Isolation of a Cationic Platinum(II) σ-Silane Complex

被引:28
作者
Rios, Pablo
Fouilloux, Hugo
Vidossich, Pietro [3 ,4 ]
Diez, Josefina [5 ]
Lledos, Agusti [3 ]
Conejero, Salvador [1 ,2 ]
机构
[1] CSIC, Ctr Innovac Quim Avanzada ORFEO CINCA, Dept Quim Inorgan, IIQ, Avda Americo Vespucio 49, Seville 41092, Spain
[2] Univ Seville, Avda Americo Vespucio 49, Seville 41092, Spain
[3] Univ Autonoma Barcelona, Dept Quim, Ctr Innovac Quim Avanzada ORFEO CINCA, Campus UAB, Cerdanyola Del Valles 08193, Spain
[4] Univ Andes, Dept Chem, COBO Computat Bioorgan Chem Bogota, Bogota, Colombia
[5] Univ Oviedo, Dept Quim Organ & Inorgan, Unidad Asociada CSIC, Lab Compuestos Organomet & Catalisis, E-33006 Oviedo, Spain
关键词
density-functional calculations; platinum; silane; structure elucidation; x-ray diffraction; SI-H; SPECTROSCOPIC CHARACTERIZATION; BOND ACTIVATION; C-H; ETA(2)-SILANE; COORDINATION; RUTHENIUM; DYNAMICS; H-2;
D O I
10.1002/anie.201712791
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The platinum complex [Pt((IBuPr)-Bu-t-Pr-i')((IBuPr)-Bu-t-Pr-i)][BArF] interacts with tertiary silanes to form stable (<0 degrees C) mononuclear Pt-II sigma-SiH complexes [Pt((IBuPr)-Bu-t-Pr-i')((IBuPr)-Bu-t-Pr-i)(eta(1)-HSiR3)][BArF]. These compounds have been fully characterized, including X-ray diffraction methods, as the first examples for platinum. DFT calculations (including electronic topological analysis) support the interpretation of the coordination as an unusual eta(1)-SiH. However, the energies required for achieving a eta(2)-SiH mode are rather low, and is consistent with the propensity of these derivatives to undergo Si-H cleavage leading to the more stable silyl species [Pt(SiR3)((IBuPr)-Bu-t-Pr-i)(2)]-[BArF] at room temperature.
引用
收藏
页码:3217 / 3221
页数:5
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