Pregled bibliografske jedinice broj: 652060
Solvent dependent dynamics of the retinal chromophore
Solvent dependent dynamics of the retinal chromophore // Bridging Scales in Theoretical Chemistry
Erlagen, 2013. (poster, međunarodna recenzija, sažetak, ostalo)
CROSBI ID: 652060 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Solvent dependent dynamics of the retinal chromophore
Autori
Novak, Jurica ; Mališ, Momir ; Došlić, Nađa
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Izvornik
Bridging Scales in Theoretical Chemistry
/ - Erlagen, 2013
Skup
49th Symposium on Theoretical Chemistry
Mjesto i datum
Erlangen, Njemačka, 22.09.2013. - 26.09.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
protonirana Schiffova baza retinala; neadijabatska dinamika
(protonated Schiff base of retinal; nonadiabatic dynamics)
Sažetak
The all-trans protonated Schiff base of retinal (at-PSBR) is the chromophore of bacteriorhodopsin. The light triggered isomerization of the chromophore in the protein pocket is ultrafast (~500 fs), occurs with high quantum yield (0.64) and is highly specific (13-cis PSBR is the main photoproduct). In the solution, the quantum yield is lower (0.27 and 0.17 in CH3CN and CH2Cl2 (DCM), respectively), the isomerization dynamics is slower (~4 ps) and less specific (11-cis PSBR is dominant product). Recent pump-dump-probe experiments have demonstrated that the initially excited S1 state of PSBR relaxes to the ground state via one reactive and one or two nonreactive channels depending on the solvent. Ground state molecular dynamics simulations, multidimensional anharmonic frequency calculations and IR titration experiments have shown that the all-trans Schiff base of retinal (nSBR) and the trifluoroacetic acid (TFA) form ion pairs in DCM. TDDFT based QM/MM nonadiabatic dynamics simulations of at-PSBR with explicit TFA- counter-ions in DCM revealed the origin of the fast non-reactive channel as charge transfer from the hydrogen bonded TFA- to the chromophore backbone. The analysis of nonadiabatic dynamics trajectories indicate that the rotation of the β-ionone ring and concomitant dynamics of a n-butyl tail might be responsible for the slow nonreactive relaxation.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
Napomena
Http://chemie.uni-erlangen.de/stc2013/
POVEZANOST RADA
Projekti:
098-0352851-2921 - Kontrola atomske i molekulske dinamike oblikovanim elektromagnetskim poljima (Došlić, Nađa, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb