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Calixarenes with exo-hydroxy groups: Synthesis, crystal and molecular structure of ortho-tert-butylphenol-based calix[4]-, calix[6]- and calix[8]arenes

✍ Scribed by Giovanni Sartori; Cecilia Porta; Franca Bigi; Raimondo Maggi; Francesco Peri; Elena Marzi; Maurizio Lanfranchi; Maria Angela Pellinghelli


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
709 KB
Volume
53
Category
Article
ISSN
0040-4020

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✦ Synopsis


Ortho-tert-butylcalixarenes 3, 4 and 5 with exo-hydroxy groups were synthesised by tin tetrachloride-promoted condensation of 2,2"-dihydroxy-3,3"-di-tert-butyldiphenylmethane 6 with formaldehyde. While tH NMR analysis of compounds 3, 4 and 5 revealed a considerable annular flexibility in CDCI3 solution, their X-ray single crystal analysis showed the presence of a strong intramolecular hydrogen bonds between the proximal OH groups.


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