Issue 29, 2009

Na+ and Ca2+ ion selective pyridylcarboxylate rings of Pd(II) and Pt(II)

Abstract

A series of dinuclear Pd(II) and Pt(II) with central rectangular cavities have been self-assembled using pyridyl carboxylates as spacers and phosphines [1,1′-bis(diphenylphosphino)ferrocene (dppf) and triphenylphosphines] as supporting ligands. Some of these function as metallacrowns by capturing adventitious alkali or alkali earth metals ions. Two of the Pt(II) rings bind selectively to Na+ whereas the Pd(II) rings prefer Ca2+. Such endocyclic association with the metal ion is facilitated by the converging carbonyl pendants and supported by coordinated triflates. Affinity and selectivity are achieved through stereo-conformational control of the pendant carbonyls and the ring which are isomerically dependent on the spacer. These intermetallic complexes are characterized by X-ray single-crystal crystallography and solution spectroscopy (NMR and ESI-MS). A varied range of local geometries of Na+ and Ca2+ are revealed.

Graphical abstract: Na+ and Ca2+ ion selective pyridylcarboxylate rings of Pd(II) and Pt(II)

Supplementary files

Article information

Article type
Paper
Submitted
28 Nov 2008
Accepted
22 May 2009
First published
29 Jun 2009

Dalton Trans., 2009, 5637-5646

Na+ and Ca2+ ion selective pyridylcarboxylate rings of Pd(II) and Pt(II)

P. Teo, L. L. Koh and T. S. A. Hor, Dalton Trans., 2009, 5637 DOI: 10.1039/B821379H

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