Hill, Jeremy N. and Perutz, Robin N. and Rooney, A. Denise
(1995)
Laser-Induced Fluorescence of Molybdenocene and Tungstenocene in Low-Temperature Matrices.
Journal of Physical Chemistry A, 99.
pp. 538-543.
ISSN 1089-5639
Abstract
The reactive metallocenes, tungstenocene and molybdenocene (M(t75-C5H5)2; M = Mo, W), have been generated
by photolysis of the corresponding dihydride complexes, M(í;5-C5H5)2H2, in argon and nitrogen matrices at
12 K. The metallocenes have been probed by laser-induced fluorescence with a pulsed tunable laser and by
UV/vis absorption spectroscopy. Structured emission is observed from the LMCT excited states (lifetimes
< 10 ns). The spectra are complicated by multiple sites/conformers, but emission spectra of a single site/
conformer may be obtained with appropriate selection of matrix and excitation wavelength. Corresponding
excitation spectra are measured from the area of selected emission peaks as a function of excitation wavelength.
Vibrational progressions are dominated by the ring—metal-ring symmetric stretching mode (v4 ~ 300 cm-1).
Nevertheless, this mode changes in frequency by <4 cm-1 (< 1.3%) in the LMCT excited state. The bestresolved
peaks have a full width at half-maximum of ca. 10 cm-1. Most of the emission is vibrationally fully
relaxed, but weak emission peaks arising from ' = 1 states are found for MoCp2 in N2 matrices.
Item Type: |
Article
|
Additional Information: |
Cite as: J. Phys. Chem. 1995, 99, 2, 538–543 |
Keywords: |
Laser-Induced; Fluorescence; Molybdenocene; Tungstenocene; Low-Temperature; Matrices; |
Academic Unit: |
Faculty of Science and Engineering > Chemistry |
Item ID: |
14521 |
Identification Number: |
https://doi.org/10.1021/j100002a015 |
Depositing User: |
Dr. Denise Rooney
|
Date Deposited: |
09 Jun 2021 14:22 |
Journal or Publication Title: |
Journal of Physical Chemistry A |
Publisher: |
American Chemical Society |
Refereed: |
Yes |
URI: |
|
Use License: |
This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA).Details of this licence are available here |
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