Issue 45, 2025

Reactivity of an aza-dipyrrin and an aza-BODIPY motif bearing two 2-pyridyl units: an emissive NNN binding pocket

Abstract

The synthesis and reactivity of an aza-dipyrrin and an aza-BODIPY motif each featuring two 2-pyridyl rings appended to the pyrrolic units are reported. The tricoordinate NNN binding domain was complexed to various metals, with Zn(II) analogues isolated and crystallographically characterised. Furthermore, the addition of alcohols across the aza-fulvenium unit provided an amino-decorated framework that served as a convenient pro-ligand for turn-on emissive metal sensing.

Graphical abstract: Reactivity of an aza-dipyrrin and an aza-BODIPY motif bearing two 2-pyridyl units: an emissive NNN binding pocket

Supplementary files

Article information

Article type
Paper
Submitted
15 Oct 2025
Accepted
24 Oct 2025
First published
03 Nov 2025
This article is Open Access
Creative Commons BY-NC license

Org. Biomol. Chem., 2025,23, 10391-10397

Reactivity of an aza-dipyrrin and an aza-BODIPY motif bearing two 2-pyridyl units: an emissive NNN binding pocket

R. L. Gapare, R. M. Diaz-Rodriguez, V. A. Williams, M. Atwood, M. J. Cotnam, J. W. Hilborn, E. R. Johnson, K. N. Robertson and A. Thompson, Org. Biomol. Chem., 2025, 23, 10391 DOI: 10.1039/D5OB01628B

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements