BINAS - synthesis and use of a new ligand for propylene hydroformylation

BINAS is a new, very efficient ligand for propylene hydroformylation. BINAS is made by the sulfonation of NAPHOS. Different synthetic routes to NAPHOS are discussed. A new two step synthesis starting from 2,2′-bis(bromomethyl)-1,1′-binaphthyl is described.     

Electron impact ionization mass spectra of 2,4,5,5-tetrasubstituted 1,2,4-triazolidine-3-thiones. The effect of the ethoxycarbonyl group at position 4

The electron impact ionization mass spectra of 2,4,5,5-tetrasubstituted 1,2,4-triazolidine-3-thiones studied confirmed that the substituent at position 4 has the most dramatic influence on the fragmentation pattern. When the substituent is a methylallyl group the molecular ions exhibit four main routes of fragmentation, but when it is an ethoxycarbonyl/acetyl or a methyl group these direct decompositions of the molecular ion become less abundant. Interestingly all 4-ethoxycarbonyl derivatives and the 4-acetyl derivative exhibited the ions [M-R⁴-COOC₂H₄]⁺ and [M-R⁴-COCH₂]⁺, respectively, with the same composition.     

A Preparatively Simple Access to Homochiral Heterocyclic α-Hydroxy Acids and their Derivatives

 The synthesis of homochiral heterocyclic α-hydroxy acids starting from (S)- and (R)-malic acid using hexafluoroacetone as protecting and activating agent is described. The new compounds are useful building blocks for peptide and depsipeptide modification.     

Die Benzonitril‐Addukte [Ho2Cl6(PhCN)6] und [HoCl3(PhCN)]: Synthese,Kristallstrukturen, FIR‐ und MIR‐Spektroskopische Untersuchungen

The Benzonitrile Adducts [Ho₂Cl₆(PhCN)₆] and equation/tex2gif-stack-4.gif [HoCl₃(PhCN)]: Syntheses, Crystal Structures, FarIR and MIR Spectroscopy Investigations Transparent light pink crystals of the compound [Ho₂Cl₆(PhCN)₆] were obtained by the reaction of a mixture of HoCl₃ and AlCl₃ with benzonitrile at 150μ °C. Transparent pink crystals of the compound equation/tex2gif-stack-5.gif[HoCl₃(PhCN)] were obtained by the same reaction under solvothermal conditions at 200μ °C. [Ho₂Cl₆(PhCN)₆] exhibits a dimeric structure of linked pentagonal bipyramids whereas equation/tex2gif-stack-6.gif[HoCl₃(PhCN)] forms a layer structure of trigonal Cl prisms around Ho, linked via corners and separated by coordinating PhCN molecules.     

Preparative uv-laser photochemistry of the azoalkane spiro(2,3-diazabicyclo [2.2.1]hept-2-ene-7′,1-cyclopropane): Trapping of the 1,4-Diradical 2-(3-Cyclopentenyl) ethyl by Molecular Oxygen

Photo-extrusion of nitrogen from the azoalkane 1 in the presence of molecular oxygen gave besides the hydrocarbons 3 and 5, the endoperoxide 10 and hydroperoxide 11, the former via trapping of the 1,4-diradical 4 by triplet oxygen, the latter by ene-reaction-6f hydrocarbon 5 with singlet oxygen.     

Determination of Aroma Compounds from Alcoholic Beverages in Spiked Blood Samples by Means of Dynamic Headspace GC–MS

Some aroma compounds found in alcoholic beverages are characteristic of a certain beverage (i.e. 2,4-decadienoic acid ethyl ester is characteristic of pear spirit and 5-butyltetrahydro-4-methylfuran-2-on “whiskey lactone” is characteristic of aged spirits like whiskey). These substances were detectable in beverages but not in blood samples. The aim of this investigation was to find a sensitive sampling technique for aroma compounds in whole blood samples. This technique may be used in forensic toxicology for examination of drinking claims. The method comprises dynamic headspace sampling using a purge and trap concentrator, followed by quantitative gas chromatography–mass spectrometry (dynamic HS–GC–MS). The influence of sample preparation, trap adsorbents and sample temperature as well as desorption time and purge time on the quality of the analytical results were investigated. The following optimal parameters were determined: stirred and diluted whole blood sample without salt addition, use of Carbotrap C as trap material, sample temperature at 80 °C, desorption time 20 min and purge time 30 min. These optimal parameters were used for the determination of detection limits (LOD). The LOD of aroma compounds by means of dynamic headspace sampling were compared with the results of conventional sampling: the static headspace technique. Limits of detection for the aroma compounds with conventional static headspace GC are in the range 400–10,000 μg L^?1. Dynamic headspace–GC was found to be a more sensitive sampling technique for most of the aroma compounds investigated (e.g. C₄–C₈ ethyl esters, benzoic acid ethyl ester, linalool oxide and 4-ethylguaiacol) with detection limits between 1 and 50 μg L^?1, but there were also limits to the sampling of substances with lower volatility like decanoic acid ethyl ester, 2,4-decadienoic acid ethyl ester, eugenol and whiskey lactone with detection limits of about 1,000 μg L^?1.     

Performance of an in-plane detection cell with integrated waveguides for UV/Vis absorbance measurements on microfluidic separation devices

A microfluidic device with integrated waveguides and a long path length detection cell for UV/Vis absorbance detection is presented. The 750 microm U-cell detection geometry was evaluated in terms of its optical performance as well as its influence on efficiency for electrophoretic separations in the microdevice. Stray light was found to have a strong effect on both, the sensitivity of the detection and the available linear range. The long path length U-cell showed a 9 times higher sensitivity when compared to a conventional capillary electrophoresis (CE) system with a 75 microm inner diameter (ID) capillary, and a 22 times higher sensitivity than with a 50 microm ID capillary. The linear range was comparable to that achieved in a 75 microm ID capillary and more than twice as large as in a 50 microm ID capillary. The use of the 750 microm U-cell did not contribute significantly to band broadening; however, a clear quantification was made difficult by the convolution of several other band broadening sources.     

Generalized quantum mechanical two-centre problems

If χ _i (χ _k ) is an exact generalized diatomic orbital (solution of Eq. (1) of text), a sequence of functions χ _i ^(N) converging to χ _i may be constructed so that matrix elements of frequently occurring operators between χ _i ^(N) and χ _k ^(N) may be computed without any numerical integration. Exact expectation values are given for kinetic and potential energy, dipole moment, θ ²=x ²+y ², and quadrupole moment 3z ²?r ², for various ratios of nuclear charges Z ₁,Z ₂ and for several distances R. Special subjects discussed in terms of computed expectation values are:

1. R-dependence of the contributions to total energy of HeH²⁺ in state 2pσ and of LiH³⁺ in state 3dσ
2. RZ-and λ-dependence of dipole and quadrupole moment functions in state 1sσ
3. Some properties of those generalized diatomic orbitals which approach, for R going to 0, Slater-type atomic functions.

     

Location of saddle points and minimum energy paths by a constrained simplex optimization procedure

Two methods are proposed, one for the location of saddle points and one for the calculation of steepest-descent paths on multidimensional surfaces. Both methods are based on a constrained simplex optimization technique that avoids the evaluation of gradients or second derivative matrices. Three chemical reactions of increasing structural complexity are studied within the PRDDO SCF approximation. Predicted properties of reaction hypersurfaces are in good overall agreement with those determined by gradient minimization and gradient following algorithms in connection with various ab initio SCF methods. Computational efforts required by the new procedures are discussed.     

A 3D QSAR study on a set of dopamine D4 receptor antagonists

The molecular alignments obtained from a previously reported pharmacophore model have been employed in a three-dimensional quantitative structure-activity relationship (3D QSAR) study, to obtain a more detailed insight into the structure-activity relationships for D(2) and D(4) receptor antagonists. The frequently applied CoMFA method and the related CoMSIA method were used. Statistically significant models have been derived with these two methods, based on a set of 32 structurally diverse D(2) and D(4) receptor antagonists. The CoMSIA and the CoMFA methods produced equally good models expressed in terms of q(2) values. The predictive power of the derived models were demonstrated to be high. Graphical interpretation of the results, provided by the CoMSIA method, brings to light important structural features of the compounds related to either low- or high-affinity D(2) or D(4) antagonism. The results of the 3D QSAR studies indicate that bulky N-substituents decrease D(2) binding, whereas D(4) binding is enhanced. Electrostatically favorable and unfavorable regions exclusive to D(2) receptor binding were identified. Likewise, certain hydrogen-bond acceptors can be used to lower D(2) affinity. These observations may be exploited for the design of novel dopamine D(4) selective antagonists.