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Fig. 2.7 Time evolutions of the luminescence intensity in [Pt(en) 2 ][Pt(en) 2 Br 2 ](ClO 4 ) 4 -I. The
experimental results are shown by solid lines . Dotted lines shown the simulations (see [ 61 ]).
(Reprinted figure with permission from [ 61 ]. Copyright (1999) by the American Physical Society)
investigate nature and dynamical aspects of the gap states in that compound. To
solve this problem, Pt-Br and Pt-I chain compounds were subsequently studied, in
which photoinduced gap states are mobile and their dynamical aspects could be
clarified. Here, we introduce the comparative studies of the homometal compound,
[Pt(en) 2 ][Pt(en) 2 Br 2 ](ClO 4 ) 4 -II, and the heterometal compound, [Pd(en) 2 ][Pt
(en) 2 Br 2 ](ClO 4 ) 4 , using PA and PESR measurements [ 52 ]. As mentioned in
Sect. 2.2.2, the CDW ground states are degenerate in the former and nondegenerate
in the latter, so that solitons are stabilized only in the former. Such a difference in the
two compounds enables us to obtain a clear evidence for the photogeneration of
solitons. In [Pt(en) 2 ][Pt(en) 2 Br 2 ](ClO 4 ) 4 , two monoclinic polymorphisms with the
space group P 2 1 /m and C 2/m were obtained [ 10 , 11 ] and labeled as I and II,
respectively, as already used. Hereafter, [Pt(en) 2 ][Pt(en) 2 Br 2 ](ClO 4 ) 4 -II and
[Pd(en) 2 ][Pt(en) 2 Br 2 ](ClO 4 ) 4 are abbreviated as Pt-Br-Pt-II and Pd-Br-Pt,
respectively.
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