A preliminary study of perylene-CO van der Waals complexes has been conducted. The spectroscopy of the major in-plane and out-of-plane features ofthe I : 1 and 1:2 perylene-CO aggregates hasbeen analyzed. Little perturbation to the G 'butterfly" outof-plane mode is seen in the complex, indicating th
Rotational coherence spectroscopy and structure of the perylene-benzene van der Waals complex
β Scribed by Paul W. Joireman; Leslie L. Connell; Shane M. Ohline; Peter M. Felker
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 781 KB
- Volume
- 182
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
β¦ Synopsis
Rotational coherence spectroscopy has been used to measure rotational constants for four isotopomers of the aromatlc-aromatic dimer petylene-benzene. Possibilities for the vibrationally averaged dimer geometry have been deduced from the measured values. In the geometries the benzene moiety is close to centrally bound to the perylene and such that its ring plane is parallel or nearly parallel to the plane of the perylene. The geometries are discussed in terms of both the intermolecular forces between the spccics and the structural results for other aromatic dimcrs.
π SIMILAR VOLUMES
The fluorescence excitation spectra obtained on further complexation of perylene-benzene by other species m quatemary supersonic expansions have been used to confirm a number of important structural assignments in molecular complexes. The interpretation of spectra of species such as perylene-Ar, is
Van der Waals complexes of perylene with I-chlorobutane, prepared under supersonic jet conditions, exist in three distinct isomeric forms distinguishable by their spectral red-shifts of 265,238 and 184 cm-'. Following vibronic excitation at 355 cm-', two of these isomers yield similarly shaped and b
The dissociation energy of the complex C6H6'H20 was determined by the threshold difference method. These complexes were produced in molecular beams via the expansion of a mixture of helium, and benzene and water vapors in the ratio of 96: 3: 1. The method requires the ionization potential of C6H 6