A series of Mn(i) photo-activated carbon monoxide-releasing molecules with benzimidazole coligands: synthesis, structural characterization, CO releasing properties and biological activity evaluation. Issue 36 (2nd July 2019)

• Record Type: Journal Article
• Authors: Hu, Mixia; Yan, YaLi; Zhu, Baohua; Chang, Fei; Yu, Shiyong; Alatan, Gaole
• Is Part Of: RSC advances. Volume 9:Issue 36(2019)
• Page Start: 20505
• Page End: 20512
• Publication Date: 2019-07-02
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c9ra01370a
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Five Mn(i ) photo-activated carbon monoxide-releasing molecules were synthesized by reactions of MnBr(CO)5 with L1–L4, and characterized via single crystal X-ray diffraction, 1 H-NMR, 13 C-NMR, IR, UV-vis and fluorescence spectroscopy. Abstract : Five Mn(i ) photo-activated carbon monoxide-releasing molecules (photo-CORMs) with benzimidazole coligands, namely [MnBr(CO)3 L1] (1, L1 = 2-(2-pyridyl)benzimidazole), [Mn(CO)2 L1(PPh3 )2 ](ClO4 ) (2 ), [MnBr(CO)3 L2] (3, L2 = 2, 2′-bisbenzimidazole), [MnBr(CO)3 L3]·CH3 OH (4, L3 = 2, 6-bis(benzimidazole-2′-yl)pyridine) and fac -[MnBr(CO)3 L4] (5, L4 = 2, 4-bis(benzimidazole-2′-yl) pyridine) were synthesized by reactions of MnBr(CO)5 with complexes L1–L4, respectively, and characterized via single crystal X-ray diffraction, elemental analysis, 1 H-NMR, 13 C-NMR, IR, UV-vis and fluorescence spectroscopy. The CO-release properties of1–5 were investigated using the myoglobin assay and CO detection, and the results show that all of the complexes could release CO rapidly upon exposure to 365 nm UV light. Comparing their half-lives of CO release, we found that increasing the degree of unsaturation and conjugation of the ligand frame could be advantageous for prolonging the time of CO-release, and that the luminescence intensity of1–5 could gradually be enhanced. The cellular fluorescence imaging tests demonstrate that these Mn(i ) photo-CORMs can be taken up by human liver cells (HL-7702) and liver cancer cells (SK-Hep1), and exhibit good capabilities for bioimaging. A cell viability assay for SK-Hep1 shows that the anticancer activity of3 is better than that of other complexes.