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Photoinduced electron transfer from PbS quantum dots to cobalt(III) Schiff base complexes: light activation of a protein inhibitor

机译:从PbS量子点到钴(III)Schiff碱配合物的光诱导电子转移:蛋白抑制剂的光活化

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摘要

This paper describes the activation of a biologically inert Co(III) Schiff base (SB) complex to its protein inhibitor form by photoinduced electron transfer (PET) from a colloidal PbS quantum dot (QD, radii = 1.5 – 1.7 nm) to the cobalt center, with a charge separation time constant of 125 ns. Reduction of the Co(III)-SB initiates release of the native axial ligands, promoting replacement with the histidine mimic 4-methylimidazole. The rate of ligand displacement increases by approximately a factor of eight upon exposure of the PbS QD/Co(III)-SB mixture to light of energy greater than the energy of the first excitonic state of the QDs, from which PET occurs. These results suggest an approach for the preparation of inorganic therapeutic agents that can be specifically coupled to a biologically active site by cooperative redox-binding ligation.
机译:本文描述了通过从胶体PbS量子点(QD,半径= 1.5 – 1.7 nm)到钴的光致电子转移(PET),将一种生物惰性的Co(III)Schiff碱(SB)复合物激活为其蛋白抑制剂的形式。中心,电荷分离时间常数为125 ns。 Co(III)-SB的还原引发天然轴向配体的释放,促进用组氨酸模拟物4-甲基咪唑替代。当PbS QD / Co(III)-SB混合物暴露于大于QDs的第一个激子态能量的光中时,配体置换的速率增加大约八分之一。这些结果提示了一种制备无机治疗剂的方法,该方法可以通过协同氧化还原结合连接而特异性地偶联至生物活性位点。

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