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Ohne ZusammenfassungDiese Abhandlung ist schon im Maihefte der Sitzungsberichte erschienen, war auch für das entsprechende fünfte Heft der Monatshefte bestimmt, ist aber durch ein Versehen aus demselben weggeblieben.  相似文献   
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Observations on the steric layers formed by the adsorption of low-molecular-weight polyacrylic acid (PAA) were taken using the colloidal probe method in an atomic force microscope. The effects of divalent barium ions and of monovalent potassium ions at varying concentrations were observed on the repulsive interaction profiles. High ionic concentrations screened double-layer forces to small distances, whereby the acting forces were reduced to steric interactions. De Gennes scaling theory was used to model the effect of electrolyte on an aqueous barium titanate system, which was stabilized with PAA. The brush model was found to represent the force curves better than the mushroom model. The collapse of PAA layers with increasing salt approximated a grafted polymer brush in monovalent electrolyte, but the addition of barium ions caused markedly less steric collapse. It is suggested that the formation of a Ba(2+)-PAA complex in the adsorbed layer increases its compressibility parameter.  相似文献   
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Halochromic Molecules. Synthesis and Acidobasic Properties of 3′-substituted 6,11-dihydrospiro[[1]benzopyrano[4,3-b]indol-6,9′?9′9′H-xanthenes] We have synthesized a series of 3′-substituted 6,11-ihydrospiro[6H-chromeno[4,3-b]indol–6,9′?9′H-xanthenes] and one of their respective aza analogues. 1H-MR data as well as the fragmentation in the mass spectra of starting and final products supported the postulated structures. With acid, the spiro compounds form ring-opened intensely coloured xanthylium salts. UV/VIS spectra of these salts are listed and discussed. The ?pH* curves in buffered MeOH/H2O solutions and the pK* values are determined. The title compounds could possibly be used in ‘pressure sensitive papers’.  相似文献   
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Most p-block metal amides irreversibly react with metal alkoxides when subjected to alcohols, making reversible transformations with OH-substrates a challenging task. Herein, we describe how the combination of a Lewis acidic square-planar-coordinated aluminum(iii) center with metal–ligand cooperativity leverages unconventional reactivity toward protic substrates. Calix[4]pyrrolato aluminate performs OH-bond activation of primary, secondary, and tertiary aliphatic and aromatic alcohols, which can be fully reversed under reduced pressure. The products exhibit a new form of metal–ligand cooperative amphoterism and undergo counterintuitive substitution reactions of a polar covalent Al–O bond by a dative Al–N bond. A comprehensive mechanistic picture of all processes is buttressed by isolation of intermediates, spectroscopy, and computation. This study delineates how structural constraints can invert thermodynamics for seemingly simple addition reactions and invert common trends in bond energies.

The combination of structural constraint and metal–ligand cooperativity in calix[4]pyrrolato aluminate inverts common trends of bond energies and enables reversible OH-bond activation.  相似文献   
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This paper presents a 3D topology optimization approach for designing shell structures with a porous or void interior. It is shown that the resulting structures are significantly more robust towards load perturbations than completely solid structures optimized under the same condi-tions. The study indicates that the potential benefit of using porous structures is higher for lower total volume fractions. Compared to earlier work dealing with 2D topology opti-mization, we found several new effects in 3D problems. Most notably, the opportunity for designing closed shells signifi-cantly improves the performance of porous structures due to the sandwich effect. Furthermore, the paper introduces improved filter boundary conditions to ensure a completely uniform coating thickness at the design domain boundary.  相似文献   
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