4.6 Article

One-electron-reduced and -oxidized stages of donor-substituted 1,1,4,4-tetracyanobuta-1,3-dienes of different molecular architectures

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 14, 期 25, 页码 7638-7647

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.200800716

关键词

charge transfer; conjugation; cycloaddition; donor-acceptor systems; EPR spectroscopy

资金

  1. ETH Research Council, EWE (Austria) [P20019-N17]
  2. NCCR Nanoscale Science

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A series of monomeric and oligomeric donor-substituted 1, 1 4,4-tetracyanobuta-1,3-dienes (TCBDs) with various topologies have been synthesized by means of thermal [2+2] cycloaddition between tetracyanoethylene (TCNE) and donor-substituted alkynes, followed by retro-electrocyclization. One-electron-reduced and -oxidized stages of the donor-substituted TCBDs were generated by chemical methods. The obtained radical anions and radical cations were studied by using electron paramagnetic resonance/electron nuclear double resonance (EPR/ENDOR) spectroscopy, supported by density functional theory (DFT) calculations. ne extent of pi-electron delocalization in the paramagnetic species was investigated in terms of the EPR parameters. Despite favorable molecular orbital (MO) coefficients, the EPR results suggest that in radical anions the spin and charge are confined to the electron-withdrawing TCBD moieties on the hyperfine EPR timescale. The observed spin localization is presumably caused by an interplay between the nonplanarity of the studied pi systems, limited pi-electron conjugation, and very likely counterion effects. In radical cations, an analogous spin and charge localization confined to the electron-donating N,N-dialkylaniline moieties was found. In this case, an efficient electron delocalization is disabled by small MO coefficients at the joints between the donor and acceptor portions of the studied TCBDs.

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