Association between CMR-derived hepatic T1-time, tricuspid regurgitation and survival.

Background: Cardiac magnetic resonance (CMR) derived hepatic T1-time is associated with outcome. However, the interplay between tricuspid regurgitation (TR), which can cause congestive hepatopathy and liver T1-time is unclear.

Methods: We measured hepatic T1-time in CMR all-comers, who underwent echocardiography within 3 weeks of CMR.

Thermally-induced covalent coupling of cobalt porphyrin molecules on Au(111).

We investigated the thermally induced covalent coupling of cobalt porphyrin (CoP) molecules on an Au(111) surface using scanning tunnelling microscopy and first-principle calculations. While CoP molecules deposited at room temperature remain isolated due to electrostatic repulsion, annealing the substrate leads to their aggregation into chain-like structures with covalent bonding. Three distinct bonding motifs are identified, with calculations revealing weak magnetic coupling between theS=1/2Co ions.

Femtosecond Spin-State Switching Dynamics of Fe(II) Complexes Condensed in Thin Films.

The tailoring of spin-crossover films has made significant progress over the past decade, mostly motivated by the prospect in technological applications. In contrast to spin-crossover complexes in solution, the investigation of the ultrafast switching in spin-crossover films has remained scarce. Combining the progress in molecule synthesis and film growth with the opportunities at X-ray free-electron lasers, we study the photoinduced spin-state switching dynamics of a molecular film at room temperature.

Large Orbital Moment and Dynamical Jahn-Teller Effect of AlCl-Phthalocyanine on Cu(100).

Submonolayer amounts of chloroaluminum-phthalocyanine on Cu(100) were studied with scanning tunneling spectroscopy. The molecule can be prepared in a fourfold symmetric state whose conductance spectrum exhibits a zero-bias feature similar to a Kondo resonance. In magnetic fields, however, this resonance splits far more than expected from the spin of a single electron.

Spin-State Switching of Spin-Crossover Complexes on Cu(111) Evidenced by Spin-Flip Spectroscopy.

Spin-crossover compounds can be switched between two stable states with different magnetic moments, conformations, electronic, and optical properties, which opens appealing perspectives for technological applications including miniaturization down to the scale of single molecules. Although control of the spin states is crucial their direct identification is challenging in single-molecule experiments. Here we investigate the spin-crossover complex [Fe(HB(1,2,4-triazol-1-yl))] on a Cu(111) surface with scanning tunneling microscopy and density functional theory calculations.

Variable-temperature lightwave-driven scanning tunneling microscope with a compact, turn-key terahertz source.

We report on a lightwave-driven scanning tunneling microscope based on a home-built microscope and a compact, commercial, and cost-effective terahertz-generation unit with a repetition rate of 100 MHz. The measurements are performed in an ultrahigh vacuum at temperatures between 8.5 and 300 K.

Molybdenum(0)-Tricarbonyl Complex Supported by an Azacalix-pyridine Ligand: Synthesis, Characterization, Surface Deposition and Conversion to a Molybdenum(VI)-Trioxo Complex with O.

Adsorption of metal-organic complexes on metallic surfaces to produce well-defined single site catalysts is a novel approach combining the advantages of homogeneous and heterogeneous catalysis. To avoid the "surface trans-effect" a dome-shaped molybdenum(0) tricarbonyl complex supported by an tolylazacalix[3](2,6)pyridine ligand is synthesized. This vacuum-evaporable complex both activates CO and reacts with molecular oxygen (O) to form a Mo(VI) trioxo complex which in turn is capable of catalytically mediating oxygen transfer.

Spin-Crossover and Fragmentation of Fe(neoim) on Silver and Gold.

The neutral spin crossover complex Fe(neoim), neoim being the deprotonated form of the ionogenic ligand 2-(1-imidazol-2-yl)-9-methyl-1,10-phenanthroline (neoimH), is investigated on the (111) surfaces of Au and Ag using scanning tunneling microscopy and density functional theory calculations. The complex sublimates and adsorbs intact on Ag(111), where it exhibits an electron-induced spin crossover. However, it fragments on Au.

Defying the inverse energy gap law: a vacuum-evaporable Fe(ii) low-spin complex with a long-lived LIESST state.

The novel vacuum-evaporable complex [Fe(pypypyr)] (pypypyr = bipyridyl pyrrolide) was synthesised and analysed as bulk material and as a thin film. In both cases, the compound is in its low-spin state up to temperatures of at least 510 K. Thus, it is conventionally considered a pure low-spin compound.

Large Orbital Moment of Two Coupled Spin-Half Co Ions in a Complex on Gold.

The magnetic properties of transition-metal ions are generally described by the atomic spins of the ions and their exchange coupling. The orbital moment, usually largely quenched due the ligand field, is then seen as a perturbation. In such a scheme, = 1/2 ions are predicted to be isotropic.

Surgical Metastasectomy for Visceral and Bone Prostate Cancer Metastases: A Mini-Review.

Despite growing interest in metastasis-directed therapy (MDT) for prostate cancer (PCa), little is known regarding the feasibility and effectiveness of surgical metastasectomy for isolated lesions. We performed a narrative review of the available evidence supporting metastasectomy for M1b-c lesions in men diagnosed with oligometastatic or oligorecurrent PCa. The case series and case reports we identified indicate that surgical MDT is a safe and feasible treatment option for well-selected patients with a small number of PCa metastases diagnosed via molecular imaging.

Spin Crossover in a Cobalt Complex on Ag(111).

The Co-based complex [Co(H B(pz)(pypz)) ] (py=pyridine, pz=pyrazole) deposited on Ag(111) was investigated with scanning tunneling microscopy at ≈5 K. Due to a bis(tridentate) coordination sphere the molecules aggregate mainly into tetramers. Individual complexes in these tetramers undergo reversible transitions between two states with characteristic image contrasts when current is passed through them or one of their neighbors.

Electron-Induced Spin-Crossover in Self-Assembled Tetramers.

The spin crossover compound Fe(HB(pyrazole)(pyridylpyrazole)) was investigated in detail on Ag(111) with scanning tunneling microscopy (STM). A large fraction of the deposited molecules condenses into gridlike tetramers. Two molecules of each tetramer may be converted between two states by current injection.

Inducing and Controlling Molecular Magnetism through Supramolecular Manipulation.

Diamagnetic H phthalocyanine molecules are probed on superconducting Pb(100) using a low-temperature scanning tunneling micoscope (STM). In supramolecular arrays made with the STM, the molecules acquire a spin as detected the emergence of Yu-Shiba-Rusinov resonances. The spin moments vary among the molecules and are determined by the electrostatic field that results from polar bonds in the surrounding Pc molecules.

Iron in a Cage: Fixation of a Fe(II)tpy Complex by Fourfold Interlinking.

The coordination sphere of the Fe(II) terpyridine complex 1 is rigidified by fourfold interlinking of both terpyridine ligands. Profiting from an octa-aldehyde precursor complex, the ideal dimensions of the interlinking structures are determined by reversible Schiff-base formation, before irreversible Wittig olefination provided the rigidified complex. Reversed-phase HPLC enables the isolation of the all-trans isomer of the Fe(II) terpyridine complex 1, which is fully characterized.

Coverage-Controlled Superstructures of C -Symmetric Molecules: Honeycomb versus Hexagonal Tiling.

The competition between honeycomb and hexagonal tiling of molecular units can lead to large honeycomb superstructures on surfaces. Such superstructures exhibit pores that may be used as 2D templates for functional guest molecules. Honeycomb superstructures of molecules that comprise a C symmetric platform on Au(111) and Ag(111) surfaces are presented.

Rotation of Ethoxy and Ethyl Moieties on a Molecular Platform on Au(111).

Molecular rotors have attracted considerable interest for their prospects in nanotechnology. However, their adsorption on supporting substrates, where they may be addressed individually, usually modifies their properties. Here, we investigate the switching of two closely related three-state rotors mounted on platforms on Au(111) using low-temperature scanning tunneling microscopy and density functional theory calculations.

Reversible coordination-induced spin-state switching in complexes on metal surfaces.

Molecular spin switches are attractive candidates for controlling the spin polarization developing at the interface between molecules and magnetic metal surfaces, which is relevant for molecular spintronics devices. However, so far, intrinsic spin switches such as spin-crossover complexes have suffered from fragmentation or loss of functionality following adsorption on metal surfaces, with rare exceptions. Robust metal-organic platforms, on the other hand, rely on external axial ligands to induce spin switching.

Spin in a Closed-Shell Organic Molecule on a Metal Substrate Generated by a Sigmatropic Reaction.

Inert metal surfaces present more chances of hosting organic intact radicals than other substrates, but large amounts of delocalized electronic states favor charge transfer and thus spin quenching. Lowering the molecule-substrate interaction is a usual strategy to stabilize radicals on surfaces. In some works, thin insulating layers were introduced to provide a controllable degree of electronic decoupling.

The Kondo resonance line shape in scanning tunnelling spectroscopy: instrumental aspects.

In the scanning tunnelling microscope, the many-body Kondo effect leads to a zero-bias feature of the differential conductance spectra of magnetic adsorbates on surfaces. The intrinsic line shape of this Kondo resonance and its temperature dependence in principle contain valuable information. We use measurements on a molecular Kondo system, all- trans retinoic acid on Au(1 1 1), and model calculations to discuss the role of instrumental broadening.

Disentangling Magnetic Hardening and Molecular Spin Chain Contributions to Exchange Bias in Ferromagnet/Molecule Bilayers.

We performed ferromagnetic resonance and magnetometry experiments to clarify the relationship between two reported magnetic exchange effects arising from interfacial spin-polarized charge transfer in ferromagnetic metal (FM)/molecule bilayers: the magnetic hardening effect and spinterface-stabilized molecular spin chains. To disentangle these effects, we tuned the metal phthalocyanine molecule central site's magnetic moment to enhance or suppress the formation of spin chains in the molecular film. We find that both effects are distinct, and additive.

Scale-Up of Innovative Honeycomb Reactors for Power-to-Gas Applications - The Project Store&Go.

The German "Energiewende" is heavily based on electric power and, therefore, requests solutions to serve non-electric energy uses and to store electric energy in large scale. Synthetic natural gas (SNG) produced with hydrogen from water electrolysis and with CO from mainly renewable sources is one approach. For the catalytic SNG production efficient removal and utilization of the reaction heat is the main issue.

Light-Induced Spin Crossover in an Fe(II) Low-Spin Complex Enabled by Surface Adsorption.

Understanding and controlling the spin-crossover properties of molecular complexes can be of particular interest for potential applications in molecular spintronics. Using near-edge X-ray absorption fine structure spectroscopy, we investigated these properties for a new vacuum-evaporable Fe(II) complex, namely [Fe(pypyr(CF))(phen)] (pypyr = 2-(2'-pyridyl)pyrrolide, phen = 1,10-phenanthroline). We find that the spin-transition temperature, well above room temperature for the bulk compound, is drastically lowered for molecules arranged in thin films.

Ligand-Induced Energy Shift and Localization of Kondo Resonances in Cobalt-Based Complexes on Cu(111).

Magnetic sandwich complexes are of particular interest for molecular spintronics. Using scanning tunneling microscopy, we evidence the successful deposition of 1,3,5-tris(η-borabenzene-η-cyclopentadienylcobalt) benzene, a molecule composed of three connected magnetic sandwich units, on Cu(111). Scanning tunneling spectra reveal two distinct spatial-dependent narrow resonances close to the Fermi level for the trimer molecules as well as for molecular fragments composed of one and two magnetic units.