《Unexpected right-handed helical nanostructures co-assembled from L-phenylalanine derivatives and achiral bipyridines》 was published in Chemical Science in 2017. These research results belong to Liu, Guofeng; Liu, Jinying; Feng, Chuanliang; Zhao, Yanli. Application of 64479-78-3 The article mentions the following:
The construction of chiral supramol. systems with desirable handedness is of great importance in materials science, chem., and biol. since chiral nanostructures exhibit fascinating photophys. properties and unique biol. effects. Herein, we report that achiral bipyridines can co-assemble with L-phenylalanine derivatives into unexpected right-handed helical nanostructures rather than a left-handed helix via intermol. hydrogen bonding interactions formed between the pyridyl and carboxylic groups. This study opens up a route to develop chiral nanostructures with desirable handedness via the co-assembly of simple mol. building blocks and provides a straightforward insight into the chirality control of nanostructures in supramol. systems. In addition to this study using N-(Pyridin-4-yl)isonicotinamide, there are many other studies that have used N-(Pyridin-4-yl)isonicotinamide(cas: 64479-78-3Application of 64479-78-3) was used in this study.
N-(Pyridin-4-yl)isonicotinamide(cas: 64479-78-3) belongs to amides.Application of 64479-78-3 Amides include many other important biological compounds, as well as many drugs like paracetamol, penicillin and LSD. Low-molecular-weight amides, such as dimethylformamide, are common solvents.
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics