The recently disclosed general structure of violene/cyanine hybrids is exte
nded to a new variant. The groups X and Y complete the structure for cyanin
es, oxonols or merocyanines in the formula (Scheme 2, at the right side). T
herefore, both the addition and removal of two electrons is possible. To te
st if this general motif is applicable to ring-closed compounds, tetrapyrid
inium thiophene 4(OX)(4+) was prepared, and studied using cyclic voltammetr
y, spectroelectrochemistry and PM3 calculations covering all five redox sta
tes of 4.