Exploiting the B–N/C–C Isosterism Yields Nile‐Red Inspired Organoboron Dyes Capable of Singlet‐Oxygen Photosensitization
Open Access
- 23 September 2026
- journal article
- Published by Wiley in ChemistryEurope
- Vol. 4 (9)
Abstract
Small dyes are indispensable tools for probing biological processes. Among them, Nile Red (NR) is widely used for imaging lipid‐rich environments. However, the structural diversification of its phenoxazine core remains limited. Herein, we exploit B─N/C─C isosterism to connect the western and eastern fragments of NR through a B─N linkage, enabling the design of NR‐inspired boronic acid‐derived salicylidenehydrazone (NR‐BASHY) dyes with enhanced structural and functional versatility. This strategy allows the modular one‐pot synthesis of NR‐BASHY dyes, which exhibit promising photophysical properties. These include intense absorption ( ε up to 50,800 M –1 cm –1 ) and high brightness ( ε × Φ f up to 17,000 M –1 cm –1 ) and a pronounced solvatofluorochromism with emission spanning the red to near‐infrared spectral region. In strong contrast to NR, NR‐BASHY can act as photosensitizers, featuring efficient singlet‐oxygen generation ( Φ Δ up to 0.8) and photoinduced cytotoxicity against the U87 glioblastoma cell line in the submicromolar range (IC 50 ca. 0.5 μM), while maintaining low dark toxicity (>100 μM). Moreover, the modular architecture of NR‐BASHY dyes enables click‐reaction mediated bioconjugation with the GV1001 peptide, highlighting the potential of this platform for targeted bioimaging applications.Keywords
Funding Information
- Ministerio de Ciencia, Innovación y Universidades (PID2023‐152556NB‐I00)
- Ministerio de Ciencia, Innovación y Universidades (PRE2023‐001520)
- Fundação para a Ciência e a Tecnologia (UID/04138/2025)
- Fundação para a Ciência e a Tecnologia (UID/PRR/04138/2025)
- Fundação para a Ciência e a Tecnologia (UID/PRR2/04138/2025)
- Fundação para a Ciência e a Tecnologia (LISBOA2030‐FEDER‐00719700)
- Fundação para a Ciência e a Tecnologia (2023.14170.PEX, 2021.04125.CEECIND)
- European Research Council (GA 681679)
- Agence Nationale de la Recherche (ANR‐10‐IDEX‐0001‐02 PSL)
- Xunta de Galicia (ED481B‐2023‐123)
This publication has 50 references indexed in Scilit:
- Engineering the BASHY Dye Platform toward Architectures with Responsive FluorescenceChemistry – A European Journal, 2023
- Rationally designed monoamine oxidase A‐activatable AIE molecular photosensitizer for the specific imaging and cellular therapy of tumorsAggregate, 2022
- Cyanine‐Like Boronic Acid‐Derived Salicylidenehydrazone Complexes (Cy‐BASHY) for Bioimaging ApplicationsChemistry – A European Journal, 2020
- Discerning the Chemistry in Individual Organelles with Small‐Molecule Fluorescent ProbesAngewandte Chemie International Edition, 2016
- B=N Units as Part of Extended π‐Conjugated Oligomers and PolymersChemistry – A European Journal, 2016
- Nile Red and Nile Blue: Applications and Syntheses of Structural AnaloguesChemistry – A European Journal, 2016
- A Three‐Component Assembly Promoted by Boronic Acids Delivers a Modular Fluorophore Platform (BASHY Dyes)Chemistry – A European Journal, 2015
- A Four‐Component Reaction for the Synthesis of DioxadiazaborocinesAngewandte Chemie International Edition, 2015
- BN/CC Isosteric Compounds as Enzyme Inhibitors: N‐ and B‐Ethyl‐1,2‐azaborine Inhibit Ethylbenzene Hydroxylation as Nonconvertible Substrate AnaloguesAngewandte Chemie International Edition, 2013
- Boron Mimetics: 1,2‐Dihydro‐1,2‐azaborines Bind inside a Nonpolar Cavity of T4 LysozymeAngewandte Chemie International Edition, 2009