divalent platinum
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2019 ◽  
Vol 55 (82) ◽  
pp. 12400-12403 ◽  
Author(s):  
Benjamin J. Frogley ◽  
Anthony F. Hill

The lithiocarbyne [W]CLi ([W] = W(CO)2(Tp*); Tp* = tris(dimethylpyrazolyl)borate) with divalent platinum complexes afford access to μ-carbido, μ-methylidyne and carbyne-based metallo-ligand complexes.


2013 ◽  
Vol 32 (24) ◽  
pp. 7451-7459 ◽  
Author(s):  
Nedaossadat Mirzadeh ◽  
Steven H. Privér ◽  
Martin A. Bennett ◽  
Jörg Wagler ◽  
Suresh K. Bhargava

1983 ◽  
Vol 69 (3) ◽  
pp. 432-441 ◽  
Author(s):  
Robin S. Goldstein ◽  
Gilbert H. Mayor ◽  
Ronald L. Gingerich ◽  
Jerry B. Hook ◽  
Robert W. Rosenbaum ◽  
...  

1981 ◽  
Vol 46 (5) ◽  
pp. 1222-1228 ◽  
Author(s):  
Jiří Pangrác ◽  
Jana Podlahová

Diphenylphosphineacetic acid (HA) acts as a monodentate P-donor towards divalent platinum; the anion acts as a bidentate P,O-donor. Three types of complexes have been prepared, PtX2(HA)2, PtXA(HA) and PtA2 (X = Cl, Br, I, SCN), whose formation is determined primarily by the type of X, the acidity of the medium and the polarity of the solvent. It follows from electronic, infrared and 31P-NMR spectra that all the prepared complexes are cis-square planar in structure.


Author(s):  
N. N. Zheligovskaya ◽  
S. V. Loginov ◽  
L. V. Popov ◽  
V. I. Spitsyn

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