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September 16, 2025Chemical Communications3 citations

The photoluminescence behaviour of monosubstituted non-benzenoid polycyclic-aromatic-substituted ortho-carboranes

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AMAdam V. MarshAWAndrew J. P. WhiteMHMartin Heeney

Key Points

  • Optical studies reveal intramolecular charge transfer and aggregation-induced emission in modified ortho-carboranes.
  • Two new ortho-carborane compounds exhibit unique electronic behaviors, such as excimer emission, upon substitution.
  • The research highlights the stimuli-responsive optical behavior of non-benzenoid polycyclic aryl compounds.
  • Findings may enable the development of advanced optical materials based on novel ortho-carborane derivatives.

Abstract

Ortho-Carborane is a cluster compound known for its ability to exhibit stimuli-responsive optical behaviour when substituted with aromatic fluorophores. Here, we describe the synthesis of two such compounds: 1-(4'-naphtho2,3-bthiophenyl)-ortho-carborane and 1-(4'-benzo1,2-b;4,5-b'dithiophenyl)-ortho-carborane. Optical studies reveal complex electronic and photoluminescent behaviour including intramolecular charge transfer (ICT), excimer emission, and aggregation-induced emission (AIE).

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Cite This Study

Marsh et al. (2025) studied this question.

synapsesocial.com/papers/68d46ccf31b076d99fa68f80https://doi.org/10.1039/d5cc02672e
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