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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.

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

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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