Picosecond time-resolved infrared investigation into the nature of the lowest excited state of fac-[Re(Cl)(CO)3(CO2Et-dppz)] (CO2Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester)

Marina K. Kuimova; David C. Grills; Pavel Matousek; Anthony W. Parker; Xue Zhong Sun; Michael Towrie; Michael W. George

doi:10.1016/j.vibspec.2004.01.019

Picosecond time-resolved infrared investigation into the nature of the lowest excited state of fac-[Re(Cl)(CO)₃(CO₂Et-dppz)] (CO₂Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester)

Marina K. Kuimova, David C. Grills, Pavel Matousek, Anthony W. Parker, Xue Zhong Sun, Michael Towrie, Michael W. George

Research output: Journal Publication › Conference article › peer-review

22 Citations (Scopus)

Abstract

The photophysics of the fac-[Re(Cl)(CO)₃(CO₂Et-dppz)] (CO₂Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester) was studied with picosecond time-resolved infrared (ps-TRIR) spectroscopy in metal carbonyl (2100-1800cm^-1) and organic ester (1800-1600cm^-1) spectral regions. The ps-TRIR spectra in both regions give evidence for the formation of a metal-to-ligand charge transfer (MLCT) excited state. The magnitude of ν(C≡O) shift in the metal carbonyl region of the excited state relative to those of the ground state allows the excited state to be described more precisely as a dπ(Re) → π* (phenazine) ³MLCT state.

Original language	English
Pages (from-to)	219-223
Number of pages	5
Journal	Vibrational Spectroscopy
Volume	35
Issue number	1-2
DOIs	https://doi.org/10.1016/j.vibspec.2004.01.019
Publication status	Published - 17 Jun 2004
Externally published	Yes
Event	The 2nd International Conference on Advanced Vibrational Spectroscopy - Nottingham, United Kingdom Duration: 24 Aug 2003 → 29 Aug 2003

Keywords

MLCT
Phenazine
Time-resolved

ASJC Scopus subject areas

Spectroscopy

Access to Document

10.1016/j.vibspec.2004.01.019

Cite this

Kuimova, M. K., Grills, D. C., Matousek, P., Parker, A. W., Sun, X. Z., Towrie, M., & George, M. W. (2004). Picosecond time-resolved infrared investigation into the nature of the lowest excited state of fac-[Re(Cl)(CO)₃(CO₂Et-dppz)] (CO₂Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester). Vibrational Spectroscopy, 35(1-2), 219-223. https://doi.org/10.1016/j.vibspec.2004.01.019

@article{5f7e5966d7484fa1a80029be6bb20bfc,

title = "Picosecond time-resolved infrared investigation into the nature of the lowest excited state of fac-[Re(Cl)(CO)3(CO2Et-dppz)] (CO2Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester)",

abstract = "The photophysics of the fac-[Re(Cl)(CO)3(CO2Et-dppz)] (CO2Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester) was studied with picosecond time-resolved infrared (ps-TRIR) spectroscopy in metal carbonyl (2100-1800cm-1) and organic ester (1800-1600cm-1) spectral regions. The ps-TRIR spectra in both regions give evidence for the formation of a metal-to-ligand charge transfer (MLCT) excited state. The magnitude of ν(C≡O) shift in the metal carbonyl region of the excited state relative to those of the ground state allows the excited state to be described more precisely as a dπ(Re) → π* (phenazine) 3MLCT state.",

keywords = "MLCT, Phenazine, Time-resolved",

author = "Kuimova, {Marina K.} and Grills, {David C.} and Pavel Matousek and Parker, {Anthony W.} and Sun, {Xue Zhong} and Michael Towrie and George, {Michael W.}",

note = "Funding Information: We thank the EPSRC (GR/M40486), ThermoNicolet, Edinburgh Instruments, ORS (MKK) and The University of Nottingham for financial support. MWG is grateful for the support of The Sir Edward Frankland Fellowship of the Royal Society of Chemistry.; The 2nd International Conference on Advanced Vibrational Spectroscopy ; Conference date: 24-08-2003 Through 29-08-2003",

year = "2004",

month = jun,

day = "17",

doi = "10.1016/j.vibspec.2004.01.019",

language = "English",

volume = "35",

pages = "219--223",

journal = "Vibrational Spectroscopy",

issn = "0924-2031",

publisher = "Elsevier",

number = "1-2",

}

Kuimova, MK, Grills, DC, Matousek, P, Parker, AW, Sun, XZ, Towrie, M & George, MW 2004, 'Picosecond time-resolved infrared investigation into the nature of the lowest excited state of fac-[Re(Cl)(CO)₃(CO₂Et-dppz)] (CO₂Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester)', Vibrational Spectroscopy, vol. 35, no. 1-2, pp. 219-223. https://doi.org/10.1016/j.vibspec.2004.01.019

Picosecond time-resolved infrared investigation into the nature of the lowest excited state of fac-[Re(Cl)(CO)₃(CO₂Et-dppz)] (CO₂Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester). / Kuimova, Marina K.; Grills, David C.; Matousek, Pavel et al.
In: Vibrational Spectroscopy, Vol. 35, No. 1-2, 17.06.2004, p. 219-223.

Research output: Journal Publication › Conference article › peer-review

TY - JOUR

T1 - Picosecond time-resolved infrared investigation into the nature of the lowest excited state of fac-[Re(Cl)(CO)3(CO2Et-dppz)] (CO2Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester)

AU - Kuimova, Marina K.

AU - Grills, David C.

AU - Matousek, Pavel

AU - Parker, Anthony W.

AU - Sun, Xue Zhong

AU - Towrie, Michael

AU - George, Michael W.

N1 - Funding Information: We thank the EPSRC (GR/M40486), ThermoNicolet, Edinburgh Instruments, ORS (MKK) and The University of Nottingham for financial support. MWG is grateful for the support of The Sir Edward Frankland Fellowship of the Royal Society of Chemistry.

PY - 2004/6/17

Y1 - 2004/6/17

N2 - The photophysics of the fac-[Re(Cl)(CO)3(CO2Et-dppz)] (CO2Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester) was studied with picosecond time-resolved infrared (ps-TRIR) spectroscopy in metal carbonyl (2100-1800cm-1) and organic ester (1800-1600cm-1) spectral regions. The ps-TRIR spectra in both regions give evidence for the formation of a metal-to-ligand charge transfer (MLCT) excited state. The magnitude of ν(C≡O) shift in the metal carbonyl region of the excited state relative to those of the ground state allows the excited state to be described more precisely as a dπ(Re) → π* (phenazine) 3MLCT state.

AB - The photophysics of the fac-[Re(Cl)(CO)3(CO2Et-dppz)] (CO2Et-dppz = dipyrido[3,2a:2′,3′c]phenazine-11- carboxylic ethyl ester) was studied with picosecond time-resolved infrared (ps-TRIR) spectroscopy in metal carbonyl (2100-1800cm-1) and organic ester (1800-1600cm-1) spectral regions. The ps-TRIR spectra in both regions give evidence for the formation of a metal-to-ligand charge transfer (MLCT) excited state. The magnitude of ν(C≡O) shift in the metal carbonyl region of the excited state relative to those of the ground state allows the excited state to be described more precisely as a dπ(Re) → π* (phenazine) 3MLCT state.

KW - MLCT

KW - Phenazine

KW - Time-resolved

UR - http://www.scopus.com/inward/record.url?scp=2342496791&partnerID=8YFLogxK

U2 - 10.1016/j.vibspec.2004.01.019

DO - 10.1016/j.vibspec.2004.01.019

M3 - Conference article

AN - SCOPUS:2342496791

SN - 0924-2031

VL - 35

SP - 219

EP - 223

JO - Vibrational Spectroscopy

JF - Vibrational Spectroscopy

IS - 1-2

T2 - The 2nd International Conference on Advanced Vibrational Spectroscopy

Y2 - 24 August 2003 through 29 August 2003

ER -