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Synthesis and characterization of conformationally flexible phosphonated cyclophanes

Giuseppe A Consiglio 1
Giuseppe A Consiglio
, 
Salvatore Failla 2
Salvatore Failla
, 
Paolo Finocchiaro 1
Paolo Finocchiaro
10.1070/MC1999v009n03ABEH001109
Published 1999-05-27
Communication , Volume 9, Issue 3, 90-92
6
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Consiglio G. A., Failla S., Finocchiaro P. Synthesis and characterization of conformationally flexible phosphonated cyclophanes // Mendeleev Communications. 1999. Vol. 9. No. 3. pp. 90-92.
GOST all authors (up to 50) Copy
Consiglio G. A., Failla S., Finocchiaro P. Synthesis and characterization of conformationally flexible phosphonated cyclophanes // Mendeleev Communications. 1999. Vol. 9. No. 3. pp. 90-92.
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TY - JOUR
DO - 10.1070/MC1999v009n03ABEH001109
UR - https://mendcomm.colab.ws/publications/10.1070/MC1999v009n03ABEH001109
TI - Synthesis and characterization of conformationally flexible phosphonated cyclophanes
T2 - Mendeleev Communications
AU - Consiglio, Giuseppe A
AU - Failla, Salvatore
AU - Finocchiaro, Paolo
PY - 1999
DA - 1999/05/27
PB - Mendeleev Communications
SP - 90-92
IS - 3
VL - 9
ER -
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@article{1999_Consiglio,
author = {Giuseppe A Consiglio and Salvatore Failla and Paolo Finocchiaro},
title = {Synthesis and characterization of conformationally flexible phosphonated cyclophanes},
journal = {Mendeleev Communications},
year = {1999},
volume = {9},
publisher = {Mendeleev Communications},
month = {May},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1999v009n03ABEH001109},
number = {3},
pages = {90--92},
doi = {10.1070/MC1999v009n03ABEH001109}
}
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Consiglio, Giuseppe A., et al. “Synthesis and characterization of conformationally flexible phosphonated cyclophanes.” Mendeleev Communications, vol. 9, no. 3, May. 1999, pp. 90-92. https://mendcomm.colab.ws/publications/10.1070/MC1999v009n03ABEH001109.

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.

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