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
    The @journal of physical chemistry 〈Washington, DC〉 51 (1947), S. 262-277 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 434-444 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The Cs(7P)+H2→CsH (X 1Σ+) (v‘=0,J‘)+H reaction has been studied in a crossed-beam experiment, with electronic excitation of Cs atoms and laser-induced fluorescence detection of CsH products. The Doppler technique has been applied to determine the center of mass angular scattering probability of CsH products, for all rotational levels between 1 and 14 (in v‘=0) and for various values of the collision energy between 0.03 and 0.13 eV. We have used two complementary arrangements of the analysis laser beam: With a "parallel'' arrangement (the laser beam is along the collision axis), the shape analysis of fluorescence profiles leads directly to the angular scattering probability but experimental constraints limit the range of measurements; with a "perpendicular'' arrangement (the laser beam is perpendicular to the collision plane), fluorescence profiles are symmetrical and "forward'' contributions cannot be separated from "backward'' ones. However, extensive shape analyses have been performed with this perpendicular arrangement, since the direction of scattering was determined earlier by recording several profiles with the parallel arrangement. For the title reaction, it is shown unambiguously that, in the center of mass, CsH products scatter preferentially at small angle, in the forward direction with respect to the Cs initial velocity. The angular scattering probability varies with the collision energy but is independent of the rotational level of the product molecule (thus of its recoil velocity). These results are compatible with the harpooning mechanism which was suggested for the reaction.
    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 95 (1991), S. 3347-3360 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The Cs(7P)+H2→CsH(X 1Σ+)(v‘=0,J‘)+H harpooning reaction has been studied in a crossed-beam experiment, with electronic excitation of Cs atoms and laser-induced fluorescence detection of CsH products performed in a coherent saturation regime. Measurements of reactive cross sections have been achieved as a function of two parameters: The collision energy Ec (0.015≤Ec≤0.15 eV) and the rotational quantum number J‘ of CsH products (0≤J‘≤16, in v‘=0). For Ec=0.09 eV, the total reactive cross sections corresponding to the two 7P fine structure levels of Cs are σ(Cs(7P1/2)+H2)=4.2×10−16 cm2 and σ(Cs(7P3/2)+H2)=10−16 cm2. These cross sections are much smaller than expected for a harpooning reaction. This is interpreted from ab initio potential energy and quantal dynamics calculations which show that the efficiency of the photochemical reaction (Cs atoms in the 7P state) is limited by the quenching processes associated with the underlying potential energy surfaces connected with Cs atoms in the 6S, 6P, 5D, and 7S states. From the present measurements, one deduces that the rate of these quenching processes is larger than 90%. The rotational distributions of products in v‘=0 measured at two collision energies (Ec=0.045 and 0.09 eV) are close to "prior'' statistical distributions, with the same "surprisal.'' The energy dependence of rotationally resolved cross sections (J‘ fixed, Ec variable) confirms the reaction thresholds and shows that there is no potential barrier higher than 0.015 eV on the entrance valley and the exit valley of the reactive system; it is in agreement with the dependence predicted by hemiquantal dynamical calculations performed in the frame of a harpooning model. The uncertainty on the measurement of absolute cross sections is larger than 70%, but of the order of 20% for relative cross sections.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 16 (1968), S. 500-504 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    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 101 (1994), S. 3973-3980 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Multireference configuration interaction calculations (MRD-CI) were carried out in order to obtain the bending and stretching potential energy curves of several low-lying electronic states of the fluoroformyl radical FCO. The study of interactions between valence and Rydberg states as well as that of the dissociative behavior is included in the investigation.
    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 104 (1996), S. 5558-5571 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Extensive multireference configuration interaction calculations were carried out in order to obtain complete two-dimensional (2D) potential energy surfaces for the amidogen (NH2) radical as functions of both N–H bond lengths keeping the bond angle fixed at its experimental ground state equilibrium value. The eight lowest-lying states (four of each symmetry, A′ and A″) were treated mainly for the purpose of using these surfaces in subsequent studies of the photodissociation dynamics. In analogy with the neighboring dihydrides CH2 and H2O the photodissociation of NH2 into NH+H (hydrogen abstraction) takes place preferentially after excitation of the first two Rydberg s states (3 2A′/2 2A1 and 2 2A″/2 2B1) found closely together at about 7.6 eV. The transition dipole moments connecting the ground state with these two states are large (0.44 a.u. and 0.66 a.u.) in the Franck–Condon region, but the behavior of the potentials in the dissociation channel is quite different. The 3 2A′/2 2A1 state is weakly repulsive whereas the 2 2A″/2 2B1 state is strongly repulsive. This will result in differences in the dissociation dynamics for the two states.The next higher state which should play a role in the NH2 photodissociation is the 4 2A″/3 2B1 Rydberg s state at 9.4 eV, because of its large transition dipole moment with the ground state (0.36 a.u.). Close to this state, many Rydberg p states were found. Due to the high density of states in the region above 9.0 eV, interactions of these states are expected and should lead to complicated dissociation dynamics. Contrary to CH2, the two low-lying valence states for NH2 are found at lower energies [2.2 eV (1 2A1) and 6.5 eV (1 2B2)], well separated from the first members of the Rydberg series. These states are less important for the photodissociation of NH2, compared with CH2, because the first state is bound and the transition to the other is dipole-forbidden in C2v symmetry. For H2O, the valence states are missing. © 1996 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 101 (1994), S. 3981-3988 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Results of an ab initio study of the vibrational structure of several electronic spectral systems of FCO are presented. An interpretation of hitherto recorded spectra, as well as a prediction of features of yet unobserved electronic transitions is given. The absorption spectra observed in the uv spectral region are ascribed to the transitions involving the first excited states of 2A' and 2A‘ character. The emission spectrum obtained by Toby and Toby [J. Phys. Chem. 85, 4071 (1981)] is assigned to the transition X 2A'←2 2A‘. Reassignment of some observed vibrational bands is proposed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 13569-13570 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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 111 (1999), S. 1926-1936 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A sub-Doppler experiment involving an effusive beam of lithium dimers and a continuous wave (cw) tunable dye laser is used to record the absorption spectrum of the B–X system. Predissociation due to tunneling through the potential barrier of the B state is studied in a small range of energy above the Li(2p)+Li(2s) dissociation limit by analyzing the shape of homogeneously broadened absorption lines and by measuring the fluorescence intensity of Li atoms. Experimental data are interpreted in the frame of a semiclassical dynamical model involving the shape of the potential barrier. Their accuracy should address an improvement of the potential shape through a full quantal dynamical model. © 1999 American Institute of Physics.
    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 107 (1997), S. 2930-2941 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The ground-state potential energy surface (PES) for linear arrangements of the N2H+ molecular ion is numerically computed by the multireference single- and double-excitation configuration interaction (MRD-CI) technique. An analytical representation of the potential energy function is obtained by fitting a power series in the Simons–Parr–Finlan coordinates to the numerical data. For investigating the intramolecular dynamics we describe the nuclear motion by a Gaussian wave packet located initially in the strong interaction region of the PES. The vibrational eigenvalue spectrum is calculated by Fourier transforming the time autocorrelation function. The spectrum is then analyzed statistically in the light of random matrix theory (RMT) to understand the nature of the intramolecular dynamics. We examine the short-range correlation in the spectrum through the nearest neighbor level spacing distribution P(s) and the long-range correlation through Δ3 and Σ2 statistics. The spectrum in the time domain is analyzed by computing the ensemble averaged survival probability 〈〈P(t)〉〉. The above four quantities obtained from the spectrum are compared with the distribution predicted for regular, irregular, and mixed (intermediate) spectra by the RMT. We find the system is of mixed type and the fractional irregularity is 0.7±0.05. In order to reveal a possible correspondence to the classical dynamics, we have carried out the spectral analysis of the dynamical variables for classical trajectories over a wide range of internal energies. In addition the classical dynamics of proton collisions with N2 molecules has also been preliminarily studied on the same PES, in particular the dependence of the final vibrational action nf on the initial vibrational phase φi of N2 and, furthermore, the Poincaré surface-of-section superimposed with the zero-order separatrix; we find a large number of trapped trajectories. © 1997 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...