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Supramolecular Helical Assemblies of Dirhodium(II) Paddlewheels with 1,4-Diazabicyclo[2.2.2]octane: A Remarkable Substituent Effect on the Helical Sense Preference and Amplification of the Helical Handedness Excess of Metallo-Supramolecular Helical Polymers

Shogo Okuda, Naoki Ousaka, Takuya Iwata, Riku Ishida, Akio Urushima, Nozomu Suzuki, Shusaku Nagano, Tomoyuki Ikai, Eiji Yashima

2022Journal of the American Chemical Society34 citationsDOIOpen Access PDF

Abstract

-dodecyl chains assembled with DABCO to form an almost one-handed helix (the "majority rule" (MR) effect), whereas the three other nonracemic copolymers showed a weak MR effect.

Topics & Concepts

ChemistrySupramolecular chemistryCircular dichroismSubstituentCrystallographyChirality (physics)StereochemistryEnantiomerLyotropicPolymerCrystal structureOrganic chemistryNambu–Jona-Lasinio modelLiquid crystallineChiral symmetry breakingQuarkPhysicsQuantum mechanicsSupramolecular Self-Assembly in MaterialsSynthesis and Properties of Aromatic CompoundsSupramolecular Chemistry and Complexes
Supramolecular Helical Assemblies of Dirhodium(II) Paddlewheels with 1,4-Diazabicyclo[2.2.2]octane: A Remarkable Substituent Effect on the Helical Sense Preference and Amplification of the Helical Handedness Excess of Metallo-Supramolecular Helical Polymers | Litcius