⌘+K

Pulse Explore Communities Researchers Journals

Home Communities Explore

January 17, 2002Chemical Communications

Helix versus zig-zag: control of supramolecular topology via carboxylic acid conformations in ortho-substituted phenyl amines

Jason E. Field D. Venkataraman

View at Publisher

Ask AI

Bookmark

Share

Abstract

ortho-Substituted phenyl amines form supramolecular helices or zig-zag structures, depending on the conformation of the carboxylic acid substituents--which can be controlled by an intramolecular hydrogen-bonding interaction.

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Field et al. (2002) studied this question.

synapsesocial.com/papers/6a72f00d256db8d1b21cf4c0 https://doi.org/10.1039/b110049a

View at Publisher

Ask AI

Bookmark

Share

Keep reading

Synapse has enriched 5 related papers. Consider them for comparative context:

1Light-activated thiomaleimide crosslinking stabilizes collagen mimetic peptide triple helixChemical Communications · Thu,
2Macrocyclic stibine-bridged [1.1.1] and [1.1.1.1] ferrocenophanesChemical Communications · Thu,
3Excited-State Palladium-Catalyzed Defluorinative Arylation of PolyfluoroarenesChemical Communications · Thu,
4Evaporation-Induced Formation of Blue-Emissive Guanine-Based Spherulitic MicrostructuresChemical Communications · Thu,
5Harnessing heteroatomic S/P coordination effects of FeCo dual-atomic catalysts for enhanced ORR performanceChemical Communications · Thu,

More from Chemical Communications

Core engineering within BINOL-based porous organic polymers for efficacious sequestration of iodine and methyl orangeThu,
Soft catalytic platforms: Hydrogel-catalyst synergies for spatiotemporally controlled therapyThu,
Reversible pH-Responsive Switching of Strong Circularly Polarized Luminescence in the Polysaccharide-Templated Co-assembliesThu,
Electrochemical deoxygenative sulfenylation of aminopyrazoles with sodium sulfinatesThu,
Back coverThu,