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Ternary Iron(III) complex showing photocleavage of DNA in the photodynamic therapy window

机译:三元铁(III)配合物在光动力治疗窗口中显示DNA的光裂解

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摘要

A new ternary iron(III) complex [FeL(dpq)] containing dipyridoquinoxaline (dpq) and 2,2-bis(3,5-di-tert-butyl-2-hydroxybenzyl)aminoacetic acid (H3L) is prepared and structurally characterized by X-ray crystallography. The high-spin complex with a FeN3O3 core shows a quasi-reversible iron(III)/iron(II) redox couple at -0.62 V (vs SCE) in DMF/0.1 M TBAP and a broad visible band at 470 nm in DMF/Tris buffer. Laser photoexcitation of this phenolate (L)-to-iron(III) charge-transfer band at visible wavelengths including red light of >= 630 nm leads to cleavage of supercoiled pUC19 DNA to its nicked circular form via a photoredox pathway forming hydroxyl radicals.
机译:制备了一种新的三元铁(III)配合物[FeL(dpq)],其中含有二吡啶并喹喔啉(dpq)和2,2-双(3,5-二叔丁基-2-羟基苄基)氨基乙酸(H3L)通过X射线晶体学。具有FeN3O3核的高自旋复合物在DMF / 0.1 M TBAP中在-0.62 V(vs SCE)处显示准可逆铁(III)/铁(II)氧化还原对,在DMF / S中在470 nm处显示宽可见带Tris缓冲区。在可见光波长(包括> = 630 nm的红光)上对该酚盐(L)-铁(III)电荷转移带进行激光光激发,会导致超螺旋的pUC19 DNA通过形成羟基的光氧化还原途径裂解成带切口的环状。

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