Abstract

Novel heteroleptic ZnII bis(dipyrrinato) complexes were prepared as intriguing emitters. With our tailor-made design, we achieved far-red emissive complexes with a photoluminescence quantum yield up to 45% in dimethylsulfoxide and 70% in toluene. This means that heteroleptic ZnII bis(dipyrrinato) complexes retain very intense emission also in polar solvents, in contrast to their homoleptic counterparts, which we prepared for comparing the photophysical properties. It is evident from the absorption and excitation spectra that heteroleptic complexes present the characteristic features of both ligands: the plain dipyrrin (Lp) and the π-extended dipyrrin (Lπ). On the contrary, the emission comes exclusively from the π-extended dipyrrin Lπ, suggesting an interligand nonradiative transition that causes a large pseudo-Stokes shift (up to 4,600 cm−1). The large pseudo-Stokes shifts and the emissive spectral region of these novel heteroleptic ZnII bis(dipyrrinato) complexes are of great interest for bioimaging applications. Thus, their high biocompatibiliy with four different cell lines make them appealing as new fluorophores for cell imaging.

Highlights

  • Far-red and near-infrared (NIR) fluorophores are highly desired probes for bioimaging and sensing applications in living organisms

  • SBCT is very appealing in potential applications such as artificial photosynthesis (Alqahtani et al, 2019; Tungulin et al, 2019) or photovoltaics, (Bartynski et al, 2015), it is not advantageous for other applications such as imaging, where high emission in polar solvents is of utmost importance

  • Green-emitting homoleptic bis(dipyrrinato) zinc complexes were employed as selective probes for cancer cells and as photodynamic therapy photosensitisers (Karges et al, 2019a; Karges et al, 2019b; Karges et al, 2020)

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Summary

Introduction

Far-red and near-infrared (NIR) fluorophores are highly desired probes for bioimaging and sensing applications in living organisms. Heteroleptic Zn Bis(Dipyrrinato) Complexes for Bioimaging electronically degenerate excited states of the identical dipyrrins. In heteroleptic bis(dipyrrinato) zinc complexes, the electronically excited states of the two dipyrrinato ligands are energetically different.

Results
Conclusion

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