Facile preparation of graphene oxide silver aerogel for antibacterial

We report a simple and straightforward method for the preparation of graphene oxide-silver aerogel (GOAg) via microwave irradiation. Graphene oxide (GO) was used as a substrate for the growth of silver nanoparticles (AgNPs) and silver complex was used as a precursor. The GOAg were prepared by rapidly expose mixture of GO and silver complexes with microwave for 30 s under an ambient atmosphere. For the nanocomposites, GOAg solution were lyophilized in a freeze-dryer for 24 hours to form an aerogel. The obtained GO and GOAg nanocomposites were characterized by X-ray diffractometer (XRD) and Ultraviolet-visible spectroscopy (UV-Vis). XRD confirmed the formation GO, and GOAg while GOAg display antibacterial properties against Methicillin-resistant Staphylococcus aureus (MRSA) and Aeromonas hydrophila bacteria. We demonstrate

Synthesis and coordination chemistry of silver(I), gold(I) and gold(III) complexes with picoline-functionalized benzimidazolin-2-ylidene ligands

The reactions of N-alkyl-N′-picolyl-benzimidazolium bromides or N,N′-dipicolyl-benzimidazolium bromide with silver oxide yielded the silver dicarbene complexes of the type [Ag(NHC)2][AgBr2] 1–4 (NHC = picoline-functionalized benzimidazolin-2-ylidene). The silver complexes 1–4 have been used in carbene transfer reactions to yield the gold(I) complexes of the type [AuCl(NHC)] 5–8 in good yields. A halide exchange at the metal center of complexes 5–8 with lithium bromide yielded the gold bromide complexes 9–12. Finally, the oxidation of the gold(I) centers in complexes 9–12 with elemental bromine gave the gold(III) complexes of the type [AuBr3(NHC)] 13–16. Molecular structures of selected Au(I) and Au(III) complexes have been determined by X-ray diffraction studies.

Facile N9-Alkylation of Xanthine Derivatives and Their Use as Precursors for N-Heterocyclic Carbene Complexes

The xanthine-derivatives 1,3,7-trimethylxanthine, 1,3-dimethyl-7-benzylxanthine and 1,3-dimethyl-7-(4-chlorobenzyl)xanthine are readily ethylated at N9 using the cheap alkylating agents ethyl tosylate or diethyl sulfate. The resulting xanthinium tosylate or ethyl sulfate salts can be converted into the corresponding PF6- and chloride salts. The reaction of these xanthinium salts with silver(I) oxide results in the formation of different silver(I) carbene-complexes. In the presence of ammonia, ammine complexes [Ag(NHC)(NH3)]PF6 are formed, whilst with Et2NH, the bis(carbene) salts [Ag(NHC)2]PF6 were isolated. Using the xanthinium chloride salts neutral silver(I) carbenes [Ag(NHC)Cl] were prepared. These silver complexes were used in a variety of transmetallation reactions to give the corresponding gold(I), ruthenium(II) as well as rhodium(I) and rhodium(III) complexes. The compounds were characterized by various spectroscopic methods as well as X-ray diffraction.

Synthesis, structural characterization, and properties of three Ag(I) complexes with oxazoline-containing chiral ligands

The two enantiopure chiral organic ligands 2-[(S)-4-isopropyl-2-oxazolyl]quinoline (L1) and 2-[(S)-4-benzyl-2-oxazolyl]quinoline (L2) react with different silver salts to give rise to three new silver complexes [Ag(L1)2](SbF6) (1), [Ag(L1)(CH3CN)](ClO4) (2), and [Ag(L2)(NO3)] (3), which have been characterized by single-crystal X-ray diffraction, IR spectroscopy, elemental and thermogravimetric analyses. Complexes 1–3 all display discrete mononuclear structures. The nonlinear optical properties of 1–3 were investigated.