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硅酞菁染料在 X 射线照射下的配体释放。

Ligand release from silicon phthalocyanine dyes triggered by X-ray irradiation.

机构信息

Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita-ku, Sapporo 060-0812, Japan.

Graduate School of Veterinary Medicine, Hokkaido University, Kita-ku, Sapporo 060-0818, Japan.

出版信息

Org Biomol Chem. 2022 Sep 21;20(36):7270-7277. doi: 10.1039/d2ob00957a.

Abstract

Ligand release from silicon phthalocyanine (SiPc) dyes triggered by near-infrared (NIR) light is a key photochemical reaction involving caged compounds based on SiPc. Although NIR light is relatively permeable compared with visible light, this light can be attenuated by tissue absorption and scattering; therefore, using light to induce photochemical reactions deep inside the body is difficult. Herein, because X-rays are highly permeable and can produce radicals through the radiolysis of water, we investigated whether the axial ligands of SiPcs can be cleaved using X-ray irradiation. SiPcs with different axial ligands (alkoxy, siloxy, oxycarbonyl, and phenoxy groups) were irradiated with X-rays under hypoxic conditions. We found that the axial ligands were cleaved reactions with hydrated electrons (e), not OH radicals, generated from water in response to X-ray irradiation, and SiPc with alkoxy groups exhibited the highest cleavage efficiency. A quantitative investigation revealed that X-ray-induced axial ligand cleavage proceeds a radical chain reaction. The reaction is expected to be applicable to the molecular design of X-ray-activatable functional molecules in the future.

摘要

硅酞菁(SiPc)染料的配体在近红外(NIR)光的触发下释放是一种涉及基于 SiPc 的笼状化合物的关键光化学反应。尽管与可见光相比,NIR 光的穿透能力相对较强,但这种光会被组织吸收和散射衰减;因此,用光诱导体内深处的光化学反应是困难的。在这里,由于 X 射线具有很强的穿透能力,并可以通过水的辐射分解产生自由基,我们研究了 SiPcs 的轴向配体是否可以通过 X 射线照射来断裂。在缺氧条件下,用 X 射线辐照具有不同轴向配体(烷氧基、硅氧基、氧羰基和苯氧基)的 SiPcs。我们发现,轴向配体被断裂与水合电子(e)发生反应,而不是来自水的 OH 自由基,对 X 射线辐照作出反应,并且具有烷氧基的 SiPc 表现出最高的断裂效率。定量研究表明,X 射线诱导的轴向配体断裂是一个自由基链式反应。该反应有望在未来应用于 X 射线激活功能分子的分子设计。

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