Synthesis, structure and properties of SrAu3In3 and EuAu3In3—New indides with gold zig-zag chains

New indides SrAu₃In₃ and EuAu₃In₃ were synthesized by induction melting of the elements in sealed tantalum tubes. Both indides were characterized by X-ray diffraction on powders and single crystals. They crystallize with a new orthorhombic structure type: Pmmn, Z=2, a=455.26(9), b=775.9(2), c=904.9(2) pm, wR2=0.0425, 485 F² values for SrAu₃In₃ and a=454.2(2), b=768.1(6), c=907.3(6) pm, wR2=0.0495, 551 F² values for EuAu₃In₃ with 26 variables for each refinement. The gold and indium atoms build up three-dimensional [Au₃In₃] polyanionic networks, which leave distorted hexagonal channels for the strontium and europium atoms. Within the networks one observes Au2 atoms without Au-Au contacts and gold zig-zag chains (279 pm Au1-Au1 in EuAu₃In₃). The Au-In and In-In distances in EuAu₃In₃ range from 270 to 290 and from 305 to 355 pm. The europium atoms within the distorted hexagonal channels have coordination number 14 (8 Au+6 In). EuAu₃In₃ shows Curie-Weiss behavior above 50 K with an experimental magnetic moment of 8.1(1) μB/Eu atom. ¹⁵¹Eu Mössbauer spectra show a single signal at δ=−11.31(1) mm/s, compatible with divalent europium. No magnetic ordering was detected down to 3 K.     

Negative magnetoresistance in Cr-containing diamond-like carbon-based heterostructures

We have characterized the local structure around the Cr atom, as a function of Cr content, in films of chromium-doped hydrogenated amorphous diamond-like carbon (Cr-DLC) synthesized by plasma-enhanced chemical vapor deposition (PECVD). The composition appears to be related to the structure and forward bias magnetoresistance in heterojunction devices. Chromium in diamond-like carbon (DLC) has a chemical state much like chromium carbide and, at low Cr content, the Cr is dissolved in an amorphous DLC matrix forming an atomic-scale composite. At higher Cr content, Cr is present as nano-composite and chromium carbide precipitates preferentially form at the surface of the film. In these films of higher chromium concentration, a large coefficient of negative magnetoresistance is observed in heterojunction devices with n-type silicon.     

Bi-Poisson Structures and Integrability of Geodesic Flow on Homogeneous Spaces

Let G/K be a semisimple orbit of the adjoint representation of a real connected reductive Lie group G. Let K₁ be any closed subgroup of K containing the commutant of the identity component of K. We prove that the geodesic flow on the symplectic manifold T*(G/K₁), corresponding to a G-invariant pseudo-Riemannian metric on G/K₁ which is induced by a bi-invariant pseudo-Riemannian metric on G, is completely integrable in the class of real analytic functions, polynomial in momenta. To this end we study the Poisson geometry of the space of G-invariant functions on T*(G/K) using a one-parameter family of moment maps.     

A total synthesis of (±)-dihydropalustrine

Dihydropalustrine has been synthesized by a β-lactam-imino ether coupling route. A dehydro precursor previously considered to represent palustrine has now been shown to be nonidentical with the natural product.     

Gd-doping of HfO2

An increase in the density of states between the oxygen 2p bands and the Fermi level is seen with increasing Gd concentrations. In addition, for the Gd-doped HfO₂ films, the Gd 4f photoexcitation peak at 5.5 eV below the valence band maximum was identified using resonant photoemission. Electrical measurements show pronounced rectification properties for lightly-doped Gd:HfO₂ films on p-Si and for heavily-doped Gd:HfO₂ films on n-Si, suggesting a crossover from n-type to p-type behavior with increasing doping level. In addition, there is an increase in the reverse bias current with neutron irradiation.     

Infinite Gold Zig‐Zag Chains as Structural Motif in Ca3Au3In – A Ternary Ordered Variant of the Ni4B3 Type

New auride Ca₃Au₃In was synthesized from the elements in a sealed tantalum tube in a high‐frequency furnace. Ca₃Au₃In was investigated by X‐ray powder and single crystal diffraction: ordered Ni₄B₃ type, Pnma, a = 1664.1(6), b = 457.3(2), c = 895.0(3) pm, wR2 = 0.0488, 1361 F² values, and 44 variables. The three crystallographically independent boron positions of the Ni₄B₃ type are occupied by the gold atoms, while the four nickel sites are occupied by calcium and indium in an ordered manner. All gold atoms have trigonal prismatic coordination, i.e. Ca₆ prisms for Au1 and Au2 and Ca₄In₂ prisms for Au3. While the Au3 atoms are isolated, we observe Au1–Au1 and Au2–Au2 zig‐zag chains at Au–Au distances of 292 and 284 pm. These slabs resemble the CrB type structure of CaAu. Consequently Ca₃Au₃In can be considered as a ternary auride. Together the Au2, Au3 and indium atoms build up a three‐dimensional [Au₂In] polyanionic network (281–293 pm Au–In) in which the chains of Au1 centered trigonal prisms are embedded. The crystal chemical similarities with the structures of Ni₄B₃, CaAuIn, and CaAu are discussed.     

Nonwettable thin films from hybrid polymer brushes can be hydrophilic

Hybrid brushes composed of two liquid polymers, poly(dimethylsiloxane) (PDMS) and a highly branched ethoxylated polyethylenimine (EPEI), were synthesized on Si wafers by the "grafting to" method and by applying a combinatorial approach (fabrication of gradient brushes). The combinatorial approach revealed a strong effect of "layer assisted tethering", which allowed us to synthesize hybrid brushes twice as thick as the reference homopolymer brushes. The hybrid brushes are stable thin films that can rapidly and reversibly switch between hydrophilic and hydrophobic states in water and air, respectively. The switching in water affects a rapid release of amino functional groups which can be used to regulate adhesion and reactivity of the material. The switching in air rapidly returns the brush to a hydrophobic state. The hybrid brush is hydrophilic because of two mechanisms: (1) exposure of EPEI chains to the brush-water interface under water, and (2) retention of some fraction of water via swollen EPEI chains (the EPEI chains swell by 2-3 times), which are conserved by a PDMS cap in air. The hybrid brush is wettable under water, and at the same time, the brush is nonwettable in air because water droplets are trapped in a metastable state when the water contact angle is above 90 degrees .     

An electrochemical gate based on a stimuli-responsive membrane associated with an electrode surface

The electrochemical gate based on a chemical signal-responsive membrane was assembled on a Au electrode surface. The polyelectrolyte gel membrane was capable to bind cholesterol because of the hydrogen bonding between cholesterol and the polymer backbone resulting in the gel swelling. The membrane channels were reversibly closed and opened upon addition and washing out cholesterol, respectively. Thus, the electrochemical process of a soluble redox probe, [Fe(CN)(6)](3-/4-), at the membrane-modified electrode was reversibly switched "on-off" by the cyclic addition and washing out cholesterol. The electrochemical reaction was also tuned by the variation of the concentration of the added cholesterol that controlled the extent of the channels closing. The switchable and tuneable operation of the chemically controlled electrochemical gate was characterized by Faradaic impedance spectroscopy and atomic force microscopy, indicating that the extent of the pores opening and closing is controlled by the concentration of the membrane-associated cholesterol. The chemical-responsive electrochemical gate was suggested to be a part of future biochemical/electrochemical systems with logic operations.