Solvent- and concentration-induced self-assembly of an amphiphilic perylene dye
- 19 December 2019
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 44 (3) , 892-899
Abstract
A new amphiphilic perylene dye bearing two carboxylic and two amidic chains (PDA-CA) has been synthesized and the ability to form π–π driven aggregates or folded structures has been investigated in aqueous or organic solvents at different concentrations, by means of NMR spectroscopy, theoretical calculations and optical characterization. The 1H NMR data showed the coexistence of supramolecular aggregates due to a synergetic effect of π–π stacking, hydrogen bonding and hydrophobic/hydrophilic interactions. The ratio between these species has been evaluated by concentration- and temperature-dependent 1H NMR experiments and also by the effect of aqueous or organic solvents. UV-Vis measurements are in agreement with NMR data evidencing the presence of more organized structures in organic solvents and aggregated species in aqueous solution. The π-stacking ability and the role intermolecular hydrogen bonds in the formation of different aggregated structures, was also estimated by density functional theory.Keywords
Funding Information
- Agentúra na Podporu Výskumu a Vývoja (APVV-15-0053)
- Vedecká Grantová Agentúra MŠVVaŠ SR a SAV (2/0161/17)
- Vedecká Grantová Agentúra MŠVVaŠ SR a SAV (1/0601/15)
This publication has 42 references indexed in Scilit:
- Solvent-induced self-assembly of hydrogen bonded P4VP-perylenebisimide comb polymerJournal of Materials Chemistry C, 2013
- Aromatic Core Extension in the Series of N‐Cyclic Bay‐Substituted Perylene G‐Quadruplex Ligands: Increased Telomere Damage, Antitumor Activity, and Strong Selectivity for Neoplastic over Healthy CellsChemMedChem, 2012
- Ammonia Sensory Properties Based on Single-Crystalline Micro/Nanostructures of Perylenediimide Derivatives: Core-Substituted EffectThe Journal of Physical Chemistry C, 2011
- Universal Solvation Model Based on Solute Electron Density and on a Continuum Model of the Solvent Defined by the Bulk Dielectric Constant and Atomic Surface TensionsThe Journal of Physical Chemistry B, 2009
- Solvent Effect on the Self-Assembled Structure of an Amphiphilic Perylene Diimide DerivativeThe Journal of Physical Chemistry B, 2008
- Selective Bromination of Perylene Diimides under Mild ConditionsThe Journal of Organic Chemistry, 2007
- How does basis set superposition error change the potential surfaces for hydrogen-bonded dimers?The Journal of Chemical Physics, 1996
- Density-functional exchange-energy approximation with correct asymptotic behaviorPhysical Review A, 1988
- Development of the Colle-Salvetti correlation-energy formula into a functional of the electron densityPhysical Review B, 1988
- The crystal and molecular structure of peryleneProceedings of the Royal Society of London. A. Mathematical and Physical Sciences, 1953