Journal
NEW JOURNAL OF CHEMISTRY
Volume 45, Issue 19, Pages 8563-8571Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nj01257f
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Funding
- Czech Science Foundation [20-08667S, A2_FCHT_2021_087]
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The oxidation of 2,14-dithiacalix[4]arene led to the selective formation of S-spiro derivatives, indicating that the thiacalixarene fragment is more prone to spirocyclization than the calixarene one. Acid-induced rearrangement of the S-spiro compound resulted in a novel phenoxathiin-based calixarene macrocycle. The conformational preferences of these new inherently chiral macrocycles were studied using NMR spectroscopy, single-crystal X-ray analysis, and DFT calculations.
The oxidation of 2,14-dithiacalix[4]arene with formation of the corresponding mono- and di-spirodienone derivatives was studied to find out which part of the molecule determines the chemical behaviour of this mixed-bridge macrocycle. Interestingly, applying procedures well established in thia- and/or classical calixarene chemistry, for the macrocycle with alternating thiacalixarene and calixarene structural fragments, resulted in the selective formation of the S-spiro derivative. Similar selectivity was also observed for dispiro compounds, indicating that the thiacalixarene fragment (Ar-S-Ar) is much more prone to spirocyclization than the calixarene one (Ar-CH2-Ar). The acid-induced rearrangement of the S-spiro compound led to the corresponding phenoxathiin-based calixarene, representing a novel macrocyclic system. The conformational preferences of the new inherently chiral macrocycles were studied with NMR spectroscopy and single-crystal X-ray analysis complemented by DFT calculations.
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