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一系列具有苯并咪唑共配体的锰(Ⅰ)光活化一氧化碳释放分子:合成、结构表征、一氧化碳释放性质及生物活性评价

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

作者信息

Hu Mixia, Yan YaLi, Zhu Baohua, Chang Fei, Yu Shiyong, Alatan Gaole

机构信息

College of Chemistry and Chemical Engineering, Inner Mongolia University Hohhot 010021 China

Key Lab of Fine Organic Synthesis Inner Mongolia Autonomous Region Hohhot 010021 China.

出版信息

RSC Adv. 2019 Jul 2;9(36):20505-20512. doi: 10.1039/c9ra01370a. eCollection 2019 Jul 1.

Abstract

Five Mn(i) photo-activated carbon monoxide-releasing molecules (photo-CORMs) with benzimidazole coligands, namely [MnBr(CO)L1] (1, L1 = 2-(2-pyridyl)benzimidazole), Mn(CO)L1(PPh) (2), [MnBr(CO)L2] (3, L2 = 2,2'-bisbenzimidazole), [MnBr(CO)L3]·CHOH (4, L3 = 2,6-bis(benzimidazole-2'-yl)pyridine) and -[MnBr(CO)L4] (5, L4 = 2,4-bis(benzimidazole-2'-yl) pyridine) were synthesized by reactions of MnBr(CO) with complexes L1-L4, respectively, and characterized single crystal X-ray diffraction, elemental analysis, H-NMR, C-NMR, IR, UV-vis and fluorescence spectroscopy. The CO-release properties of 1-5 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 of 1-5 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 of 3 is better than that of other complexes.

摘要

合成了五种带有苯并咪唑共配体的锰(Ⅰ)光活化一氧化碳释放分子(光CORMs),即[MnBr(CO)L1](1,L1 = 2-(2-吡啶基)苯并咪唑)、Mn(CO)L1(PPh)(2)、[MnBr(CO)L2](3,L2 = 2,2'-双苯并咪唑)、[MnBr(CO)L3]·CHOH(4,L3 = 2,6-双(苯并咪唑-2'-基)吡啶)和[MnBr(CO)L4](5,L4 = 2,4-双(苯并咪唑-2'-基)吡啶),它们分别通过MnBr(CO)与配合物L1 - L4反应合成,并通过单晶X射线衍射、元素分析、1H-NMR、13C-NMR、红外光谱、紫外-可见光谱和荧光光谱进行表征。使用肌红蛋白测定法和CO检测研究了1 - 5的CO释放特性,结果表明所有配合物在暴露于365 nm紫外光时都能快速释放CO。比较它们的CO释放半衰期,我们发现增加配体框架的不饱和程度和共轭程度有利于延长CO释放时间,并且1 - 5的发光强度可以逐渐增强。细胞荧光成像测试表明,这些锰(Ⅰ)光CORMs可以被人肝细胞(HL-7702)和肝癌细胞(SK-Hep1)摄取,并表现出良好的生物成像能力。对SK-Hep1的细胞活力测定表明,3的抗癌活性优于其他配合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f79d/9065806/888d3964a55e/c9ra01370a-f1.jpg

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