Synthesis and characterization of Di-π-cyclopentadienyl- metal pentasulfides of titanium(IV) and vanadium (IV):an operational test of the influence of an unpaired electron on the molecular geometry

Our preparation of Ti(h⁵?C₅H₅)₂ S₅ by the reaction of elemental sulfur with Ti(h⁵?C₅H₅)₂(CO)₂ in hexane and of V(h⁵?C₅H₅)₂S₅?$\text{1}\text{2}$ H₂O by the reacti of V(h⁵?C₅H₅)₂ Cl₂ with Na₂S₅ in THF and structural analyses by single crystal X-ray diffraction (together with infrared, solution EPR, and temperaturedependent magnetic susceptibility measurements) represent an extension of our previous work on M(h⁵?C₅H₅)₂ (SC₆H₅)₂ (M = Ti, V). The crystallographic results provide further support of our previous conclusions that the Ballhausen—Dahl model is not valid for M(h⁵?C₅H₅)₂L₂ systems. The structuralfeatures of the chair-like titanium and vanadium pentasulfide molecules are compared to the corresponding phenylmercapto analogs and to the chair-like cyclohexasulfur molecule in rhombohedral sulfur. Ti(h⁵?C₅H₅)₂S₅ was isolated as a mixture of monoclinic and orthorhombic Crystalline phases-which were both characterized by preliminary X-ray data. A complete Structural determination and refinement of the monoclinic phase, which contains two independent molecules in a cell of dimensions a 22.843(2), b 7.958(1), c 14.465(1) Å, β 90.074(4)° and symmetry P2₁/c, yielded R₁ 5.3 % and R₂ 5.9 % for 2168 independent diffractometry-collected data with I≥ 2.5o(I). V(h⁵?C₅H₅)₂S₅-$\text{1}\text{2}$ H₂O contains four V(h⁵?C₅H₅)₂S₅ molecules and two water molecules of hydration (of crystallographic site symmetry C₂-2) in onorthorhombic unit cell of symmetry P2₁2₁2 and of dimensions a 13.491(1), b 12.748(1), c 7.715(1) Å. Least-squares refinement of 750 diffractometry data with I≥2.0σ(I) gave R₁ 2.4% and R₂ 3.0% Both of these compounds were independently synthesized and Spectroscopically characterized by Köpf and co-workers, and-a Complete X-ray diffraction study was performed by Epstein and Bernal on a different monoclinic phase of Ti(h⁵?C₅H₅)₂S₅ (isolated by-Köpf). An extraction of V(h⁵?C₅H₅)₂S₅ with re fluxing benzene under nitrogen atmosphere in a Soxhlet apparatus led to the formation of the previously reported [V₂ (h⁵?C₅H₅)₂S₅]_n compound which was characterized by physical measurements including a preliminary X-ray diffraction study.     

3',4'-trans-linked bicyclic nucleosides locked in S-type conformations

A novel class of 3',4'-trans-linked bicyclic nucleosides with locked S-type furanose conformations is introduced by synthesis of two model derivatives; one was obtained by cyclic ether formation and the other by ring-closing metathesis methodology.     

Importance of the choice of assumptions and models in the estimation of analytical quality specifications

The validity of any model depends on its ability to imagine the situation or problem to which it is applied. Further, the assumptions made in relation to the model are determining for the actual outcome. Within the field of clinical biochemistry a lot of models for analytical quality specifications, based on a variety of concepts and ’clinical settings’, have been proposed. A hierarchical structure for application of these approaches and models has been agreed on at several occasions in 1999. In this hierarchy, the highest rank is given to evaluation of analytical quality specifications based on ’clinical settings’/’clinical outcome’ models, followed by specifications based on biological variation and on ’clinicians opinions’. This contribution, deals with the problems of combining random and systematic errors and the implications of application of different models to a variety of clinical settings. Received: 1 June, 2002 Accepted: 17 July 2002 Presented at the European Conference on Quality in the Spotlight in Medical Laboratories, 7–9 October 2001, Antwerp, Belgium     

Synthese und Charakterisierung funktionalisierter β‐Hydroxydithiozimtsäuren und deren Ester. Komplexchemisches Verhalten gegenüber Nickel(II), Palladium(II) und Platin(II)

Synthesis and Analytical Characterization of Functionalized β‐Hydroxydithiocinnamic Acids and their Esters. Complex Chemistry towards Nickel(II), Palladium(II), and Platin(II) Starting from silyl‐protected 4‐hydroxy acetophenone ( 1 ) the 1,1‐ethenedihiolato complexes 3 – 5 were synthesised using carbon disulfide and potassium‐tert‐butylate as a base. After being deprotected, the resulting 4‐hydroxy‐substituted complexes 6 – 8 were esterified with DL‐α‐lipoic acid to obtain the compounds 9 – 11 . The resulting complexes were characterized using NMR spectroscopy, mass spectrometry and IR spectroscopy. 3‐substituted β‐hydroxydithiocinnamic acid methyl ester ( 12 ) was obtained via an analogous path of reaction using silyl‐protected 3‐hydroxy acetophenone ( 2 ), carbon disulfide and methyl iodide. After removing of the silyl group the resulting hydroxy group was esterified with DL‐α‐lipoic acid. Using the dithioacid ester 14 as a ligand the Ni^II ( 15 ), Pd^II ( 16 ) and Pt^II ( 17 ) [O,S] complexes were obtained.     

Crystallization Temperature Limit of (Ba,Sr)TiO<Subscript>3</Subscript> Thin Films Prepared by a Non Oxocarbonate Phase Forming CSD Route

A new chemical solution deposition (CSD) route for the fabrication of Ba_0.7Sr_0.3TiO₃ (BST) thin films has been developed which completely prevents the formation of an intermediate oxo-carbonate phase. The latter has been reported previously by several authors to be responsible for increased crystallization temperatures. Barium and strontium diaminoethoxides were synthesized starting from pure barium and strontium metal and aminoethanol. These alkoxides were found to be readily soluble in a wide range of solvents and thus were excellent candidates for the CSD process. To prepare a stable precursor solution the aminoalkoxides were dissolved in 2-butoxyethanol and then used for the deposition of BST thin films. We conclude that the minimum crystallization temperature of 600C to be independent of the formation of the oxo-carbonate phase. DTA-TGA were performed on the precursors and their solutions to study their decomposition behaviour. All films annealed at different temperatures were physically characterized by XRD, IR, and SEM. The films prepared by this route at 650C were found to have high dielectric constant and the leakage currents were comparable to BST films prepared by normal carboxylate based routes at 750C.     

Tachibana-type theorems and special Holonomy

Annals of Global Analysis and Geometry - In the present paper, we consider star-shaped mean convex hypersurfaces of the real, complex and quaternionic hyperbolic space evolving by a class of...     

Mechanisch-chemische Reaktionen in künstlichen organischen Fasern

Zusammenfassung Die beim Verstrecken sowie Mahlen von künstlichen organischen Fasermaterialien (Polyester-, Polyamid- und Viskosefasern) als Folge homolytischer Kettenspaltungen auftretende Freiradikalbildung wurde untersucht.

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Mechanochemical reactions in synthetic organic fibres

The formation of free radicals due to homolytic chain fission occurring in the course of stretching and grinding of synthetic organic fibres (polyester, polyamide, and viscose fibres) has been investigated by means of ESR spectroscopy.

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Die Elektronspinresonanz-Messungen wurden im Chemischen Institut der Sir George Williams University, Montreal, Canada, durchgeführt.     

Perfect crystals andq-deformed Fock spaces

In [S], [KMS] the semi-infinite wedge construction of level 1U _q (A _n ⁽¹⁾ ) Fock spaces and their decomposition into the tensor product of an irreducibleU _q (A _n ⁽¹⁾ )-module and a bosonic Fock space were given. Here a general scheme for the wedge construction ofq-deformed Fock spaces using the theory of perfect crystals is presented.LetU _q (g) be a quantum affine algebra. LetV be a finite-dimensionalU _q (g)-module with a perfect crystal base of levell. LetV _aff V [z,z ^–1] be the affinization ofV, with crystal base (L _aff,B _aff). The wedge spaceV _aff V _aff is defined as the quotient ofV _aff V _aff by the subspace generated by the action ofU _q (g) [z ^a z ^b +z ^b z ^a ]_a,b onv v (v an extremal vector). The wedge space ^r V _aff (r ) is defined similarly. Normally ordered wedges are defined by using the energy functionH :B _aff B _aff . Under certain assumptions, it is proved that normally ordered wedges form a base of ^r V _aff.Aq-deformed Fock space is defined as the inductive limit of ^r V _aff asr , taken along the semi-infinite wedge associated to a ground state sequence. It is proved that normally ordered wedges form a base of the Fock space and that the Fock space has the structure of an integrableU _q (g)-module. An action of the bosons, which commute with theU _q (g)-action, is given on the Fock space. It induces the decomposition of theq-deformed Fock space into the tensor product of an irreducibleU _q (g)-module and a bosonic Fock space.As examples, Fock spaces for typesA _2n ⁽²⁾ ,B _n ⁽¹⁾ ,A _2n ^–1/(2) ,D _n ⁽¹⁾ andD _n ^+1/(2) at level 1 andA ₁ ⁽¹⁾ at levelk are constructed. The commutation relations of the bosons in each of these cases are calculated, using two point functions of vertex operators.     

Yields of Br* (4P1/2) as a function of wavelength in the photodissociation of Br2 and IBr

A flashlamp-pumped tunable dye laser has been used to study the photochemical production of Br* (4²P_1/2) atoms from Br₂ and IBr exc     

A DANREF certified reference plastic for measurement of overall migration into the food simulant olive oil by single sided testing

A reference material for the determination of overall migration from a plastic coextrudate into the fatty food simulant olive oil was produced and certified in an interlaboratory study. The analyses were carried out according to the ENV 1186 standard from the European Committee for Standardization (CEN) [ 1, 2, 3] with exposure of the coextrudate to olive oil for 10 days at 40 degrees C. After an initial preliminary interlaboratory study eight laboratories participated in the certification round, and two different methods were used to obtain single sided exposure of the plastic to the oil. The certified value was determined as the mean of laboratory mean values. No outliers were found. A reference value of 8.6 mg/dm2 +/- 1.4 mg/dm2 (+/- half width of the 95% confidence interval) was obtained which is within the range relevant for the regulatory limit (10 mg/ dm2), making this reference material suitable for laboratories measuring according to the EU overall migration limit [4]. The material has been found stable over 45 months.