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2,2′-Bithiazolyl-p-tert-butylcalix[4]arene podands. Synthesis and fluorescence properties

✍ Scribed by Stephane Pellet-Rostaing; Jean-Bernard Regnouf-de-Vains; Roger Lamartine

Publisher
Elsevier Science
Year
1996
Tongue
French
Weight
323 KB
Volume
37
Category
Article
ISSN
0040-4039

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p-terbButylcalix arene analogs in which up to four methylene bridges were replaced by sulfur bridge(s) were synthesized. NMR studies indicated that the thiacalixarenes were conformationally much more fle~dble than the parent calixarene in CDCh solution; the flexibility was greater with increasing nu