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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.

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

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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