PreprintCC BY-NCChemRxiv
Synthesis and Reactivity of Fluorene-Bridged Cyclic Diaryliodonium Salts
- 1Institute for Organic and Analytical Chemistry, University of Bremen, Leobener Straße 7, Bremen, Germany, 28359
- 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 -