Litcius/Paper detail

Highly Regioselective and Helix-Sense Selective Living Polymerization of Phenyl and Alkoxyallene Using Chiral Nickel(II) Catalysts

Li Zhou, Chonglong Li, Run‐Tan Gao, Shu‐Ming Kang, Lei Xu, Xun-Hui Xu, Na Liu, Zong‐Quan Wu

2021Macromolecules32 citationsDOI

Abstract

Facile synthesis of high optically active helical polymers from achiral monomers still remains a great challenge. In this work, two chiral Ni(II) catalysts bearing chiral R- or S-2a ligands were facilely prepared which can efficiently initiate the living/controlled polymerization of allene monomers and afford well-defined polyallenes in high yields with controlled molecular masses (Mns) and low molecular mass distributions (Mw/Mns). The catalysts showed interesting regioselectivity on the cumulated double bonds of allene monomers, as the polymerizations were highly selective which occurred on 2,3-double bonds. Moreover, the polymerization of achiral allene monomers using chiral Ni(II) catalysts showed remarkable helix-sense selectivity. The yielded polyallenes exhibited high optical activity due to the formation of a predominant one-handed helix as revealed by circular dichroism, UV–vis, and direct atomic force microscopy (AFM) observations as well. The predominant one-handed helicity of the generated polyallenes was solely determined by the chirality of the Ni(II) catalysts.

Topics & Concepts

AlleneMonomerPolymerizationChirality (physics)Helix (gastropod)ChemistryRegioselectivityCircular dichroismPolymer chemistryCotton effectCatalysisPolymerPhotochemistryCrystallographyOrganic chemistrySnailBiologyPhysicsEcologyQuarkNambu–Jona-Lasinio modelChiral symmetry breakingQuantum mechanicsSynthesis and Properties of Aromatic CompoundsSupramolecular Self-Assembly in MaterialsAxial and Atropisomeric Chirality Synthesis
Highly Regioselective and Helix-Sense Selective Living Polymerization of Phenyl and Alkoxyallene Using Chiral Nickel(II) Catalysts | Litcius