Issue 13, 2003

Chemical and biological studies of the dichloro(2-phenylpyridine) gold(iii) complex and its derivatives

Abstract

Four new derivatives of the type [Au(ppy)X2] (ppy = 2-phenylpyridine) together with [Au(ppy)Cl2] (1) have been synthesized and characterized [X = ac = CH3COO (2), bz = C6H5COO (3); mal = CH2(COO)2 (4), cbdca = C4H6(COO)2 (5)]. The crystal structures of 2 and 3 are similar in which two carboxylate groups are bound to gold through oxygen, but the two Au–O distances are inequivalent. The crystal structure of 5 shows that gold is bound to σ-C,N-phenylpyridine (ppy) and O,O-cbdca, forming a five-membered and a six-membered chelate ring, respectively. In all four structures the Au(III) center exhibits a square planar coordination geometry and the trans influence of the σ-bonded phenyl group is apparent. The σ-bonded phenyl group contributes to stabilizing these complexes in reducing, biological media. The reaction between 5 and chloride has been investigated by 1H NMR spectroscopy and reveals slow replacement of cbdca by chlorides through an intermediate [Au(ppy)(O-cbdca)Cl]. All five complexes have been tested for cytotoxic properties in vitro against MOLT-4 (human leukemia) and C2C12 (mouse tumour) cell lines. The results show that these complexes have similar cytotoxicity profile to cisplatin against MOLT-4 but are inactive on C2C12, except for complex 5.

Graphical abstract: Chemical and biological studies of the dichloro(2-phenylpyridine) gold(iii) complex and its derivatives

Supplementary files

Article information

Article type
Paper
Submitted
24 Mar 2003
Accepted
19 May 2003
First published
30 May 2003

Dalton Trans., 2003, 2680-2685

Chemical and biological studies of the dichloro(2-phenylpyridine) gold(III) complex and its derivatives

D. Fan, C. Yang, J. D. Ranford, P. F. Lee and J. J. Vittal, Dalton Trans., 2003, 2680 DOI: 10.1039/B303297C

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