1.3-Diondioxime und ihre Metall(II)-Komplexe mit den Ionen Nickel(II), Palladium(II) und Platin(II) / 1,3-Dionedioximes and their Metal(II) Complexes with Ions Niekel(II), Palladium(II) and Platinum(II)

1978 ◽  
Vol 33 (4) ◽  
pp. 399-402 ◽  
Author(s):  
N. Gottstein ◽  
H. J. Keller

Several alkyl and aryl substituted 1,3-dionedioximes, like acetylacetonedioxime, have been reacted with nickel(II), palladium(II) and platinum(II) in aqueous or alcoholic solution. Two kinds of complexes were obtained:(i) those with stoichiometry metal: ligand = 1 : 1 and(ii) bis(l,3-dionedioximato)metal(II) complexes.None of the isolated solid compounds showed any sign of appreciable intermolecular metal metal interactions. An attempt to enhance intermolecular interaction by oxidizing the compounds with iodine lead to the destruction of all of the complexes.

2014 ◽  
Vol 2 (44) ◽  
pp. 9331-9341 ◽  
Author(s):  
Masayoshi Higuchi

Based on the metal–ligand or metal–metal interactions, metallo-supramolecular polymer films showed stimuli-responsive electro- and photo-chemical properties such as electrochromism.


1998 ◽  
Vol 51 (5) ◽  
pp. 371 ◽  
Author(s):  
Ian G. Phillips ◽  
Peter J. Steel

Thirteen mononuclear, homobinuclear and heterobinuclear transition metal complexes of 4,6-di(2- pyridyl)pyrimidine have been prepared. Assignments of the 1H n.m.r. spectra of the molybdenum(0) and ruthenium(II) complexes were achieved by a combination of one- and two-dimensional n.m.r. techniques, especially 1D-TOCSY. For the ruthenium complexes, electronic absorption spectroscopy and cyclic voltammetry were used to probe the nature of the metal{ligand and, for the binuclear complexes, metal-metal interactions. The complexes have low HOMO−LUMO energy gaps. Meta-metal interactions are shown to be of similar magnitude to those in complexes of the better-studied ligands 2,2′-bipyrimidine and 2,3-di(2-pyridyl)pyrazine.


Author(s):  
Peter Werner Roesky ◽  
Milena Dahlen ◽  
Niklas Reinfandt ◽  
Chengyu Jin ◽  
Michael T. Gamer ◽  
...  

2021 ◽  
Author(s):  
Qiuran Wang ◽  
Sam H. Brooks ◽  
Tianchang Liu ◽  
Neil C. Tomson

This Feature Article describes recent advances in the design of multinucleating ligands that support small molecule activation chemistry.


2004 ◽  
Vol 108 (3) ◽  
pp. 959-964 ◽  
Author(s):  
Shu-Yi Lin ◽  
I-Wen Peter Chen ◽  
Chun-hsien Chen ◽  
Ming-Hsun Hsieh ◽  
Chen-Yu Yeh ◽  
...  

2016 ◽  
Vol 128 (7) ◽  
pp. 2452-2456 ◽  
Author(s):  
Daniël L. J. Broere ◽  
Dieuwertje K. Modder ◽  
Eva Blokker ◽  
Maxime A. Siegler ◽  
Jarl Ivar van der Vlugt

1994 ◽  
Vol 368 ◽  
Author(s):  
M. Malaty ◽  
D. Singh ◽  
R. Schaeffer ◽  
S. Jansen ◽  
S. Lawrence

ABSTRACTStudies of the mixed-metal interface in metal impregnated alumina have indicated the possibility of much metal-metal and metal-substrate interaction. Studies were carried out on NiCu/Al2O3 system which was evaluated to develop a better understanding of the forces that drive modification of the catalytic selectivity of Ni in the presence of Cu. Electron Paramagnetic Resonance (EPR), Powder X-ray Photoelectron Spectroscopy (XPS), X-ray Diffraction (XRD) and theoretical calculations were carried out on this bimetallic system, using Ni,Ag/Al2O3 as a reference as Ni shows negligible electron perturbation on co-adsorbance with Ag onto alumina. XRD results indicate that gross modification of the electronic fields of Ni and Cu are due to direct coupling and intercalation into the alumina matrix. As a result of this phenomena, these materials may form a good base for the development of novel ceramics based on mixed-metal interactions where the intermetallic perturbations are driven by the substrate effects.


1990 ◽  
Vol 52 (3-4) ◽  
pp. 337-357 ◽  
Author(s):  
Wiesław Barabasz ◽  
Bogusława Hetmańska ◽  
Piotr Tomasik

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