Unknown

Dataset Information

0

BODIPY dyads and triads: synthesis, optical, electrochemical and transistor properties.


ABSTRACT: A series of D-A dyads and D-A-D triads molecular systems based on triphenylamine and 9-ethyl-carbarzole as donor (D) and BODIPY as acceptor (A) has been designed and synthesized. The optoelectronic properties including optical, electrochemical, and charge carrier mobility of these molecules have been investigated. We found that the D-A-D triads exhibited broader absorption, raising the HOMO energy levels and increase hole carrier mobilities. Analysis surface morphology revealed that BODIPY containing carbazole demonstrated smooth film and no macro phase aggregation was observed upon thermal annealing.

SUBMITTER: Wanwong S 

PROVIDER: S-EPMC5945575 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

BODIPY dyads and triads: synthesis, optical, electrochemical and transistor properties.

Wanwong Sompit S   Khomein Piyachai P   Thayumanavan S S  

Chemistry Central journal 20180511 1


A series of D-A dyads and D-A-D triads molecular systems based on triphenylamine and 9-ethyl-carbarzole as donor (D) and BODIPY as acceptor (A) has been designed and synthesized. The optoelectronic properties including optical, electrochemical, and charge carrier mobility of these molecules have been investigated. We found that the D-A-D triads exhibited broader absorption, raising the HOMO energy levels and increase hole carrier mobilities. Analysis surface morphology revealed that BODIPY conta  ...[more]

Similar Datasets

| S-EPMC6225113 | biostudies-literature
| S-EPMC4382992 | biostudies-literature
| S-EPMC7066649 | biostudies-literature
| S-EPMC9033462 | biostudies-literature
| S-EPMC8596797 | biostudies-literature
| S-EPMC7570900 | biostudies-literature
| S-EPMC4578393 | biostudies-literature
| S-EPMC6273483 | biostudies-literature
| S-EPMC7277623 | biostudies-literature
| S-EPMC6207649 | biostudies-literature