Synthesis and study of platinum silylene complexes of the type (R3P)2Pt=SiMes2 (Mes = 2,4,6-trimethylphenyl)

2003 ◽  
Vol 81 (11) ◽  
pp. 1127-1136 ◽  
Author(s):  
Jay D Feldman ◽  
Gregory P Mitchell ◽  
Jörn-Oliver Nolte ◽  
T Don Tilley

The synthesis and characterization of neutral platinum silylene complexes (R3P)2Pt=SiMes2 (R = i-Pr (1) or cyclohexyl (2), Mes = 2,4,6-trimethylphenyl) is reported. The dimesitylsilylene ligand in 2 is displaced by a number of ligands including phosphines, alkenes, alkynes, and O2. Complex 2 reacts with ROH substrates (R = H, Me, Et) to give (Cy3P)2Pt and Mes2Si(OR)(H) and with H2 to give trans-(Cy3P)2Pt(H)SiHMes2 (3). Reaction of H2SiMes2 with (Cy3P)2Pt gave cis-(Cy3P)2Pt(H)SiHMes2 (4). EXSY NMR experiments of 4 reveal that exchange of silicon and platinum hydrides occurs via reductive elimination – oxidative addition and not via a silylene intermediate.Key words: silylene, EXSY, platinum, hydride.


2011 ◽  
Vol 4 (1) ◽  
pp. 109 ◽  
Author(s):  
R. Begum ◽  
S. M. S. Islam

Synthesis of two methoxy bridged bis(silylene) complexes (CpMe4)W(CO)2 {(Et2Si)••OMe••(SiMe2)}(3) and (CpMe)W(CO)2 {(Et2Si)••OMe••(SiMe2)}(4) have been synthesized. Both the compounds contain chiral tungsten center and formed via oxidative addition of an Si-H bond to a coordinatively unsaturated metal center. The complexes were characterized by 1H, 13C, 29Si NMR, IR and elemental analysis. A plausible mechanism of formation is also suggested.Keywords:  Coordinatively unsaturated; Chiral tungsten; Oxidative addition.© 2012 JSR Publications. ISSN: 2070-0237 (Print); 2070-0245 (Online). All rights reserved.doi: http://dx.doi.org/10.3329/jsr.v4i1.7890J. Sci. Res. 4 (1), 109-118 (2012)



1987 ◽  
Vol 6 (11) ◽  
pp. 2453-2455 ◽  
Author(s):  
Claudio. Bianchini ◽  
Andrea. Meli ◽  
Maurizio. Peruzzini ◽  
Alberto. Vacca ◽  
Fabrizio. Zanobini


Author(s):  
José Ruiz ◽  
J. F. Javier López ◽  
Venancio Rodríguez ◽  
José Pérez† ◽  
M. Carmen Ramírez de Arellano ◽  
...  


1987 ◽  
Vol 40 (9) ◽  
pp. 1565 ◽  
Author(s):  
TG Appleton ◽  
JR Hall ◽  
MA Williams

Reactions of cyanide with the dimethylplatinum (IV) complexes, [PtMe2(OH) (H20)1.5 n, [PtMe2Br2]n and fac-PtMe2Br(H2O)3+, have been studied, principally by 1H, 13C and 195Pt n.m.r. Cyanide rapidly displaces the ligands trans to the methyl groups. Subsequent reactions cis to the methyl groups occur more slowly with heating, or, for bromo complexes, on ultraviolet irradiation. These substitution reactions compete with reductive elimination of groups from the platinum(IV) compounds to produce platinum(II) products. All attempts to prepare solutions of fac-PtMe2(CN)(H2O)3+ were unsuccessful. Oxidative addition of ICN to cis-PtMe2( py )2 ( py = pyridine) gave PtMe2I(CN)( py )2, from which a solution of fac-PtMe2(CN)( MeOH )3+ in methanol could be obtained. Addition of water or aqueous acid to this solution gave a very insoluble precipitate of [PtMe2(CN)(OH)n. The cis and trans influences on Jpt -C and δC of the cyanide ligands have been evaluated.





1993 ◽  
Vol 12 (11) ◽  
pp. 4368-4375 ◽  
Author(s):  
Juan Fornies ◽  
Consuelo Fortuno ◽  
Miguel A. Gomez ◽  
Babil Menjon ◽  
Eberhardt Herdtweck


1996 ◽  
Vol 15 (8) ◽  
pp. 2185-2188 ◽  
Author(s):  
Wanzhi Chen ◽  
Andrew J. Edwards ◽  
Miguel A. Esteruelas ◽  
Fernando J. Lahoz ◽  
Montserrat Oliván ◽  
...  




1996 ◽  
Vol 35 (5) ◽  
pp. 1250-1256 ◽  
Author(s):  
María L. Buil ◽  
Pablo Espinet ◽  
Miguel A. Esteruelas ◽  
Fernando J. Lahoz ◽  
Agustí Lledós ◽  
...  


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