Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 101 (1979), S. 6468-6470 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Accounts of chemical research 20 (1987), S. 120-126 
    ISSN: 1520-4898
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 3662-3673 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Total dephasing decay profiles of the ν12 (1002 cm−1) ring-stretching mode of toluene have been measured in the time domain in a range extending from the low viscosity, normal liquid (380 K, 0.26 cP) to the high viscosity, supercooled liquid (140 K, 4600 cP). In the region from 1 to 5 cP (250 to 200 K), the profile makes a transition from exponential to partially Gaussian, consistent with a loss of motional narrowing. In contrast to many interpretations of dephasing in terms of collisional dynamics, these data clearly indicate an important role for diffusive dynamics in vibrational dephasing. Above 10 cP, oscillations appear, and their period decreases with increasing viscosity. An analysis of the low to moderate viscosity region with a Kubo model shows that the frequency modulation time is dependent on the viscosity. The dephasing decay profiles are used to test a recent viscoelastic theory of dephasing [Chem. Phys. 233, 257 (1998)], which attributes the perturbation of the vibrational frequency to shear fluctuations in the liquid. A second dephasing process must be included to obtain reasonable fits in the viscosity range below 10 cP. The second process is consistent with a Gaussian frequency modulation whose modulation time is weakly viscosity dependent or has no viscosity dependence. We speculate that this process is due to rapid rotation about the toluene z axis and that the same process also causes the oscillations seen at higher viscosity. There is a good correspondence between the value of the infinite frequency shear modulus found from fitting the Raman free-induction-decay data and the value recently found by Larsen, Ohta, and Fleming by fitting photon-echo-peak-shift measurements in toluene [J. Chem. Phys. 111, 8970 (1999)]. This correspondence supports the idea that both vibrational dephasing and nonpolar electronic solvation are caused by the same physical mechanism. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 113 (2000), S. 3233-3242 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The two-pulse echo sequence is examined for the case in which the frequency modulation time τm of the transition is intermediate between the well known limiting cases of very fast modulation (motional narrowing) and very slow or static modulation (inhomogeneous broadening). Within this spectral diffusion regime, the interpretation of the echo decay differs markedly from standard treatments. If the frequency-frequency correlation function initially decays as 1−tβ, the echo decay time TE is proportional to τmβ/(β+2). These results reduce to those of Yan and Mukamel [J. Chem. Phys. 94, 179 (1991)] for β=1. Drawing on a viscoelastic model, the theoretical results are compared to viscosity and temperature dependent vibrational echo experiments on myoglobin–CO. A τm1/3 dependence is observed, as is predicted for an exponential decay of the frequency–frequency correlation function. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 115 (2001), S. 4212-4222 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Dichroism experiments with 150 fs time resolution on anthracene in benzyl alcohol are presented as a function of viscosity from 14.4 cP (274 K) to 2.7 cP (329 K). These measurements test a qualitative prediction of the viscoelastic picture of liquid dynamics, specifically that earlier "inertial" dynamics have a viscosity independent rate, whereas later "diffusive" dynamics have a rate directly proportional to viscosity. This paper focuses on two components of the dichroism decay that are assigned to rotational motion. A third component is assigned to electronic-state solvation and is analyzed in a companion paper [J. Chem. Phys. 115, 4231 (2001)]. The longest component is due to rotational diffusion and is very well described by a hydrodynamic model with slip boundary conditions. A fast decay component in the subpicosecond region is found and shown to have a viscosity-independent rate. It is assigned to inertial rotation by comparison to the computer simulations of Jas et al. [J. Chem. Phys. 107, 8800 (1997)]. Inertial rotation extends out to at least 1 ps, longer than the range commonly assumed for inertial dynamics. Over much of this range, the inertial rotation is not free-rotor-like, but is strongly modified by interaction with the solvent. The inertial rotation also accounts for the "missing" anisotropy found when the rotational diffusion fits are extrapolated to zero time. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 115 (2001), S. 4231-4238 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Results on single-wavelength transient hole burning (SW-THB) developed in paper II [J. Chem. Phys. 115, 4223 (2001)] are applied to the dichroism experiments on anthracene in benzyl alcohol reported in paper I [J. Chem. Phys. 115, 4212 (2001)]. The intermediate component of the dichroism decay is assigned to a SW-THB effect caused by nonpolar electronic solvation. The presence of a solvation component in dichroism experiments has not been demonstrated previously. The sparseness of anthracene's electronic spectrum eliminates vibrational dynamics from the solvation measurement. Because data collection is focused on a single dimension, the viscosity dependence of the nonpolar solvation is determined with greater accuracy than in our previous two-dimensional transient hole-burning studies. The solvation time is obtained as a function of viscosity/temperature from 14.4 to 2.7 cP (1–56 °C). The times show good agreement with a viscoelastic theory of the diffusive component of nonpolar solvation. Combining the results of this paper with those of paper I allows for comparison of solvation and rotation dynamics within a single system. A correlation between the ratio of diffusive solvation and rotation times and the magnitude of the inertial rotation is suggested. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 115 (2001), S. 4223-4230 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Experiments to determine the frequency autocorrelation function of an electronic transition (the "solvation function") inherently depend on a multidimensional response function. However, a degenerate transient absorption experiment, or "single-wavelength transient hole burning" (SW-THB), provides a one-dimensional cut through this multidimensional space with sufficient information to uniquely determine the desired solvation function. We derive an analytical formula that relates the solvation function to the one-dimensional SW-THB signal. Sample calculations examine the effects of strong versus weak coupling to the solvent, the wavelength of the laser relative to the absorption spectrum and of unresolved fast relaxation components. We conclude that for many systems, SW-THB provides a simpler alternative to multidimensional methods for measuring solvation dynamics. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 5787-5795 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The results of transient hole burning of the nonpolar solute dimethyl-s-tetrazine (DMST) in glycerol, glycerol triacetate, sorbitol hexaacetate, squalane, and hexane solutions are reported. Despite the high viscosity and diversity of chemical types of the solvents, the solvent-induced perturbations of the electronic states of DMST relax in less than 1 ps in all cases. This contrasts strongly with the relaxation of polar electronic states, which are typically slow in viscous solvents. A new type of solvent-interaction mechanism appears to be important. We suggest that short-range repulsions modulated by phonon-like solvent modes are responsible.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 2413-2424 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A number of limitations to hole burning in the liquid phase are identified. As spectral diffusion becomes more rapid, a point is reached where the narrowest hole width no longer measures the homogeneous linewidth. Spectral congestion of the solute is also shown to limit the fastest detectable spectral diffusion rate. An optimal pulse length is found which allows observation of the most rapid spectral diffusion. In addition, the coherence effect observed when the pulses overlap is shown to have resonances at both the excited and ground state vibrational spacings. The coherence effect greatly resembles the hole burning spectrum, but contains no dynamical information. Because of these limitations, hole burning may not be observed even when the homogeneous spectrum is well resolved and spectral diffusion is slow. Experimental confirmation is found in the hole burning spectrum of iodine in hexane, which shows no hole burning despite having a narrow homogeneous linewidth.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 8577-8588 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The viscoelastic (VE) continuum model of solvation developed in the first paper of this series [J. Phys. Chem. A 102, 17 (1998)] is applied to solvation of the electron in water and is compared to the computer simulations of Rossky and co-workers. The theory correctly predicts both the inertial and diffusive solvation times for both injected electrons and electrons excited to the p state. These times are associated with the speed of phonon propagation and the rate of shear relaxation respectively. The ability of the VE model to predict the inertial solvation time shows that continuum models are a valuable first approximation, even at very short times. The full solvation response function, the time-dependent cavity shape and the effect of deuteration are also all reproduced accurately for solvation of the p state. The effect of a shape change in the excited state of the electron is compared to the effect of a size change. A shape change produces a low amplitude, picosecond tail in the solvation response function, which is not present with a purely spherical size change. The theory is extended to include quadratic terms in the solvation difference potential. This nonlinearity accounts for the largest differences between the solvation response function in the ground and excited states of the electron. All the major features seen in the simulations can be accounted for by mechanical relaxation of the solvent. At present, there is no compelling indication of a significant role for dielectric relaxation, although the issue merits further investigation. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...