Departamento de Química Inorgánica, Facultad de Química, Universidad de Sevilla, Aptdo 1203, 41071, Sevilla, Spain.
Dalton Trans. 2010 Jan 21;39(3):900-7. doi: 10.1039/b914788h. Epub 2009 Nov 16.
The copper catalysed aerobic oxidation of selected alcohol substrates in supercritical carbon dioxide (scCO(2)), employing a range of simple copper(II) catalyst compounds, is here described. The copper acetate complex of polydimethylsiloxane (PDMS) functionalised pyridine (1), compound 2, has previously been synthesised and characterised by us and its solubility in scCO(2) demonstrated. Due to this solubility we anticipated that the selective aerobic oxidation of alcohols to aldehydes could be homogeneously catalysed by this compound in scCO(2) in combination with the co-catalyst 2,2,6,6-tetramethylpiperidin-1-yloxy free radical (TEMPO). Our initial results showed that complete oxidation of 4-nitrobenzyl alcohol was achieved within 4 h of reaction. However, the activities of analogous copper derivatives containing simpler pyridine substituents, Cu(AcO)(2)(py) and Cu(AcO)(2)(4VP) (4VP = 4-vinylpyridine), were shown to be similar, in spite of their negligible solubility in scCO(2). When we repeated the reactions in highly non-polar hexane rather than scCO(2) similar observations were made. In both cases, as 2 is soluble and the pyridine analogues are not, a much higher reaction rate was anticipated for 2 as it is the only compound capable of homogeneous catalysis. However, in some cases slightly better activities were observed for Cu(AcO)(2)(py) rather than for the PDMS functionalised analogue, 2. Thus, despite poor catalyst solubility typically being very inhibitory in this type of catalytic process, in this system solubilisation of the catalyst is not necessary. In continuation the activity of silica supported copper complexes was therefore investigated. Employing such catalysts the 4-nitrobenzyl and benzyl alcohol substrates were completely oxidised to the corresponding aldehydes in scCO(2), this time employing lower catalyst loadings. Other types of alcohol substrate showed more limited conversions however. To conclude, alcohol oxidation in the non-conventional green solvent scCO(2), with the benign terminal oxidant, dioxygen, and simple, cheap, easily prepared metal catalyst compounds was demonstrated. This is the first copper-TEMPO catalysed alcohol oxidation system in scCO(2) to be described.
本文描述了在超临界二氧化碳(scCO2)中使用一系列简单的铜(II)催化剂化合物,对选定的醇底物进行铜催化的有氧氧化。我们之前已经合成并表征了聚二甲基硅氧烷(PDMS)功能化吡啶(1)的铜醋酸盐配合物,即化合物 2,并证明了其在 scCO2 中的溶解度。由于这种溶解度,我们预计这种醇的选择性有氧氧化可以通过该化合物在 scCO2 中与共催化剂 2,2,6,6-四甲基哌啶-1-氧基自由基(TEMPO)的均匀催化来实现。我们的初步结果表明,在反应 4 小时内,4-硝基苄醇完全氧化。然而,含有更简单吡啶取代基的类似铜衍生物[Cu(AcO)(2)(py)](2)和[Cu(AcO)(2)(4VP)](2)(4VP=4-乙烯基吡啶)的活性相似,尽管它们在 scCO2 中的溶解度可以忽略不计。当我们在高度非极性己烷中而不是在 scCO2 中重复这些反应时,也得到了类似的观察结果。在这两种情况下,由于 2 可溶而吡啶类似物不可溶,因此预计 2 的反应速率要高得多,因为它是唯一能够进行均相催化的化合物。然而,在某些情况下,[Cu(AcO)(2)(py)](2)的活性略高于 PDMS 功能化类似物 2。因此,尽管在这种类型的催化过程中,催化剂的溶解度通常很差,但在该体系中,催化剂的溶解不是必需的。因此,我们继续研究了负载在硅胶上的铜配合物的活性。在 scCO2 中使用这种催化剂,4-硝基苄基和苄基醇底物完全氧化为相应的醛,此时使用的催化剂负载量较低。然而,其他类型的醇底物的转化率则受到了更大的限制。总之,在非传统的绿色溶剂 scCO2 中,使用温和的末端氧化剂氧气和简单、廉价、易于制备的金属催化剂化合物,实现了醇的氧化。这是 scCO2 中首次描述的铜-TEMPO 催化的醇氧化体系。