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Andrés Arregui

Researcher at Complutense University of Madrid

Publications -  9
Citations -  279

Andrés Arregui is an academic researcher from Complutense University of Madrid. The author has contributed to research in topics: Excited state & Photodissociation. The author has an hindex of 8, co-authored 9 publications receiving 259 citations.

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The photodissociation of CH 3 I in the red edge of the A-band: Comparison between slice imaging experiments and multisurface wave packet calculations

TL;DR: A general qualitative good agreement has been found between theory and experiment, the most important discrepancies being in the I((2)P(3/2)/I( *)((2) P(1/2)) branching ratios.
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Slice imaging of the photodissociation of acetaldehyde at 248 nm. Evidence of a roaming mechanism

TL;DR: The photodissociation of acetaldehyde in the molecular channel yielding CO and CH(4) at 248 nm has been studied, probing different rotational states of the CO(nu = 0) fragment by slice ion imaging using a 2+1 REMPI scheme.
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Imaging the radical channel in acetaldehyde photodissociation: Competing mechanisms at energies close to the triplet exit barrier

TL;DR: The photodissociation of acetaldehyde in the radical channel has been studied at wavelengths between 315 and 325 nm using the velocity-map imaging technique, and the fragments' KER is characterized, as well as the energy partitioning for the radical fragments are determined.
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Imaging the molecular channel in acetaldehyde photodissociation: roaming and transition state mechanisms.

TL;DR: The roaming dynamics in the photodissociation of acetaldehyde is studied through the first absorption band, in the wavelength interval ranging from 230 nm to 325 nm, using a combination of the velocity-map imaging technique and rotational resonance enhanced multiphoton ionization spectroscopy of the CO fragment.
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Solvent-Free MALDI Investigation of the Cationization of Linear Polyethers with Alkali Metals

TL;DR: The MALDI technique with solvent-free sample preparation has been applied to evaluate relative gas-phase affinities of polyether chain polymers with alkali metal cations and shows that the polyether-cation aggregation efficiencies decrease systematically with growing cation size.