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)/

Citation
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
Citations number
57
Categorie Soggetti
Chemistry Physical","Material Science
Journal title
ISSN journal
08974756
Volume
6
Issue
8
Year of publication
1994
Pages
1413 - 1418
Database
ISI
SICI code
0897-4756(1994)6:8<1413:FRMOCP>2.0.ZU;2-U
Abstract
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.