Supramolecular self-assembly of soft matter have received many attention for various applications such as liquid crystals, sensors, catalysts, and optics due to its precise control and easily tunable characteristics. Particularly, benzene-1,3,5-tricarboxamides (BTAs) as p- stacked organic motif were recognized for formation of liquid crystals materials; however, these BTAs were only reported bearing different short alkyl or aromatic side chains in order to have liquid crystalline properties. Herein, self-assemblies of BTAs (CRNH-BTA, where R = 10, 12, 14, 16, and 18) via hydrogen bonding interactions have been demonstrated as mesophase liquid crystalline materials by simply tuning its long hydrophobic alkyl chains attached to amide. Series ...
The self-assembly in aqueous solution of benzene-1,3,5-tricarboxamide (BTA) bearing one alkyl chain ...
The synthesis of C3- and C2-symmetric benzene-1,3,5-tricarboxamides (BTAs) containing well-defined o...
The self-assembly of small and well-defined molecules using noncovalent interactions to generate var...
The self-assembly of N, N’, N’’-trialkylbenzene-1,3,5-tricarboxyamides (BTAs) has been reported to l...
International audienceAs the benzene 1,3,5-tricarboxamide (BTA) moiety is commonly used as the centr...
After their first synthesis in 1915 by Curtius, benzene-1,3,5-tricarboxamides (BTAs) have become inc...
AbstractA dendritic unit based on a benzenetricarboxamide core and three triarylamine arms has been ...
This work reports the synthesis and characterization of a new family of star-shaped tricarboxamides ...
N-Centred benzene-1,3,5-tricarboxamides (N-BTAs) composed of chiral and achiral alkyl substituents w...
Understanding the self-assembly of small molecules in water is crucial for the development of respon...
Synthetic water-compatible supramolecular polymers based on benzene-1,3,5-tricarboxamides (BTAs) hav...
The self-assembly in aqueous solution of benzene-1,3,5-tricarboxamide (BTA) bearing one alkyl chain ...
The synthesis of C3- and C2-symmetric benzene-1,3,5-tricarboxamides (BTAs) containing well-defined o...
The self-assembly of small and well-defined molecules using noncovalent interactions to generate var...
The self-assembly of N, N’, N’’-trialkylbenzene-1,3,5-tricarboxyamides (BTAs) has been reported to l...
International audienceAs the benzene 1,3,5-tricarboxamide (BTA) moiety is commonly used as the centr...
After their first synthesis in 1915 by Curtius, benzene-1,3,5-tricarboxamides (BTAs) have become inc...
AbstractA dendritic unit based on a benzenetricarboxamide core and three triarylamine arms has been ...
This work reports the synthesis and characterization of a new family of star-shaped tricarboxamides ...
N-Centred benzene-1,3,5-tricarboxamides (N-BTAs) composed of chiral and achiral alkyl substituents w...
Understanding the self-assembly of small molecules in water is crucial for the development of respon...
Synthetic water-compatible supramolecular polymers based on benzene-1,3,5-tricarboxamides (BTAs) hav...
The self-assembly in aqueous solution of benzene-1,3,5-tricarboxamide (BTA) bearing one alkyl chain ...
The synthesis of C3- and C2-symmetric benzene-1,3,5-tricarboxamides (BTAs) containing well-defined o...
The self-assembly of small and well-defined molecules using noncovalent interactions to generate var...