2016
DOI: 10.1039/c6tc02555b
|View full text |Cite
|
Sign up to set email alerts
|

Energy transfer in pendant perylene diimide copolymers

Abstract: We report the synthesis, characterisation and polymerisation of two novel asymmetric perylene diimide acrylate monomers. The novel monomers form a sensitiser-acceptor pair capable of undergoing Förster resonance energy transfer, and were incorporated as copolymers with tert-butyl acrylate. The tert-butyl acrylate units act as spacers along the polymer chain allowing high concentrations of dye while mitigating aggregate quenching, leading to persistent fluorescence in the solid state at high concentrations of u… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

3
49
0
1

Year Published

2017
2017
2024
2024

Publication Types

Select...
8

Relationship

3
5

Authors

Journals

citations
Cited by 30 publications
(55 citation statements)
references
References 52 publications
3
49
0
1
Order By: Relevance
“…Moreover, when the PDA in PDI–PDA is thermally transformed from its blue phase to red phase, emission from the PDI chromophore is recovered. Although energy transfer processes were monitored with PDI and other chromophores, PDA has never been used as an FRET donor/acceptor with a PDI. Second, PDI–PDA displays reversible thermochromism in that the red‐phase PDA formed by heat treatment is converted to the original blue‐phase PDA upon cooling.…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, when the PDA in PDI–PDA is thermally transformed from its blue phase to red phase, emission from the PDI chromophore is recovered. Although energy transfer processes were monitored with PDI and other chromophores, PDA has never been used as an FRET donor/acceptor with a PDI. Second, PDI–PDA displays reversible thermochromism in that the red‐phase PDA formed by heat treatment is converted to the original blue‐phase PDA upon cooling.…”
Section: Introductionmentioning
confidence: 99%
“…Все используемые растворители очищали стандартными методами. Соединения 1 [13], 6 [14] и 7 [15] синтезированы по литературным методикам. Спектры ЯМР 1 Н и 13 С регистрировали на спектрометре Bruker Avance-400 с использованием CDCl 3 в качестве внутреннего стандарта.…”
Section: экспериментальная частьunclassified
“…Previously, we demonstrated energy transfer from the sensitizer to the emitter through the Förster mechanism. 17 Förster transfer efficiency is highly sensitive to the distance between the sensitizer and emitter. 18 To reduce this distance without creating an excessive concentration of fluorophores, we created a copolymer of sensitizer and emitter, which is illustrated in Fig.…”
Section: Introductionmentioning
confidence: 99%