1124353-53-2

Upstream product

• 14235-81-5 4-Ethynylaniline 
• 130296-37-6 N-(1-hexylheptyl)-perylene-3,4,9,10-tetracarboxylic-3,4-carboximide-9,10-anhydride 
• 1257338-42-3 2-(1-hexylheptyl)-9-(4-trimethylsilanylethynylphenyl)anthra[2,1,9-def;6,5,10-d'e'f']diisoquinoline-1,3,8,10-tetraone 

Downstream Products

• 1124353-55-4 N-[4-(1-benzyl-1H-[1,2,3]triazol-4-yl)phenyl]-N'-(1-hexylheptyl)perylene-3,4:9,10-tetracarboxdiimide 
• 1257338-40-1 2-(4-bromoethynylphenyl)-9-(1-hexylheptyl)anthra[2,1,9-def;6,5,10-d'e'f']diisoquinoline-1,3,8,10-tetraone 

Relevant academic research and scientific papers

Foerster resonant energy transfer in orthogonally arranged chromophores

We investigate the ultrafast resonant energy transfer of a perylene bisimide dyad by pump-probe spectroscopy, chemical variation, and calculations. This dyad undergoes transfer with near-unit quantum efficiency, although the transition dipole moments of t

A click reaction for fluorescent labelling: Application of the 1,3-dipolar cycloaddition reaction

The copper-catalysed 1,3-dipolar cycloaddition of azides with terminal alkynes was use to introduce a highly fluorescent and photostable perylene-tetracarboxdiimide label. Fluorescent labelling of human hormones and applications are discussed. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.