Chemistry Reference
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Fig. 7
Linear 1D infinite chains formed on self-assembly of bidentate and self-
complementary modules where donor and acceptor sites axes are parallel and coaxial (
A
),
of bidentate donor and acceptor modules where donor and acceptor sites axes are paral-
lel and coaxial (
B
), or are parallel and translated from each other in the XB donor (
C
)or
acceptor (
D
) module, respectively
DITFB/1,4-bis(
N
,
N
-dimethylamino)benzene [64], diiodobutadiyne/dicyano
and diiodobutadiyne/dipyridyl derivatives [80, 81]). Similarly, the stepped in-
finite chains geometry is obtained when XB acceptor tectons with collinear
sites interact with stepped XB donors. Examples are the chains formed by TIE
(e.g. with phenazine [129]), by (
E
)-1,2-diiododifluoroethene (e.g. with 1,4-
BPY[164]),andby
-diiodoperfluoroalkanes, or their dibromo analogues
(e.g. with 1,4-BPY, pyrazine and its derivatives) wherein the perfluoroalkyl
chain typically adopts a
trans
conformation along the carbon chain [124,
165-167]. Stepped 1D networks are generated also on self-assembly of tec-
tons, both of which have parallel and translated binding sites (e.g.
α
,
ω
α
,
ω
-
dicyanoalkanes/
-diiodoperfluoroalkane adducts [168] and TMEDA/(
E
)-
1,2-diiododifluoroethene adduct [164]).
When the binding sites axes on starting modules are not parallel but form
an angle, the resulting self-assembled chains assume a herringbone arrange-
ment, the angles along the chain corresponding to the angles of binding sites
α
,
ω
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