Visible‐Light‐Driven Chemoselective Hydrogenation of Nitroarenes to Anilines in Water through Graphitic Carbon Nitride Metal‐Free Photocatalysis

Green and efficient procedures are essential for the chemoselective hydrogenation of functionalized nitroarenes to form industrially important anilines. Herein, it is shown that visible‐light‐driven, chemoselective hydrogenation of functionalized nitroarenes with groups sensitive to forming anilines can be achieved in good to excellent yields (82–100 %) in water under relatively mild conditions and catalyzed by low‐cost and recyclable graphitic carbon nitride. The process is also applicable to gram‐scale reaction, with a yield of aniline of 86 %. A study of the mechanism reveals that visible‐light‐induced electrons are responsible for the hydrogenation reactions, and thermal energy can also promote the photocatalytic activity. A study of the kinetics shows that this reaction possibly occurs through one‐step hydrogenation or stepwise condensation routes. A wide range of applications can be expected for this green, efficient, and highly selective photocatalysis system in reduction reactions for the synthesis of fine chemicals.     

Über die Affinitätsconstanten der mehrbasischen Säuren und der Estersäuren

Ohne Zusammenfassung     

Kolloidmühlen

Ohne Zusammenfassung     

Perturbation calculations on the hydrogen bond in the water dimer for different proton acceptor orientations

Using perturbation theory of intermolecular forces (including exchange effects) hydrogen-bond energies are calculated for a simple model representing the water dimer. Several orientations of the proton acceptor with respect to the O...O axis are considered and it is found that the optimum orientation depends sensitively on the oxygen lone-pair hybridization assumed. The main orientation-dependent energy term is found to be the classical electrostatic energy between the unperturbed molecules. The relation of the present results to the structures of the ices I and Ic, and to the results of recent SCF studies are discussed briefly.

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Zusammenfassung Die Energien von Wasserstoffbindungen werden für ein einfaches Modell des dimeren Wassers mit Hilfe der Störungstheorie für intermolekulare Kräfte (mit Austauscheffekten) berechnet. Verschiedene Orientierungen des Protonen-Akzeptors bezüglich der O ... O-Achse werden untersucht; man findet, daß die optimale Orientierung empfindlich von der angenommen Hybridisierung des einsamen Elektronenpaars des Sauerstoffs abhängt. Der hauptsächliche, von der Orientierung abhängige Energieterm ist die klassische elektrostatische Energie zwischen den beiden ungestörten Molekülen. Die Beziehung der vorliegenden Ergebnisse zu den Strukturen von Eis I und Ic sowie zu den Ergebnissen kürzlicher SCF-Rechnungen wird kurz diskutiert.

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For some recent CNDO/2 calculations on (H₂O)₂ which concentrate mainly on rotations of the donor see Ref. [5].     

Flocculation of silver iodide sols by hydrolysed cations in the presence of a non-ionic surface active agent

Summary Previous studies have indicated that non-ionic surface active agents, such as n-dodecylhexaoxyethylene glycol monoether, confer considerable protection on silver iodide sols to flocculation by inorganic cations. In the present study the effects of hydrolysis of the flocculating cations, lanthanum, aluminium and thorium have been examined. It was found that with the hydrolysed cations the protective action of the non-ionic surface active agent was considerably diminished. It was deduced that the hydrolysed species are more strongly adsorbed than the nonionic surface active agent and either displace the latter from the surface or form species which are large enough to cause flocculation by interparticle bridging.

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Zusammenfassung Vorausgehende Untersuchungen haben gezeigt, daß nichtionische oberflächenaktive Substanzen wie n-Dodecylhexaoxyäthylen-glykol-monoäther beträchtliche Schutzwirkung Silberjodidsolen gegenüber Flokkung durch anorganische Kationen verleihen. In der vorliegenden Untersuchung wird die Wirkung der Hydrolyse flockender Kationen, Lanthan, Aluminium und Thorium, geprüft. Es wurde gefunden, daß durch die hydrolisierten Kationen die Schutzwirkung der nichtionischen oberflächenaktiven Substanz beträchtlich vermindert wird. Daraus ist zu schließen, daß die hydrolisierte Ionenart stärker als das nichtoberflächenaktive Agens adsorbiert wird und deshalb das letztere von der Oberfläche entfernt wird oder genügend große interpartikuläre Brücken, bildet, um Flockung zu verursachen.

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With 6 figures and 1 table     

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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Mit 3 Abbildungen

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

Oligo-Quinolylene–Vinylene Foldamers

Quinoline based aromatic amide foldamers are known to adopt stable folded conformations. We have developed a synthetic approach to produce similar oligomers where all amide bonds, or part of them, have been replaced by an isosteric vinylene group. The results of solution and solid state structural studies show that oligomers exclusively containing vinylene linkages are not well folded, and adopt predominantly flat conformations. In contrast, a vinylene segment flanked by helical oligoamides also folds in a helix, albeit with a slightly lower curvature. The presence of vinylene functions also result in an extension of π-conjugation across the oligomer that may change charge transport properties. Altogether, these results pave the way to foldamers in which both structural control and specific electronic properties may be engineered.     

Isomers of B←N-Fused Dibenzo-azaacenes: How B←N Affects Opto-electronic Properties and Device Behaviors?

The B←N unit has a large dipole and it is isoelectronic to C−C moiety with no dipole. Incorporating B←N units into π-conjugated system is a powerful strategy to design organic small molecules and polymers with intriguing opto-electronic properties and excellent opto-electronic device performance. However, it is unclear how the B←N unit affects electronic structures and opto-electronic properties of large π-conjugated molecules. In this work, to address this question, we developed three dibenzo-azaacene molecules in which two B←N units were introduced at different positions. Although the dibenzo-azaacene skeleton is fully π-conjugated, the effect of B←N unit on the electronic structures of the adjacent rings is much stronger than that of the distant rings. As a result, the three molecules with isomerized B←N incorporation patterns possess different electronic structures and exhibit tunable opto-electronic properties. Among the three molecules, the centrosymmetrical molecule exhibits higher LUMO/HOMO energy levels than those of the two axisymmetrical molecules. When used as the active layer in organic field-effect transistors (OFETs), while the two axisymmetrical molecules show unipolar electron transporting property, the centrosymmetrical molecule exhibits ambipolar hole and electron transporting behavior. This work not only deepens our understanding on organoboron π-conjugated molecules, but also indicates a new strategy to tune opto-electronic properties of organic semiconductors for excellent device performance.     

Synthesis of Lignans Based on a Borate-mediated One-pot Sequential Suzuki-Miyaura Coupling of Cyclic Boranes

Lignans are a group of polyphenolic phytochemicals that possess a large spectrum of chemical structures and biological activities. Here the syntheses of lignans – anwulignan, burseran, dehydroxycubebin, ruburisandrin B, and sesamin – are achieved based on a borate-mediated one-pot sequential Suzuki-Miyaura coupling of cis- and trans-fused bicyclic boranes, which were prepared by diastereoselective cyclic hydroboration of exo-cyclic diene with cyclopentyl- and thexylboranes, respectively. A one-pot sequential Suzuki-Miyaura coupling of each cyclic borate with various aryl bromides initiated by activation of the cyclic borane with the carbon nucleophile provided 2,3-dibenzylbutane derivatives with different aromatic substituents. Finally, the syntheses of naturally occurring lignans were accomplished in several steps from the products of Suzuki-Miyaura coupling.