219477-53-9Relevant academic research and scientific papers
Thermal Si-C bond cleavage of LRhH(SiAr3)(μ-H) (μ-Cl)RhH(SiAr3)L (Ar = C6H5, C 6H4F-p; L = P(i-Pr)3) to give LRhH(μ-SiAr3)(μ-SiAr2)(μ-Cl)RhHL containing sym
Koizumi, Take-Aki,Osakada, Kohtaro,Yamamoto, Takakazu
, p. 5721 - 5727 (2008/10/08)
The reaction of dinuclear rhodium complex LRhH(SiPh3)(μ-H) (μ-Cl)RhH(SiPh3)L (1; L = P(i-Pr)3) with excess HSi(C6H4F-p)3 leads to replacement of the SiPh3 ligands with the Si-(C
A new series of mono- and dinuclear hydridosilylrhodium(iii) complexes, RhCl(H)(SiAr3)L2 and RhL(SiAr3)H(μ-C1)(μ-H)RhH(SiAr3)L (L = P(i-Pr3)). Preparation by oxidative addition of HSiAr3 and molecular structures of the complexes
Osakada, Kohtaro,Koizumi, Take-Aki,Yamamoto, Takakazu
, p. 2063 - 2069 (2008/10/08)
Reactions of triarylsilanes such as HSiPh3, HSi(C6H4Me-p)3, HSi(C6H4OMe-p)3, HSi(C6H4Cl-p)3, HSi(C6H4F-p)3, and HSi(C6H4CF3-p)3 with RhC(H)(SiA3)L2 = P(i-Pr)3) give a series of hydrido(triarylsilyl)rhodium(III) complexes, RhCl(H)(SiAr3)L2 (1, Ar = Ph; 2, Ar = C6H4Me-p; 3, Ar = C6H4OMe-p; 4, Ar = C6H4Cl-p; 5, Ar = C6H4F-p; 6, Ar = C6H4CF3-p). Tris(phenylethynyl)silane also reacts with the Rh(I) complex to give another oxidative-addition product, RhCl(H)[Si(C≡CPh)3]L2 (7). X-ray analyses of 1 and 7 show a distorted-squarepyramidal coordination around the Rh center with the silyl ligand at the apical position. Prolonged reactions of HSiPh3 and of HSi(C6H4OCF3-p)3 with RhClL2 give dinuclear complexes, RhL(SiAr3)H(μ-Cl)(μ-H)RhH(SiAr3)L (8, Ar = Ph; 9, Ar = C6H4OCF3-p). X-ray crystallography of 9 shows a molecular structure containing two Rh centers bridged with hydrido and chloro ligands. 1,1,3,3-Tetraisopropyldisiloxane undergoes oxidative addition of the Si - H bonds to RhClL2 to give a symmetric dinuclear Rh(III) complex with bridging hydrido, chloro, and disiloxanyl ligands, RhL(H)(μ-H)(μ-Cl)[μ-(i-Pr)2Si - O - Si-(i-Pr)2]Rh(H)L (10).
