1589028-36-3

Upstream product

• 54845-07-7 2-(3,5-dihydroxyphenyl)isoindoline-1,3-dione 
• 62921-74-8 2-(2-(2-methoxyethoxy)ethoxy)ethyl p-toluenesulfonate 
• 1589028-28-3 C₂₈H₃₇NO₁₀ 
• 1589028-31-8 3,5-bis(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)aniline 
• 1589028-33-0 C₆₈H₉₁NO₁₄ 

Downstream Products

• 1589028-55-6 C₅₂H₄₇N₃O₁₆ 
• 1589028-39-6 C₅₀H₅₂N₂O₁₄ 
• 1589028-53-4 C₄₆H₄₄N₂O₁₄ 

Relevant academic research and scientific papers

Self-assembly and phase separation of amphiphilic dyads based on 4,7-bis(2-thienyl)benzothiodiazole and perylene diimide

To get highly ordered organic structures at the nanoscale, a series of new electronic donor-acceptor (D-A) dyads were synthesized. The dyads bearing different side chains (lipophilic or amphiphilic) or linkers (Long or Short) showed variable self-assembly behaviour. Long-linker dyads can fold in dilute solution, but the folding of short-linker dyads was not observed. Intermolecular D-A interactions and acceptor-acceptor (A-A) aggregation were proved to co-occur in chloroform for all four dyads. In the bulk state, amphiphilic dyads could overcome the intrinsic D-A interactions and achieve better D-A phase separation than lipophilic ones due to the incompatibility of the side chains. The dyad with a short-linker and amphiphilic side chains, Samphi, had the ability to form a gel, and both of the amphiphilic dyads could form nanofibres. This journal is the Partner Organisations 2014.