Magnetic and spectral properties of two five-coordinate Lewis-base adducts of cobalt(II) Schiff-base complexes with a N3O2 ligand environment

Polyhedron ◽  
2000 ◽  
Vol 19 (13) ◽  
pp. 1643-1648 ◽  
Author(s):  
Floriana Tuna ◽  
Luminita Patron* ◽  
Eric Rivière ◽  
Marie-Laure Boillot*
Molecules ◽  
2019 ◽  
Vol 24 (13) ◽  
pp. 2514 ◽  
Author(s):  
Consiglio ◽  
Oliveri ◽  
Failla ◽  
Di Bella

The zinc(II) ion forms stable complexes with a wide variety of ligands, but those related to Schiff-bases are among the most largely investigated. This review deals with the peculiar aggregation characteristics of Zn(II) Schiff-base complexes from tetradentate N2O2 salen-type ligands, L, derivatives from salicylaldehydes and 1,2-diamines, and is mostly focused on their spectroscopic properties in solution. Thanks to their Lewis acidic character, ZnL complexes show interesting structural, nanostructural, and aggregation/deaggregation properties in relation to the absence/presence of a Lewis base. Deaggregation of these complexes is accompanied by relevant changes of their spectroscopic properties that can appropriately be exploited for sensing Lewis bases. Thus, ZnL complexes have been investigated as chromogenic and fluorogenic chemosensors of charged and neutral Lewis bases, including cell imaging, and have shown to be selective and sensitive to the Lewis basicity of the involved species. From these studies emerges that these popular, Lewis acidic bis(salicylaldiminato)Zn(II) Schiff-base complexes represent classical coordination compounds for modern applications.


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