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Ruthenium catalyzed reactions of aldehydes: Molecular structures of ruthenium complexes with aldehyde ligands

机译:钌催化的醛反应:带有醛配体的钌配合物的分子结构

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[RuCl(H)(CO)(PPh_3)_3] (2) was found to catalyze,in the presence of H_2C = CHSiMe_3 (3),the trimerisation of aldehydes RCHO [R = Et (4a),i-Bu (4b)} yielding 1,3,5-trioxanes (5) and the aldol condensation yielding alpha,beta-unsaturated aldehydes (6).When (4a) was used as a reactant,from these reaction mixtures,the ruthenium complex [RuCl_2(CO)(PPh_3)_2(EtCH=CMe-CHO-kappaO)] (7) having the aldol condensation product as the ligand crystallized.In the analogous reaction with (4b),the complex [RuCl_2(CO)(PPh_3)_2(i-BuCHO-kappaO)] (8) with the aldehyde as ligand was obtained.The constitution of these complexes was established by single-crystal X-ray diffraction measurements.The ruthenium centers are octahedrally coordinated having the aldehyde and the car-bonyl ligand in mutually trans positions (coordination index: OC-6-12).The aldehydes are monodentately coordinated via the carbonyl oxygen atom (kappaO).The coordination induced elongations of the C=O double bonds [1.242(4) A (7),1.234(4) A (8)} indicate an activation of the aldehydes.Furthermore,the Ru-CO bond lengths [1.842(4) A (7),1.823(4) A (8)] exhibit a relatively low trans influence of the aldehyde ligands.The formation of the complexes (7) and (8) give an indication that the Lewis acidity of the ruthenium center is of importance for aldehyde activation in the catalytic process.
机译:发现[RuCl(H)(CO)(PPh_3)_3](2)在H_2C = CHSiMe_3(3)的存在下催化醛RCHO [R = Et(4a),i-Bu(4b)的三聚。 )}生成1,3,5-三恶烷(5),醛醇缩合生成α,β-不饱和醛(6)。当(4a)用作反应物时,这些反应混合物中的钌络合物[RuCl_2(CO )(PPh_3)_2(EtCH = CMe-CHO-kappaO)](7),其中有醛醇缩合产物作为配体结晶。在与(4b)的类似反应中,配合物[RuCl_2(CO)(PPh_3)_2(i -(BuCHO-kappaO)](8),以醛为配体。通过单晶X射线衍射测量确定了这些配合物的结构。钌中心是八面体配位的,醛和羰基配体在相互反位(配位指数:OC-6-12)。醛通过羰基氧原子(kappaO)单齿配位。配位诱导的C = O双键伸长[1.242(4)A(7),1.234 (4) A(8)}表示醛的活化。此外,Ru-CO键长[1.842(4)A(7),1.823(4)A(8)]对醛配体的反式影响较小。配合物(7)和(8)的形成表明,钌中心的路易斯酸度对于催化过程中的醛活化很重要。

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