No data available.
Please log in to see this content.
You have no subscription access to this content.
No metrics data to plot.
The attempt to load metrics for this article has failed.
The attempt to plot a graph for these metrics has failed.
Vibrational and rotational dynamics of cyanoferrates in solution
1.V. Rusanov, S. Stankov, and A. X. Trautwein, Hyperfine Interact. 144, 307 (2002).
2.K. Szacilowski and Z. Stasicka, Coord. Chem. Rev. 229, 17 (2002).
3.P. Gutlich, Y. Garcia, and T. Woike, Coord. Chem. Rev. 219, 839 (2001).
4.C. G. Garcia, J. F. de Lima, and N. Y. M. Iha, Coord. Chem. Rev. 196, 219 (2000).
5.P. G. Wang, M. Xian, X. P. Tang, X. J. Wu, Z. Wen, T. W. Cai, and A. J. Janczuk, Chem. Rev. (Washington, D.C.) 102, 1091 (2002).
6.Y. X. Weng, Y. Q. Wang, J. B. Asbury, H. N. Ghosh, and T. Q. Lian, J. Phys. Chem. B 104, 93 (2000).
7.M. Yang, D. W. Thompson, and G. J. Meyer, Inorg. Chem. 41, 1254 (2002).
8.C. Matranga, B. L. Wehrenberg, and P. Guyot-Sionnest, J. Phys. Chem. B 106, 8172 (2002).
9.C. Matranga and P. Guyot-Sionnest, J. Chem. Phys. 112, 7615 (2000).
10.N. A. Anderson, K. Hang, J. B. Asbury, and T. Q. Lian, Chem. Phys. Lett. 329, 386 (2000).
11.V. Lenchenkov, J. Kloepfer, V. Vilchiz, and S. E. Bradforth, Chem. Phys. Lett. 342, 277 (2001).
12.P. J. Reid, C. Silva, P. F. Barbara, L. Karki, and J. T. Hupp, J. Phys. Chem. 99, 2609 (1995).
13.D. C. Arnett, P. Vohringer, and N. F. Scherer, J. Am. Chem. Soc. 117, 12262 (1995).
14.S. K. Doorn, R. B. Dyer, P. O. Stoutland, and W. H. Woodruff, J. Am. Chem. Soc. 115, 6398 (1993).
15.A. V. Tivansky, C. F. Wang, and G. C. Walker, J. Phys. Chem. A 107, 9051 (2003).
16.C. F. Wang, B. K. Mohney, B. B. Akhremitchev, and G. C. Walker, J. Phys. Chem. A 104, 4314 (2000).
17.B. Kushkuley and S. S. Stavrov, Biochim. Biophys. Acta 1341, 238 (1997).
18.A. Bonamore, E. Chiancone, and A. Boffi, Biochim. Biophys. Acta 1549, 174 (2001).
19.K. Bian and F. Murad, Front. Biosci. 8, D264 (2003).
20.S. Chowdhary and J. N. Townend, Clin. Sci. 97, 5 (1999).
21.H. Schutte, F. Grimminger, J. Otterbein, R. Spriestersbach, K. Mayer, D. Walmrath, and W. Seeger, J. Pharmacol. Exp. Ther. 282, 985 (1997).
22.K. G. Spears, X. N. Wen, and R. H. Zhang, J. Phys. Chem. 100, 10206 (1996).
23.K. G. Spears, X. N. Wen, and S. M. Arrivo, J. Phys. Chem. 98, 9693 (1994).
24.S. M. Arrivo, T. P. Dougherty, W. T. Grubbs, and E. J. Heilweil, Chem. Phys. Lett. 235, 247 (1995).
25.T. P. Dougherty and E. J. Heilweil, Chem. Phys. Lett. 227, 19 (1994).
26.W. T. Grubbs, T. P. Dougherty, and E. J. Heilweil, Chem. Phys. Lett. 227, 480 (1994).
27.E. J. Heilweil, R. R. Cavanagh, and J. C. Stephenson, Chem. Phys. Lett. 134, 181 (1987).
28.E. J. Heilweil, R. R. Cavanagh, and J. C. Stephenson, J. Chem. Phys. 89, 230 (1988).
29.E. J. Heilweil, M. P. Casassa, R. R. Cavanagh, and J. C. Stephenson, Annu. Rev. Phys. Chem. 40, 143 (1989).
30.A. Tokmakoff, B. Sauter, and M. D. Fayer, J. Chem. Phys. 100, 9035 (1994).
31.A. Tokmakoff, R. S. Urdahl, D. Zimdars, R. S. Francis, A. S. Kwok, and M. D. Fayer, J. Chem. Phys. 102, 3919 (1995).
32.A. Tokmakoff and M. D. Fayer, J. Chem. Phys. 103, 2810 (1995).
33.J. D. Beckerle, M. P. Casassa, R. R. Cavanagh, E. J. Heilweil, and J. C. Stephenson, Chem. Phys. 160, 487 (1992).
34.J. Childs and J. D. Beckerle, J. Chem. Phys. 107, 319 (1997).
35.A. Tokmakoff, B. Sauter, A. S. Kwok, and M. D. Fayer, Chem. Phys. Lett. 221, 412 (1994).
36.E. J. Heilweil, F. E. Doany, R. Moore, and R. M. Hochstrasser, J. Chem. Phys. 76, 5632 (1982).
37.P. Hamm, M. Lim, and R. M. Hochstrasser, J. Chem. Phys. 107, 10523 (1997).
38.M. Li, J. Owrutsky, M. Sarisky, J. P. Culver, A. Yodh, and R. M. Hochstrasser, J. Chem. Phys. 98, 5499 (1993).
39.J. C. Owrutsky, Y. R. Kim, M. Li, M. J. Sarisky, and R. M. Hochstrasser, Chem. Phys. Lett. 184, 368 (1991).
40.J. C. Owrutsky, D. Raftery, and R. M. Hochstrasser, Annu. Rev. Phys. Chem. 45, 519 (1994).
41.Q. Zhong, A. P. Baronavski, and J. C. Owrutsky, J. Chem. Phys. 118, 7074 (2003).
42.Q. Zhong, A. P. Baronavski, and J. C. Owrutsky, J. Chem. Phys. 119, 9171 (2003).
43.J. Assmann, A. Charvat, D. Schwarzer, C. Kappel, K. Luther, and B. Abel, J. Phys. Chem. A 106, 5197 (2002).
44.R. M. Whitnell, K. R. Wilson, and J. T. Hynes, J. Chem. Phys. 96, 5354 (1992).
45.B. M. Ladanyi and R. M. Stratt, J. Chem. Phys. 111, 2008 (1999).
46.D. A. Yarne, M. E. Tuckerman, and M. L. Klein, Chem. Phys. 258, 163 (2000).
47.J. Vieceli, I. Chorny, and I. Benjamin, J. Chem. Phys. 117, 4532 (2002).
48.D. A. V. Kliner, J. C. Alfano, and P. F. Barbara, J. Chem. Phys. 98, 5375 (1993).
49.There are numerous studies of organometallic photochemistry that result in vibrationally excited products. These often involve monitoring changes in high frequency (CO) stretch absorption bands. Generally, there are two ways that the photoproduct IR bands (or those of hot parent molecules following geminate recombination) can appear “hot.” If high frequency modes are excited, it typically results in a resolved, anharmonically red-shifted absorption band, since states with only one or a few quanta are populated. On the other hand, as a result of populating various levels with many quanta in low frequency modes for a comparable amount of energy, the band is often broadened and red-shifted. Photochemical studies provide a way, one of the only ways, to measure VER for low frequency modes and indicates that it is much faster than IVR for high frequency modes.
50.K. Ohta, H. Maekawa, and K. Tominaga, Chem. Phys. Lett. 386, 32 (2004).
51.K. Ohta, H. Maekawa, and K. Tominaga, J. Phys. Chem. A 108, 1333 (2004).
52.M. E. C. Villalba, E. L. Varetti, and P. J. Aymonino, Spectrochim. Acta, Part A 55, 1545 (1999).
53.D. A. Estrin, L. M. Baraldo, L. D. Slep, B. C. Barja, J. A. Olabe, L. Paglieri, and G. Corongiu, Inorg. Chem. 35, 3897 (1996).
54.In our experiment, we expect the magnitude of the transient signals to scale as where is the integrated band intensity, which relates to excitation for a broadband pump pulse that which overlaps the entire band, and I is due to frequency resolved probe, which is narrower than the band width. This trend accounts for the relative signal strengths observed, but quantitative agreement is difficult to establish due to other contributing factors, such as competitive solvent absorption, variations in pump power, and sample concentrations.
55.Q. Zhong, D. A. Steinhurst, E. E. Carpenter, and J. C. Owrutsky, Langmuir 18, 7401 (2002).
56.A. Seilmeier and W. Kaiser, in Ultrashort Laser Pulses and Applications, edited by W. Kaiser (Springer, New York, 1993), p. 279.
57.J. C. Deak, L. K. Iwaki, and D. D. Dlott, J. Phys. Chem. A 103, 971 (1999).
58.C. G. Elles, D. Bingemann, M. M. Heckscher, and F. F. Crim, J. Chem. Phys. 118, 5587 (2003).
59.J. Assmann, R. von Benton, A. Charvat, and B. Abel, J. Phys. Chem. A 107, 1904 (2003).
60.K. D. Rector and M. D. Fayer, J. Chem. Phys. 108, 1794 (1998).
61.M. L. Horng, J. A. Gardecki, and M. Maroncelli, J. Phys. Chem. A 101, 1030 (1997).
62.L. H. Jones, Inorg. Chem. 2, 777 (1963).
63.M. C. G. Lebrero, D. A. Scherlis, G. L. Estiu, J. A. Olabe, and D. A. Estrin, Inorg. Chem. 40, 4127 (2001).
64.K. Szacilowski, W. Macyk, G. Stochel, Z. Stasicka, S. Sostero, and O. Traverso, Chem. Rev. (Washington, D.C.) 208, 277 (2000).
65.J. R. Sprague, S. M. Arrivo, and K. G. Spears, J. Phys. Chem. 95, 10528 (1991).
66.K. Wynne and R. M. Hochstrasser, Chem. Phys. 171, 179 (1993).
67.S. Raghavan, R. S. Knox, and J. H. Eberly, Chem. Phys. Lett. 326, 207 (2000).
68.A. A. Ferro and D. M. Jonas, J. Chem. Phys. 115, 6281 (2001).
69.W. Qian and D. M. Jonas, J. Chem. Phys. 119, 1611 (2003).
70.K. R. Naqvi and R. E. Dale, Chem. Phys. Lett. 357, 147 (2002).
71.M. E. Schmidt and P. GuyotSionnest, J. Chem. Phys. 104, 2438 (1996).
72.J. C. Owrutsky, M. Li, B. Locke, and R. M. Hochstrasser, J. Phys. Chem. 99, 4842 (1995).
73.J. R. Hill, C. J. Ziegler, K. S. Suslick, D. D. Dlott, C. W. Rella, and M. D. Fayer, J. Phys. C 100, 18023 (1996).
74.J. R. Hill, A. Tokmakoff, K. A. Peterson, B. Sauter, D. Zimdars, D. D. Dlott, and M. D. Fayer, J. Phys. Chem. 98, 11213 (1994).
75.J. R. Heiks, M. K. Barnett, L. V. Jones, and E. Orban, J. Phys. C 58, 488 (1954).
76.S. A. Angel, P. A. Hansen, E. J. Heilweil, and J. C. Stephenson, in Ultrafast Phenomena VII, edited by A. H. Zewail (Springer, Berlin, 1990), p. 480.
77.K. D. Dobson and A. J. McQuillan, Phys. Chem. Chem. Phys. 2, 5180 (2000).
78.Other CN stretching modes in the cyanoferrates are close in energy so they could be thermally populated, which was the mechanism attributed to the mode of (Ref. 35). It is interesting that in the latter study, they had enough sensitivity to detect population in the somewhat higher lying state but did not observe any, which indicated that coupling is not determined by energetics alone and may be symmetry constrained.
Article metrics loading...
Full text loading...
Most read this month
Most cited this month