Westerhausen Matthias, Gärtner Martin, Fischer Reinald, Langer Jens, Yu Lian, Reiher Markus
Institute of Inorganic and Analytical Chemistry, Friedrich-Schiller-Universität Jena, August-Bebel-Strasse 2, 07743 Jena, Germany.
Chemistry. 2007;13(22):6292-306. doi: 10.1002/chem.200700558.
Compounds of the type aryl--M--X, with M=Ca, Sr, Ba and X as any kind of ligand (such as halide, phosphanide, amide, aryl), are presented. The low reactivity of the heavy alkaline earth metals calcium, strontium, and barium enforces an activation prior to use for the direct synthesis. The insertion of these metals into C--I bonds of aryl iodides (direct synthesis) yields aryl metal iodides and has to be performed at low temperatures and in THF. Aryl alkaline-earth-metal compounds show some characteristics: 1) the ease of ether cleavage enforces low reaction temperatures, 2) for Sr and Ba the Schlenk equilibrium is shifted towards homoleptic MI2 and MPh2, 3) high solubility of diaryl alkaline-earth-metal derivatives in THF even at low temperatures initiated quantum chemical investigations on the aggregation behavior, and 4) a strong low field shift of the 13C resonances of the ipso carbon atoms in NMR spectra was observed. First results from quantum chemical calculations on diaryl dicalcium(I) suggest a long Ca--Ca bond with a considerable Ca--Ca bond dissociation energy. Initial results on a selection of applications such as metallation, metathesis, and addition reactions of aryl calcium compounds are presented as well.
本文介绍了芳基-M-X型化合物,其中M = Ca、Sr、Ba,X为任何类型的配体(如卤化物、膦化物、酰胺、芳基)。重碱土金属钙、锶和钡的低反应活性使得在直接合成之前需要进行活化。将这些金属插入芳基碘的C-I键(直接合成)会生成芳基金属碘化物,且必须在低温下于四氢呋喃(THF)中进行。芳基碱土金属化合物具有一些特性:1)醚键易于断裂,这要求反应温度较低;2)对于Sr和Ba,施伦克平衡向同配体MI2和MPh2偏移;3)即使在低温下,二芳基碱土金属衍生物在THF中的高溶解度引发了关于聚集行为的量子化学研究;4)在核磁共振(NMR)光谱中观察到,本位碳原子的13C共振有很强的低场位移。关于二芳基二钙(I)的量子化学计算的初步结果表明,存在一个具有相当大的Ca-Ca键解离能的长Ca-Ca键。还展示了芳基钙化合物在金属化、复分解和加成反应等一系列应用方面的初步结果。