Insight into chirality on molecular stacking for tunable ultralong organic phosphorescence

Chaoqun Ma; Huili Ma; Kun Ling; Ruilin Zheng; Mingxing Gu; Lulu Song; Zhongfu An; Huifang Shi; Wei Huang

doi:10.1039/c8tc03297a

Insight into chirality on molecular stacking for tunable ultralong organic phosphorescence

Chaoqun Ma, Huili Ma, Kun Ling, Ruilin Zheng, Mingxing Gu, Lulu Song, Zhongfu An, Huifang Shi, Wei Huang

Institute of Flexible Electronics

Research output: Contribution to journal › Article › peer-review

16 Scopus citations

Abstract

A new levorotatory compound ((S)-9,9′-(6-(1-phenylethoxy)-1,3,5-triazine-2,4-diyl)bis(9H-carbazole)) and its corresponding racemic compound show different intermolecular interactions to restrain nonradiative transition, resulting in an enhanced ultralong organic phosphorescence lifetime from 229.0 ms to 419.8 ms. This work will provide a new insight into the chirality of organic molecules to adjust the ultralong phosphorescence.

Original language	English
Pages (from-to)	10179-10183
Number of pages	5
Journal	Journal of Materials Chemistry C
Volume	6
Issue number	38
DOIs	https://doi.org/10.1039/c8tc03297a
State	Published - 2018

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title = "Insight into chirality on molecular stacking for tunable ultralong organic phosphorescence",

abstract = "A new levorotatory compound ((S)-9,9′-(6-(1-phenylethoxy)-1,3,5-triazine-2,4-diyl)bis(9H-carbazole)) and its corresponding racemic compound show different intermolecular interactions to restrain nonradiative transition, resulting in an enhanced ultralong organic phosphorescence lifetime from 229.0 ms to 419.8 ms. This work will provide a new insight into the chirality of organic molecules to adjust the ultralong phosphorescence.",

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T1 - Insight into chirality on molecular stacking for tunable ultralong organic phosphorescence

AU - Ma, Chaoqun

AU - Ma, Huili

AU - Ling, Kun

AU - Zheng, Ruilin

AU - Gu, Mingxing

AU - Song, Lulu

AU - An, Zhongfu

AU - Shi, Huifang

AU - Huang, Wei

PY - 2018

Y1 - 2018

N2 - A new levorotatory compound ((S)-9,9′-(6-(1-phenylethoxy)-1,3,5-triazine-2,4-diyl)bis(9H-carbazole)) and its corresponding racemic compound show different intermolecular interactions to restrain nonradiative transition, resulting in an enhanced ultralong organic phosphorescence lifetime from 229.0 ms to 419.8 ms. This work will provide a new insight into the chirality of organic molecules to adjust the ultralong phosphorescence.

AB - A new levorotatory compound ((S)-9,9′-(6-(1-phenylethoxy)-1,3,5-triazine-2,4-diyl)bis(9H-carbazole)) and its corresponding racemic compound show different intermolecular interactions to restrain nonradiative transition, resulting in an enhanced ultralong organic phosphorescence lifetime from 229.0 ms to 419.8 ms. This work will provide a new insight into the chirality of organic molecules to adjust the ultralong phosphorescence.

UR - http://www.scopus.com/inward/record.url?scp=85054542293&partnerID=8YFLogxK

U2 - 10.1039/c8tc03297a

DO - 10.1039/c8tc03297a

M3 - 文章

AN - SCOPUS:85054542293

SN - 2050-7534

VL - 6

SP - 10179

EP - 10183

JO - Journal of Materials Chemistry C

JF - Journal of Materials Chemistry C

IS - 38

ER -

Insight into chirality on molecular stacking for tunable ultralong organic phosphorescence

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