Site selectivity in carbon monoxide insertion into a PtC σ-bond of the binuclear complex [(CH3)ClPt(μ-Cl) (μ-Ph2PPy) Pt(CH3)(DMSO)]DMSO. Structural characterization of the derivatives [(CH3CO)ClPt(μ-Cl)(μ-Ph2 PPy)Pt(CH3)(DMSO)] and [(CH3)ClPt(μ-Ph2PPy)2Pt(COCH3)]+

1994 ◽  
Vol 484 (1-2) ◽  
pp. 71-80 ◽  
Author(s):  
Carmela G. Arena ◽  
Gianfranco Ciani ◽  
Dario Drommi ◽  
Felice Faraone ◽  
Davide M. Proserpio ◽  
...  
1998 ◽  
Vol 120 (30) ◽  
pp. 7502-7510 ◽  
Author(s):  
William K. Russell ◽  
Christina M. V. Stålhandske ◽  
Jinqiang Xia ◽  
Robert A. Scott ◽  
Paul A. Lindahl

2014 ◽  
Vol 92 (3) ◽  
pp. 194-200 ◽  
Author(s):  
Colin M. Kelly ◽  
Adam J. Ruddy ◽  
Craig A. Wheaton ◽  
Orson L. Sydora ◽  
Brooke L. Small ◽  
...  

We report herein on the synthesis and spectroscopic/crystallographic characterization of the first isolable, formally 16-electron Cp*Ru(κ2-P∼N) species, which are supported by N-phosphinoamidinate ligands. Despite the stability of such complexes, they have been shown to readily coordinate two-electron (L) donors including carbon monoxide and 2,6-xylylisocyanide, affording crystallographically characterized 18-electron Cp*Ru(L)(κ2-P∼N) adducts. Preliminary reactivity studies confirm that such complexes are capable of extruding hydrogen from ammonia borane.


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