首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Red-light activated photoCORMs of Mn(I) species bearing electron deficient 2,2 '-azopyridines
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Red-light activated photoCORMs of Mn(I) species bearing electron deficient 2,2 '-azopyridines

机译:带有电子缺陷的2,2'-偶氮吡啶的Mn(I)物种的红光激活photoCORM

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摘要

The realization of CO releasing molecules triggered by light (photoCORMs) within the phototherapeutic window (lambda > 600 nm) constitutes an important goal for potential therapeutic applications of the molecules. The activation of photoCORMs with red/NIR light would enable exploiting the higher depth of penetration of this radiation with respect to higher energy photons. In this article we report a family of carbonyl Mn(I) complexes capable of releasing CO when triggered with red light (>= 625 nm). Such complexes are based on 2,2'-azopyridine ligands modified by the introduction of electron-donating or electron-withdrawing substituents. Our results indicate that electron deficient ligands induce a gradual decrease of the HOMO-1/LUMO gap of the species (i.e. of the orbitals involved in the lowest energy transition), thus enabling a fine tuning of their visible absorption maxima between 630 and 693 nm. The synthesis of the complexes and their photodecomposition behaviour towards CO release are described. We suggest that this approach could be generalized for further development of low-energy activated photoCORMs.
机译:在光疗窗(λ> 600 nm)内由光(photoCORM)触发的释放CO的分子的实现,构成了分子潜在治疗应用的重要目标。用红色/近红外光激活photoCORMs将使该辐射相对于更高能量的光子具有更高的穿透深度。在本文中,我们报告了一个羰基Mn(I)配合物家族,当被红光(> = 625 nm)触发时能够释放CO。此类络合物基于通过引入给电子或吸电子取代基而修饰的2,2'-偶氮吡啶吡啶配体。我们的结果表明,缺乏电子的配体会引起物种HOMO-1 / LUMO间隙的逐渐减小(即,参与最低能量跃迁的轨道),从而能够在630至693 nm之间对其可见吸收最大值进行微调。 。描述了配合物的合成及其对CO释放的光分解行为。我们建议这种方法可以推广到低能量激活photoCORMs的进一步发展。

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