Abstract
Many photoactive proteins contain chromophores based on para-substituted phenolate anions which are an essential component of their electronic structure. Here, we present a reductionist approach to gain fundamental insight into the evolution of electronic structure as the chromophore increases in complexity from phenolate to that in GFP. Using frequency- and angle-resolved photoelectron spectroscopy, in combination with electronic structure theory, the onset of excited states that are responsible for the characteristic spectroscopic features in biochromophores are determined. A comprehensive, yet intuitive picture of the effect of phenolate functionalisation is developed based on simple Hückel theory. Specifically, the first two bright excited states can be constructed from a linear combination of molecular orbitals localised on the phenolate and para-substituent groups. This essential interaction is first observed for p-vinyl-phenolate. This bottom-up approach offers a readily accessible framework for the design of photoactive chromophores.
| Original language | English |
|---|---|
| Pages (from-to) | 29772-29779 |
| Number of pages | 8 |
| Journal | Physical chemistry chemical physics : PCCP |
| Volume | 19 |
| Issue number | 44 |
| DOIs | |
| Publication status | Published - 15 Nov 2017 |
Keywords
- Anions
- Luminescent Proteins/chemistry
- Models, Molecular
- Phenols
- Photoelectron Spectroscopy