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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Synthesis and properties of a dendritic FRET donor-acceptor system with cationic iridium(iii) complex core and carbazolyl periphery
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Synthesis and properties of a dendritic FRET donor-acceptor system with cationic iridium(iii) complex core and carbazolyl periphery

机译:具有阳离子铱(iii)配合物核和咔唑基外围的树枝状FRET供体-受体体系的合成和性能

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摘要

In order to enhance the photoluminescence of cyclometalated iridium(iii) complexes, which are potentially useful for biolabeling and bioimaging, a series of benzyl ether branched dendritic moieties with carbazolyl termini were introduced to the cyclometalating CN ligands of the heteroleptic Ir(iii) complexes. The complexes also contain a bidentate bipyridine ligand with a carboxyl group for further bioconjugation or functionalization. The dendritic benzyl ether moieties with carbazolyl peripheral groups have demonstrated a dual function as both a F?rster resonance energy transfer (FRET) donor and an oxygen shield to the Ir(iii) complex core. The peripheral carbazolyl groups absorb UV light more intensively and transfer energy efficiently to the Ir(iii) complex core via the FRET effect, and thus the photoluminescence of the Ir(iii) complex at around 560 nm is significantly enhanced. Furthermore, the benzyl ether dendrimers containing carbazolyl termini can shield the Ir(iii) complex core to weaken the oxygen quenching effect, which leads to a further enhancement of the PL of the Ir(iii) complex.
机译:为了增强可能对生物标记和生物成像有用的环金属化铱(iii)配合物的光致发光,将一系列带有咔唑基末端的苄基醚支化树枝状部分引入到杂化Ir(iii)配合物的环金属化CN配体中。该复合物还含有带有羧基的二齿联吡啶配体,用于进一步的生物缀合或功能化。具有咔唑基外围基团的树枝状苄基醚部分已显示出双重功能,既可以作为Fster共振能量转移(FRET)供体,也可以作为对Ir(iii)配合物核的氧屏蔽。外围的咔唑基团更密集地吸收紫外光,并通过FRET效应将能量有效地转移到Ir(iii)配合物核心,因此Ir(iii)配合物在560 nm附近的光致发光显着增强。此外,含咔唑基末端的苄基醚树枝状大分子可以屏蔽Ir(iii)配合物的核心,从而减弱氧的猝灭作用,从而进一步提高Ir(iii)配合物的PL。

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