Research on the formation and properties of clusters of aromatic molecules bonded to numerous solvents is rapidly expanding. Recently much attention has been paid to these adduct species with the objective of clarifying nucleation phenomena. Photophysical and photochemical studies of these clusters give information on solvent effects, intracluster reactions and charge-transfer processes. Model calculations of potential surfaces of vdW adducts have provided knowledge of the intracluster binding energy and vdW vibrational modes in a few systems. Here, data are reported on resonant two-photon ionization R2PI mass spectra and on spectroscopic shifts of styrenes clustered with various atoms and molecules.

RESONANT 2-PHOTON IONIZATION PROCESSES OF VAN-DER-WAALS ADDUCTS - SPECTROSCOPY AND REACTIVITY OF STYRENES CLUSTERED WITH VARIOUS MOLECULES

SNELS M
1993

Abstract

Research on the formation and properties of clusters of aromatic molecules bonded to numerous solvents is rapidly expanding. Recently much attention has been paid to these adduct species with the objective of clarifying nucleation phenomena. Photophysical and photochemical studies of these clusters give information on solvent effects, intracluster reactions and charge-transfer processes. Model calculations of potential surfaces of vdW adducts have provided knowledge of the intracluster binding energy and vdW vibrational modes in a few systems. Here, data are reported on resonant two-photon ionization R2PI mass spectra and on spectroscopic shifts of styrenes clustered with various atoms and molecules.
1993
Inglese
2nd International Conference on Solar Energy Storage and Applied Photochemistry
105
773
782
10
Sì, ma tipo non specificato
JAN 06-11, 1993
AIN SHAMS UNIV, CAIRO, EGYPT
1
none
GIARDINIGUIDONI, A ; MELE, A; PICCIRILLO, S ; CORENO, M; SNELS, M
273
info:eu-repo/semantics/conferenceObject
04 Contributo in convegno::04.01 Contributo in Atti di convegno
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/123495
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