People | Locations | Statistics |
---|---|---|
Naji, M. |
| |
Motta, Antonella |
| |
Aletan, Dirar |
| |
Mohamed, Tarek |
| |
Ertürk, Emre |
| |
Taccardi, Nicola |
| |
Kononenko, Denys |
| |
Petrov, R. H. | Madrid |
|
Alshaaer, Mazen | Brussels |
|
Bih, L. |
| |
Casati, R. |
| |
Muller, Hermance |
| |
Kočí, Jan | Prague |
|
Šuljagić, Marija |
| |
Kalteremidou, Kalliopi-Artemi | Brussels |
|
Azam, Siraj |
| |
Ospanova, Alyiya |
| |
Blanpain, Bart |
| |
Ali, M. A. |
| |
Popa, V. |
| |
Rančić, M. |
| |
Ollier, Nadège |
| |
Azevedo, Nuno Monteiro |
| |
Landes, Michael |
| |
Rignanese, Gian-Marco |
|
Djuran, Miloš I.
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (7/7 displayed)
- 2020Zinc(II) complexes with aromatic nitrogen-containing heterocycles as antifungal agents: Synergistic activity with clinically used drug nystatincitations
- 2020Modulation of the structure of octahedral 1,3-pdta-nickel(II) complex by introducing methyl substituents at the central 1,3-propanediamine carbon atom: Stereospecific formation and the crystal structure of [Mg(H2O)5Ni(2,2-diMe-1,3-pdta)]·1.5H2Ocitations
- 2017Mononuclear gold(iii) complexes with l-histidine-containing dipeptides: tuning the structural and biological properties by variation of the N-terminal amino acid and counter anioncitations
- 2017Mononuclear gold(III) complexes with phenanthroline ligands as efficient inhibitors of angiogenesis: A comparative study with auranofin and sunitinibcitations
- 2011Structural diversification of the coordination mode of divalent metals with 1,3-propanediaminetetraacetate (1,3-pdta): The missing crystal structure of the s-block metal complex [Sr<inf>2</inf>(1,3-pdta)(H<inf>2</inf>O) <inf>6</inf>]·H<inf>2</inf>Ocitations
- 2008Coordination behaviour and two-dimensional-network formation in poly[[μ-aqua-diaqua-(μ5-propane-1,3-diyldinitrilo-tetra-acetato) -dilithium(I)-cobalt(II)] dihydrate]: The first example of an M <sup>II</sup>-1,3-pdta complex with a monovalent metal counter-ioncitations
- 2005Highly selective crystallization of metal(II) ions with 1,3-pdta ligand: Syntheses and crystal structures of the [Mg(H<inf>2</inf>O)<inf>6</inf>][Cd(1,3- pdta)(H<inf>2</inf>O)]·2H<inf>2</inf>O and two isomorphic [Zn(1,3-pdta)]<sup>2-</sup> complexescitations
Places of action
Organizations | Location | People |
---|
article
Structural diversification of the coordination mode of divalent metals with 1,3-propanediaminetetraacetate (1,3-pdta): The missing crystal structure of the s-block metal complex [Sr<inf>2</inf>(1,3-pdta)(H<inf>2</inf>O) <inf>6</inf>]·H<inf>2</inf>O
Abstract
<p>This paper reports the synthesis and X-ray characteristics of the missing homonuclear s-block metal complex {[Sr<sub>2</sub>(1,3-pdta)(H <sub>2</sub>O)<sub>6</sub>]·H<sub>2</sub>O}<sub>n</sub>. In the title compound, the hexadentate 1,3-propanediaminetetraacetate (1,3-pdta) ligand joins to two Sr(II) centers via the diamine chain. Moreover, each Sr(II) is bridged through two carboxylate O atoms and a water molecule to two neighboring Sr(II) ions. The coordination sphere around each Sr(II) ion consists of one diamine nitrogen, four carboxylate oxygens and four water molecules. Comparison with the previously reported M(II)-1,3-pdta complexes reveals that increasing of the ion size results in the incorporation of water molecules into its first coordination sphere and consequent increase of the coordination number (C.N.) from six to seven or eight, while keeping the hexadentate coordination mode of the ligand. Further increase of the metal ion size leads to the loss of the chelating properties of the diamine and formation of a bis-tridentate complex. Associated with it is the change in the binding mode of the carboxylate groups. This forms the basis for classification of divalent metal 1,3-pdta complexes into five distinct structural classes. Additionally, in the present study X-ray powder diffraction and IR spectroscopy were used to distinguish the different structural types of M(II)-1,3-pdta complexes, including Ba[Ba(1,3-pdta)] ·2H<sub>2</sub>O which has been used for their preparation. © 2011 Elsevier Ltd. All rights reserved.</p>