Premium
Combining classical molecular dynamics and quantum mechanical methods for the description of electronic excitations: The case of carotenoids
Author(s) -
Prandi Ingrid G.,
Viani Lucas,
Andreussi Oliviero,
Mennucci Benedetta
Publication year - 2016
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.24286
Subject(s) - photoprotection , quantum , degrees of freedom (physics and chemistry) , molecular dynamics , singlet state , excited state , dynamics (music) , carotenoid , statistical physics , physics , chemistry , chemical physics , biological system , classical mechanics , quantum mechanics , photosynthesis , biochemistry , acoustics , biology , food science
Carotenoids are important actors both in light‐harvesting (LH) and in photoprotection functions of photosynthetic pigment–protein complexes. A deep theoretical investigation of this multiple role is still missing owing to the difficulty of describing the delicate interplay between electronic and nuclear degrees of freedom. A possible strategy is to combine accurate quantum mechanical (QM) methods with classical molecular dynamics. To do this, however, accurate force–fields (FF) are necessary. This article presents a new FF for the different carotenoids present in LH complexes of plants. The results show that all the important structural properties described by the new FF are in very good agreement with QM reference values. This increased accuracy in the simulation of the structural fluctuations is also reflected in the description of excited states. Both the energy order and the different nature of the lowest singlet states are preserved during the dynamics when the new FF is used, whereas an unphysical mixing is found when a standard FF is used. © 2016 Wiley Periodicals, Inc.