Abstract
The synthesis of three novel macrocycles 3-5 based on the two
electron donors bis(2,5-dimethyl-
pyrrolo)[3,4-d]tetrathiafulvalene (1) and 1,4-hydroquinone is
presented. Their abilities to include the electron acceptor
paraquat (6) have been investigated by UV/Vis and sup 1 H NMR
spectroscopy and an X-ray crystallographic analysis. Also, the
complex formation between the cyclic acceptor
cyclobis(paraquat-p-phenylene) (7) and different
tetrathiafulvalene derivatives has been studied. A strong
association between 1 and 7 facilitates the self-assembly of
catenanes from the macrocycles 3-5. However, the preferred
position of the cyclic acceptor 7 in the catenanes around either
the pyrrolo-annelated TTF or around the hydroquinone donor relies
on a fine balance between all the individual noncovalent forces
acting in cooperation.
Original language | English |
---|---|
Journal | European Journal of Organic Chemistry |
Pages (from-to) | 3335-3341 |
ISSN | 1434-193X |
Publication status | Published - 1999 |