Azobenzene chains complexation

Recently, this methodology has been applied by Liu and co-workers to obtain bimetallic ruthenium Tp complexes with cr,cr -bridging azobenzene chains. ... 

Perez et al. [128] investigated the crystal structure of 4-(4 -ethoxybezoy-loxy)-2-butoxy-4 -(4-butoxysalicylaldimine)azobenzene. This compound contains four rings in the main core and a lateral alkoxy branch on one of the inner rings. The lateral butoxy chain is nearly perpendicular to the long axis of the main core. This molecular conformation induces the molecules to make a very complex network in the solid. The crystal cohesion is due to van der Waals interactions. The change of the lateral chain conformation in the solid and nematic phases is discussed. 

RA and transmission techniques [3], and applied it to the studies of LB films of cadmium stearate [3], azobenzene-containing long-chain fatty acids and their barium salts [4], dipalmitoylphosphatidylcholine (DPPC) [5], and polyion complexes [6]. Furthermore, we explored the relationship between the molecular orientation evaluated by this method and pyroelectricity in alternating (noncentrosymmetric) Y-type LB films consisting of a phenylpyrazine-containing long-chain fatty acid and deuterated stearic acid and of their barium salts [7]. 

Inclusion properties of molecular nanotubes composed of crosslinked a-cyclodextrin was investigated [47], Induced circular dichroism was used to probe the formation and dissociation of complexes between the nanotubes and azobenzene modified polyethylene glycol), either with or without a hydrophobic alkyl chain. The inclusion complex between the nanotubes and polymers formed at room temperature, and the polymers dissociated from the nanotubes with increasing temperature. 

Several problems occurring in polyelectrolyte complexes can be circumvented by attaching the azobenzene inoiety covalently to a pplymer chain. Seki and Ichimiura used poly(vinylalcohol) as a hydrophilic backbone and attached azobenzene fatty acids 32 (n = 5,10) to this backbone. 

Orthometallated complexes are intermediates in numerous cyclic carbonylation reactions involving aromatics with nitrogen donor groups in their side chains. For example, aromatic ketoximes and azobenzene are carbonylated at elevated temperatures and pressures with a cobalt carbonyl catalyst to form five-membered ring heterocycles in which a carbonyl group has replaced the metal in the presumed orthometallated intermediate ... 

The development of H-bonded complexes is now considered. An influence of UV irradiation on optical properties of low-molecular-weight azobenzene-con-taining material (Fig. 2.4b) has been investigated (Aoki et ah, 2000) on the basis of such interactions. The first observation of photoinduced optical anisotropy in H-bonded complexes of azobenzene dyes and copolymers (Fig. 2.4b) has been recently demonstrated (Medvedev et ah, 2005). In this case, the induced anisotropy was stable, and the maximum dichroic ratio of 2 has been observed. A kinetics of the induction of birefringence (maximum value of ca. 0.01) in one of these complexes is shown in Fig. 2.5. An influence of H-bonding on the mesomorphic and photoorientation properties was recently demonstrated (Cui and Zhao, 2004). In this approach, the amorphous azopyridine side-chain polymer was converted into liquid crystalline polymers through self-assembly with a series of commercially available, aliphatic, and aromatic carboxylic acids (Fig. 2.4d). 

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