Synthesis, structural characterization and NMR studies of group 10 metal complexes with macrocyclic amine N-heterocyclic carbene ligands

2018 ◽  
Vol 47 (12) ◽  
pp. 4282-4292
Author(s):  
Taotao Lu ◽  
Zhiming Liu ◽  
Carlos A. Steren ◽  
Fan Fei ◽  
Tabitha M. Cook ◽  
...  

Two conformers of Ni(ii), Pd(ii) and Pt(ii) complexes with two types of tetradentate macrocyclic amine-NHC ligands have been revealed.

RSC Advances ◽  
2014 ◽  
Vol 4 (18) ◽  
pp. 9383-9394 ◽  
Author(s):  
Lorena Soria ◽  
Paloma Ovejero ◽  
Mercedes Cano ◽  
José Vicente Heras ◽  
M. Rosario Torres ◽  
...  

Novel metal complexes containing dipyridylpyrazole ligands as efficient examples of isomerism are investigated.


2021 ◽  
Vol 330 ◽  
pp. 115522
Author(s):  
Ola A. El-Gammal ◽  
Farid Sh. Mohamed ◽  
Ghada N. Rezk ◽  
Ashraf A. El-Bindary

2004 ◽  
Vol 23 (4) ◽  
pp. 755-764 ◽  
Author(s):  
Xile Hu ◽  
Ingrid Castro-Rodriguez ◽  
Kristian Olsen ◽  
Karsten Meyer

Author(s):  
Vignesh Vasu ◽  
Joon-Sung Kim ◽  
Hyun-Seok Yu ◽  
William I. Bannerman ◽  
Mark E. Johnson ◽  
...  
Keyword(s):  

2014 ◽  
Vol 18 (01n02) ◽  
pp. 115-122 ◽  
Author(s):  
Srinivas Banala ◽  
Klaus Wurst ◽  
Bernhard Kräutler

We report here the preparation (in "one-pot") of a tetra-β″-sulfoleno-meso-aryl-porphyrin in about 80% yield by using an optimized modification of Lindsey's variant of the Adler–Longo approach. The Zn ( II )-, Cu ( II )- and Ni ( II )-complexes of the symmetrical porphyrin were prepared and characterized spectroscopically. Crystal structures of the fluorescent Zn ( II )- and of the non-fluorescent Ni ( II )-tetra-β″-sulfoleno-meso-aryl-porphyrinates showed the highly substituted porphyrin ligands to be nearly perfectly planar. The Zn ( II )-complex of this porphyrin has been used as a thermal precursor of a reactive diene, and — formally — of lateral and diagonal bis-dienes, of a tris-diene and of a tetra-diene, which all underwent [4 + 2]-cycloaddition reactions in situ with a range of dienophiles. Thus, the tetra-β″-sulfoleno-meso-aryl-porphyrin and its metal complexes represent reactive building blocks, "programmed" for the syntheses of symmetrical and highly functionalized porphyrins.


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