Ruiz-Varilla Andrea M, Baquero Edwin A, Silbestri Gustavo F, Gonzalez-Arellano Camino, de Jesús Ernesto, Flores Juan C
Departamento de Química Orgánica y Química Inorgánica, Universidad de Alcalá, Campus Universitario, 28871 Alcalá de Henares, Madrid, Spain.
Dalton Trans. 2015 Nov 14;44(42):18360-9. doi: 10.1039/c5dt02622a. Epub 2015 Sep 8.
A series of water-soluble (NHC)Pt(0)(dvtms) and (NHC)Pt(0)(AE) complexes containing different sulfonated NHC ligands (dvtms = divinyltetramethyldisiloxane and AE = diallyl ether) are reported. The dvtms compounds have been found to be quite robust and to display some conformational rigidity, whereas their AE counterparts are less stable and more flexible. The catalytic evaluation of these complexes in the hydrosilylation of alkynes in water revealed no benefits in favor of the complexes containing the more labile spectator diene (AE), and a fairly regular catalytic behavior for all complexes that restricts the location of the sulfonate group to the proximity of the metal site.
报道了一系列含有不同磺化N-杂环卡宾配体的水溶性(NHC)Pt(0)(dvtms)和(NHC)Pt(0)(AE)配合物(dvtms = 二乙烯基四甲基二硅氧烷,AE = 二烯丙基醚)。已发现dvtms化合物相当稳定,并表现出一定的构象刚性,而它们的AE对应物稳定性较差且更具柔性。这些配合物在水中炔烃的硅氢化反应中的催化评估表明,含更不稳定旁观二烯(AE)的配合物并无优势,且所有配合物都具有相当规则的催化行为,这将磺酸根基团的位置限制在金属位点附近。