in the gas phase and contrasted to time-dependent density functional theory computations

Law Libraries and Laboratories: The Legacies of Langdell and His Metaphor

Law Librarians and others have often referred to Harvard Law School Dean C.C. Langdell’s statements that the law library is the lawyer’s laboratory. Professor Danner examines the context of what Langdell through his other writings, the educational environment at Harvard in the late nineteenth century, and the changing perceptions of university libraries generally. He then considers how the “laboratory metaphor” has been applied by librarians and legal scholars during the twentieth century and into the twenty-first. The article closes with thoughts on Langdell’s legacy for law librarians and the usefulness of the laboratory metaphor

Paradoxical enhancement of chemoreceptor detection sensitivity by a sensory adaptation enzyme

A sensory adaptation system that tunes chemoreceptor sensitivity enables motile Escherichia coli cells to track chemical gradients with high sensitivity over a wide dynamic range. Sensory adaptation involves feedback control of covalent receptor modifications by two enzymes: CheR, a methyltransferase, and CheB, a methylesterase. This study describes a CheR function that opposes the signaling consequences of its catalytic activity. In the presence of CheR, a variety of mutant serine chemoreceptors displayed up to 40-fold enhanced detection sensitivity to chemoeffector stimuli. This response enhancement effect did not require the known catalytic activity of CheR, but did involve a binding interaction between CheR and receptor molecules. Response enhancement was maximal at low CheR:receptor stoichiometry and quantitative analyses argued against a reversible binding interaction that simply shifts the ON-OFF equilibrium of receptor signaling complexes. Rather, a short-lived CheR binding interaction appears to promote a long-lasting change in receptor molecules, either a covalent modification or conformation that enhances their response to attractant ligands

The Tim54p–Tim22p Complex Mediates Insertion of Proteins into the Mitochondrial Inner Membrane

We have identified a new protein, Tim54p, located in the yeast mitochondrial inner membrane. Tim54p is an essential import component, required for the insertion of at least two polytopic proteins into the inner membrane, but not for the translocation of precursors into the matrix. Several observations suggest that Tim54p and Tim22p are part of a protein complex in the inner membrane distinct from the previously characterized Tim23p-Tim17p complex. First, multiple copies of the TIM22 gene, but not TIM23 or TIM17, suppress the growth defect of a tim54-1 temperature-sensitive mutant. Second, Tim22p can be coprecipitated with Tim54p from detergent-solubilized mitochondria, but Tim54p and Tim22p do not interact with either Tim23p or Tim17p. Finally, the tim54-1 mutation destabilizes the Tim22 protein, but not Tim23p or Tim17p. Our results support the idea that the mitochondrial inner membrane carries two independent import complexes: one required for the translocation of proteins across the inner membrane (Tim23p–Tim17p), and the other required for the insertion of proteins into the inner membrane (Tim54p–Tim22p)