首页> 外文期刊>Inorganics >P -Fluorous Phosphines as Electron-Poor/Fluorous Hybrid Functional Ligands for Precious Metal Catalysts: Synthesis of Rh(I), Ir(I), Pt(II), and Au(I) Complexes Bearing P -Fluorous Phosphine Ligands
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P -Fluorous Phosphines as Electron-Poor/Fluorous Hybrid Functional Ligands for Precious Metal Catalysts: Synthesis of Rh(I), Ir(I), Pt(II), and Au(I) Complexes Bearing P -Fluorous Phosphine Ligands

机译:P氟膦作为贵金属催化剂的电子贫/氟杂化功能配体:合成含P氟膦配体的Rh(I),Ir(I),Pt(II)和Au(I)配合物

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P -Fluorous phosphine (R 2 PR f ), in which the perfluoroalkyl group is directly bonded to the phosphorus atom, is a promising ligand because it has a hybrid functionality, i.e., electron-poor and fluorous ligands. However, examples of P -fluorous phosphine–metal complexes are still rare, most probably because the P -fluorous group is believed to decrease the coordination ability of the phosphines dramatically. In contrast, however, we have succeeded in synthesizing a series of P -fluorous phosphine–coordinated metal complexes such as rhodium, iridium, platinum, and gold. Furthermore, the electronic properties of R 2 P n C 10 F 21 are investigated by X-ray analysis of PtCl 2 (Ph 2 P n C 10 F 21 ) 2 and the infrared CO stretching frequency of RhCl(CO)(R 2 P n C 10 F 21 ) 2 . IrCl(CO)(Ph 2 P n C 10 F 21 ) 2 - and AuCl(R 2 P n C 10 F 21 )-catalyzed reactions are also demonstrated.
机译:全氟烷基直接键合到磷原子上的P-氟膦(R 2 PR f)是一种很有前途的配体,因为它具有杂化功能,即贫电子配体和氟配体。但是,P-氟膦-金属配合物的例子仍然很少,最可能是因为据信P-氟基团会显着降低膦的配位能力。但是,相比之下,我们已经成功地合成了一系列由P-氟膦配位的金属配合物,例如铑,铱,铂和金。此外,通过X射线分析PtCl 2(Ph 2 P n C 10 F 21)2和RhCl(CO)(R 2 P)的红外CO拉伸频率,研究了R 2 P n C 10 F 21的电子性质。 n C 10 F 21)2。还证明了IrCl(CO)(Ph 2 P n C 10 F 21)2-和AuCl(R 2 P n C 10 F 21)催化的反应。

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