The role of isomorphism in synthetic analysis. Pruning the search tree by finding disjoint isomorphic substructures

Isomorphism is an equivalence relation that is less stringent than identity (equality), and it is useful for synthetic analysis, since it allows one to find reflexive routes for targets even when they do not have an element of symmetry.     

Pattern formation and ordering in thin films of crystallisable block copolymers

We show that tapping-mode atomic force microscopy provides real-space and time-resolved observations of morphology and pattern formation resulting from crystallisation of annealed thin films of polyethelenoxide or microphase-separated low-molecular-weight hydrogenated poly(butadiene-b-ethyleneoxide) diblock copolymers. Differences in viscoelastic properties allow distinguishing crystalline and molten (amorphous) areas with a nanometer resolution.     

Ein neues Verfahren zur Bestimmung des Stickstoffs in Kohle und Koks

Ohne Zusammenfassung     

Simulation of Complexes between a Charged Dendrimer and a Linear Polyelectrolyte with Finite Rigidity

Complexes comprising a 4th‐generation dendrimer with 32 positively charged end‐groups and an oppositely charged linear polyelectrolyte along with explicit counterions are studied in an athermal solvent using MC simulations. The excluded volume between monomers, the full Coulomb potential between charges and the bending energy of the chain bonds are taken into account. The chain flexibility parameter is varied in a wide range, including the limiting cases of rigid and flexible chains. As the chains become more rigid, they take locally extended conformations within the complex. The conformations of the condensed chains are described in terms of loops, trains, and tails. In the limit of strong electrostatic coupling and high rigidity, long chains show a release of tails from the complex.

     

A new, fast and efficient synthesis of 3-aryl indenones: intramolecular cyclization of 1,3-diarylpropynones in superacids

1,3-Diarylpropynones were cleanly converted to the corresponding 3-arylindenones in various superacidic media. This new, simple, one-pot reaction proved to be efficient (yields up to 95%) and very fast (reaction time less than 30 min).     

Apparent Specific Volume Measurements of Poly(ethylene oxide), Poly(butylene oxide), Poly(propylene oxide), and Octadecyl Chains in the Micellar State as a Function of Temperature

Apparent specific densities of aqueous solutions of the diblock copolymers C18(EO)100, C18(EO)20, and (EO)92(BO)18 and the triblock copolymers (EO)25(PO)40(EO)25 and (EO)21(PO)47(EO)21 in the micellar state have been measured over a temperature range from 10 to 90 degrees C at concentrations between 1% and 5%, using an oscillating tube densitometer. From these measurements, apparent specific volumes of poly(ethylene oxide) (PEO), poly(propylene oxide) (PPO), poly(butylene oxide) (PBO), and octadecane in the micellar state have been determined. The composition of the block copolymers was checked by NMR spectroscopy. Results were compared with published data for the polymers and bulk values for octadecane, respectively. The apparent specific density of PEO chains in the dissolved state was also measured for PEG4600 solutions at different concentrations and compared with results in the micellar state. The results presented in the paper are crucial in connection with analysis and modeling of small-angle X-ray scattering (SAXS) data from polymer and block copolymer micellar systems. PEO and PPO have a relatively low apparent partial specific volume in water at low temperatures. It is associated with water molecules making strong hydrogen bonds with the oxygen atoms on the polymer backbone. These water molecules gradually become disordered when the temperature is increased and the polymer apparent specific volume increases. For PBO in the micellar cores of PBO-PEO block copolymer micelles and in PNiPAM microgels, pronounced temperature dependence with the same origin is also found. The application of the derived results for the apparent specific volume of PEO for deriving contrast factors is demonstrated and the results are used in the analysis of SAXS data for semidilute solutions of PEG4600 in a broad temperature range.     

Quantitative measurement of the Brönsted acid sites in solid acids: toward a single-site design of Mo-modified ZSM-5 zeolite

On the basis of our previous H/D exchange studies devoted to the quantification of the number of Br?nsted acid sites in solid acids, we report here an innovative approach to determine both the amount and the localization of Mo atoms inside the Mo/ZSM-5 catalyst, commonly used for the methane dehydroaromatization reaction. The influence of Mo introduction in the MFI framework was studied by means of BET, X-ray diffraction, 27Al magic angle spinning NMR, NH3 temperature-programmed desorption, and H/D isotopic exchange techniques. A dependence was found between the decrease of acidic OH groups and the Mo content. Depending on the Si/Al ratio of the zeolite, i.e., the proximity of two Br?nsted acid sites, the Mo atoms substitute a different number of OH groups. Consequently, a chemical structure was proposed to describe the geometry of the Mo complex in the channels of the ZSM-5 zeolite.