799559-80-1

Upstream product

• 17789-14-9 3-(1,3-dioxolan-2-yl)-phenylbromide 
• 840531-04-6 N-(3-(1,3-dioxolan-yl)phenyl)-N-phenylpyren-1-amine 
• 65838-93-9 N-phenyl-1-aminopyrene 
• 840531-08-0 N-(3-(hydroxymethyl)phenyl)-N-phenylpyren-1-amine 

Downstream Products

• 840531-10-4 {3,5-bis-[3-(phenyl-pyren-1-yl-amino)-benzyloxy]-phenyl}-methanol 
• 903561-93-3 {3-benzyloxy-5-[3-(phenyl-pyren-1-yl-amino)-benzyloxy]-phenyl}-methanol 
• 903561-94-4 [3-(3-benzyloxy-5-bromomethyl-phenoxymethyl)-phenyl]-phenyl-pyren-1-yl-amine 
• 903561-96-6 (3-{3-benzyloxy-5-[3-(3,5-bis-benzyloxy-benzyloxy)-5-bromomethyl-phenoxymethyl]-phenoxymethyl}-phenyl)-phenyl-pyren-1-yl-amine 
• 903561-95-5 [3-{3-benzyloxy-5-[3-(phenyl-pyren-1-yl-amino)-benzyloxy]-benzyloxy}-5-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-methanol 
• 840531-11-5 C₆₅H₄₅BrN₂O₂ 

Relevant academic research and scientific papers

Dendrimer analogues of linear molecules to evaluate energy and charge-transfer properties

We have designed and synthesized difunctionalized dendrimers containing two donors in the periphery and an acceptor at the core to serve as scaffolds for comparison with linear analogues to investigate the advantage of dendritic scaffolds for energy and c

Energy and electron transfer in bifunctional non-conjugated dendrimers

Nonconjugated dendrimers, which are capable of tunneling energy from the periphery to the core followed by a charge-transfer process from the core to the periphery, have been synthesized. The energy and electron donors involve a diarylaminopyrene unit and