Time-resolved infrared spectroscopy of excited states of transition metal species

J. J. Turner; M. W. George; F. P.A. Johnson; J. R. Westwell

doi:10.1016/0010-8545(93)85011-R

Time-resolved infrared spectroscopy of excited states of transition metal species

J. J. Turner^*
, M. W. George
, F. P.A. Johnson
, J. R. Westwell

^*Corresponding author for this work

Research output: Journal Publication › Article › peer-review

70 Citations (Scopus)

Abstract

This article describes examples of the application of time-resolved infrared Spectroscopy (TRIR) to the probing of the excited states of transition metal species. Other "direct" methods for excited states include time-resolved absorption Spectroscopy, and, more importantly, time-resolved resonance Raman Spectroscopy (TR³). Both of these techniques have limitations and hence TRIR is of value in complementing them. The common "indirect" methods are absorption, emission, and excitation spectroscopies, to which has been more recently added, resonance Raman, particularly in the time-dependent formulation. The relevance of these methods is also discussed.

Original language	English
Pages (from-to)	101-114
Number of pages	14
Journal	Coordination Chemistry Reviews
Volume	125
Issue number	1-2
DOIs	https://doi.org/10.1016/0010-8545(93)85011-R
Publication status	Published - May 1993
Externally published	Yes

ASJC Scopus subject areas

General Chemistry
Materials Chemistry
Inorganic Chemistry
Physical and Theoretical Chemistry

Access to Document

10.1016/0010-8545(93)85011-R

Cite this

@article{2b6ce61c0b42438eb349342cd2930e87,

title = "Time-resolved infrared spectroscopy of excited states of transition metal species",

abstract = "This article describes examples of the application of time-resolved infrared Spectroscopy (TRIR) to the probing of the excited states of transition metal species. Other {"}direct{"} methods for excited states include time-resolved absorption Spectroscopy, and, more importantly, time-resolved resonance Raman Spectroscopy (TR3). Both of these techniques have limitations and hence TRIR is of value in complementing them. The common {"}indirect{"} methods are absorption, emission, and excitation spectroscopies, to which has been more recently added, resonance Raman, particularly in the time-dependent formulation. The relevance of these methods is also discussed.",

author = "Turner, \{J. J.\} and George, \{M. W.\} and Johnson, \{F. P.A.\} and Westwell, \{J. R.\}",

note = "Funding Information: The authorsa re gratefult o Drs. l? Glyn, W. H. Woodruffa nd C. A. Bignoui, and Miss S. L. Morrison, for very helpful discussions, and to Messrs. K. R. Stanley, D. Lichfiekl,a nd R. Parsons for technicala ssistance. Work at Nottinghamh as been supported by SERC, EEC, NATO, Miitek Gmbh, Perkin-Elmer Ltd., Edinburgh Instrumentsa nd the Paul InstrumentF und of the Royal Society.",

year = "1993",

month = may,

doi = "10.1016/0010-8545(93)85011-R",

language = "English",

volume = "125",

pages = "101--114",

journal = "Coordination Chemistry Reviews",

issn = "0010-8545",

publisher = "Elsevier B.V.",

number = "1-2",

}

TY - JOUR

T1 - Time-resolved infrared spectroscopy of excited states of transition metal species

AU - Turner, J. J.

AU - George, M. W.

AU - Johnson, F. P.A.

AU - Westwell, J. R.

N1 - Funding Information: The authorsa re gratefult o Drs. l? Glyn, W. H. Woodruffa nd C. A. Bignoui, and Miss S. L. Morrison, for very helpful discussions, and to Messrs. K. R. Stanley, D. Lichfiekl,a nd R. Parsons for technicala ssistance. Work at Nottinghamh as been supported by SERC, EEC, NATO, Miitek Gmbh, Perkin-Elmer Ltd., Edinburgh Instrumentsa nd the Paul InstrumentF und of the Royal Society.

PY - 1993/5

Y1 - 1993/5

N2 - This article describes examples of the application of time-resolved infrared Spectroscopy (TRIR) to the probing of the excited states of transition metal species. Other "direct" methods for excited states include time-resolved absorption Spectroscopy, and, more importantly, time-resolved resonance Raman Spectroscopy (TR3). Both of these techniques have limitations and hence TRIR is of value in complementing them. The common "indirect" methods are absorption, emission, and excitation spectroscopies, to which has been more recently added, resonance Raman, particularly in the time-dependent formulation. The relevance of these methods is also discussed.

AB - This article describes examples of the application of time-resolved infrared Spectroscopy (TRIR) to the probing of the excited states of transition metal species. Other "direct" methods for excited states include time-resolved absorption Spectroscopy, and, more importantly, time-resolved resonance Raman Spectroscopy (TR3). Both of these techniques have limitations and hence TRIR is of value in complementing them. The common "indirect" methods are absorption, emission, and excitation spectroscopies, to which has been more recently added, resonance Raman, particularly in the time-dependent formulation. The relevance of these methods is also discussed.

UR - https://www.scopus.com/pages/publications/0011267968

U2 - 10.1016/0010-8545(93)85011-R

DO - 10.1016/0010-8545(93)85011-R

M3 - Article

AN - SCOPUS:0011267968

SN - 0010-8545

VL - 125

SP - 101

EP - 114

JO - Coordination Chemistry Reviews

JF - Coordination Chemistry Reviews

IS - 1-2

ER -

Time-resolved infrared spectroscopy of excited states of transition metal species

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this