2018
DOI: 10.1039/c8sc00833g
|View full text |Cite
|
Sign up to set email alerts
|

Mechanically triggered reversible stepwise tricolor switching and thermochromism of anthracene-o-carborane dyad

Abstract: A novel single organic molecule–carborane conjugate, CAN, was synthesized in a high yield via a modified nickel-catalyzed cross-coupling reaction incorporating an anthracene unit and an o-carborane moiety.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

2
86
0

Year Published

2019
2019
2022
2022

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 143 publications
(88 citation statements)
references
References 52 publications
2
86
0
Order By: Relevance
“…In addition, their emission spectra in solution are analogoust ot hat of Py-NC in dilute solution (Figures 3, S8 and S9), demonstrating that the emission of 1 and 2 at % 400 nm might be originated from the locally excited state. [39] We tentatively speculate that such diversity between Py-NC and gold complexes (1 and 2)m ight be due to the introduction of large groups,s uch as fluorobenzyl-gold(I) groups, which hinder the formation of excimers in the concentrated solution.…”
Section: Photophysical Properties and Dft Calculationmentioning
confidence: 85%
“…In addition, their emission spectra in solution are analogoust ot hat of Py-NC in dilute solution (Figures 3, S8 and S9), demonstrating that the emission of 1 and 2 at % 400 nm might be originated from the locally excited state. [39] We tentatively speculate that such diversity between Py-NC and gold complexes (1 and 2)m ight be due to the introduction of large groups,s uch as fluorobenzyl-gold(I) groups, which hinder the formation of excimers in the concentrated solution.…”
Section: Photophysical Properties and Dft Calculationmentioning
confidence: 85%
“…Other types of AIE‐active o ‐carborane derivatives are listed in Table and Scheme . Influences on AIE properties were investigated by changing the substituents on the o ‐carborane unit ( 44 – 75 ) . For these compounds, solid‐state excimer emission, single‐molecule white emission, aggregation‐induced electrochemiluminescence, and thermally activated delayed fluorescence were observed.…”
Section: Aggregation‐induced Emissionmentioning
confidence: 99%
“…The interest in carboranes and metallacarboranes as potential units for molecular materials might be endorsed to their remarkable chemical, thermal, and biological stabilities [7][8][9][10][11][12][13][14][15][16][17]. Owing to the properties above of carboranes, they have been used as exceptional building blocks for developing a large variety of fluorescent carborane-containing molecules, in which the cluster is usually linked to a fluorescent π-conjugated organic system, either directly by the C c [18][19][20][21][22][23][24][25][26][27][28][29][30] or through one spacer [7][8][9][31][32][33][34][35][36][37][38][39].…”
Section: Introductionmentioning
confidence: 99%