A naphthalenediimide (NDI)-based synthetic peptide molecule forms gels in a particular solvent mixture (chloroform/aromatic hydrocarbon, 4:1) through charge-transfer (CT) complex formation; this is evident from the corresponding absorbance and fluorescence spectra at room temperature. Various aromatic hydrocarbon based solvents, including benzene, toluene, xylene (ortho, meta and para) and mesitylene, have been used for the formation of the CT complex. The role of different solvent molecules with varying electron-donation capacities in the formation of CT complexes has been established through spectroscopic and computational studies
\u3cp\u3eThe remarkable ability of a charge-transfer (CT) complex prepared from a pyrene-based donor...
Here is reported a solubility method for studying one : one charge transfer complex formation in non...
A series of eight synthetic self-assembling terminally blocked tripeptides have been studied for gel...
The peptide-driven formation of charge transfer supramolecular gels featuring both directional hydro...
The peptide-driven formation of charge transfer (CT) supramolecular gels featuring both directional ...
International audienceGels are made of large amounts of solvent trapped within a 3D molecular networ...
This article describes two-component charge-transfer interaction mediated organogels (CT-gels) deriv...
This thesis describes the formation of supramolecular hydrogels and organogels from different synthe...
In recent years, the self-assembly of various organic π-systems, mediated by non-covalent bonding, h...
The remarkable ability of a charge-transfer (CT) complex prepared from a pyrene-based donor (Py-D) a...
Cation−π and charge-transfer (CT) interactions are ubiquitous in nature and involved in several biol...
Following a supramolecular synthon rationale, a dicarboxylic acid derivative having a naphthalenedii...
This thesis reports the results of a study of some donor-acceptor complexes in solution by a variety...
In this article we present dual-component charge-transfer interaction (CT) induced organogel formati...
Coupling of peptide self-assembly to dynamic sequence exchange provides a useful approach for the di...
\u3cp\u3eThe remarkable ability of a charge-transfer (CT) complex prepared from a pyrene-based donor...
Here is reported a solubility method for studying one : one charge transfer complex formation in non...
A series of eight synthetic self-assembling terminally blocked tripeptides have been studied for gel...
The peptide-driven formation of charge transfer supramolecular gels featuring both directional hydro...
The peptide-driven formation of charge transfer (CT) supramolecular gels featuring both directional ...
International audienceGels are made of large amounts of solvent trapped within a 3D molecular networ...
This article describes two-component charge-transfer interaction mediated organogels (CT-gels) deriv...
This thesis describes the formation of supramolecular hydrogels and organogels from different synthe...
In recent years, the self-assembly of various organic π-systems, mediated by non-covalent bonding, h...
The remarkable ability of a charge-transfer (CT) complex prepared from a pyrene-based donor (Py-D) a...
Cation−π and charge-transfer (CT) interactions are ubiquitous in nature and involved in several biol...
Following a supramolecular synthon rationale, a dicarboxylic acid derivative having a naphthalenedii...
This thesis reports the results of a study of some donor-acceptor complexes in solution by a variety...
In this article we present dual-component charge-transfer interaction (CT) induced organogel formati...
Coupling of peptide self-assembly to dynamic sequence exchange provides a useful approach for the di...
\u3cp\u3eThe remarkable ability of a charge-transfer (CT) complex prepared from a pyrene-based donor...
Here is reported a solubility method for studying one : one charge transfer complex formation in non...
A series of eight synthetic self-assembling terminally blocked tripeptides have been studied for gel...