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首页> 外文期刊>Journal of Organometallic Chemistry >WATER-SOLUBLE ORGANOMETALLIC COMPOUNDS .5. THE REGIO-SELECTIVE CATALYTIC HYDROGENATION OF UNSATURATED ALDEHYDES TO SATURATED ALDEHYDES IN AN AQUEOUS TWO-PHASE SOLVENT SYSTEM USING 1,3,5-TRIAZA-7-PHOSPHAADAMANTANE COMPLEXES OF RHODIUM
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WATER-SOLUBLE ORGANOMETALLIC COMPOUNDS .5. THE REGIO-SELECTIVE CATALYTIC HYDROGENATION OF UNSATURATED ALDEHYDES TO SATURATED ALDEHYDES IN AN AQUEOUS TWO-PHASE SOLVENT SYSTEM USING 1,3,5-TRIAZA-7-PHOSPHAADAMANTANE COMPLEXES OF RHODIUM

机译:水溶性有机化合物.5。使用铑的1,3,5-三氮杂-7-磷酸金刚烷络合物在两相溶剂体系中将不饱和醛进行区域选择性催化加氢成饱和醛

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The water-soluble phosphine complex of Rh(I), [Rh(PTAH)(PTA)(2)Cl]Cl (1), has been synthesized from RhCl3 and 1,3,5,-triaza-7-phosphaadamantane (PTA) in 96% ethanol. This complex is an effective catalyst for the regioselective reduction of unsaturated aldehydes to saturated aldehydes. The rate of hydrogenation of trans-cinnamaldehyde with sodium formate as reductant was studied as a function of catalyst, substrate, and sodium formate concentration. The presence of an excess of PTA was found to inhibit hydrogenations completely. This reaction was also found to be partially inhibited by cyclo-octatetraene and Hg(O), leading to the conclusion that both heterogeneous and homogeneous mechanisms are operating. Recycling experiments show complex 1 to be quite robust, with minimal leaching into the organic phase in a biphasic system. The complex resulting from the addition of an excess of PTA to 1, [Rh(PTAH)(3)(PTA)CL]Cl-3 (2), has been prepared and structurally characterized by a single crystal X-ray diffraction study. P-31 and H-1 NMR, IR, and UV-VIS spectroscopy and pH titrametric measurements were employed to study the reactivity of the various rhodium PTA complexes in aqueous solutions. [References: 67]
机译:Rh(I)的水溶性膦络合物[Rh(PTAH)(PTA)(2)Cl] Cl(1)是由RhCl3和1,3,5,-triaza-7-phosphaadamantane(PTA)合成的)的96%乙醇溶液。该络合物是用于将不饱和醛区域选择性还原为饱和醛的有效催化剂。研究了以肉桂酸钠为还原剂的反式肉桂醛的氢化速率与催化剂,底物和甲酸钠浓度的关系。发现过量的PTA的存在完全抑制氢化。还发现该反应受到环辛酸酯和Hg(O)的部分抑制,从而得出结论,即异质和均相机理均在起作用。再循环实验表明,复合物1非常坚固,在双相系统中几乎没有浸出到有机相中。由过量的PTA加至1 [Rh(PTAH)(3)(PTA)CL] Cl-3(2)制成的配合物已经制备,并通过单晶X射线衍射研究对其结构进行了表征。使用P-31和H-1 NMR,IR和UV-VIS光谱以及pH滴定法研究水溶液中各种铑PTA配合物的反应性。 [参考:67]

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