Lensless Fourier holography for digital holographic interferometry on biological samples

Digital holography as a tool for highly sensitive, interferometric non-destructive testing has several advantages compared to holographic measurements based on conventional storage media like an all-digital processing and a direct access to the phase of the object wave. Experimental results of interferometric investigations of heart valve bio-prostheses with a setup for lensless Fourier holography are presented which demonstrate that this technique is applicable to such biological samples with their wet and unstable surfaces. Limitations on size and resolution of the reconstructed object caused by the properties of the CCD sensor are discussed.     

Cycloaddition reactions of 2H-benzo[b]thiete and conjugated cyclic dienes

2H-Benzo[b]thiete 1 reacts with cyclopentadiene 3 in consecutive [8π + 2π]cycloadditions yielding the condensed heterocycles 6–8 . Tetracyclone 9 on the other hand gives only the monoadduct 10 . An [8π + 8π]cycloaddition can be observed for 1 and diphenylisobenzofuran 11 . The related π system 13 shows again consecutive [477π + 27π]processes ( 1 + 13 ← 14, 15 ).     

In-line Particle Size Analysis in the fines outlet of an air classifier

Laser diffraction (LD), with reference to the analysis time, is highly advantageous for the automation of particle size analysis. The high measuring frequencies alloy quasi-continous measuring operation. The fineness values obtained form the particle size distribution (PSD) can be transformed into electrical signals for automatic process control. For industrial purposes, an encapsulated measuring cell was developed where the laser beam penetrates the dispersed fines stream via two optical windows. Thus, hazardous materials can also be measured, specifically pharmaceutical or chemical products, or applications requiring explosion-proof plant design are possible. Great efforts had to be made to keep the inner side of the windows clean form product dust. Ultimately, batches running for more than 8 h could be analysed continuously without any contamination of the windows. For the PSD measurements, a standard LD instrument was used with a measuring range of 0.5/0.9–175 μm. As product fineness is monitored continuously in-stream, and virtually without delay, any changes in the fineness during classifier operation can be detected immediately. On the one hand, this opens up a new field for studies of classifier performance. On the other, immediate quality control of even very small batches is possible during the micronization process. The results demonstrate very clearly, for example, the importance of controlling the feed rate to the classifier. Therefore, fineness control by means of this in-line technique gives superior advantages for direct adjustment of the classifier speed.     

Dynamic mechanical investigations of different substituted cellulose o-silyl ethers

In contrast to many cellulose derivatives, the cellulose O-silyl ethers with bulky side groups exhibit scarcely a change in glass transition temperature by a variation of the degree of substitution (DS) or degree of polymerization (DP) or by introducing phenyl carbamate groups for the remaining hydroxyls along the main chain. However, a substitution of these hydroxyls by flexible acetate groups lowers the glass transition temperature considerably. The secondary dispersion (relaxation) behavior is strongly influenced by the various substituents and can be correlated to specific motions of the molecules. The dynamic mechanical properties are also dependent on the kind of preconditioning of the samples.     

Uncertainty Relations in the Madelung Picture

Madelung showed how the complex Schrödinger equation can be rewritten in terms of two real equations, one for the phase and one for the amplitude of the complex wave function, where both equations are not independent of each other, but coupled. Although these equations formally look like classical hydrodynamic equations, they contain all the information about the quantum system. Concerning the quantum mechanical uncertainties of position and momentum, however, this is not so obvious at first sight. We show how these uncertainties are related to the phase and amplitude of the wave function in position and momentum space and, particularly, that the contribution from the phase essentially depends on the position–momentum correlations. This will be illustrated explicitly using generalized coherent states as examples.     

Hindered organoboron groups in organic synthesis. 17 [1]. Synthesis of 2,4,6-triisopropylphenylborane (TripBH2)2, a useful alternative to thexylborane

2,4,6-Triisopropylphenylborane (tripylborane, TripBH₂) resembles thexylborane in having a single, bulky organic group attached to boron, but the group is aromatic rather than aliphatic. The compound has been synthesized by two alternative routes, one involving direct reduction of dimethoxytripylborane and the other involving redistribution between ditripylborane and borane. It is a solid which is considerably more stable than thexylborane.     

Formation of polymer - polymer complexes in the system poly(methacrylic acid) - hydroxyethylcellulose

An interpolymer complex was prepared by mixing aqueous solutions of poly(methacrylic acid) and hydroxyethylcellulose (molar substitution 2.5) and studied by using viscometric method. The hydrogen bonding is primarily involved in these complexations, but the hydrophobic interaction plays also an important role. The complex composition is not changing with the solvents used and is stable in the temperature range 25 °C - 65 °C.     

New mechanistic insights into the Claisen rearrangement of chorismate – a Unified Reaction Valley Approach study

ABSTRACT

The Bacillus subtilis chorismate mutase catalysed Claisen rearrangement of chorismate to prephenate is one of the few pericyclic processes in biology, and as such provides a rare opportunity for understanding how Nature promotes such rearrangements so successfully. The major focus of this work is on (i) Exploring the hypothesis that the mechanism of the chorismate rearrangement is the same in the gas phase, in the aqueous solution and in the enzyme; (ii) Investigating current suggestions that the enzyme lowers the barrier via transition state stabilisation rather than via space confinement; and (iii) A comparison of Nature's way of catalysing the reaction with a gold(I) catalysed chorismate rearrangement. Based the Unified Reaction Valley Approach (URVA), for the first time, a detailed one-to-one comparison of the rearrangement in the gas phase, in the aqueous solution and in the enzyme is presented. URVA confirms that the actual chemical process of CO bond breaking and CC bond forming is the same for all media and unravels the unique catalytic function of the enzyme as a combination of shortening the process of positioning the enolpyruvyl side chain over the cyclohexadienyl ring by space confinement in concert with facilitating CO cleavage by enhanced charge polarisation. The transition state does not play a signifiant role for the rearrangement. In contrast, the gold catalyst changes the chemical process. The rearrangement is split into two steps by switching between Au[I]-π and Au[I]-σ complexation, thus avoiding the energy consuming CO breakage in the first step. Suggestions are made for metalloenzyme analogues combining both strategies.     

Dynamics in nanoporous materials probed by 2H solid state NMR: estimation of self-diffusion coefficients

Adsorption - 2H solid-state NMR represents a reliable method for probing the dynamics of the molecules in confined geometries, including microporous and mesoporous materials such as zeolites or...