The chemical shape of molecules: an introduction to dynamic stereochemistry

1990 ◽  
Vol 94 (26) ◽  
pp. 8872-8880 ◽  
Author(s):  
Raphael D. Levine
1988 ◽  
Vol 121 (5) ◽  
pp. 917-922 ◽  
Author(s):  
Axel Meyer ◽  
Karl Schlögl ◽  
Ulrike Lerch ◽  
Emanuel Vogel

1975 ◽  
Vol 29b ◽  
pp. 741-748 ◽  
Author(s):  
Arild J. Dale ◽  
Paul Frøyen ◽  
Mona Grönlund ◽  
Anna-Britta Hörnfeldt ◽  
Rolf Servin ◽  
...  

1975 ◽  
Vol 53 (17) ◽  
pp. 2558-2574 ◽  
Author(s):  
Thomas R. Jack ◽  
John Powell

A series of dimeric tertiary phosphine carboxylate complexes of palladium(II) of the general types [(PR3)Pd(O2CR)2]2 and [(PR3)Pd(O2CR)(O2CR)]2 have been synthesized and struc-turally characterized. The dynamic stereochemistry of the complexes where PR3 = Me2PhP has been investigated using variable temperature n.m.r. techniques. Exchange of the stereochemically nonequivalent methyl groups of the coordinated Me2PhP ligand occurs via a solvent assisted process involving ring opening of the "Pd2(OCO)2" bridged structure. For the trifluoroacetate complexes solution equilibria between monomer and dimer are readily apparent at low temperatures in the 19F n.m.r. The observed equilibrium constants are a function of the solvent and the size of the PR3 ligand. The reaction of [(PMe2Ph)Pd(O2CCF3)2]2 with excess AgO2CCF3 gives an unusual crystalline complex of stoichiometry Ag[(PMe2Ph)Pd(O2CCF3)3]. A quantitative measure of the ability of a coordinated carboxylate to stabilize intermediate species via chelation has been obtained from a variable temperature n.m.r. study of [(Π-2-methylallyl)Pd(O2CR)(Me2PhP)] (R=CH3, CH2Cl, CHCl2, CCl3, CF3, CMe3, CPh3, CH2Ph).


1986 ◽  
Vol 22 (2) ◽  
pp. 206-210
Author(s):  
B. A. Puodzhyunaite ◽  
R. A. Yanchene ◽  
Z. A. Stumbryavichyute ◽  
P. P. Mikul'skis

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