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ATTO-CONTROL SIGNED

Attosecond X-ray Molecular Dynamics and Strong-Field Control

Total Cost €

0

EC-Contrib. €

0

Partnership

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 ATTO-CONTROL project word cloud

Explore the words cloud of the ATTO-CONTROL project. It provides you a very rough idea of what is the project "ATTO-CONTROL" about.

nuclear    opened    subfemtosecond    chemistry    transient    place    experiments    molecules    absorption    leone    internal    photochemical    butadiene    mutations    time    ones    uv    bio    packages    fundamental    fs    velocity    electronic    individual    complutense    atas    firstly    resolution    dynamics    ba    avenues    pi    schemes    powerful    xuv    experimental    university    berkeley    sources    ray    ares    nitroethylene    trans    damage    supervision    secondly    madrid    attosecond    temporal    biology    polyatomic    regime    carbon    photoisomerization    pioneering    organic    performed    color    femtosecond    fellowship    citosine    spectra    incoming    conversion    ultimately    divided    vmi    biological    excited    pump    disentangle    united    investigation    ntilde    underlying    thymine    employed    california    understand    imaging    cis    notch    observe    chromophores    transbutadiene    map    reactions    technologies    light    ultrashort    experiment    spain    probe    dna    chemical    atom    doorway    prof   

Project "ATTO-CONTROL" data sheet

The following table provides information about the project.

Coordinator
UNIVERSIDAD COMPLUTENSE DE MADRID 

Organization address
address: AVENIDA DE SENECA 2
city: MADRID
postcode: 28040
website: http://www.ucm.es

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Spain [ES]
 Total cost 245˙732 €
 EC max contribution 245˙732 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-GF
 Starting year 2019
 Duration (year-month-day) from 2019-05-20   to  2022-05-19

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSIDAD COMPLUTENSE DE MADRID ES (MADRID) coordinator 245˙732.00
2    THE REGENTS OF THE UNIVERSITY OF CALIFORNIA US (OAKLAND CA) partner 0.00

Map

 Project objective

The development in recent years of ultrashort light sources in the attosecond regime has opened new avenues for the investigation of electronic and nuclear dynamics. In particular, the current development of UV-XUV or UV-X-ray pump-probe schemes with subfemtosecond temporal resolution represents a doorway to study chemical reactions in excited states of molecules in real-time, including biological reactions, such as e.g. those related to DNA damage and mutations. The aim of this project is to understand and ultimately control photochemical reactions in excited states of polyatomic molecules, especially relating to two fundamental processes in biology and chemistry: (i) cis-trans photoisomerization and (ii) the internal conversion of pi-pi*/n-pi* states in organic chromophores. Two top-notch experimental methods will be employed to achieve this goal: attosecond X-ray transient absorption (X-ATAS) at the University of California at Berkeley (United States), where the fellowship will be carried out under the supervision of Prof. S. Leone, and three-color femtosecond pump-probe velocity map imaging (fs-VMI) at Complutense University of Madrid (Spain), where the incoming phase will take place under the supervision of Prof. L. Bañares. The project is divided in three specific objectives and work-packages. Firstly, the powerful X-ATAS method will be employed to observe dynamics in real-time through individual carbon atom spectra and disentangle the dynamics underlying these processes in two polyatomic targets –nitroethylene and transbutadiene– and two bio-relevant ones –thymine and citosine. Secondly, attosecond control in real-time using X-ATAS on the pi-pi*/ n-pi* internal conversion in thymine will be performed in a pioneering experiment. Finally, effective femtosecond control with fs-VMI of these processes in nitroethylene and trans-butadiene, molecules of interest for technologies, will be performed based on the relevant results from the X-ATAS experiments.

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