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@ARTICLE{Maansson:474803,
author = {Maansson, Erik and Latini, Simone and Covito, Fabio and
Wanie, Vincent and Galli, Mara and Perfetto, Enrico and
Stefanucci, Gianluca and De Giovannini, Umberto and
Castrovilli, Mattea Carmen and Trabattoni, Andrea and
Frassetto, Fabio and Greenwood, Jason B. and Légaré,
François and Nisoli, Mauro and Rubio, Angel and Calegari,
Francesca},
title = {{U}ltrafast dynamics of adenine following {XUV} ionization},
journal = {JPhys photonics},
volume = {4},
issn = {2515-7647},
address = {Bristol},
publisher = {IOP Publishing},
reportid = {PUBDB-2022-01010},
pages = {034003},
year = {2022},
note = {The article is Open Access so I don't upload the
publisher's PDF here.HAllo zusammen in L, finde das ist ok,
ich verstehe auch nicht so richtig, warum bei OPen Access
die PDFs mit hochgeladen werden müssen. VG Daniela},
abstract = {The dynamics of biologically relevant molecules exposed to
ionizing radiation contains many facets and spans several
orders of magnitude in time and energy. In the extreme
ultraviolet (XUV) spectral range, multi-electronic phenomena
and bands of correlated states with inner-valence holes must
be accounted for in addition to a plethora of vibrational
modes and available dissociation channels. The ability to
track changes in charge density and bond length during
ultrafast reactions is an important endeavor toward more
general abilities to simulate and control photochemical
processes, possibly inspired by those that have evolved
biologically. By using attosecond XUV pulses extending up to
35 eV and few-femtosecond near-infrared pulses, we have
previously time-resolved correlated electronic dynamics and
charge migration occurring in the biologically relevant
molecule adenine after XUV-induced sudden ionization. Here,
using additional experimental data, we comprehensively
report on both electronic and vibrational dynamics of this
nucleobase in an energy range little explored to date with
high temporal resolution. The time-dependent yields of
parent and fragment ions in the mass spectra are analyzed to
extract exponential time constants and oscillation periods.
Together with time-dependent density functional theory and
ab-initio Green's function methods, we identify different
vibrational and electronic processes. Beyond providing
further insights into the XUV-induced dynamics of an
important nucleobase, our work demonstrates that yields of
specific dissociation outcomes can be influenced by
sufficiently well-timed ultrashort pulses, therefore
providing a new route for the control of the
multi-electronic and dissociative dynamics of a DNA building
block.},
cin = {FS-ATTO / CFEL-MPT},
ddc = {530},
cid = {I:(DE-H253)FS-ATTO-20170403 / I:(DE-H253)CFEL-MPT-20160915},
pnm = {632 - Materials – Quantum, Complex and Functional
Materials (POF4-632) / STARLIGHT - Steering attosecond
electron dynamics in biomolecules with UV-XUV LIGHT pulses
(637756) / DFG project 390715994 - EXC 2056: CUI: Advanced
Imaging of Matter (390715994) / QSpec-NewMat - Quantum
Spectroscopy: exploring new states of matter out of
equilibrium (694097) / CoExAN - Collective Excitations in
Advanced Nanostructures (644076) / MaX - MAterials design at
the eXascale. European Centre of Excellence in materials
modelling, simulations, and design (824143) / DFG project
170620586 - SFB 925: Licht-induzierte Dynamik und Kontrolle
korrelierter Quantensysteme (170620586)},
pid = {G:(DE-HGF)POF4-632 / G:(EU-Grant)637756 /
G:(GEPRIS)390715994 / G:(EU-Grant)694097 /
G:(EU-Grant)644076 / G:(EU-Grant)824143 /
G:(GEPRIS)170620586},
experiment = {EXP:(DE-MLZ)NOSPEC-20140101},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000802816600001},
doi = {10.1088/2515-7647/ac6ea5},
url = {https://bib-pubdb1.desy.de/record/474803},
}