One-pot Synthesis of Stable NIR Tetracene Diimides Via Double Cross-coupling
Overview
Affiliations
Tetracene tetracarboxylic diimides have been synthesized based on direct double ring extension of electron-deficient naphthalene diimides involving metallacyclopentadienes. Atomic structure and electronic transitions responsible for their NIR absorption spectra are investigated with quantum-chemical calculations. In light of their unique structure and admirable photophysical and electronic properties, this new molecular skeleton is promising candidate for n-type semiconductors.
Synthesis and characterization of 1,2,3,4-naphthalene and anthracene diimides.
Bass A, Castellanos D, Calicdan X, Cao D Beilstein J Org Chem. 2024; 20:1767-1772.
PMID: 39076299 PMC: 11285063. DOI: 10.3762/bjoc.20.155.
Bergman H, Beattie D, Kiel G, Handford R, Liu Y, Don Tilley T Chem Sci. 2022; 13(19):5568-5573.
PMID: 35694352 PMC: 9116291. DOI: 10.1039/d2sc00397j.
Ricci G, Canola S, Dai Y, Fazzi D, Negri F Molecules. 2021; 26(14).
PMID: 34299394 PMC: 8307299. DOI: 10.3390/molecules26144119.
A NIR dye with high-performance n-type semiconducting properties.
Xie J, Shi K, Cai K, Zhang D, Wang J, Pei J Chem Sci. 2018; 7(1):499-504.
PMID: 29861996 PMC: 5952312. DOI: 10.1039/c5sc03045e.
Zirconacyclopentadiene-Annulated Polycyclic Aromatic Hydrocarbons.
Kiel G, Ziegler M, Don Tilley T Angew Chem Int Ed Engl. 2017; 56(17):4839-4844.
PMID: 28334480 PMC: 5671771. DOI: 10.1002/anie.201700818.