Functional Molecular Thin Films: Topological Templates for the Chemoselective Ligation of Antigenic Peptides to Self-Assembled Monolayers

The combination of self-assembly and regioselective surface chemistry has made it possible to immobilize peptide recognition sites 1 on a template attached to a gold surface. Each of the seven individual reaction steps, including the final functional biomolecular recognition, was controlled in situ with surface-sensitive detection techniques. The presented strategy is of general importance for the formation of complex supramolecular structures with biologically interesting functionalities at the interfaces.     

Plaquette ground state in the two-dimensional SU(4) spin-orbital model

In order to understand the properties of Mott insulators with strong ground state orbital fluctuations, we study the zero temperature properties of the SU(4) spin-orbital model on a square lattice. Exact diagonalizations of finite clusters suggest that the ground state is disordered with a singlet-multiplet gap and possibly low-lying SU(4) singlets in the gap. An interpretation in terms of plaquette SU(4) singlets is proposed. The implications for LiNiO₂ are discussed. Received 6 July 2000     

Magnetic properties of the S = 1/2 one-dimensional antiferromagnet MgVO

The magnetic susceptibility and the electron spin resonance in the X-band of the transition metal oxide compound MgVO₃ are reported. We show that this compound, made of weakly coupled infinite chains of VO₅ pyramids, behaves as a S =1/2 one-dimensional Heisenberg antiferromagnet. From the ESR and magnetic experiments we deduce the Néel temperature K, the in-chain coupling constant K and the g-factor values g x = g z =1.972(2), g y =1.946(1) for V⁴⁺ ions in MgVO₃. Received 14 July 1999     

Determination of selected pesticides in environmental water by employing liquid-phase microextraction and liquid chromatography–tandem mass spectrometry

An optimised extraction and cleanup method for the analysis of pesticide in natural water samples is presented. Sixteen pesticides of different polarity and from the different chemical classes (organophosphates, triazines, benzimidazoles, carbamates, carbamides, neonicotinoides, methylureas, phenylureas and benzohydrazides), most frequently used in Serbia, were selected for the analysis. Liquid-phase microextraction in a single hollow fibre (HF-LPME) has been applied for sample preparation. The concentrations of pesticides were determined using HPLC-MS/MS method with electrospray ionisation. The extraction behaviour and selection of the experimental conditions was predicted based on log D and pK _a values of targeted pesticides, which were calculated applying the computer software ACD/Labs PhysChem Suite v12. The influence of the donor pH and concentration of pesticides, organic phase composition as well as the extraction time on the extraction efficiency was investigated. Optimum extraction conditions were evaluated with respect to the investigated parameters of the extraction. The extraction method was validated for 10 out of 16 studied pesticides. Linear range of the pesticides was 0.1–5 μg L⁻¹ with the correlation coefficient from 0.991 to 0.9998, and the relative standard deviation for three standard measurements was between 0.2 and 11.8%. The limits of detections ranged from 0.026 to 0.237 μg L⁻¹ and the limits of quantifications from 0.094 to 0.793 μg L⁻¹. The optimised two-phase HF-LPME method was successfully applied for determination of moderately polar as well low-polar pesticides in the environmental water samples.     

Determination of pesticides in surface and ground waters by liquid chromatography-electrospray-tandem mass spectrometry

The sensitive multiresidual analytical method for simultaneous analysis of 14 most commonly used agricultural pesticides in Serbia was developed and optimized. The selected insecticides, fungicides and herbicides belong to seven chemical classes (organophosphates, neonicotinoids, carbamates, diacylhydrazines, benzimidazoles, triazines and phenylureas). The method was based on solid-phase extraction followed by liquid chromatography-tandem mass spectrometry. The following parameters that may affect the SPE procedure efficiency were optimized: the sorbent type in combination with different elution solvents, the sample pH and the sample volume. For each pesticide, MSⁿ analysis was performed and distinctive ions and transitions were selected for identification and quantification, as well as for confirmation purposes. External matrix-matched calibration method was used to eliminate variable matrix effect and ensure precise quantification. Good recoveries (72-129%), and low limits of detection (0.4-5.5 ng L⁻¹) and quantification (1.1-18.2 ng L⁻¹) were achieved for all selected pesticides. The developed and optimized method was successfully applied in the analysis of several river waters, as well as ground waters in Serbia, influenced by agriculture. The most frequently detected pesticide was carbendazim. Dimethoate, carbofuran and propazine were also found in the investigated samples.     

Quadrupolar phases of the s=1 bilinear-biquadratic Heisenberg model on the triangular lattice

Using mean-field theory, exact diagonalizations, and SU(3) flavor theory, we have precisely mapped out the phase diagram of the S = 1 bilinear-biquadratic Heisenberg model on the triangular lattice in a magnetic field, with emphasis on the quadrupolar phases and their excitations. In particular, we show that ferroquadrupolar order can coexist with short-range helical magnetic order, and that the antiferroquadrupolar phase is characterized by a remarkable 2/3 magnetization plateau, in which one site per triangle retains quadrupolar order while the other two are polarized along the field. Implications for actual S=1 magnets are discussed.     

Silver selenide modification of polyamide fabric

Formation of a silver selenide layer on silicone coated polyamide cloth was investigated. Fabric samples were selenized in potassium selenotrithionate (K₂SeS₂O₆) solution then treated with AgNO₃ solution. Formation of a silver selenide particle layer on the surface was confirmed by a change in appearance, X-ray diffraction, and EDX analysis. XRD revealed two phases: orthorhombic naumannite (Ag₂Se) and monoclinic selenium (Se₈). SEM showed that the fabric macrostructure and the multifilament yarn microstructure was preserved. The silver selenide particles ranged from 100 nm to more than 20 µm.