Abstract

Two-dimensional (2D) Fourier transform (FT) infrared spectroscopy is performed by using a collinear pulse-pair pump and probe geometry with conventional optics. Simultaneous collection of the third-order response and pulse-pair timing permit automated phasing and rapid acquisition of 2D absorptive spectra. To demonstrate the ability of this method to capture molecular dynamics, couplings and structure found in the conventional boxcar 2D FT spectroscopy, a series of 2D spectra of a metal carbonyl, and a β-sheet protein are acquired.

© 2007 Optical Society of America

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References

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    [CrossRef] [PubMed]

2007 (1)

S. H. Shim, D. B. Strasfeld, and M. T. Zanni, Proc. Natl. Acad. Sci. U.S.A. 104, 14197 (2007).
[CrossRef] [PubMed]

2004 (4)

M. Khalil, N. Demirdöven, and A. Tokmakoff, J. Chem. Phys. 121, 362 (2004).
[CrossRef] [PubMed]

N. Demirdöven, C. M. Cheatum, H. S. Chung, M. Khalil, J. Knoester, and A. Tokmakoff, J. Am. Chem. Soc. 126, 7981 (2004).
[CrossRef] [PubMed]

V. Cervetto, J. Helbing, J. Bredenbeck, and P. Hamm, J. Phys. Chem. 121, 5935 (2004).
[CrossRef]

T. Brixner, I. V. Stoipkin, and G. R. Fleming, Opt. Lett. 29, 884 (2004).
[CrossRef] [PubMed]

2003 (4)

P. Tian, D. Keusters, Y. Suzaki, and W. S. Warren, Science 300, 1553 (2003).
[CrossRef] [PubMed]

M. Khalil, N. Demirdöven, and A. Tokmakoff, Phys. Rev. Lett. 90, 47401 (2003).
[CrossRef]

M. Khalil, N. Demirdoven, and A. Tokmakoff, J. Phys. Chem. A 107, 5258 (2003).
[CrossRef]

D. M. Jonas, Annu. Rev. Phys. Chem. 54, 397 (2003).
[CrossRef]

1999 (1)

S. M. Gallagher Faeder and D. M. Jonas, J. Phys. Chem. A 103, 10489 (1999).
[CrossRef]

1997 (1)

Annu. Rev. Phys. Chem. (1)

D. M. Jonas, Annu. Rev. Phys. Chem. 54, 397 (2003).
[CrossRef]

J. Am. Chem. Soc. (1)

N. Demirdöven, C. M. Cheatum, H. S. Chung, M. Khalil, J. Knoester, and A. Tokmakoff, J. Am. Chem. Soc. 126, 7981 (2004).
[CrossRef] [PubMed]

J. Chem. Phys. (1)

M. Khalil, N. Demirdöven, and A. Tokmakoff, J. Chem. Phys. 121, 362 (2004).
[CrossRef] [PubMed]

J. Phys. Chem. (1)

V. Cervetto, J. Helbing, J. Bredenbeck, and P. Hamm, J. Phys. Chem. 121, 5935 (2004).
[CrossRef]

J. Phys. Chem. A (2)

S. M. Gallagher Faeder and D. M. Jonas, J. Phys. Chem. A 103, 10489 (1999).
[CrossRef]

M. Khalil, N. Demirdoven, and A. Tokmakoff, J. Phys. Chem. A 107, 5258 (2003).
[CrossRef]

Opt. Lett. (2)

Phys. Rev. Lett. (1)

M. Khalil, N. Demirdöven, and A. Tokmakoff, Phys. Rev. Lett. 90, 47401 (2003).
[CrossRef]

Proc. Natl. Acad. Sci. U.S.A. (1)

S. H. Shim, D. B. Strasfeld, and M. T. Zanni, Proc. Natl. Acad. Sci. U.S.A. 104, 14197 (2007).
[CrossRef] [PubMed]

Science (1)

P. Tian, D. Keusters, Y. Suzaki, and W. S. Warren, Science 300, 1553 (2003).
[CrossRef] [PubMed]

Other (1)

P. Hamm and R. M. Hochstrasser, in Ultrafast Infrared and Raman Spectroscopy, M.D.Fayer, ed. (Marcel Dekker, 2001), pp. 273-347.

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Figures (3)

Fig. 1
Fig. 1

Experimental setup of the 2D IR spectrometer, including (A) acquisition of 2D spectra, (B) interferometric autocorrelation, and (C) stage calibration.

Fig. 2
Fig. 2

(a),(b) ZZYY 2D FT spectrum of RDC in CDCl 3 and RDC in Hexane. (c)–(f) ZZZZ 2D FT waiting time series of RDC in CDCl 3 .

Fig. 3
Fig. 3

ZZYY 2D FT spectrum of Concanavalin A.

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