Multivalued Logic with a Tristable Fluorescent Switch

Ferreira, R; Remon, P; Pischel, Uwe

HERO ID

3575463

Reference Type

Journal Article

Year

2009

HERO ID 3575463
In Press No
Year 2009
Title Multivalued Logic with a Tristable Fluorescent Switch
Authors Ferreira, R; Remon, P; Pischel, Uwe
Journal Journal of Physical Chemistry C
Volume 113
Issue 14
Page Numbers 5805-5811
Abstract A fluorophorel-spacer-receptor-spacer-fluorophore, dyad was prepared and photophysically characterized. The two spectrally well-differentiated fluorophores are 1,8-naphthalimide and its 4-amino-substituted derivative, the latter showing strong ICT emission. The receptor unit consists of a tertiary amine, which leads to site-selective PET (only the 1,8-naphthalimide part gets quenched). This process can be blocked by protonation of the tertiary amine, which, on the other hand, results in enhanced singlet-singlet energy transfer between the 1,8-naphthalimide and 4-amino-1,8-naphthalimide parts (Phi(EET) = 0.27 and 0.59 for neutral and monoprotonated form, respectively). In acetonitrile, the monoprotonated form can be deprotonated by sufficiently basic anions like fluoride in micromolar concentration (<20 mu M). The observed fluorescence\ quenching, due to PET-reactivation, is ca. 41%. Further addition of fluoride in concentrations > 1 mM leads to deprotonation of the 4-amino group of one of the naphthalimides, which is accompanied by more fluorescence quenching (ca. 93%). The resulting double-sigmoidal titration curve enables the implementation of ternary logic. Using fluoride anions as degenerate inputs results in a ternary NOR logic gate, which is demonstrated for the first time.
Doi 10.1021/jp809527d
Wosid WOS:000264805700065
Is Certified Translation No
Dupe Override No
Is Public Yes