Polyphosphorylated triphenylenes: synthesis, crystal structure, and selective catechol recognition.


Designed as a multivalent hydrogen bond acceptor, new receptors, Discopus 1a,b, were built from a triphenylene core surrounded by six (diaryl)phosphinate groups. An efficient synthesis was developed to prepare these elaborated structures in a high overall yield. The X-ray structure of receptor 1b showed strong cooperative hydrogen bonds with two water molecules and intermolecular CH-pi contacts. In chloroform, Discopus 1a,b displayed recognition properties toward dihydroxybenzenes, selectively forming complexes with catechol derivatives 4a-c in a 1:2 (host:guest) stoichiometry. According to NMR and microcalorimetry titrations, association constants were found in the 30-2837 M(-1) range, which were larger than those reported for curvated catechol receptors (14-120 M(-1)). Interestingly, Discopus present two distinct catechol binding sites. Weak hydrogen bonding between host phosphinates and guest hydroxyl groups was shown by infrared spectroscopy and (31)P NMR. Molecular dynamics simulations and recognition experiments suggested that a stronger hydrogen bond assisted by a pi-interaction between the Discopus core and one catechol molecule could exist within the 1:2 complex.

DOI: 10.1021/jo802015k

Cite this paper

@article{Givelet2009PolyphosphorylatedTS, title={Polyphosphorylated triphenylenes: synthesis, crystal structure, and selective catechol recognition.}, author={C{\'e}cile Givelet and Bernard Tinant and Luc Van Meervelt and T. Buffeteau and Nathalie Marchand-Geneste and Brigitte Bibal}, journal={The Journal of organic chemistry}, year={2009}, volume={74 2}, pages={652-9} }