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Fig. 8 A view of both types of I
···
Iinteractionsin(EDT-TTF-I 2 )(I 3 )
Table 3 Halogen bond distances and angles in various salts with I 3 -
Interaction
D anis
Br(I)I
θ 1
θ 2
Refs.
(A)
(A)
( C)
( C)
(BTM - TTF - Br 2 ) 2 (I 3 )
C - Br ··· I
3.67
3.635(1)
163.6(3)
72.08(3)
[61, 64]
(EDT - TTF - Br 2 ) 2 (I 3 )
C - Br
···
I
3.67
3.51(5)
165.3(1)
110.48(2)
[66]
···
(EDO - TTF - I 2 )(I 3 )
C - I
I
3.89
3.40(2)
173.2(2)
133.1(3)
[67]
3.399(8)
163.4(2)
71.54(2)
(EDT - TTF - I 2 ) 2 (I 3 )
C - I
···
I
3.89
3.55(5)
164.8(2)
107.21(2)
[66]
1 Scm -1 , a large value when compared with other
β
β -
structures such as
(BEDT-TTF) 2 (ICl 2 ).
3.3.1.3
Halometallate Anions as Halogen Bond Acceptors
Only a few recent examples of halogen bonding of halogenated TTFs with
halometallate anions have been described and this most probably represents
a broad development field in this area. Indeed, these halometallate salts of-
fer a wide variety of complexes and specifically here a large variation of
the ratio of anion charge vs number of halide atoms, as already discussed
above in the comparison between Br - and I 3 - salts. This point is illustrated
by the superb structures of two salts of EDT-TTF-I 2 with the polymeric
one-dimensional PbI 3 -
6 I 2 ) 3
(Fig. 9) and two-dimensional (Pb 5 / 6
anions
1
/
I anion contacts are observed with the linear PbI 3 - chains
where shorter C - I
···
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