Instituto de Tecnología Química (UPV-CSIC), Universidad Politécnica de Valencia, Consejo Superior de Investigaciones Científicas, Avenida de los Naranjos s/n 46022-Valencia, Spain.
Chem Soc Rev. 2011 Jul;40(7):3835-53. doi: 10.1039/c0cs00183j. Epub 2011 Mar 16.
Azobenzenes are ubiquitous motifs very important in many areas of science. Azo compounds display crucial properties for important applications, mainly for the chemical industry. Because of their discovery, the main application of aromatic azo compounds has been their use as dyes. These compounds are excellent candidates to function as molecular switches because of their efficient cis-trans isomerization in the presence of appropriate radiation. The classical methods for the synthesis of azo compounds are the azo coupling reaction (coupling of diazonium salts with activated aromatic compounds), the Mills reaction (reaction between aromatic nitroso derivatives and anilines) and the Wallach reaction (transformation of azoxybenzenes into 4-hydroxy substituted azoderivatives in acid media). More recently, other preparative methods have been reported. This critical review covers the various synthetic methods reported on azo compounds with special emphasis on the more recent ones and their mechanistic aspects (170 references).
偶氮苯是许多科学领域中无处不在的重要基序。偶氮化合物具有重要应用的关键性质,主要用于化学工业。由于它们的发现,芳香族偶氮化合物的主要应用是将其用作染料。由于它们在适当辐射存在下的高效顺反异构化,这些化合物是作为分子开关的优秀候选物。偶氮化合物的经典合成方法是偶氮偶联反应(重氮盐与活化芳香族化合物的偶联)、米尔斯反应(芳香族亚硝基衍生物与苯胺之间的反应)和瓦拉赫反应(在酸性介质中将偶氮苯转化为 4-羟基取代的偶氮衍生物)。最近,还报道了其他一些制备方法。本综述涵盖了有关偶氮化合物的各种合成方法,特别强调了最近的方法及其机理方面(170 篇参考文献)。