601488-61-3

Upstream product

• 494859-11-9 N,N-dimethyl-4-{(3Z)-6-[4-(dimethylamino)phenyl]-3,4-bis[(triisopropylsilyl)ethynyl]hex-3-ene-1,5-diyn-1-yl}benzenamine 

Downstream Products

• 601488-56-6 C₈₈H₈₂N₂Si₂ 
• 601488-57-7 4-((9Z)-18-[4-(dihexylamino)phenyl]-3,16-bis{[4-(dihexylamino)phenyl]ethynyl}-9,10-bis{[4-(dimethylamino)phenyl]ethynyl}-4,15-bis[(triisopropylsilyl)ethynyl]octadeca-3,9,15-triene-1,5,7,11,13,17-hexayn-1-yl)-N,N-dihexylbenzenamine 

Relevant academic research and scientific papers

Donor-substituted perethynylated dehydroannulenes and radiaannulenes: Acetylenic carbon sheets featuring intense intramolecular charge transfer

In this article, we report the preparation of unprecedented φ-conjugated macrocycles (Fig. 1) by acetylenic scaffolding using modular tetraethynylethene (TEE, 3,4-diethynylhex-3-ene-1,5-diyne) building blocks. A novel photochemical access to (Z)-bisdeprot

π-electron conjugation effects in antiaromatic dehydro[12]- and aromatic dehydro[18]-annulenes

N,N-Dimethylanilino-substituted perethynylated dehydro[12]- and dehydro[18]-annulenes were prepared by oxidative acetylenic coupling of cis-bisdeprotected tetra-ethynylethene derivatives obtained by a new photochemical route; they display strongly bathoch