4.5 Article

Tetrakis{[(p-dodecacarboranyl)methyl]stilbenyl}ethylene: A Luminescent Tetraphenylethylene (TPE) Core System

Journal

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume -, Issue 38-39, Pages 4575-4580

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201700453

Keywords

Boron clusters; Carboranes; Luminescence; Stilbene; Density functional calculations

Funding

  1. Spanish Ministerio de Economia y Competitividad, MINECO [CTQ2013-44670-R]
  2. Severo Ochoa Program for Centers of Excellence in RD [SEV-2015-0496]
  3. Generalitat de Catalunya [2014/SGR/149]
  4. MINECO [CTQ2014-58801]
  5. Campus of International Excellence (CEI) UAM+CSIC
  6. PAIP
  7. PAPIIT (UNAM) [IN216616]
  8. CONACyT
  9. CSIC
  10. EC through the CO-FUND program AMAROUT
  11. Severo Ochoa program for Centers of Excellence in RD (MINECO) [SEV-2016-0686]

Ask authors/readers for more resources

The synthesis and spectroscopic characterization of the first set of tetrakis{[(p-dodecacarboranyl)methyl]stilbenyl}ethylenes (TDSE), substituted either with a methyl or a phenyl group in the 2-position (C-cluster) of the ortho-carborane, are described. The complex absorption properties are elucidated by TD-DFT calculations, stressing the importance of through-bond conjugation. Enhanced conjugation and restriction of the conformational space are identified as the main factors for boosted luminescence properties in solution, compared with the tetraphenylethylene (TPE) core, effectively reducing internal conversion (IC). IC is further reduced when aggregate suspensions of our compounds are formed in water, providing highly luminescent materials of quasi-isolated (very weakly interacting) emitters.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available