Jia-Ning Wang , Chuan-Qi Shen , Jin Liu , Zi-Ang Nan , Qing Li , You-Gui Huang
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引用次数: 0
Abstract
Two hexanuclear titanium-oxo clusters, [Ti6O6(OiPr)6L16]·2CH3CN (1) and [Ti6O4(OiPr)10(OiPrL2)2L22] (2), were synthesized via solvothermal reactions (HL1 = o-nitrobenzoic acid and H2L2 = 1,3-bisbenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid). Compound 1 is a cluster with an octahedral {Ti6O6} core, while compound 2 features as a cluster with chair-shaped {Ti6O4} core. Both the compounds show strong UV absorptions, but their activities to radicals including 2,2-diphenylpicrylhydrazyl (DPPH), hydroxyl, and azinobis-(3-ethylbenzthiazoline-6-sulphonate) (ABTS) are significantly different. In contrast to the silence of all of the three radicals to compound 1, compound 2 is able to efficiently scavenge all of them. This obvious difference is attributed to that compound 2 shows higher reducibility, which is probably intrinsically related to electronic donating ligands L2 and OiPrL2. The coexistence of strong UV absorption and great antioxidant activity enables compound 2 to protect skin against photoaging and enhance skin health effectively. These results indicate titanium-oxo clusters bearing redox active ligands are potential for next-generation skincare products.
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