AI Article Synopsis

  • The study presents and characterizes a monometallic and three bimetallic ruthenium nitrosyl complexes, highlighting their novel ligands.
  • Crystal structures of specific bimetallic complexes are described alongside their spectroscopic behavior, which aligns with computational predictions.
  • A significant increase in two-photon absorption cross-section is noted in the bimetallic complexes, making them potential candidates for drug delivery applications by releasing nitric oxide upon light irradiation.

Article Abstract

One monometallic and three bimetallic ruthenium nitrosyl (RuNO) complexes are presented and fully characterized in reference to a parent monometallic complex of formula [FTRu(bpy)(NO)] , where FT is a fluorenyl-substituted terpyridine ligand, and bpy the 2,2'-bipyridine. These new complexes are built with the new ligands FFT, TFT, TFFT, and TF-CC-TF (where an alkyne C≡C group is inserted between two fluorenes). The crystal structures of the bis-RuNO and bis-RuNO complexes built from the TFT ligand are presented. The evolution of the spectroscopic features (intensities and energies) along the series, at one-photon absorption (OPA) correlates well with the TD-DFT computations. A spectacular effect is observed at two-photon absorption (TPA) with a large enhancement of the molecular cross-section (σ ), in the bimetallic species. In the best case, σ is equal to 1523±98 GM at 700 nm, in the therapeutic window of transparency of biological tissues. All compounds are capable of releasing NO⋅ under irradiation, which leads to promising applications in TPA-based drug delivery.

Download full-text PDF

Source
http://dx.doi.org/10.1002/chem.202201692DOI Listing

Publication Analysis

Top Keywords

bimetallic ruthenium
8
ruthenium nitrosyl
8
two-photon absorption
8
complexes built
8
complexes
4
nitrosyl complexes
4
complexes enhanced
4
enhanced two-photon
4
absorption properties
4
properties nitric
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!