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Article

Synthesis and Antimicrobial Activity of Novel Ag-N-Hetero-cyclic Carbene Complexes

by
İlknur Özdemir
1,*,
Emine Özge Özcan
1,
Selami Günal
2 and
Nevin Gürbüz
1,*
1
Department of Chemistry, Faculty of Science and Art, İnönü University, 44280 Malatya, Turkey
2
Department of Microbiology, Faculty of Medicine, İnönü University, 44280 Malatya, Turkey
*
Authors to whom correspondence should be addressed.
Molecules 2010, 15(4), 2499-2508; https://doi.org/10.3390/molecules15042499
Submission received: 16 March 2010 / Revised: 29 March 2010 / Accepted: 7 April 2010 / Published: 8 April 2010
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Abstract

:
A series of imidazolidinium ligand precursors are metallated with Ag2O to give silver(I) N-heterocyclic carbene complexes. All compounds were fully characterized by elemental analyses, 1H-NMR, 13C-NMR and IR spectroscopy techniques. All compounds studied in this work were screened for their in vitro antimicrobial activities against the standard strains: Enterococcus faecalis (ATCC 29212), Staphylococcus aureus (ATCC 29213), Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853) and the fungi Candida albicans and Candida tropicalis. The new imidazolidin-2-ylidene silver complexes have been found to display effective antimicrobial activity against a series of bacteria and fungi.

Graphical Abstract

1. Introduction

With metallopharmaceuticals playing a significant role in therapeutic and diagnostic medicine, the discovery and development of new metallodrugs remain an ever-growing area of research in medicinal inorganic chemistry [1,2,3]. Metallic silver, silver salts and silver complexes have been used in a variety of applications like water purification, wound management, eye-drops, anti-infective coatings in medical devices and in burn treatment because they have potent antimicrobial properties but with low human toxicity [4,5,6,7,8,9]. Among the various silver containing species, silver complexes are particularly interesting since the antimicrobial activity can be changed by varying type of ligands coordinated to silver. The Ag(I) imidazolate complex has antibacterial and antifungal properties [10]. The phosphine adduct of Ag(I) imidazolate has essentially no antimicrobial activity [11]. In addition, an anticancer activity of silver and silver complexes has been demonstrated recently [12,13].
The biomedical applications of metal complexes based on N-heterocyclic carbine (NHC) [14,15,16,17,18] are just beginning to unfold, despite such complexes being phenomenally successful in homogeneous catalysis [19,20,21]. N-Heterocyclic carbene complexes of Ag are commonplace in the organometallic literature. The interest in Ag-NHC complexes is largely due to their ease of synthesis and their ability to serve as useful to other NHC-metal complexes by NHC transfer reactions [22].In addition, their diverse properties in bonding and structure and potential applications in medicine [23,24,25,26,27,28], nanomaterials [29], liquid crystals [30] and organic catalysis [31] also contribute to the attraction of Ag-NHCs.
Ag-carbene complexes derived from imidazolium salts were synthesized and characterized for the first time by Arduengo in 1993 [32]. These complexes were obtained by reaction of the free carbene with silver triflate. Bertrand and co-workers first used silver acetate as a silver base to react triazolium salts to synthesize polymeric Ag-NHC complexes [33]. The use of silver oxide to give silver complexes of 1,3-diethylbenzimidazole-2-ylidine was pioneered by Lin and co-worker [34]. More recently, Danopoulos and co-workers reported the use of silvercarbonate to deprotonate imidazolium salts to give silver-NHC complexes [35].
The finding silver based antimicrobials active against bacteria, we report the preparation and characterization of the imidazolidin-2-ylidene silver(I) (1) isolated high yield, by complete elemental analyses, FT-IR, 1H and 13C-NMR spectroscopy.

2. Results and Discussion

2.1. Preparation of silver-carbene complexes 1a-f

Three common approaches towards the synthesis of Ag–NHC complexes are: i) the reaction of a free NHC with silver salts [32], ii) the reaction of azolium salts with silver salts under basic phase-transfer conditions [36,37] and iii) the reaction of azolium salts with silver bases [30,38,39]. The latter method, in which Ag2O is used as a base is now by far the most commonly employed [22]. Soon after the first report in 199 [34], the Ag2O route was recognized for its attractive features, such as its stability towards air and the tolerance towards other reactive hydrogen atoms. This method was used for the preparation of complexes 1a-1f.
The ligand precursor 1,3-dialkylimidazolidinium chloride was obtained according to literature [40]. Treatment of the imidazolidinium salts with 0.5 equiv. of Ag2O in CH2Cl2 afforded quantitavely after 24 hours the expected carbenes 1a-1f (Scheme 1). Silver-carbene complexes 1a‑f were obtained as white solids in 91–95% yields. The silver carbene complexes (1a–f) were soluble in halogenated solvents and insoluble in non-polar solvents.
Molecules 15 02499 g001 550
Scheme 1. Synthesis of silver-carbene complexes.
Scheme 1. Synthesis of silver-carbene complexes.
Molecules 15 02499 g001
Their 1H and 13C-NMR spectra are consistent with the proposed formula. In the 1H-NMR and 13C-NMR spectra of this solid product in DMSO-d6 and CDCl3 loss of the imidazolidinium proton (NCHN) and imidazolidinium carbon (NCHN) signal suggests the formation of the silver-NHC complexes. The 13C-NMR spectra exhibit singlets at 203.1, 202.1 and 202.9 ppm for 1b, 1c and 1f respectively characteristic of the carbenic carbon resonance. The chemical shift is well consistent with those of the knows silver-NHC complexes in the range of 213-163 ppm [41,42]. In the other complexes, the resonances for carbene carbons were not detected, which was also mentioned in the literature and given a reason of the fluxional behavior of the NHCs complexes [43,44,45]. Ag-NHC complexes exhibit a characteristic υ(NCN) band typically at 1,501, 1,500, 1,515, 1,502, 1,507 and 1,508 cm-1,respectively, for 1a-f.

2.2. Antimicrobial properties of silver-NHC complexes

The antimicrobial activity was reported in terms of the minimum inhibitory concentration (MIC) values, which are defined as the lowest concentration of an antimicrobial that visibly inhibits the growth of the bacteria after an overnight incubation [46]. The usefulness of 1a-f as antimicrobial agents was evaluated. Minimal inhibitory concentrations for each compound were investigated against standard bacterial strains; Staphylococcus aureus ATCC 29213, Enterococcus faecalis ATCC 29212, Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853 and the fungal strains Candida albicans and Candida tropicalis. The test organism was laboratory strains used to test a range of concentration of the silver compounds for minimum inhibitory concentration determination. Antimicrobial activities of the Ag (I)-NHC complexes were determined by using agar dilution procedure and were tested with different concentrations of the compounds. The minimum inhibitory concentration (MIC) of synthesized silver complexes against Gram positive, Gram negative bacteria and fungus are summarized in Table 1. Ampicillin, ciprofloxacin and fluconazole were used as standard drugs for comparison.
Table
Table 1. Minimum inhibitory concentration (μg/mL) of silver NHC complexes tested against bacterial and fungus.
Table 1. Minimum inhibitory concentration (μg/mL) of silver NHC complexes tested against bacterial and fungus.
Ag-NHCE. coliS. aureusE. faecalisP. aerug.C. albicansC. tropicalls
1a1001001001005012.5
1b20020020020010050
1c2002002002006.256.25
1d200100100200100100
1e1001001001002525
1f100100100100506.25
Ampicillin3.123.121.56---
Ciprofloxacin1.560.390.783.12--
Fluconazole----3.123.12
As shown in the table, antimicrobial activity against bacteria and fungi was observed in the silver-NHC complexes tested at 200–6.25 μg/mL concentrations. The new complexes showed effective activities against Gram-positive, Gram-negative bacteria and fungi. The complexes were found effective in inhibiting the growth of Gram-positive and Gram-negative bacteria with MICs values between 100–200 µg/mL. The tested compounds showed antifungal activity with a range of the MICs between 6.25 and 100 μg/mL. However, among the silver complexes tested 1a, 1c and 1f shoved high activity against the fungi C. albians and C. tropicalls with a range of MICs between 6.25–50 µg/mL. Incorporation of same groups at positions 2 and 3 on aromatic group (1a and 1b) exhibit difference in activity (1a is more active than 1b). In case of incorporation of an i-propyl group at position 4 on aromatic ring (1d) decreases the activity. The ethyl group on aromatic ring (1c) particularly enhanced the antifungal activity. From the data obtained in this work, it is suggested that the substituents on the N-atom may play a crucial role in the antimicrobial activity.

3. Experimental

3.1. General

All reactions for the preparation of imidazolidinium salts and silver (NHC) complexes were carried out under argon in flame-dried glassware using standard Schlenk techniques. The solvents used were purified by distillation over the drying agents indicated and were transferred under Ar: Et2O (Na/K alloy), CH2Cl2 (P4O10), hexane, toluene (Na). Melting points were determined in glass capillaries under air with an Electrothermal-9200 melting point apparatus. FTIR spectra were recorded as KBr pellets in the range 400–4000 cm–1 with an ATI UNICAM 1000 spectrometer. 1H-NMR and 13C-NMR spectra were recorded with a Varian AS 400 Merkur spectrometer operating at 400 MHz (1H), 100 MHz (13C) in CDCl3 and DMSO-d6 with tetramethylsilane as an internal reference. Elemental analyses were performed by Turkish Research Council (Ankara, Turkey) Microlab.

3.2. General method for the preparation of silver NHC complexes

A solution of imidazolidinium salt (1.0 mmol), Ag2O (0.5 mmol) and activated 4Ǻ molecular sieves in dichloromethane (30 mL) was stirred room temperature for 24 hours. The reaction mixture was filtered through celite and the solvent removed under reduced pressure. The crude product was recrystallized from dichloromethane/hexane at room temperature.
Chloro-1,3-bis(2-methylbenzyl)imidazolidin-2-ylidenesilver (I) (1a). Yield: 0.20 g; 90%, m.p.: 155–156 °C; υ(CN) = 1,501 cm -1. 1H-NMR (CDCl3) δ: 2.37 (s, 6H, CH2C6H4(CH3)-2), 3.44 (s, 4H, NCH2CH2N), 4.78 (s, 4H, CH2C6H4(CH3)-2), 7.11–7.29 (m, 8H, CH2C6H4(CH3)-2). 13C{H}-NMR (CDCl3) δ: 19.2 (CH2C6H2(CH3)-2), 48.6 (NCH2CH2N), 53.5 (CH2C6H4(CH3)-2), 127.0, 128.4, 128.5, 131.0, 136.7 ve 138.1 (CH2C6H4(CH3)-2). Anal. Calcd for C19H23AgClN2: C, 53.98; H, 5.48; N, 6.63%; found: C, 53.90; H, 5.43; N, 6.59.
Chloro-1,3-bis(4-methylbenzyl)imidazolidin-2-ylidenesilver (I) (1b). Yield: 0.21 g; 95%, m.p.: 230–231 °C; υ(CN) = 1,500 cm -1. 1H-NMR (DMSO-d6) δ: 2.30 (s, 6H, CH2C6H4(CH3)-4), 3.49 (s, 4H, NCH2CH2N), 4.66 (s, 4H, CH2C6H4(CH3)-4), 7.09–7.24 (m, 8H, CH2C6H4(CH3)-4). 13C{H}-NMR (DMSO-d6) δ: 21.2 (CH2C6H2(CH3)-4), 48.9 (NCH2CH2N), 54.2 (CH2C6H4(CH3)-4), 128.2, 129.8, 133.6, 137.6 (CH2C6H4(CH3)-4), 203.1 (Ccarb). Anal. Calcd for C19H23AgClN2: C, 53.98; H, 5.48; N, 6.63%; found: C, 53.96; H, 5.40; N, 6.62%.
Chloro-1,3-bis(4-ethylbenzyl)imidazolidin-2-ylidenesilver (I) (1c). Yield: 0.20 g; 92%, m.p.: 97–98 °C; υ(CN) = 1,515 cm -1. 1H-NMR (DMSO-d6) δ: 1.12 (t, J = 7.5 Hz, 6H, CH2C6H4(CH2CH3)-4), 2.54 (q, J = 7.5 Hz, 4H, CH2C6H4(CH2CH3)-4), 3.46 (s, 4H, NCH2CH2N), 4.52 (s, 4H, CH2C6H4(CH2CH3)-4), 7.07 ve 7.22 (d, J = 7.8 Hz, 8H, CH2C6H4(CH2CH3)-4). 13C{H}-NMR (DMSO-d6) δ: 14.6 (CH2C6H2(CH2CH3)-4), 27.3 (CH2C6H2(CH2CH3)-4), 46.3 (NCH2CH2N), 50.5 (CH2C6H4(CH2CH3)-4), 127.3, 128.2, 128.7, 143.2 (CH2C6H4(CH2CH3)-4), 202.1 (Ccarb). Anal. Calcd for C21H27AgClN2: C, 55.95; H, 6.04; 7.86; N, 6.21%; found: C, 55.90; H, 5.98; N, 6.26%.
Chloro-1,3-bis(4-i-propylbenzyl)imidazolidin-2-ylidenesilver (I) (1d). Yield: 0.20 g; 94%, m.p.: 194–195 °C; υ(CN) = 1,503 cm -1. 1H-NMR (DMSO-d6) δ: 1.88 (d, J = 6.9 Hz, 12H, CH2C6H4(CH(CH3)2)-4), 2.87 (h, J = 6.9 Hz, 2H, CH2C6H4(CH(CH3)2)-4), 3.56 (s, 4H, NCH2CH2N), 4.6 (s, 4H, CH2C6H4(CH(CH3)2)-4), 7.18 ve 7.29 (d, J = 5.1 Hz, 8H, CH2C6H4(CH(CH3)2)-4). 13C{H}-NMR (DMSO-d6) δ: 22.6 (CH2C6H2(CH(CH3)2)-4), 33.4 (CH2C6H2(CH(CH3)2)-4), 46.6 (NCH2CH2N), 53.0 (CH2C6H4(CH(CH3)2)-4), 126.2, 127.9, 129.8, 148.9 (CH2C6H4(CH3)-4). Anal. Calcd for C23H31AgClN2: C, 57.69; H, 6.53; N, 5.85%; found: C, 57.63; H, 6.50; N, 5.83%.
Chloro-1,3-bis(4-diethylaminobenzyl)imidazolidin-2-ylidenesilver (I) (1e). Yield: 0.19g; 91%, m.p.: 163–165 °C; υ(CN) = 1,507 cm -1. 1H-NMR (CDCl3) δ: 1.15 (t, J = 7.05 Hz, 12H, CH2C6H4N(CH2CH3)2-4), 3.36 (q, J = 6.9 Hz, 8H, CH2C6H4N(CH2CH3)2-4), 3.69 (s, 4H, NCH2CH2N), 4.57 (s, 4H, CH2C6H4N(CH2CH3)2-4), 6.61 ve 6.64 (d, J = 9.0 Hz, 8H, CH2C6H4N(CH2CH3)2-4). 13C{H}-NMR (CDCl3) δ: 12.5 (CH2C6H2N(CH2CH3)2-4), 44.3 (CH2C6H2N(CH2CH3)2-4), 48.2 (NCH2CH2N), 52.0 (CH2C6H4N(CH2CH3)2-4), 111.7, 121.1, 130.3, 147.7 (CH2C6H4N(CH2CH3)2-4). Anal. Calcd for C25H37AgClN4: C, 55.93; H, 6.95; N, 10.44%; found: C, 55.90; H, 6.93; 6.63; N, 10.42%.
Chloro-1,3-bis(3,4-dimethoxybenzyl)imidazolidin-2-ylidenesilver (I) (1f). Yield: 0.19 g; 93%, m.p.:134–135 °C; υ(CN) = 1,508 cm -1. 1H-NMR (DMSO-d6) δ: 3.36 (s, 4H, NCH2CH2N), 3.53 (s, 6H, CH2C6H3(OCH3)2-3), 3.75 (s, 6H, CH2C6H3(OCH3)2-4), 4.63 (s, 4H, CH2C6H3(OCH3)2-3,4), 6.76-7.01(m, 6H, CH2C6H3(OCH3)2-3,4). 13C{H}-NMR (DMSO-d6) δ: 49.0 (NCH2CH2N), 54.2 (CH2C6H3(OCH3)2-3), 55.9 (CH2C6H3(OCH3)2-4), 56.0 (CH2C6H3(OCH3)2-3,4), 112.1, 112.4, 120.4, 129.0, 148.9, 149.3 (CH2C6H3(OCH3)2-3,4), 202.9 (Ccarb). Anal. Calcd for C21H27AgClN2O4: C, 49.00; H, 5.29; N, 5.44; O, 12.43%; found: C, 49.02; H, 5.30; N, 5.40; O, 12.44%.

3.3. Antimicrobial activities of silver NHC complexes

Antimicrobial activities of the Ag (I) complexes with N-Heterocyclic carbene ligand were determined using the agar dilution procedure recommended by the Clinical and Laboratory Standards Institute [47,48]. Minimal inhibitory concentrations for each compound were investigated against standard bacterial strains; Staphylococcus aureus ATCC 29213, Enterococcus faecalis ATCC 29212, Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853 were obtained from American Type Culture Collection (Rockville, MD.) and the fungal strains Candida albicans and Candida tropicalis obtained from the Department of Microbiology, Faculty of Medicine, Ege University (Turkey). Bacterial strains were subcultured on Muller Hinton Broth (HiMedia Laboratories Pvt. Ltd. Mumbai-India) and fungal strains were also on RPMI 1640 Broth (Sigma-Aldrich Chemie GmbH Taufkirchen, Germany). Their turbidities matched that of a McFarland no. 0.5 turbidity standard [49]. The stock solution of all compounds was prepared in dimethyl sulfoxide (DMSO). All of the dilutions were done with distilled water. The concentrations of the tested compounds were 800, 400, 200, 100, 50, 25, 12.5 and 6.25 µg/mL. Ampicillin and ciprofloxacin were used as antibacterial standard drugs, while fluconazole were used as antifungal standard drugs whose minimum inhibitory concentration (MIC) values are provided. A loopful (0.01 mL) of the standardised inoculums of the bacteria and yeasts (106 CFUs/mL) was spread over the surface of agar plates. All the inoculated plates were incubated at 35 °C and results were evaluated after 16–20 h of incubation for bacteria and 48 h for yeasts. The lowest concentration of the compounds that prevented visible growth was considered to be the minimal inhibitory concentration (MIC).

4. Conclusions

In summary, six Ag(I)-NHC complexes were synthesized starting from 1,3-dialkylimidazolidinium chloride, following a common procedure. The silver-NHC complexes characterized by 1H-NMR, 13 C- NMR, IR and elemental analysis. Also, antimicrobial activities of the new complexes are reported. The silver complexes 1a, 1c and 1f showed better antimicrobial activity against the fungi than other complexes, even at the much lower concentrations. Although the mechanism of antimicrobial activity is not known, it was found that substituents on the N-atom have an effect on antimicrobial activity in this work. Detailed investigations focusing on new silver-NHC complexes and other biomedical applications are ongoing.

Acknowledgements

This work was financially supported by the Technological and Scientific Research Council of Turkey TUBİTAK [TBAG (108T411)].
  • Sample Availability: Samples of the compounds are available from the authors.

References and Notes

  1. Mascini, M.; Bagni, G.; Pietro, M.L.D.; Ravera, M.; Baracco, S.; Osella, D. Electrochemical biosensor evaluation of the interaction between DNA and metallo-drugs. BioMetals 2006, 19, 409–418. [Google Scholar] [CrossRef]
  2. Kostova, I. Platinum complexes as anticancer agents. Recent Pat. Anti-Cancer Drug Discover. 2006, 1, 1–22. [Google Scholar] [CrossRef]
  3. Guo, Z.; Sadler, P.J. Advances in Inorganic Chemistry; Academic Press: San Diego, CA, USA, 2000; Volume 1, pp. 1–22. [Google Scholar]
  4. Farrell, N. Inorganic Complexes as Drugs and Chemotherapeutic Agents. In Comprehensive Coordination Chemistry, 2nd; McCleverty, J.A., Meyer, T.J., Eds.; Elsevier Pergamon: Oxford, UK, 2004; Volume 9, pp. 809–840. [Google Scholar]
  5. Clement, J.L.; Jarret, P.S. Antibacterial Silver. Metal-Based Drugs 1994, 1, 467–482. [Google Scholar] [CrossRef]
  6. Tambe, S.M.; Sampath, L.; Modak, S.M. In-vitro evaluation of the risk of developing bacterial resistance to antiseptics and antibiotics used in medical devices. J. Antimicrob. Chemother. 2001, 47, 589–598. [Google Scholar] [CrossRef]
  7. Jakupec, M.A.; Unfried, P.; Keppler, B.K. In vitro evaluation of the risk of developing bacterial resistance to antiseptics and antibiotics used in medical devices. Rev. Physiol. Biochem. Pharmacol. 2005, 153, 101–111. [Google Scholar]
  8. Nomiya, K.; Takahashi, S.; Noguchi, R.; Nemoto, S.; Takayama, T.; Oda, M. Synthesis and Characterization of Water-Soluble Silver(I) Complexes with l-Histidine (H2his) and (S)-(−)-2-Pyrrolidone-5-carboxylic Acid (H2pyrrld) Showing a Wide Spectrum of Effective Antibacterial and Antifungal Activities. Crystal Structures of Chiral Helical Polymers [Ag(Hhis)]n and {[Ag(Hpyrrld)]2}n in the Solid State. Inorg. Chem. 2000, 39, 3301–3311. [Google Scholar]
  9. Kasuga, N.C.; Sugie, A.; Nomiya, K. Syntheses, structures and antimicrobial activities of water-soluble silver(I)-oxygen bonding complexes with chiral and racemic camphanic acid (Hca) ligands. Dalton Trans. 2004, 3732–3740. [Google Scholar]
  10. Nomiya, K.; Tsuda, K.; Sudoh, T.; Oda, M. Ag(I)-N bond-containing compound showing wide spectra in effective antimicrobial activities: Polymeric silver(I) imidazolate. J. Inorg. Biochem. 1997, 68, 39–44. [Google Scholar] [CrossRef]
  11. Nomiya, K.; Noguchi, R.; Oda, M. Synthesis and crystal structure of coinage metal(I) complexes with tetrazole (Htetz) and triphenylphosphine ligands, and their antimicrobial activities. A helical polymer of silver(I) complex [Ag(tetz)(PPh3)2]n and a monomeric gold(I) complex [Au(tetz)(PPh3)]. Inorg. Chim. Acta. 2000, 298, 24–32. [Google Scholar] [CrossRef]
  12. Liu, J.J.; Galettis, P.; Farr, A.; Maharaj, L.; Samarasinha, H.; McGechan, A.C.; Baguley, B.C.; Bowen, R.J.; Berners-Price, S.J.; McKeage, M.J. In vitro antitumour and hepatotoxicity profiles of Au(I) and Ag(I) bidentate pyridyl phosphine complexes and relationships to cellular uptake. J. Inorg. Biochem. 2008, 102, 303–310. [Google Scholar] [CrossRef]
  13. Thati, B.; Noble, A.; Creaven, B.S.; Walsh, M.; McCann, M.; Kavanagh, K.; Devereux, M.; Egan, D.A. In vitro anti-tumour and cyto-selective effects of coumarin-3-carboxylic acid and three of its hydroxylated derivatives, along with their silver-based complexes, using human epithelial carcinoma cell lines. Cancer Lett. 2007, 248, 321–331. [Google Scholar] [CrossRef]
  14. Kascatan-Nebioglu, A.; Melaiye, A.; Hindi, K.; Durmus, S.; Panzner, M.J.; Hogue, L.A.; Mallett, R.J.; Hovis, C.E.; Coughenour, M.; Crosby, S.D.; Milsted, A.; Ely, D.L.; Tessier, C.A.; Cannon, C.L.; Youngs, W.J. Synthesis from Caffeine of a Mixed N-Heterocyclic Carbene−Silver Acetate Complex Active against Resistant Respiratory Pathogens. J. Med. Chem. 2006, 49, 6811–6818. [Google Scholar]
  15. Melaiye, A.; Sun, Z.; Hindi, K.; Milsted, A.; Ely, D.; Reneker, D.H.; Tessier, C.A.; Youngs, W.J. Silver(I)−imidazole cyclophane gem-diol complexes encapsulated by electrospun tecophilic nanofibers: Formation of nanosilver particles and antimicrobial activity. J. Am. Chem. Soc. 2005, 127, 2285–2291. [Google Scholar]
  16. Garrison, J.C.; Tessier, C.A.; Youngs, W.J. Synthesis and crystallographic characterization of multi-donor N-heterocyclic carbene chelating ligands and their silver complexes: Potential use in pharmaceuticals. J. Organomet. Chem. 2005, 690, 6008–6020. [Google Scholar] [CrossRef]
  17. Barnard, P.J.; Wedlock, L.E.; Baker, M.V.; Berners-Price, S.J.; Joyce, D.A.; Skelton, B.W.; Steer, J.H. Luminescence studies of the intracellular distribution of a dinuclear gold(I) N-heterocyclic carbene complex. Angew. Chem. Int. Ed. 2006, 45, 5966–5970. [Google Scholar]
  18. Özdemir, I.; Denizci, A.; Öztürk, H.T.; Çetinkaya, B. Synthetic and antimicrobial studies on new gold(I) complexes of imidazolidin-2-ylidenes. Appl. Organomet. Chem. 2004, 18, 318–322. [Google Scholar]
  19. Herrmann, W.A. N-Heterocyclic Carbenes: A new concept in organometallic catalysis. Angew. Chem. Int. Ed. 2002, 41, 1290–1309. [Google Scholar] [CrossRef]
  20. Peris, E.; Crabtree, R.H. Recent homogeneous catalytic applications of chelate and pincer N-heterocyclic carbenes. Coord. Chem. Rev. 2004, 248, 2239–2246. [Google Scholar] [CrossRef]
  21. Gonzalez, S.D.; Maria, N.; Nolan, S.P. N-Heterocyclic Carbenes in Late Transition Metal Catalysis. Chem. Rev. 2009, 109, 3612–3676. [Google Scholar] [CrossRef]
  22. Lin, I.J.B.; Vasam, C.S. Preparation and application of N-heterocyclic carbene complexes of Ag(I). Coord. Chem. Rev. 2007, 251, 642–670. [Google Scholar]
  23. Hindi, K.M.; Ditto, A.J.; Panzeri, M.J.; Medvetz, D.A.; Han, S.D.; Hovis, C.E.; Hilliard, J.K.; Taylor, J.B.; Yun, Y.H.; Cannon, C.L.; Youngs, W.J. The antimicrobial efficacy of sustained release silver-carbene complex-loaded l-tyrosine polyphosphate nanoparticles: Characterization, in vitro and in vivo studies. Biomaterials 2009, 30, 3771–3779. [Google Scholar] [CrossRef]
  24. Kascatan-Nebioglu, A.; Panzner, M.J.; Tessier, C.A.; Cannon, C.L.; Youngs, W.J. N-Heterocyclic carbene-silver complexes: A new class of antibiotics. Coord. Chem. Rev. 2007, 251, 884–895. [Google Scholar]
  25. Hindi, K.M.; Siciliano, T.J.; Durmus, S.; Panzner, M.J.; Medvetz, D.A.; Reddy, D.V.; Hogue, L.A.; Hovis, C.E.; Hilliard, J.K.; Mallet, R.; Tessier, C.A.; Cannon, C.L.; Youngs, W.J. Synthesis, stability, and antimicrobial studies of electronically tuned Silver acetate N-heterocyclic carbenes. J. Med. Chem. 2008, 51, 1577–1583. [Google Scholar]
  26. Hindi, K.M.; Panzner, M.J.; Tessier, C.A.; Cannon, C.L.; Youngs, W.J. The Medicinal applications of imidazolium carbene−metal complexes. Chem. Rev. 2009, 109, 3859–3884. [Google Scholar] [CrossRef]
  27. Medvetz, D.A.; Hindi, K.M.; Panzner, M.J.; Ditto, A.J.; Yun, Y.H.; Youngs, W.J. Anticancer activity of Ag(I) N-heterocyclic carbene complexes derived from 4,5-dichloro-1H-imidazole. Met. Based Drugs 2008, 384010–384016. [Google Scholar]
  28. Lin, J.C.Y.; Huang, R.T.W.; Lee, C.S.; Bhattacharyya, A.; Hwang, W.S.; Lin, I.J.B. Coinage metal−N-heterocyclic carbene complexes. Chem. Rew. 2009, 109, 3561–3598. [Google Scholar] [CrossRef]
  29. Peris, E. Routes to N-Heterocyclic Carbene Complexes. Top. Organomet. Chem. 2007, 21, 83–116. [Google Scholar]
  30. Lee, C.K.; Vasam, C.S.; Huang, T.W.; Wang, H.M.J.; Yang, R.Y.; Lee, C.S.; Lin, I.J.B. Silver(I) N-heterocyclic carbenes with long N-alkyl chains. Organometallics 2006, 25, 3768–3775. [Google Scholar]
  31. Garrison, J.C.; Youngs, W.J. Ag(I) N-heterocyclic carbene complexes: Synthesis, structure, and application. Chem. Rev. 2005, 105, 3978–4008. [Google Scholar] [CrossRef]
  32. Arduengo, A.J.; Dias, H.W.R.; Calabrase, J.C.; Davidson, F. Homoleptic carbene-silver(I) and carbene-copper(I) complexes. Organometallics. 1993, 12, 3405–3409. [Google Scholar] [CrossRef]
  33. Guerret, O.; Sole´, S.; Gornitzka, H.; Trinquier, G.; Bertrand, G. 1,2,4-Triazole-3,5-diylidene: A building block for organometallic polymer synthesis. J. Am.Chem. Soc. 1997, 119, 6668–6669. [Google Scholar] [CrossRef]
  34. Wang, H.M.J.; Lin, I.J.B. Facile Synthesis of silver(I)−carbene complexes. Useful carbene transfer agents. Organometallics 1998, 17, 972–975. [Google Scholar]
  35. Tulloch, A.A.D.; Danopoulos, A.A.; Winston, S.; Kleinhenz, S.; Estham, G. N-Functionalised heterocyclic carbene complexes of silver. J. Chem. Soc. Dalton Trans. 2000, 4499–4506. [Google Scholar]
  36. Vasam, C.S.; Lin, I.J.B. Preparation and application of N-heterocyclic carbene complexes of Ag(I). Coord. Chem. Rev. 2007, 251, 642–670. [Google Scholar]
  37. Lin, I.J.B.; Vasam, C.S. Silver(I) N-heterocyclic carbenes. Comment. Inorg. Chem. 2004, 25, 75–129. [Google Scholar] [CrossRef]
  38. Wang, H.M.J.; Chen, C.Y.L.; Lin, I.J.B. Synthesis, structure, and spectroscopic properties of gold(I)−carbene complexes. Organometallics 1999, 18, 1216–1223. [Google Scholar]
  39. Lee, C.K.; Lee, K.M.; Lin, I.J.B. Inorganic−organic hybrid lamella of di- and tetranuclear silver−carbene complexes. Organometallics 2002, 21, 10–12. [Google Scholar]
  40. Gürbüz, N.; Özdemir, I.; Demir, S.; Çetinkaya, B. Improved palladium-catalyzed coupling reactions of aryl halides using saturated N-heterocarbene ligands. J. Mol. Catal. A Chem. 2004, 209, 23–28. [Google Scholar] [CrossRef]
  41. Liu, F.; Chen, W.; Wang, D. Synthesis and structural characterization of one- and two-dimensional coordination polymers based on platinum-silver metallic backbones. Dalton Trans. 2006, 3015–3024. [Google Scholar]
  42. Chen, W.; Liu, F.; Xu, D.; Matsumoto, K.; Kishi, S.; Kato, M. Luminescent amidate-Bridged one-dimensional platinum(II)−thallium(I) coordination polymers assembled via metallophilic attraction. Inorg. Chem. 2006, 45, 5552–5560. [Google Scholar] [CrossRef]
  43. Nielsen, D.J.; Cavell, K.J.; Skelton, B.W. Tetrafluoroborate anion B-F bond activation-unusual formation of a nucleophilic heterocyclic carbene:BF3 adduct. Inorg. Chim. Acta. 2003, 352, 143–148. [Google Scholar] [CrossRef]
  44. Pytkowicz, J.; Roland, S.; Mangeney, P. Synthesis of chiral silver(I) diaminocarbene complexes from (R,R)-4,5-di-tert-butylimidazoline. J. Organomet. Chem. 2001, 631, 157. [Google Scholar]
  45. Lee, H.M.; Chiu, P.L.; Hu, C.H.; Lai, C.L.; Chou, Y.C. Synthesis and structural characterization of metal complexes based on pyrazole/imidazolium chlorides. J. Organomet. Chem. 2005, 690, 403–414. [Google Scholar]
  46. Pernak, J.; Skrzypczak, A. 3-Alkylthiomethyl-1-ethylimidazolium chlorides. Correlation between critical micelle concentrations and minimum inhibitory concentrations. Eur. J. Med. Chem. 1996, 31, 901–903. [Google Scholar] [CrossRef]
  47. Clinical and Laboratory Standards Instıtute, Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically; Approved Standard-Seventh Edition; CLSI Document M7-A7, Clinical and Laboratory Standards Instıtute: Wayne, PA, USA, 2003.
  48. Clinical and Laboratory Standards Instıtute, Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts; Approved Standard-Second Edition; NCCLS document M27-A2 (ISBN 1-56238-469-4). NCCLS: Wayne, PA, USA, 2002.
  49. Hindler, J.; Hochstein, L.; Howell, A. Preparation of Routine Media and Reagents Used in Antimicrobial Susceptibility Testing. Part 1. McFarland Standards. In Clinical Microbiology Procedures Handbook; Isenberg, H.D., Ed.; American Society for Microbiology: Washington, DC, USA; Volume 1, pp. 5.19.1–5.19.6.

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Özdemir, İ.; Özcan, E.Ö.; Günal, S.; Gürbüz, N. Synthesis and Antimicrobial Activity of Novel Ag-N-Hetero-cyclic Carbene Complexes. Molecules 2010, 15, 2499-2508. https://doi.org/10.3390/molecules15042499

AMA Style

Özdemir İ, Özcan EÖ, Günal S, Gürbüz N. Synthesis and Antimicrobial Activity of Novel Ag-N-Hetero-cyclic Carbene Complexes. Molecules. 2010; 15(4):2499-2508. https://doi.org/10.3390/molecules15042499

Chicago/Turabian Style

Özdemir, İlknur, Emine Özge Özcan, Selami Günal, and Nevin Gürbüz. 2010. "Synthesis and Antimicrobial Activity of Novel Ag-N-Hetero-cyclic Carbene Complexes" Molecules 15, no. 4: 2499-2508. https://doi.org/10.3390/molecules15042499

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