Issue 48, 2024

Photo-triggered NO release of nitrosyl complexes bearing first-row transition metals and therapeutic applications

Abstract

In biological systems, nitric oxide (NO) is a crucial signaling molecule that regulates a wide range of physiological and pathological processes. Given the significance of NO, there has been considerable interest in delivering NO exogenously, particularly through light as a non-invasive therapeutic approach. However, due to the high reactivity and instability of NO under physiological conditions, directly delivering NO to targeted sites remains challenging. In recent decades, photo-responsive transition metal–nitrosyl complexes, especially based on first-row transition metals such as Mn, Fe, and Co, have emerged as efficient NO donors, offering higher delivery efficiency and quantum yields than heavy metal–nitrosyl complexes under light exposure. This review provides a comprehensive overview of current knowledge and recent developments in the field of photolabile first-row transition metal–nitrosyl complexes, focusing on the structural and electronic properties, photoreactivity, photodissociation mechanisms, and potential therapeutic applications. By consolidating the key features of photoactive nitrosyl complexes, the review offers deeper insights and highlights the potential of first-row transition metal–nitrosyl complexes as versatile tools for photo-triggered NO delivery.

Graphical abstract: Photo-triggered NO release of nitrosyl complexes bearing first-row transition metals and therapeutic applications

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Article information

Article type
Review Article
Submitted
08 Okt. 2024
Accepted
06 Nov. 2024
First published
07 Nov. 2024
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2024,15, 20155-20170

Photo-triggered NO release of nitrosyl complexes bearing first-row transition metals and therapeutic applications

S. Sun, J. Choe and J. Cho, Chem. Sci., 2024, 15, 20155 DOI: 10.1039/D4SC06820C

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