Effects of Different Substituents on the Crystal Structures and Antimicrobial Activities of Six Ag(I) Quinoline Compounds

The syntheses and single crystal
X-ray structures of [Ag­(5-nitroquinoline)2]­NO3 (1), [Ag­(8-nitroquinoline)2]­NO3·H2O (2), [Ag­(6-methoxy-8-nitroquinoline)­(NO3)]n (3), [Ag­(3-quinolinecarbonitrile)­(NO3)]n (4), [Ag­(3-quinolinecarbonitrile)2]­NO3 (5), and [Ag­(6-quinolinecarboxylic
acid)2]­NO3 (6) are described. As
an alternative to solution chemistry, solid-state grinding could be
used to prepare compounds 1 and 3, but the
preparation of 4 and 5 in this way failed.
The Ag­(I) ions in the monomeric compounds 1, 2, 5, and 6 are coordinated to two ligands
via the nitrogen atoms of the quinoline rings, thereby forming a distorted
linear coordination geometry with Ag–N bond distances of 2.142(2)–2.336(2)
Å and N–Ag–N bond angles of 163.62(13)°–172.25(13)°.
The 1D coordination polymers 3 and 4 contain
Ag­(I) centers coordinating one ligand and two bridging nitrate groups,
thereby forming a distorted trigonal planar coordination geometry
with Ag–N bond distances of 2.2700(14) and 2.224(5) Å,
Ag–O bond distances of 2.261(4)–2.536(5) Å, and
N–Ag–O bond angles of 115.23(5)°–155.56(5)°.
Hirshfeld surface analyses of compounds 1–6 are presented as dnorm and curvedness
maps. The dnorm maps show different interaction
sites around the Ag­(I) ions, i.e., Ag···Ag interactions
and possible O–H···O, C–H···O,
C–H···N, and C–H···C hydrogen
bonds. Curvedness maps are a good way of visualizing π–π
stacking interactions between molecules. The antimicrobial activities
of compounds 1, 2, and 6 were
screened against 15 different multidrug-resistant strains of bacteria
isolated from diabetic foot ulcers and compared to the antimicrobial
activities of the clinically used silver sulfadiazine (SS). Compound 2 showed activity similar to SS against this set of test organisms,
being active against all strains and having slightly better average
silver efficiency than SS (5 vs 6 μg Ag/mL). Against the standard
nonresistant bacterial strains of Staphylococcus aureus, Pseudomonas aeruginosa, Proteus mirabilis, and Streptococcus
pyogenes, compound 1 performed better
than silver nitrate, with an average MIC of 6 μg Ag/mL versus
18 μg Ag/mL for the reference AgNO3. Electrospray
ionization mass spectrometry (ESI-MS) analyses of compounds 3 and 6 in DMSO/MeOH confirm the two-coordinated
Ag+ complexes in solution, and the results of the 1H NMR titrations of DMSO solutions of 5-nitroquinoline and
8-nitroquinoline with AgNO3 in DMSO suggest that 5-nitroquinoline
is more strongly coordinated to the silver ion.