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Figure 1.14. (a) Mo 3 S 7 [(dmit) 2 ] 3 cluster and (b) view of the crystal structure
of the Mo 3 S 7 [(dmit) 2 ] 3 solid parallel to the (001) plane. C, S and Mo atoms
are represented by black, medium grey and light grey balls, respectively. P 3, a
=
1
.
944 nm, c
=
0
.
656 nm. Crystallographic data from Llusar et al. , 2004.
respectively, and E a
30 meV, respectively. The crystal structure
of Mo 3 S 7 [(dmit) 2 ] 3 is hexagonal and is shown in Fig. 1.14(b). The 3D packing
results in cavities with a diameter of 1 nm. This new semiconductor material leads
to the possibility of obtaining a series of new materials by chemically modifying
the cluster complex, which are also nanostructured, thus enabling in principle the
introduction of other molecules (guest) in their structure (host).
10 and E a
Organic metals
In 1911 H. N. McCoy and W. C. Moore predicted that it is possible to prepare
composite metallic substances from non-metallic constituent elements , inspired
by their results on the preparation of tetramethylammonium-mercury amalgams
by cold electrolysis (McCoy & Moore, 1911). The prediction has come true, as
will be evident in this section, but it was not until 1954 that a relatively stable
perylene-bromine complex with conductivities up to 1
1 cm 1 was synthesized
(Akamatu et al. , 1954). Although the material reported in this work behaved as a
semiconductor with E a =
055 eV, it can certainly be considered as the starting
point of an extremely productive field leading to a wealth of conducting organic
materials exhibiting remarkable results of fundamental interest. Since then, many
perylene-based conductors have been prepared, which are exhaustively reviewed
in Almeida and Henriques, 1997. The host of different conducting materials that
have been synthesized essentially retain the structure of a purely organic molecule
0
.
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