RUS  ENG
Full version
JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1999 Volume 9, Issue 3, Pages 90–92 (Mi mendc4541)

This article is cited in 6 papers

Synthesis and characterization of conformationally flexible phosphonated cyclophanes

G. A. Consiglioa, S. Faillab, P. Finocchiaroa

a Dipartimento di Metodologie Fisiche e Chimiche per l'Ingegneria, Universita di Catania, Catania, Italy
b Dipartimento di Ingegneria Chimica, dei Materiali delle Materie Prime e Metallurgiche, Universita di Roma 'La Sapienza', Rome, Italy

Abstract: The phosphorylated calyx[4]arenoid para- and meta-substituted cyclophane tetramers, which were synthesised in good yields starting from parent cyclic hydrocarbons, show a ‘saddle-shaped’ rigid conformation in solution, and the methylenephosphonic acid dialkyl ester groups are in a strategic position for complexation with neutral guests.

Language: English

DOI: 10.1070/MC1999v009n03ABEH001109



© Steklov Math. Inst. of RAS, 2025