FROM RACEMIC MIXTURES OF CHIRAL PI-DONOR MOLECULES TO MIXED STACKS OFH-BONDED CENTROSYMMETRICAL DIMERS OF CATION AND ANION-RADICALS WITH SINGLET-TRIPLET EXCITATIONS - THE EXAMPLE OF [(+ -)ME3TTF-C-ASTERISK-H(MEOH).+]2[TCNQ.-]2 (TTF = TETRATHIAFULVALENE - TCNQ = TETRACYANOQUINODIMETHANE)/
A. Dolbecq et al., FROM RACEMIC MIXTURES OF CHIRAL PI-DONOR MOLECULES TO MIXED STACKS OFH-BONDED CENTROSYMMETRICAL DIMERS OF CATION AND ANION-RADICALS WITH SINGLET-TRIPLET EXCITATIONS - THE EXAMPLE OF [(+ -)ME3TTF-C-ASTERISK-H(MEOH).+]2[TCNQ.-]2 (TTF = TETRATHIAFULVALENE - TCNQ = TETRACYANOQUINODIMETHANE)/, Chemistry of materials, 6(8), 1994, pp. 1413-1418
Lithiation of Me3TTF, and subsequent reaction with ClCOMe followed by
reduction with NaBH4 afford the racemic alcohol (+/-)Me3TTF-CH(Me)OH.
Single crystals of the title compound [(+/-)Me3TTF-CH(Me)OH.+]2[TCNQ
.-]2 were obtained, and their structure was determined by X-ray diffra
ction, revealing an unusual type of mixed stacking where the chiral pi
-donor and the acceptor molecule are associated within a ... DDAA... s
equence. The room temperature ESR spectrum is characteristic of two di
fferent triplet Frenkel exciton systems. From the analysis of the sing
le-crystal ESR measurements the singlet-triplet activation energy and
the fine structure tensor orientation were determined for both triplet
excitations. The relationship between these parameters and the struct
ure allowed us to propose an interpretation of the nature of both exci
tations. The role of the hydrogen bonding between the dimers of donors
and acceptors is discussed.