Influence of the spacer on the photoreactivity of flurbiprofen-tyrosine dyads
Abstract
[EN] The photoreactivity of diastereomeric dyads containing (S)- or (R)-flurbiprofen (FBP) and (S)-Tyr, either directly linked (1) or separated by a cyclic spacer (3) has been investigated. The main feature is a remarkable intramolecular quenching of FBP fluorescence, especially in 1. The process is clearly configuration dependent, being more efficient for the (R,S)- diastereomer in 1 and for the (S,S)-analogue in 3. Noteworthy, exciplex emission is detected in the 380-500 nm region in the case of 3. Fluorescence decay kinetics from the femtosecond to the nanosecond time-domains provides evidence for the dynamic nature of the quenching. In agreement with the steady-state and time-resolved observations, molecular modelling points to a more favourable geometric arrangement of the two interacting chromophores in 1 than in 3. ; Financial support from the Spanish Government (CTQ2013-47872-C2-1-P), EU (PCIG12GA-2012-334257, LASERLAB-EUROPE grant agreement no. 284464, EU FP7, and MSCA- 657465) and Generalitat Valenciana (PROMETEOII/2013/005) is gratefully acknowledged. ; Vayá Pérez, I.; Gustavsson, T.; Markovitsi, D.; Miranda Alonso, MÁ.; Jiménez Molero, MC. (2016). Influence of the spacer on the photoreactivity of flurbiprofen-tyrosine dyads. Journal of Photochemistry and Photobiology A: Chemistry. 322:95-101. https://doi.org/10.1016/j.jphotochem.2016.03.006 ; S ; 95 ; 101 ; 322
Citations
We have found one citation for you at OpenAlex.
We have found citations for you at OpenAlex.
References
We have found one reference for you at OpenAlex.
We have found references for you at OpenAlex.
Report Issue