“Majority‐Rules” Effect on Supramolecular Chirality and Optoelectronic Properties of Chiral Tetrachloro‐Perylene Diimides

Supramolecular chirality has attracted a great deal of attention as a platform for both fundamental study and chirality amplification in various research fields. Compared with the “sergeants‐and‐soldiers” principle, the “majority‐rules” principle, which affects chirality amplification in supramolecu...

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Veröffentlicht in:Advanced optical materials 2021-03, Vol.9 (6), p.n/a
Hauptverfasser: Shang, Xiaobo, Song, Inho, Han, Myeonggeun, Lee, Jeong Hyeon, Ohtsu, Hiroyoshi, Choi, Wanuk, Kim, Jin Chul, Ahn, Jaeyong, Kwak, Sang Kyu, Oh, Joon Hak
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container_issue 6
container_start_page
container_title Advanced optical materials
container_volume 9
creator Shang, Xiaobo
Song, Inho
Han, Myeonggeun
Lee, Jeong Hyeon
Ohtsu, Hiroyoshi
Choi, Wanuk
Kim, Jin Chul
Ahn, Jaeyong
Kwak, Sang Kyu
Oh, Joon Hak
description Supramolecular chirality has attracted a great deal of attention as a platform for both fundamental study and chirality amplification in various research fields. Compared with the “sergeants‐and‐soldiers” principle, the “majority‐rules” principle, which affects chirality amplification in supramolecular systems, is rarely reported for nano/microstructures. Here, chiral tetrachloro‐substituted perylene diimides are synthesized that self‐assemble into chiral supramolecules with different degrees of enantiomeric excess (ee). Interestingly, it is found that quasi‐2D crystals are gradually transferred to 1D nanowires (NWs) with ee from 100% to 0%. In the racemic system, chiral self‐discrimination is observed due to the greater thermodynamic stability of heterochiral crystals than the homochiral counterparts, judging from the theoretical studies. Circular dichroism analysis indicates that the self‐assembled system with different ee values shows different peaks due to their unique molecular ordering for supramolecular exciton coupling. On measurement in optoelectronic devices, racemic 1D NWs show better charge transport ability than enantiomeric quasi‐2D crystals. These results provide guidelines for tuning the supramolecular chirality and optoelectronic performance of self‐assembled systems via the “majority‐rules” principle. Chiral supramolecules with different enantiomeric excess (ee) are self‐assembled into quasi‐2D single crystals with different morphologies. The quasi‐2D crystals are gradually transformed to nanowires (NWs) with ee from 100% to 0%. The racemic NWs show better charge transport than enantiomeric quasi‐2D crystals. These results provide guidelines for tuning supramolecular chirality and optoelectronic performance of self‐assembled systems via the “majority‐rules” principle.
doi_str_mv 10.1002/adom.202001911
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Compared with the “sergeants‐and‐soldiers” principle, the “majority‐rules” principle, which affects chirality amplification in supramolecular systems, is rarely reported for nano/microstructures. Here, chiral tetrachloro‐substituted perylene diimides are synthesized that self‐assemble into chiral supramolecules with different degrees of enantiomeric excess (ee). Interestingly, it is found that quasi‐2D crystals are gradually transferred to 1D nanowires (NWs) with ee from 100% to 0%. In the racemic system, chiral self‐discrimination is observed due to the greater thermodynamic stability of heterochiral crystals than the homochiral counterparts, judging from the theoretical studies. Circular dichroism analysis indicates that the self‐assembled system with different ee values shows different peaks due to their unique molecular ordering for supramolecular exciton coupling. On measurement in optoelectronic devices, racemic 1D NWs show better charge transport ability than enantiomeric quasi‐2D crystals. These results provide guidelines for tuning the supramolecular chirality and optoelectronic performance of self‐assembled systems via the “majority‐rules” principle. Chiral supramolecules with different enantiomeric excess (ee) are self‐assembled into quasi‐2D single crystals with different morphologies. The quasi‐2D crystals are gradually transformed to nanowires (NWs) with ee from 100% to 0%. The racemic NWs show better charge transport than enantiomeric quasi‐2D crystals. 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Compared with the “sergeants‐and‐soldiers” principle, the “majority‐rules” principle, which affects chirality amplification in supramolecular systems, is rarely reported for nano/microstructures. Here, chiral tetrachloro‐substituted perylene diimides are synthesized that self‐assemble into chiral supramolecules with different degrees of enantiomeric excess (ee). Interestingly, it is found that quasi‐2D crystals are gradually transferred to 1D nanowires (NWs) with ee from 100% to 0%. In the racemic system, chiral self‐discrimination is observed due to the greater thermodynamic stability of heterochiral crystals than the homochiral counterparts, judging from the theoretical studies. Circular dichroism analysis indicates that the self‐assembled system with different ee values shows different peaks due to their unique molecular ordering for supramolecular exciton coupling. On measurement in optoelectronic devices, racemic 1D NWs show better charge transport ability than enantiomeric quasi‐2D crystals. These results provide guidelines for tuning the supramolecular chirality and optoelectronic performance of self‐assembled systems via the “majority‐rules” principle. Chiral supramolecules with different enantiomeric excess (ee) are self‐assembled into quasi‐2D single crystals with different morphologies. The quasi‐2D crystals are gradually transformed to nanowires (NWs) with ee from 100% to 0%. The racemic NWs show better charge transport than enantiomeric quasi‐2D crystals. 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subjects Amplification
Charge transport
Chirality
Coupling (molecular)
Crystals
Dichroism
Diimide
Excitons
Materials science
Nanowires
Optics
Optoelectronic devices
organic phototransistors
organic single crystals
self‐assembly
supramolecular chirality
“majority‐rules” principle
title “Majority‐Rules” Effect on Supramolecular Chirality and Optoelectronic Properties of Chiral Tetrachloro‐Perylene Diimides
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