Silver(I) complexes of 9-anthracenecarboxylic acid and imidazoles: synthesis, structure and antimicrobial activity
journal contribution
posted on 2014-07-23, 11:18authored byMalachy McCann, Robert Curran, Marcia Ben-Shoshan, Vickie McKee, Asif A. Tahir, Michael Devereux, Kevin Kavanagh, Bernadette S. Creaven, Andrew Kellett
[Ag2(9-aca)2] (1) (9-acaH = 9-anthracenecarboxylic acid) reacts with a series of imidazoles to give
[Ag(imidH)2.3(CH3CN)0.7](9-aca) (3), [Ag6(imidH)4(9-aca)6(MeOH)2] (4), {[Ag(1-Me-imid)2]2[Ag4(9-
aca)6]} (5), {[Ag(1-Bu-imid)2]2[Ag4(9-aca)6]} (6) and [Ag(apim)](9-aca)·H2O (7) (imidH = imidazole;
1-Me-imid = 1-methylimidazole; 1-Bu-imid = 1-butylimidazole; apim = 1-(3-aminopropyl)imidazole).
The mononuclear complex 3, hexanuclear 4–6, and polymeric 7, were all characterised using X-ray
crystallography. While many of the complexes possess excellent in vitro antifungal and antibacterial
activities they are, unanimously, more effective against fungal cells. The insect, Galleria mellonella, can
survive high doses of the Ag(I) complexes administered in vivo, and a number of the complexes offer
significant protection to larvae infected with a lethal dose of pathogenic Candida albicans cells.
Funding
Financial support from the Irish Research Council for Science,
Engineering and Technology (IRCSET) and the John and Pat
Hume Scholarship Scheme, NUI Maynooth (R. Curran) are
gratefully acknowledged.
History
School
Science
Department
Chemistry
Published in
DALTON TRANSACTIONS
Volume
41
Issue
21
Pages
6516 - 6527 (12)
Citation
McCANN, M. ... et al, 2012. Silver(I) complexes of 9-anthracenecarboxylic acid and imidazoles: synthesis, structure and antimicrobial activity. Dalton Transactions, 41(21), pp.6516-6527.