Synthesis, structure diversity, and antimicrobial studies of Ag(i) complexes with quinoline-type ligands

Compounds [Ag(5NO2Qu)2]BF4 (1) and [Ag(Qu3CN)(H2O)]BF4 (2) were prepared and studied from a structural perspective and screened for antimicrobial activity. The Ag(i) in the monomeric complex 1 is coordinated to two 5-nitroquinoline (5NO2Qu) ligands via the N-atoms of the quinoline rings with equidistant Ag-N bonds (2.146(2) \uc5) and a N-Ag-N# bond angle of 171.42(8)\ub0. The 2D coordination polymer 2 contains tetracoordinated Ag(i) with two N-atoms (N1 and N2#1) from two quinoline-3-carbonitrile (Qu3CN) ligands and two O-atoms (O1 and O1#1) from two water molecules. The Qu3CN ligand acts as a connector between the Ag(i) sites along the b-direction via two short Ag1-N1 (2.185(4) \uc5) and Ag1-N2#1 (2.204(4) \uc5) bonds. In addition, the Ag(i) is coordinated with two symmetry related water molecules which are also acting as connectors between the Ag(i) sites along the a-direction via two longer Ag1-O1 (2.470(4) \uc5) and Ag1-O1#2 (2.546(4) \uc5) bonds. Hirshfeld surface analysis confirmed the significance of the polar F⋯H contacts in the molecular packing of 1 (25.9%) and 2 (39.9%). In addition, the crystal packing of 1 showed a significant amount of polar O⋯H (23.5%) contacts. Also, both complexes displayed π-π stacking interactions. The Ag(i) complexes and the free ligand were assessed for their antimicrobial activities. It was found that 1 (MIC = 7.8 μg mL−1) and 2 (MIC = 31.25 μg mL−1) have higher antifungal potency against C. albicans than their free ligands (MIC = 125 μg mL−1). Interestingly, 1 has better antifungal activity than the standard nystatin (15.6 μg mL−1). Also, both Ag(i) complexes and the free ligands as well have better activity against P. mirabilis than the common antibiotic amoxicillin

Hybrid salt–cocrystal solvate: p-coumaric acid and quinine system

A hybrid salt–cocrystal methanol water solvate of p-coumaric acid (p-CA) and quinine (Q) with unexpected stoichiometry was prepared by the slow evaporation technique. The crystals were analysed using single crystal X-ray diffraction. The structure was solved in the monoclinic space group P21 with unit cell dimensions: a = 6.4061(4) A˚ , b = 26.232(2) A˚ , c = 10.9639(8) A˚ and b = 103.707(2). The asymmetric unit contains one quininium cation, one p-coumarate anion and one molecule of p-CA, with water and methanol molecules playing a bridging role in the crystal structure. The thermal analyses of the crystals are reported together with kinetics of desolvation for the loss of methanol.National Research Foundation (Pretoria