Harvesting greenish blue luminescence in gold(i) complexes and their application as promising bioactive molecules and cellular bioimaging agents. (14th April 2020)

• Record Type: Journal Article
• Authors: Favarin, Lis R. V.; Laranjeira, G. B.; Teixeira, Cristiane F. A.; Silva, Heveline; Micheletti, A. C.; Pizzuti, Lucas; Machulek Júnior, Amilcar; Caires, Anderson R. L.; Deflon, Victor M.; Pesci, Rafaela B. P.; Rocha, C. N. Lima; Correa, J. R.; Pinto, L. M. C.; Casagrande, Gleison Antônio
• Is Part Of: New journal of chemistry. Volume 44:Number 17(2020)
• Page Start: 6862
• Page End: 6871
• Publication Date: 2020-04-14
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/d0nj01339k
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : This work presents new gold materials as promising antitumoral and antibacterial agents and their potential use as luminescent probes for cellular bioimaging. Abstract : Three novel highly photoluminescent mononuclear Au I compounds (1, 2, and 3 ) based on mixed phosphine/thiocarbamoyl-pyrazoline materials were synthesized at good yields using a sonochemical method and then structurally characterized. X-ray diffraction studies revealed the compounds to be mononuclear cationic complexes of the [Ph3 PAu(L)]PF6 type with linear coordination geometry around Au I atoms. Investigation of photophysical properties showed an intense greenish blue emission when the complexes were excited at 305 nm in solution. The emission was attributed to mixed MLCT + IL and LLCT electronic transitions taking place after ligand complexation, as shown by DFT calculations. Full characterization of the compounds also comprised 1 H and 13 C NMR experiments, elemental analyses, infrared spectroscopy, and absorption–emission studies. Additionally, compounds 1, 2, and 3 and respective ligands were investigated as antibacterial agents against five Streptococcus aureus strains (Gram-positive) and one Escherichia coli strain (Gram-negative) with distinct antibiotic-resistance profiles. Cytotoxic activity was assessed using the MTT method against B16F10 melanoma, 4T1 mammary carcinoma, and normal BHK-21 baby hamster kidney cell lines. The synthesized Au I compounds proved more active than the respective precursors and free ligands. Tested as probes for cellular bioimaging, the complexes showed good biodistribution in the cytoplasm of MCF-7 and MDA-MB-231 (human breast adenocarcinoma cell lines).