1094159-79-1Relevant articles and documents
Supramolecular ruthenium-alkynyl multicomponent architectures: Engineering, photophysical properties, and responsiveness to nitroaromatics
Gatri, Rafik,Ouerfelli, Ines,Efrit, Mohamed Lofti,Serein-Spirau, Francoise,Lere-Porte, Jean-Pierre,Valvin, Pierre,Roisnel, Thierry,Bivaud, Sebastien,Akdas-Kilig, Huriye,Fillaut, Jean-Luc
, p. 665 - 676 (2014)
A series of H-bonded supramolecular architectures were built from monofunctional M-Ci - C-R and bifunctional R-Ci - C-M-Ci - C-R trans-alkynylbis(1,2-bis(diphenylphosphino)ethane)ruthenium(II) complexes and π-conjugated modules containing 2,5-dialkoxy-p-p
Self-assembling depsipeptide dendrimers and dendritic fullerenes with new cis- and trans-symmetric Hamilton receptor functionalized zn-porphyrins: Synthesis, photophysical properties and cooperativity phenomena
Maurer, Katja,Grimm, Bruno,Wessendorf, Florian,Hartnagel, Kristine,Guldi, Dirk M.,Hirsch, Andreas
scheme or table, p. 5010 - 5029 (2010/11/05)
Two novel supramolecular building blocks, namely cis- and trans-symmetric zinc-porphyrins bearing Hamilton receptors as their focal points (10 and 15), were self-assembled with (i) first-, second- and third-generation depsipeptide cyanurates (21-23); (ii) second-generation dendrofullerene (24), and (iii) cyanuric acid substituted fullerene (20), and probed in a series of photophysical investigations. Importantly, an overall 1:2 stoichiometry was confirmed with binding con-stants Kn, and Hill coefficients nH that indicate remarkable cooperativities. As a general feature, stronger binding evolves from the trans-symmetric porphyrin isomer, although the increased steric demand of the depsipeptide ligands means that the binding constants decrease with each generation. The self-assembly of 10 or 15 with 20 affords novel electron donor-acceptor hybrids that reveal, upon excitation, intra-hybrid charge-transfer events.