Improving the stability and inertness of Cu(ii) and Cu(i) complexes with methylthiazolyl ligands by tuning the macrocyclic structure. Issue 17 (4th April 2016)
- Record Type:
- Journal Article
- Title:
- Improving the stability and inertness of Cu(ii) and Cu(i) complexes with methylthiazolyl ligands by tuning the macrocyclic structure. Issue 17 (4th April 2016)
- Main Title:
- Improving the stability and inertness of Cu(ii) and Cu(i) complexes with methylthiazolyl ligands by tuning the macrocyclic structure
- Authors:
- Le Fur, Mariane
Beyler, Maryline
Le Poul, Nicolas
Lima, Luís M. P.
Le Mest, Yves
Delgado, Rita
Platas-Iglesias, Carlos
Patinec, Véronique
Tripier, Raphaël - Abstract:
- Abstract : A tacn bearing methylthiazolyl arms was synthesized and its copper(ii ) and (i ) complexes showed excellent stability and inertness in aqueous medium. Abstract : A tacn based ligand bearing two methylthiazolyl arms (no2th ) was synthesized with the aim to find ligands forming very stable and inert complexes with Cu(ii ) and Cu(i ) in aqueous medium for radiopharmaceutical applications. Theno2th ligand was efficiently prepared following the orthoamide intermediate synthesis. The complexes with Cu 2+ and Zn 2+ were obtained and analyzed by X-ray diffraction. The [Cu(no2th )] 2+ complex presents a pentacoordinated distorted square pyramidal coordination geometry, while the metal ion in [Zn(no2th )] 2+ adopts a hexacoordinated distorted trigonal prismatic geometry involving the coordination of a perchlorate counter ion. The acid–base properties ofno2th have been studied using potentiometric titrations, and the stability constants of Cu 2+ and Zn 2+ complexes were determined by potentiometric and UV-vis titrations using H4 edta as a competitor ligand. The stability constant determined for the Cu 2+ complex is rather high (log K CuL = 20.77 and pCu = 17.15), and moreoverno2th exhibits a high selectivity for copper(ii ) in relation to zinc(ii ). The kinetics of the copper(ii ) complexation process is very fast even in acidic medium. In addition, the [Cu(no2th )] 2+ complex was found to be inert under rather harsh conditions (up to 2 M HCl and 60 °C), displaying a veryAbstract : A tacn bearing methylthiazolyl arms was synthesized and its copper(ii ) and (i ) complexes showed excellent stability and inertness in aqueous medium. Abstract : A tacn based ligand bearing two methylthiazolyl arms (no2th ) was synthesized with the aim to find ligands forming very stable and inert complexes with Cu(ii ) and Cu(i ) in aqueous medium for radiopharmaceutical applications. Theno2th ligand was efficiently prepared following the orthoamide intermediate synthesis. The complexes with Cu 2+ and Zn 2+ were obtained and analyzed by X-ray diffraction. The [Cu(no2th )] 2+ complex presents a pentacoordinated distorted square pyramidal coordination geometry, while the metal ion in [Zn(no2th )] 2+ adopts a hexacoordinated distorted trigonal prismatic geometry involving the coordination of a perchlorate counter ion. The acid–base properties ofno2th have been studied using potentiometric titrations, and the stability constants of Cu 2+ and Zn 2+ complexes were determined by potentiometric and UV-vis titrations using H4 edta as a competitor ligand. The stability constant determined for the Cu 2+ complex is rather high (log K CuL = 20.77 and pCu = 17.15), and moreoverno2th exhibits a high selectivity for copper(ii ) in relation to zinc(ii ). The kinetics of the copper(ii ) complexation process is very fast even in acidic medium. In addition, the [Cu(no2th )] 2+ complex was found to be inert under rather harsh conditions (up to 2 M HCl and 60 °C), displaying a very high half-life time of about 15 days in 2 M HCl at 90 °C. The electrochemical reduction of the copper(ii ) complex in water leads to the reversible formation of a stable copper(i ) species. Spectroscopic studies performed by NMR, UV-vis and EPR, assisted by theoretical calculations, show that the [Cu(no2th )] 2+ complex presents a structure in solution similar to that observed in the solid state. When compared to its cyclam di- N -methylthiazolyl counterpart, the results reported in this paper unambiguously show that replacing the cyclam unit by a tacn moiety improves the stability and inertness of its Cu(ii ) and Cu(i ) complexes. … (more)
- Is Part Of:
- Dalton transactions. Volume 45:Issue 17(2016)
- Journal:
- Dalton transactions
- Issue:
- Volume 45:Issue 17(2016)
- Issue Display:
- Volume 45, Issue 17 (2016)
- Year:
- 2016
- Volume:
- 45
- Issue:
- 17
- Issue Sort Value:
- 2016-0045-0017-0000
- Page Start:
- 7406
- Page End:
- 7420
- Publication Date:
- 2016-04-04
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6dt00385k ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 61.xml