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PreprintCC BY-NCChemRxiv

Synthesis and Reactivity of Fluorene-Bridged Cyclic Diaryliodonium Salts

  1. 1Institute for Organic and Analytical Chemistry, University of Bremen, Leobener Straße 7, Bremen, Germany, 28359
  2. 2Institute for Inorganic Chemistry and Crystallography, University of Bremen, Leobener Straße 7, Bremen, Germany, 28359

Abstract

Spirocyclic organic compounds play a significant role in organic materials, particularly in the field of optoelectronics. In this study, novel spiro-bridged cyclic diaryliodonium salts were synthesised in yields of up to 78%. The structure of the parent salt was confirmed by X-ray crystallography, and the salt was functionalised in iodine-chalcogen exchanges towards highly valuable xanthene derivatives in up to 88% yield.

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BibTeX
@misc{koch2026synthesis,
  title = {{Synthesis and Reactivity of Fluorene-Bridged Cyclic Diaryliodonium Salts}},
  author = {Jan Rick Koch and Mattis Damrath and Jannis Diekmann and Oliver Fincke and Boris J. Nachtsheim},
  howpublished = {ChemRxiv},
  year = {2026},
  month = oct,
  doi = {10.26434/chemrxiv.15009931/v1},
  url = {https://chemrxiv.org/doi/full/10.26434/chemrxiv.15009931/v1},
  note = {CC BY-NC},
}
RIS
TY  - UNPB
TI  - Synthesis and Reactivity of Fluorene-Bridged Cyclic Diaryliodonium Salts
AU  - Jan Rick Koch
AU  - Mattis Damrath
AU  - Jannis Diekmann
AU  - Oliver Fincke
AU  - Boris J. Nachtsheim
PY  - 2026
DA  - 2026/10/05
PB  - ChemRxiv
DO  - 10.26434/chemrxiv.15009931/v1
UR  - https://chemrxiv.org/doi/full/10.26434/chemrxiv.15009931/v1
AB  - Spirocyclic organic compounds play a significant role in organic materials, particularly in the field of optoelectronics. In this study, novel spiro-bridged cyclic diaryliodonium salts were synthesised in yields of up to 78%. The structure of the parent salt was confirmed by X-ray crystallography, and the salt was functionalised in iodine-chalcogen exchanges towards highly valuable xanthene derivatives in up to 88% yield.
ER  -