Synthetic and antimicrobial studies on new gold(I) complexes of imidazolidin-2-ylidenes
dc.authorid | Özdemir, İsmail/0000-0001-6325-0216 | |
dc.authorid | Cetinkaya, Bekir/0000-0002-4551-8650 | |
dc.authorwosid | Özdemir, İsmail/ABI-5192-2020 | |
dc.authorwosid | Yalçın, H. Tansel/AAG-7526-2021 | |
dc.contributor.author | Özdemir, I | |
dc.contributor.author | Denizci, A | |
dc.contributor.author | Öztürk, HT | |
dc.contributor.author | Çetinkaya, B | |
dc.date.accessioned | 2024-08-04T20:30:42Z | |
dc.date.available | 2024-08-04T20:30:42Z | |
dc.date.issued | 2004 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | Six new 1,3-diorganylimidazolidin-2-ylidene (NHC) gold(I) complexes of the type [Au(NHC)(2)](+) (1-6), were synthesized by reacting [AuCl(PPh)(3)] with 1,3-dimesitylimidazolidin-2-ylidene or bis(1,3-dialkylimidazolidin-2-ylidene). The complexes 1-6 were fully characterized by elemental analyses and spectroscopic data. The placement of mesityl or para-substituted benzyl groups on the nitrogen atoms of the ring of the complexes leads to the particularly active antibacterial agents evaluated in this work. It is worth noting that the p-methoxybenzyl derivative (2) inhibited the growth of Pseudomona aeruginosa, Staphylococcus epidermidis, Staphylococcus aureus and Enterococcus faecalis with minimum inhibitory concentration (MIC) values of 3.12 mug ml(-1), 6.25 mug ml(-1), 3.12 mug ml(-1) and 3.12 mug ml(-1) respectively. In contrast, the analogous p-dimethylaminobenzyl derivative (3) is effective only against Escherichia coli (MIC = 3.12 mug ml(-1)). Copyright (C) 2004 John Wiley Sons, Ltd. | en_US |
dc.identifier.doi | 10.1002/aoc.668 | |
dc.identifier.endpage | 322 | en_US |
dc.identifier.issn | 0268-2605 | |
dc.identifier.issn | 1099-0739 | |
dc.identifier.issue | 7 | en_US |
dc.identifier.scopus | 2-s2.0-4043076287 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 318 | en_US |
dc.identifier.uri | https://doi.org/10.1002/aoc.668 | |
dc.identifier.uri | https://hdl.handle.net/11616/94474 | |
dc.identifier.volume | 18 | en_US |
dc.identifier.wos | WOS:000223270200003 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.relation.ispartof | Applied Organometallic Chemistry | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | N-heterocarbene-gold(I) complexes | en_US |
dc.subject | antimicrobial activity | en_US |
dc.subject | minimum inhibitory concentration | en_US |
dc.title | Synthetic and antimicrobial studies on new gold(I) complexes of imidazolidin-2-ylidenes | en_US |
dc.type | Article | en_US |