936217-16-2

Upstream product

• 936217-13-9 4-(2,5-dimethyl-1H-pyrrol-1-yl)-4'-bromobiphenyl 
• 24067-17-2 4-nitrophenylboronic acid 
• 288608-09-3 1-(2,5-dimethyl-1H-pyrrol-1-yl)-4-iodobenzene 
• 5467-74-3 4-Bromophenylboronic acid 

Relevant academic research and scientific papers

Synthesis of symmetrically and unsymmetrically para-functionalized p-quaterphenylenes

Oligo-p-phenylenes have proven to be versatile building blocks for the generation of self-assembled nanoaggregates with interesting optical properties via vapor deposition on solid supports. Preliminary studies have shown that both the properties and the morphologies of these aggregates can be influenced by the introduction of functional groups. To this end, we have developed general approaches to the synthesis of symmetrically and unsymmetrically 1,4?-substituted p-quaterphenylenes through the application of a reliable Suzuki cross-coupling strategy. Georg Thieme Verlag Stuttgart.

NANOFIBERS FROM FUNCTIONALIZED ORGANIC MOLECULES

The present invention relates to organic nanofibers that can be produced from organic compounds having a core according to formula (I), wherein X and/or Y are C or N and n is 2 to 4 by self-organized growth on a solid substrate upon deposition from the ga