Quadridentate Chelate Compounds. IV. Metal Complexes from Butane-2,3-dione Bis-(2'-pyridylhydrazone)

1964 ◽  
Vol 3 (4) ◽  
pp. 490-492 ◽  
Author(s):  
Barry Chiswell ◽  
Francis Lions
1973 ◽  
Vol 93 (4) ◽  
pp. 401-405
Author(s):  
YOSHINORI KIDANI ◽  
KATSUMASA ARAKAWA ◽  
HISASHI KOIKE

1964 ◽  
Vol 3 (4) ◽  
pp. 492-499 ◽  
Author(s):  
Barry Chiswell ◽  
Francis Lions ◽  
Muriel L. Tomlinson

1964 ◽  
Vol 3 (1) ◽  
pp. 110-114 ◽  
Author(s):  
Barry Chiswell ◽  
Francis Lions ◽  
Benjamin S. Morris

2013 ◽  
Vol 11 (5) ◽  
pp. 655-663 ◽  
Author(s):  
Krzysztof Zborowski ◽  
Miquel Solá ◽  
Jordi Poater ◽  
Leonard Proniewicz

AbstractChelatoaromaticity (aromaticity of chelate complexes) has been recently recognized as an important property influencing the stability of chelate compounds. In this paper, aromaticity of various forms of 8-hydroxyquinoline (anion, neutral molecule, zwitterion and cation) as well as its chelate complexes with magnesium and aluminium ions are investigated. Aromatic properties of these compounds are analyzed using several aromaticity indices based on energetic, geometric, magnetic and electronic physical manifestations of this phenomenon. Results of performed calculations have shown different aromatic properties for the two rings (pyridine and benzene) occurring in the studied ligand. Aromaticity of these rings in metal complexes of 8-hydroxyquinoline is significantly higher than that in corresponding ligand anion. This means that during complexation the aromaticity of the ligand increases and the chelatoaromatic effect stabilizes the studied metal complexes. In contrast, metallocyclic rings of studied metal complexes have non-aromatic properties, and, consequently, the metallocyclic ring is not stabilized by chelatoaromaticity. We conclude that, in the complex, every 8-hydroxyquinoline unit and the metal ion are separated p-electronic systems.


2000 ◽  
Vol 55 (9) ◽  
pp. 855-862 ◽  
Author(s):  
Winfried Hoffmüller ◽  
Roland Krämer ◽  
Michael Maurus ◽  
Kurt Polbom ◽  
Wolfgang Beck

Reactions of chloro bridged palladium compounds with di- and tripeptide esters give (Et3P)(Cl)2Pd(NH2CHR1CONHCHR2CO2CH3) and the N,N′-chelate compounds (Et3P)- (Cl)Pd(NH2CH2CONCHR1 CO2R2), [C6H4CH 2NMe2(C,N)]Pd(NH2CH2CONCH2CO2Et) and (Et3P)Pd(gly-gly-glyOMe-2H+). The structure of (Et3P)(Cl)Pd(gly-alaOMe-H+) was determined by X-ray diffraction analyses. Attempts to form open chain peptides from α-amino acid ester in the coordination sphere of palladium(II) are reported


1973 ◽  
Vol 93 (9) ◽  
pp. 1089-1093 ◽  
Author(s):  
YOSHINORI KIDANI ◽  
KENJI INAGAKI ◽  
HISASHI KOIKE

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