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Volumn 275, Issue 5296, 1997, Pages 54-57

Femtosecond dynamics of excited-state evolution in [Ru(bpy)3]2+

Author keywords

[No Author keywords available]

Indexed keywords

RUTHENIUM COMPLEX;

EID: 0031022786     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.275.5296.54     Document Type: Article
Times cited : (670)

References (60)
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    • note
    • 2+ and do not significantly affect the data illustrated in Fig. 2.
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    • It is difficult to assess vibrational relaxation dynamics given the broad, somewhat featureless nature of electronic absorption spectra. However, because charge-transfer spectra are particularly sensitive to changes in molecular structure, it is reasonable to assume that most of the structural rearrangement in the system is complete by Δt = 300 fs
    • It is difficult to assess vibrational relaxation dynamics given the broad, somewhat featureless nature of electronic absorption spectra. However, because charge-transfer spectra are particularly sensitive to changes in molecular structure, it is reasonable to assume that most of the structural rearrangement in the system is complete by Δt = 300 fs.
  • 53
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    • and references therein
    • P. V. Kumar and M. Maroncelli, ibid. 103, 3038 (1995) and references therein; M. Maroncelli, ibid. 94, 2084 (1991); D. McMorrow and W. T. Lotshaw, ibid. 95, 10395 (1991).
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    • Kumar, P.V.1    Maroncelli, M.2
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    • P. V. Kumar and M. Maroncelli, ibid. 103, 3038 (1995) and references therein; M. Maroncelli, ibid. 94, 2084 (1991); D. McMorrow and W. T. Lotshaw, ibid. 95, 10395 (1991).
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    • P. V. Kumar and M. Maroncelli, ibid. 103, 3038 (1995) and references therein; M. Maroncelli, ibid. 94, 2084 (1991); D. McMorrow and W. T. Lotshaw, ibid. 95, 10395 (1991).
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    • McMorrow, D.1    Lotshaw, W.T.2
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    • 1 relaxation process
    • 1 relaxation process.
  • 58
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    • 2 conversion in a spin-crossover complex, although the time resolution was insufficient to observe the actual formation of the lowenergy excited state. See J. K. McCusker, et al., J. Am. Chem. Soc. 115, 298 (1993).
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    • McCusker, J.K.1
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    • This research was supported by the University of California (J.K.M.), the ACS-PRF grant 31016-G6 (J.K.M.), and the U.S. Department of Energy, contract DE-AC0376SF00098 (C.V.S.). G.C. acknowledges support from a NATO fellowship
    • This research was supported by the University of California (J.K.M.), the ACS-PRF grant 31016-G6 (J.K.M.), and the U.S. Department of Energy, contract DE-AC0376SF00098 (C.V.S.). G.C. acknowledges support from a NATO fellowship.


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