Electrochemical scanning tunnelling spectroscopy of a ferrocene-modified n-Si(111)-surface: electrolyte gating and ambipolar FET behaviour

As revealed for the first time by in situ scanning tunnelling spectroscopy (STS), ferrocene-modified Si(111) substrates show ambipolar field effect transistor (FET) behaviour upon electrolyte gating.     

Fluorescence of semiconductor nanorods in liquid-crystal composites

The fluorescence of CdSe/ZnS nanorods in liquid-crystal and anisotropic polymer composites is studied. A high degree of the fluorescence anisotropy is shown. It is found that a solubilizer strongly affects the CdSe/ZnS orientation, which opens new possibilities for creating electrically controlled liquid-crystal composites.     

Image of the Spectral Measure of a Jacobi Field and the Corresponding Operators

By definition, a Jacobi field is a family of commuting selfadjoint three-diagonal operators in the Fock space The operators J(ϕ) are indexed by the vectors of a real Hilbert space H₊. The spectral measure ρ of the field J is defined on the space H₋ of functionals over H₊. The image of the measure ρ under a mapping is a probability measure ρ_K on T₋. We obtain a family J_K of operators whose spectral measure is equal to ρ_K. We also obtain the chaotic decomposition for the space L²(T₋, d_{ρ K}).     

On diagonal actions of branch groups and the corresponding characters

We introduce notions of absolutely non-free and perfectly non-free group actions and use them to study the associated unitary representations. We show that every weakly branch group acting on a regular rooted tree acts absolutely non-freely on the boundary of the tree. Using this result and the symmetrized diagonal actions we construct for every countable branch group infinitely many different ergodic perfectly non-free actions, infinitely many II₁-factor representations, and infinitely many continuous ergodic invariant random subgroups.     

New approach to the synthesis of substituted 7H‐furo[3,2‐b]pyran‐7‐ones based on 5‐hydroxy‐2‐methyl‐4H‐pyran‐4‐one derivatives

A convenient approach to the synthesis of the previously unknown 7H‐furo[3,2‐b]pyran‐7‐ones based on the intramolecular cyclization of carbonyl derivatives of 5‐hydroxy‐2‐methyl‐4H‐pyran‐4‐one has been elaborated. Key intermediates in the synthesis of the target 7H‐furo[3,2‐b]pyran‐7‐ones are 3‐hydroxy‐6‐methyl‐2‐(2‐oxo‐2‐arylethyl)‐4H‐pyran‐4‐ones. They are formed as a result of multicomponent condensation of 5‐hydroxy‐2‐methyl‐4H‐pyran‐4‐one with arylglyoxals and 4‐methoxyaniline.     

A Novel Niobium Cluster Aqua Ion with Capping μ4‐Se Ligand

The aqueous solution chemistry of niobium is underexplored, and well characterized aqua complexes are scarce. In this contribution, a new niobium aqua complex was obtained by treatment of Zn‐reduced ethanolic solution of NbCl₅ with HCl in the presence of a selenide source (ZnSe). This is the first example of selenium containing aqua complex of niobium. The yellow‐green aqua complex was isolated by cation‐exchange chromatography and transformed into corresponding isothiocyanate complex by ligand exchange, which was crystallized as (PyH)_4.5[H_1.5Nb₄SeO₅(NCS)₁₀] · 0.5H₂O. X‐ray structural analysis revealed a metal‐metal bonded tetranuclear {Nb₄(μ₄‐Se)(μ₂‐O)₅}⁴⁺ core with a capping μ₄‐Se ligand.     

Electrochemical Signal‐triggered Release of Biomolecules Functionalized with His‐tag Units

His‐tagged molecular species, a ferrocene derivative and Protein A, were immobilized on electrode surfaces (Au and graphite) through formation of a chelated complex in the presence of Cu²⁺ cations used as bridging units. The complex was cleaved and the attached molecules were released from the electrode surface by applying reductive potential to the electrodes resulting in Cu²⁺ reduction, thus decomposing the chelate complex. The molecule release process was followed by cyclic voltammetry in case of the ferrocene derivative. His‐tagged Protein A was additionally labeled with a fluorescent tag and its release was followed by fluorescence measurements in the solution and by impedance spectroscopy at the electrode. The studied release of the His‐tagged redox species and biomolecules was considered as a new generic approach to the signal‐controlled molecule release applicable in various biotechnological and biomedical applications.     

Mechanism of [3+2] Cycloaddition of Alkynes to the [Mo3S4(acac)3(py)3][PF6] Cluster

A study, involving kinetic measurements on the stopped‐flow and conventional UV/Vis timescales, ESI‐MS, NMR spectroscopy and DFT calculations, has been carried out to understand the mechanism of the reaction of [Mo₃S₄(acac)₃(py)₃][PF₆] ([ 1 ]PF₆; acac=acetylacetonate, py=pyridine) with two RC?CR alkynes (R=CH₂OH (btd), COOH (adc)) in CH₃CN. Both reactions show polyphasic kinetics, but experimental and computational data indicate that alkyne activation occurs in a single kinetic step through a concerted mechanism similar to that of organic [3+2] cycloaddition reactions, in this case through the interaction with one Mo(μ‐S)₂ moiety of [ 1 ]⁺. The rate of this step is three orders of magnitude faster for adc than that for btd, and the products initially formed evolve in subsequent steps into compounds that result from substitution of py ligands or from reorganization to give species with different structures. Activation strain analysis of the [3+2] cycloaddition step reveals that the deformation of the two reactants has a small contribution to the difference in the computed activation barriers, which is mainly associated with the change in the extent of their interaction at the transition‐state structures. Subsequent frontier molecular orbital analysis shows that the carboxylic acid substituents on adc stabilize its HOMO and LUMO orbitals with respect to those on btd due to better electron‐withdrawing properties. As a result, the frontier molecular orbitals of the cluster and alkyne become closer in energy; this allows a stronger interaction.     

Binuclear copper(II) complex with 2-imidazolylbenzothiazole and bridged chloride ligands

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