<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(8)</volume><submitter>Chen J</submitter><pubmed_abstract>Supramolecular chirality is essential for the development of functional materials. In this study, we report the synthesis of twisted nanobelts based on charge-transfer (CT) complexes using self-assembly cocrystallization starting from asymmetric components. An asymmetric donor, DBCz, and a typical acceptor, tetracyanoquinodimethane, were used to construct a chiral crystal architecture. An asymmetric alignment of the donor molecules induced polar ±(102) facets that, accompanied with free-standing growth, resulted in a twisting along the &lt;i>b&lt;/i>-axis due to the electrostatic repulsive interactions. Meanwhile, the alternately oriented ±(001) side-facets were responsible for the propensity of the helixes to be right-handed. Addition of a dopant significantly enhanced the twisting probability </pubmed_abstract><journal>Chemical science</journal><pagination>2091-2096</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9945330</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Polarization-induced nanohelixes of organic cocrystals from asymmetric components with dopant-induced chirality inversion.</pubmed_title><pmcid>PMC9945330</pmcid><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Ma S</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Xiang W</pubmed_authors><pubmed_authors>Yang C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Polarization-induced nanohelixes of organic cocrystals from asymmetric components with dopant-induced chirality inversion.</name><description>Supramolecular chirality is essential for the development of functional materials. In this study, we report the synthesis of twisted nanobelts based on charge-transfer (CT) complexes using self-assembly cocrystallization starting from asymmetric components. An asymmetric donor, DBCz, and a typical acceptor, tetracyanoquinodimethane, were used to construct a chiral crystal architecture. An asymmetric alignment of the donor molecules induced polar ±(102) facets that, accompanied with free-standing growth, resulted in a twisting along the &lt;i>b&lt;/i>-axis due to the electrostatic repulsive interactions. Meanwhile, the alternately oriented ±(001) side-facets were responsible for the propensity of the helixes to be right-handed. Addition of a dopant significantly enhanced the twisting probability </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-22T03:34:29.42Z</modification><creation>2025-04-05T20:43:53.447Z</creation></dates><accession>S-EPMC9945330</accession><cross_references><pubmed>36845927</pubmed><doi>10.1039/d2sc05942h</doi></cross_references></HashMap>