Issue 18, 2008

New fluorenyl-substituted ditopic dioxotetraamine ligands and their copper(ii) complexes—synthesis, crystal structure, magnetic properties and solution behavior

Abstract

A new fluorenyl-substituted dioxotetraamine salicylaldehyde Schiff-base ligand (L1) has been synthesized by the non-template 1 + 2 condensation of ligand 6-(9-fluorenyl)-1,4,8,11-tetraazaundecane-5,7-dione (L) with salicylaldehyde. From reduction of L1 with an excess of NaBH4, a ditopic dioxotetraamine ligand (L2) has been obtained. The copper(II) complex of L1 has been synthesized and its properties were examined by ES-MS and variable-temperature magnetic susceptibility as well as its crystal structure being determined. Detailed studies have been made on solution chemistry of Cu(II) complex of L2 by pH-potentiometric and fluorometric titration.

Graphical abstract: New fluorenyl-substituted ditopic dioxotetraamine ligands and their copper(ii) complexes—synthesis, crystal structure, magnetic properties and solution behavior

Supplementary files

Article information

Article type
Paper
Submitted
23 Nov 2007
Accepted
08 Feb 2008
First published
18 Mar 2008

Dalton Trans., 2008, 2487-2494

New fluorenyl-substituted ditopic dioxotetraamine ligands and their copper(II) complexes—synthesis, crystal structure, magnetic properties and solution behavior

Q. Li, Y. Wang, Q. Luo, X. Hu and Y. Li, Dalton Trans., 2008, 2487 DOI: 10.1039/B717866B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements