| Description: |
One Colour-Resonant Two-Photon Ionisation, coupled with a supersonic expansion was used to study the rotationally cold excited electronic states of the water clusters of ortho-, meta- and para-difluorobenzene. Ground state rotational constants obtained through ab-initio calculations allowed rotational band contour simulations of these species to be performed, elucidating structural and spectroscopic features such as rotational band types, directions of transition dipole moments and excited state geometries. Confidence in the calculated ground state geometries, obtained through successful simulation of the rotational band contours, provided strength to the credibility of the vibrational frequencies acquired via these calculations. Analysis of ground state dispersed fluorescence spectroscopy utilising these ab-initio (geometry + frequency) optimisation calculations, allowed assignment of the ground state vibrational modes of each species. Furthermore, comparison of the assigned ground state modes with the excited state spectroscopy, affirmed assignment of the low frequency Van der Waals modes along with the higher frequency aromatic ring modes of these cluster species. A novel technique that produces pseudo-selective excitation of ground state aromatic-rare gas cluster ions was used to assign the vibrational transitions of the D3[less than]D0 electronic excitation spectrum of para-Difluorobenzene+-Argonn=1,2. This technique works on the principle of providing varying degrees of excess energy to the ground state of the cluster ion, as well as altering the Franck-Condon factors for excitation to the D3 electronic state. Measurement of the redshifts for each pDFB-R (where R= Ar1, Ar2, Kr1, Kr2) cluster, revealed that the addition of a second rare-gas adatom doubled the redshift, and that Krypton ad-atoms produced a stronger redshift than argon as expected. It was also noted that the addition of a positive charge to the complex increased the redshift of the complexes, in accordance with our expectations. Rotational ... |