Peer-Reviewed Journal Details
Mandatory Fields
McCann M.;Curran R.;Ben-Shoshan M.;McKee V.;Tahir A.;Devereux M.;Kavanagh K.;Creaven B.;Kellett A.
2012
June
Dalton Transactions
Silver(i) complexes of 9-anthracenecarboxylic acid and imidazoles: Synthesis, structure and antimicrobial activity
Published
38 ()
Optional Fields
41
21
6516
6527
[Ag 2(9-aca) 2] (1) (9-acaH = 9-anthracenecarboxylic acid) reacts with a series of imidazoles to give [Ag(imidH) 2.3(CH 3CN) 0.7](9-aca) (3), [Ag 6(imidH) 4(9-aca) 6(MeOH) 2] (4), {[Ag(1-Me-imid) 2] 2[Ag 4(9-aca) 6]} (5), {[Ag(1-Bu-imid) 2] 2[Ag 4(9-aca) 6]} (6) and [Ag(apim)](9-aca)·H 2O (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. © 2012 The Royal Society of Chemistry.
1477-9226
10.1039/c2dt12166b
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