4.6 Article

Fluorescence enhancement of non-fluorescent triphenylamine: A recipe to utilize carborane cluster substituents

Journal

CHEMICAL PHYSICS LETTERS
Volume 633, Issue -, Pages 190-194

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cplett.2015.05.038

Keywords

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Funding

  1. Japan Society for the Promotion of Science (JSPS) [24310090]
  2. Ministry of Education, Culture, Sports, Science, and Technology of Japan (MEXT) [2401, 24102014, 25102516]
  3. Grants-in-Aid for Scientific Research [25102516, 24102014] Funding Source: KAKEN

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Carborane-substituted triphenylamines were prepared to demonstrate the effective fluorescent enhancement of triphenylamine as a typical non-fluorescent pi-conjugated compound on the basis of molecular design to suppress the non-radiative decay by reduced vibronic coupling. Non-fluorescent carborane substituents work to reduce only the HOMO distribution in the non-fluorescent parent pi-conjugated core, thereby leading to increase in fluorescence quantum yield by suppressing internal conversion. (C) 2015 Elsevier B.V. All rights reserved.

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