Conformational analysis of the bidentate ligand, tetramethylmethylenediphosphine dioxide, in its chelate complexes with metals

1978 ◽  
Vol 13 (3) ◽  
pp. 256-262
Author(s):  
D. G. Dashevskii ◽  
A. P. Baranov ◽  
T. Ya. Medved' ◽  
M. I. Kabachnik
2007 ◽  
Vol 62 (3) ◽  
pp. 475-482 ◽  
Author(s):  
Karsten Schubert ◽  
Helmar Görls ◽  
Wolfgang Weigand

Starting from 4-bromoacetophenone 1, the 4-bromo-β -hydroxydithiocinnamic acid 2 and the 4-bromo-β -hydroxydithiocinnamic acid hexyl ester 3 were prepared using carbon disulfide and potassium-tert-butylate as a base. Acting as a ligand, the acid gives 1,1-ethenedithiolato complexes with (Ph3P)2Pt(II) (4a), (Et3P)2Pt(II) (4b), dppePt(II) (4c), (Ph3P)2Pd(II) (4d), dppePd(II) (4e), and dppeNi(II) (4f). In contrast to the acid, the deprotonated ester 3 forms a monoanionic bidentate ligand. [O,S] Complexes of Pt(II) (5a), Pd(II) (5b) and Ni(II) (5c) were obtained. All complexes have been fully characterised using 1H NMR, 13C NMR and 31P NMR spectroscopy, mass spectrometry, infrared spectroscopy and elemental analyses. The molecular structures of the complexes 4b and 5a - 5c were determined by X-ray diffraction analyses.


1975 ◽  
Vol 97 (1) ◽  
pp. 73-80 ◽  
Author(s):  
Kenneth L. Servis ◽  
Donald J. Bowler ◽  
Cliff Ishii

1979 ◽  
Vol 34 (2) ◽  
pp. 200-207 ◽  
Author(s):  
Wolfgang Beck ◽  
Timm Kemmerich ◽  
Heiko Böhme

Abstract The preparation and characterization of a series of azido chelate complexes of cobalt(III), N3Co(chel)2B (chel = anionic bidentate ligand, B = base e.g. PPh3, P(OEt)3) and N3Co(chel′)B (chel′ = anionic tetradentate ligand) is reported. In addition, analogous chelate cobalt(III) complexes containing the pesudo halides NCO-, NCS -, CN -, C ≡ CR-, C(CN)3-, CH2NO2- have been prepared.


1972 ◽  
Vol 50 (7) ◽  
pp. 1005-1007 ◽  
Author(s):  
N. Hadjiliadis ◽  
A. Diot ◽  
T. Theophanides

The conformational analysis of the ethylenediamine molecule has been studied by the LCAO-EHMO calculation method. The results indicate that the most stable conformation of the molecule is the gauche form, in which the angle N—C—C—N is ca. 63.0° measured from the cis form. This is in agreement with experimental data and can explain the fact that the ethylenediamine in its chelate complexes is always in the gauche form. In addition, the present results indicate that the trans form is the next most stable conformation of ethylenediamine in agreement with experimental results on bridging ethylenediamine metal complexes.


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