Abstract
Electrochemical tuning and structural modification of thiophene-substituted siloles led to silole chromophores with efficient and stable electrochemiluminescence (ECL). By extending silole π conjugation with thiophene units and by constraining the applied potential range, stable radical cations favorable for ECL emission were generated (see graph for an example).
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have