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Reaction of the bis(phosphinoalkyl)silanes RSiH[(CH 2 ) n PR 1 2 ] 2 (R ) Me or Ph, n ) 2 or 3, R 1) Ph or Cy, i.e., cyclohexyl; biPSiH for R ) Me, n ) 2, R 1 ) Ph) with Pt(COD)Cl 2 (COD ) cycloocta-1,5-diene), [Ir(COD)Cl] 2 , trans-M(PPh 3 ) 2 (CO)Cl (M ) Rh or Ir), or Ru 3 (CO) 12 affords products that are complexes of tridentate biPSi silyl analogues, in which the Si center is anchored through attachment of trans P atoms at the transition-metal site. The platinum(II) compounds Pt[SiMe(CH 2 CH 2 PPh 2 ) 2 ]Cl (1), Pt[SiMe(CH 2 CH 2 PCy 2 ) 2 ]Cl (2), Pt[SiPh(CH 2 CH 2 PCy 2 ) 2 ]Cl (3), Pt[SiPh(CH 2 CH 2 PPh 2 )(CH 2 CH 2 PCy 2 )]Cl (4), Pt[SiMe(CH 2 CH 2 -CH 2 PPh 2 ) 2 ]Cl (5), Pt[SiMe(CH 2 CH 2 CH 2 PCy 2 ) 2 ]Cl (6), and Pt[SiPh(CH 2 CH 2 CH 2 PPh 2 ) 2 ]Cl ( 7), which have been characterized by 1 H, 13 C, and 31 P NMR spectroscopy, possess distinguishable square faces with Me on Si projecting in one direction and the buckled (CH 2 ) n backbones in the other. Cleavage of the Pt-Si bond in Pt(biPSi)Cl ( 5) by HCl affords a pair of diastereomers HPt[(PPh 2 CH 2 CH 2 CH 2 ) 2 Si(Cl)Me]Cl (8,8′) in which the two P atoms are also trans. The five-coordinate, 16e, d 6 Ir(III) complex IrH(biPSi)Cl ( 9) is isolated as a single diastereomer, but octahedral IrH(biPSi)(CO)Cl is formed as a 3:1 mixture of stereoisomers (10 and 11, CO or Cl trans to Si, respectively, i.e., H trans to Cl or CO) that react with SnCl 2 to afford (also 3:1) the analogues IrH(biPSi)(CO)SnCl 3 (12 and 13). Treatment of 10 and 11 (3:1) with LiAlH 4 yields a diastereomeric pair of cis-dihydrido complexes IrH 2 (biPSi)-(CO) (14,14′) (1:3), accompanied by a trans-dihydrido stereoisomer 15 and a fac-biPSi stereoisomer 16 as minor products; in 14, 14′ and 15 the hydride ligands are nonequivalent and show 2 J HHcis ) 5.1, 4.4 Hz, 2 J HHtrans ≈ 0, respectively. Similar treatment with LiAl 2 H 4 affords monodeuterioisotopomers 14a,14′a, while reaction of compound 9 with LiAlH 4 under CO gas initially affords 16 as a single product that subsequently isomerizes to 14,14′. The octahedral, 18e, d 6 Ru(II) homologues RuH[SiMe(CH 2 CH 2 PPh 2 ) 2 ](CO) 2 (17) and RuH(biPSi)-(CO) 2 (18) are formed in sealed-tube reactions at elevated temperature but in very poor yields. NMR spectroscopy suggests that in solution the biPSi backbones of 2-7 and 9-13 are equivalent, establishing planar symmetry (point group C s ) perpendicular to the ligand template, although this is not maintained in the solid state as shown crystallographically for compounds 5, 9, 13, and 18. Bond distances trans to Si are long in 5 and 13 (2.44 and 2.66 Å, to Cl or SnCl 3 , respectively), but in 9 Ir-Cl at 2.30 Å is short, occupying the equatorial plane with Si and H in a distorted TBP structure (Si-Ir-Cl 129°). The M-Si distances are 2.31 (5), 2.29 (9), 2.42 (13), and 2.46 Å (18). In 9 and 13, the H at Ir is anti vs Me on Si (of biPSi), whereas in 18, the Ir-H and Si-Me bonds are syn.

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The complex ?75-cpRuCI(PPh3)2 (cp = cyclopentadienyl) reacts with trimethyl phosphite to give 5-cpRuCI(PPh3)(P(OMe)3). The complex crystallizes in the monoclinic space group 2 ! with a = 10.168 (1) A, b = 16.622 (5) A, c = 14.964 (2) A, ß = 91.40 (1)°, Z = 4, and 4151 data with I > 3cr(J); R = 0.025, Rw = 0.038. The triphenyl phosphite analogue 7?5-cpRuCI(PPh3)(P-(OPh)3) in THF solution reacts with silver triflate and piperidine at 25 °C to give the cyclometalated complex 775-cpRu(PPh3)(P(OPh)2OC6H4).Cationic ruthenium centers of the type 7?5-cpRuL2(S)+ (cp = cyclopentadienyl) can be prepared by replacing the chloride ligand in ?75-cpRuClL3 by a coordinating solvent molecule.1 These solvated cations are of interest because the weakly bound solvent molecule can be readily replaced by a series of other donor molecules.2 Much of the earlier work with these complexes has been focused on the case where the donor ligands L are triphenylphosphine. This complex, ^6-cpRuCl(PPh3)2, has both a chloride ligand, which can be replaced by solvent, and a triphenylphosphine, which can be readily substituted.3 In order to modify the electronic and steric effects at the ruthenium center, we have synthesized the complexes ?j5-cpRuClL2 with a range of different phosphorus donor ligands L and investigated their reactions with silver triflate in dry tetrahydrofuran solvent. Experimental SectionAll reactions were carried out under dry nitrogen conditions by using cannula techniques and a Vacuum Atmospheres drybox.Solvents were dried by using standard reagents and methods. Ruthenium trichloride was supplied by Johnson Matthey, Inc. NMR spectra were measured on a Bruker AC200 spectrometer. Microanalyses were carried out by Galbraith, Inc., Knoxville, TN. Triphenylphosphine, triphenyl phosphite, and trimethyl phosphite were commercially available reagents. Infrared spectra were measured on a Mattson FT-IR spectrometer.Cyclopentadienylchlorobis(triphenylphosphine)ruthenium: ij5-cpRuCl(PPh3)2. This complex was synthesized by a method similar to the published procedure but with one modification.4 A filtered solution of hydrated ruthenium trichloride (3.0 g, 11.5 mmol) in dry ethanol (50 mL) was added in a single aliquot to a rapidly stirred refluxing solution of PPh3 (12.0 g, 46 mmol) in dry ethanol (300 mL). To this solution was immediately added freshly distilled cyclopentadiene (12 mL). The mixture (1)

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