Nanosecond Two-Dimensional Resonance Raman Correlation Spectroscopy of Benzil Radical Anion

1993 ◽  
Vol 47 (9) ◽  
pp. 1343-1344 ◽  
Author(s):  
Ken Ebihara ◽  
Hiroaki Takahashi ◽  
Isao Noda

Nanosecond two-dimensional resonance Raman spectroscopy was used to investigate the photochemistry of the production and decay of the radical anion of benzil in various solvents. A newly developed correlation formalism was applied to a set of time-resolved resonance Raman spectra of the benzil radical anion to generate two-dimensional Raman spectra. Unlike the 2D correlation method previously developed for IR spectroscopy, which was based on signals induced by a sinusoidally varying external perturbation, the new correlation formalism is generally applicable to the studies of any transient spectroscopic signals having an arbitrary waveform. This makes it ideally suited for the analysis of time-resolved spectroscopic signals following photoexcitation. 2D Raman spectra effectively accentuate certain useful information which is sometimes obscured in the original time-resolved spectra. Spectral intensity changes and peak shifts arising from the photochemical reaction processes were clearly observed by the synchronous and asynchronous correlation.

1984 ◽  
Vol 107 (4-5) ◽  
pp. 381-384 ◽  
Author(s):  
John N. Moore ◽  
George H. Atkinson ◽  
David Phillips ◽  
Patrick M. Killough ◽  
Ronald E. Hester

2015 ◽  
Vol 143 (12) ◽  
pp. 124202 ◽  
Author(s):  
Zhenkun Guo ◽  
Brian P. Molesky ◽  
Thomas P. Cheshire ◽  
Andrew M. Moran

2016 ◽  
Vol 145 (3) ◽  
pp. 034203 ◽  
Author(s):  
Brian P. Molesky ◽  
Zhenkun Guo ◽  
Thomas P. Cheshire ◽  
Andrew M. Moran

2016 ◽  
Vol 145 (18) ◽  
pp. 180901 ◽  
Author(s):  
Brian P. Molesky ◽  
Zhenkun Guo ◽  
Thomas P. Cheshire ◽  
Andrew M. Moran

1993 ◽  
Vol 47 (9) ◽  
pp. 1317-1323 ◽  
Author(s):  
I. Noda ◽  
A. E. Dowrey ◽  
C. Marcott

Recent developments in two-dimensional infrared (2D IR) correlation spectroscopy are reviewed. Since the initial introduction of the basic concept seven years ago, the field of 2D IR spectroscopy has evolved considerably. The method for generating 2D IR spectra from perturbation-induced time-dependent fluctuations of IR intensities and the properties of such 2D spectra are summarized first. Applications of 2D IR spectroscopy are then surveyed, and improvements in the instrumentation are reviewed. Different types of external perturbation schemes capable of inducing dynamic fluctuations of IR spectra are listed. Finally, a new 2D correlation method for dynamic spectral data with arbitrary time-dependence is discussed.


1990 ◽  
Vol 10 (5-6) ◽  
pp. 333-347 ◽  
Author(s):  
G. Buntinx ◽  
O. Poizat

The time-resolved Raman spectra of the first triplet state–in resonance with the Tn←T1 absorption at 370 nm–and of the radical cation transient–in resonance with the R+⋅∗←R+⋅ absorptions at 370 nm and in the 560-600 nm range-are reported for fluorene. The triplet state Raman spectra of dibenzofuran and dibenzothiophen are also given. The vibrational assignments, resonance Raman activity and intensity enhancement effects are studied. On this basis, the structures and electronic configurations of the triplet state and radical cation transients and the nature of the resonant Tn←T1 and R+⋅∗←R+⋅ transitions are discussed. It turns out from this investigation that the title molecules present close analogies with biphenyl. The insertion of a methylene group or a heteroatom does not disturb markedly the electronic properties of the ground state, the first triplet state and the radical cation transient of biphenyl.


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