Document Type
Article
Publication Date
12-1-2015
Abstract
© 2015 Elsevier B.V. A series of four BODIPYs containing one or two ortho- or para-carborane clusters were synthesized using palladium(0)-catalyzed Suzuki cross-coupling or nucleophilic substitution reactions, at the 2,6- or the 8-positions of halogenated boron dipyrromethenes (BODIPYs). The spectroscopic, structural (including one X-ray) and in vitro BBB permeability of the BODIPYs using hCMEC/D3 brain endothelial cells were investigated.
Publication Source (Journal or Book title)
Journal of Organometallic Chemistry
First Page
209
Last Page
213
Recommended Citation
Gibbs, J., Wang, H., Bhupathiraju, N., Fronczek, F., Smith, K., & Vicente, M. (2015). Synthesis and properties of a series of carboranyl-BODIPYs. Journal of Organometallic Chemistry, 798, 209-213. https://doi.org/10.1016/j.jorganchem.2015.05.009