Five-membered metal chelate rings in complexes of palladium with 2-mercaptomethylazobenzene

1997 ◽  
Vol 7 (6) ◽  
pp. 239-240 ◽  
Author(s):  
Victor A. Kogan ◽  
Stanislav G. Kochin ◽  
Alla S. Antsyshkina ◽  
Georgii G. Sadikov ◽  
Alexander D. Garnovskii
Keyword(s):  
2002 ◽  
Vol 609 (1-3) ◽  
pp. 1-9 ◽  
Author(s):  
Sonja Grubišić ◽  
Maja Gruden ◽  
S.R. Niketić ◽  
Narumi Sakagami- Yoshida ◽  
Sumio Kaizaki

2019 ◽  
Vol 48 (19) ◽  
pp. 6328-6332 ◽  
Author(s):  
Dušan P. Malenov ◽  
Snežana D. Zarić

Stacking interactions of metal–chelate rings are strong due to very strong electrostatic energy component.


1963 ◽  
Vol 2 (3) ◽  
pp. 576-580 ◽  
Author(s):  
James P. Collman ◽  
Robert P. Blair ◽  
Roger L. Marshall ◽  
Laird Slade

1968 ◽  
Vol 46 (2) ◽  
pp. 327-330 ◽  
Author(s):  
R. M. Cassidy ◽  
D. E. Ryan

A number of disubstituted hydroxamic acids were investigated as possible replacements for benzoylphenylhydroxylamine in the determination of vanadium; none is superior. At 378 mμ., p-phenylazobenzoylphenylhydroxylamine shows a marked sensitivity increase but selectivity is poor. In the visible region, there is an increase in molecular extinction coefficient as the reagent π system is extended; how ever, complete coplanarity of the aromatic and metal chelate rings is not possible and the increase is not large enough to be of much practical value.


Chemistry ◽  
2021 ◽  
Vol 4 (1) ◽  
pp. 18-30
Author(s):  
Atena B. Solea ◽  
Liangru Yang ◽  
Aurelien Crochet ◽  
Katharina M. Fromm ◽  
Christophe Allemann ◽  
...  

The complexation behavior of two novel, chiral pinene–bipyridine-type ligands ((–)-HL1 and (–)-HL2) containing a carboxylic arm towards lanthanide Ln(III) (Ln = La, Eu, Lu) ions was investigated through spectroscopic methods. The association constants of the mononuclear complexes determined from the UV-Vis titrations indicated that the ligand (–)-HL1 possessing a shorter carboxylic arm formed more stable complexes compared with (–)-HL2, whose carboxylic arm had one more methylene unit. This is due to the formation of more stable seven-member metal chelate rings in the first case as compared with the eight-member metal chelate rings in the second. IR and fluorescence spectroscopy provided additional information about the structure of these complexes.


1973 ◽  
Vol 27 ◽  
pp. 3811-3816 ◽  
Author(s):  
S. R. Niketić ◽  
F. Woldbye ◽  
Anne-Charlotte Wiehager ◽  
T. Laier ◽  
Wolfgang Nimmich

2008 ◽  
Vol 59 (11) ◽  
Author(s):  
Mircea Braban ◽  
Ionel Haiduc

The paper describes the solid state structure of a compound of composition [Cu(bipy)3][Cu(bipy)(ala) (ClO4)2]ClO4, in which both the cation and anion are octahedral complex species with copper(II) as coordination center. The cation contains three chelate rings formed by bipy; the anion contains in the quatorial plane a CuONC2 chelate ring formed by the alaninato ligand and a CuN2C2 chelate ring formed by bipy, with two monodentate perchorato ligands in axial positions completing the six-coordination. In the crystal p-p stackings lead to a supramolecular self-assembled structure.


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