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  • American Institute of Physics (AIP)  (13)
  • Blackwell Publishing Ltd  (9)
  • Wiley  (9)
  • Oxford University Press  (3)
  • American Association for the Advancement of Science (AAAS)
  • 2000-2004
  • 1995-1999  (23)
  • 1985-1989  (11)
  • 1980-1984
  • 1975-1979
  • 1970-1974
  • 1995  (23)
  • 1988  (11)
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  • 1
    Electronic Resource
    Electronic Resource
    Unimolecular dynamics following vibrational overtone excitation of HN3 v1=5 and v1=6: HN3(X˜;v,J,K)→HN(X 3Σ−;v,J,Ω)+N2 (X 1Σ+g) (1988)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 608-609 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Excitation of the NH-stretch overtone transitions of HN3 to v1=5 and 6 resulted in predissociation to HN(X) and N2(X) with lifetimes of 80+60−30 and ≤3 ns, respectively. Following excitation of either overtone, the HN fragments were formed predominantly in the symmetric F1, F3 spin–rotation states, with less than 4% population in the antisymmetric F2 levels. Fragment Doppler profiles confirmed that most of the available energy (〉96%) went into translational motion.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.455454
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  • 2
    Electronic Resource
    Electronic Resource
    Picosecond study of the population lifetime of CO(v=1) chemisorbed on SiO2-supported rhodium particles (1988)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 5342-5343 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Infrared pump–probe characterization of the excited state lifetimes reveals that CO bound to isolated metal sites (T1=140±20 ps) persists longer than the signal observed for CO bound to (approximate)35 A(ring) diameter metal particles (≤18 ps), suggesting paticipation of electron–hole excitations in the larger metal particles.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.455626
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  • 3
    Electronic Resource
    Electronic Resource
    CO(v=1) population lifetimes of metal–carbonyl cluster compounds in dilute CHCl3 solution (1988)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 230-239 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Tunable infrared picosecond pulses in the 5 μ region have been used for time-resolved pump–probe measurements of the population relaxation lifetime (T1) of CO(v=1) stretching vibrations in a series of metal–carbonyl cluster compounds in room temperature chloroform solution. T1 was the same for symmetric (ν=2084 cm−1, 90±10 ps) and antisymmetric (2014 cm−1, 87±10 ps) modes of the dicarbonyl Rh(CO)2(C5H7O2); T1 was the same for the B1 (2092 cm−1 , 710±130 ps) and B2 (2036 cm−1, 750±90 ps) modes of Rh2(CO)4Cl2. Similarly long T1 times were found for Rh4(CO)12 (2075 cm−1, 610±65 ps) and Rh6(CO)16 (2077 cm−1, 700±100 ps). The molecule Co4(CO)12 has also been compared to the corresponding rhodium analog and it exhibits an initially fast relaxation of 47±5 ps followed by a slower 396±70 ps decay. The transient response of the more complex systems to the single frequency experiment is found to be sensitive to frequency and can exhibit bleaching, absorption, and a combination of these effects. Such behavior is attributed to overlap of the IR pulse with v=1 to v=2 and higher transitions in the M4(CO)12 (M=Rh or Co) and Rh6(CO)16 molecules. The long CO(v=1) T1 values for the metal cluster molecules suggest relaxation via multiquantum transfer of vibrational energy to adjacent M–C stretch and M–C–O bend vibrations; energy transfer to vibrational or electronic states of the central metal core seems unimportant in determining T1 for these systems.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.455510
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  • 4
    Electronic Resource
    Electronic Resource
    Energetics and spin- and Λ-doublet selectivity in the infrared multiphoton dissociation DN3→DN(X 3Σ−, a 1Δ)+N2(X 1Σ+g): Experiment (1988)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 1378-1387 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Multiphoton vibrational excitation of deuterated hydrazoic acid, DN3, by a CO2 laser (I=10 GW/cm2) leads to dissociation forming DN in both X 3Σ− (spin forbidden) and a 1Δ (spin allowed) electronic states. Under collisionless conditions, the nascent DN fragments were probed via laser induced fluorescence, to determine initial product state distributions. The DN(X 3Σ−) molecules are formed predominantly in the symmetric F1 and F3 spin–rotation states with little population (≤6%) in the antisymmetric F2 levels. There is no significant population (〈3%) in excited DN(3Σ−) vibrational levels. The distribution of rotational states is Boltzmann-like, characterized by a rotational "temperature'' of about 920 K for the F1, F3 states and 500 K for F2 levels. Doppler profiles showed a large kinetic energy release of about 10 100 cm−1 total in the triplet channel. The DN(1Δ) products are formed preferentially in the symmetric Δ(A'), e-labeled lambda doublet levels: Δ(A')/Δ(A‘)=1.44. The DN(1Δ) is formed with no vibrational excitation (〈2%); the rotational states are populated Boltzmann-like with a rotational "temperature'' of 425 K. Doppler profiles give a total kinetic energy of about 1500 cm−1 in this channel. These observations give information about the distribution of energy in the reactant, the location of the barriers to dissociation, and the geometry of the transition states. Alexander, Werner, and Dagdigian (accompanying article) show that the observed DN(3Σ−) spin- and DN(1Δ) Λ-doublet selectivities reflect the symmetry properties of a planar transition state and that the low degree of DN(3Σ−) rotational and vibrational excitation is also expected from the transition state geometry.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.455137
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  • 5
    Electronic Resource
    Electronic Resource
    Time- and state-resolved measurements of nitric oxide dimer infrared photodissociation (1988)
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 1966-1976 
    Details
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Picosecond and nanosecond lasers and pulsed molecular beam techniques have been used to measure the infrared photodissociation spectra, the product state distributions, and the predissociation lifetimes of vibrationally excited nitric oxide dimer (NO)2 . Results for the ν1 (v=1) symmetric NO stretching mode and the ν4 (v=1) antisymmetric NO stretching mode are presented. Predissociation lifetimes are determined by time-resolved laser induced fluorescence probing of the NO monomer product appearance rate. A dramatic mode dependence of the predissociation lifetimes is observed with the higher energy ν1 mode decaying in approximately 1 ns, and the lower energy ν4 mode decaying in approximately 40 ps. The mode dependence is independent of which product state is probed. The product state distributions show that 75% to 80% of the available energy is channeled into relative translational energy of the fragments for both modes. Rotational state distributions are Boltzmann-like with temperatures ranging from 71 to 112 K depending on both the initially excited mode and on the NO product spin–orbit state. Predissociation from ν1 produces NO fragments in the 2Π1/2 and 2 Π3/2 states with equal probability. Predissociation from ν4 exhibits a propensity for producing the lower energy 2 Π1/2 spin–orbit state. The observations are discussed in terms of various vibrational predissociation mechanisms, including vibrational potential coupling and electronically nonadiabatic predissociation.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.455694
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  • 6
    Electronic Resource
    Electronic Resource
    Erratum: A femtojoule calorimeter using micromechanical sensors [Rev. Sci. Instrum. 65, 3793 (1994)] (1995)
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 66 (1995), S. 3083-3083 
    Details
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.1146429
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  • 7
    Electronic Resource
    Electronic Resource
    Asymmetrically cut crystals as optical elements for highly collimated x-ray beams : Proceedings of the 5th international conference on synchrotron radiation instrumentation (1995)
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 66 (1995), S. 1506-1509 
    Details
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: Asymmetrically cut perfect crystals, in both the Laue and Bragg geometries, are examined as single crystal monochromators for x-ray beams that are collimated to a small fraction of the Darwin width, as is typical in experiments with coherent x rays. Both the Laue and asymmetric Bragg geometries are plagued by an inherent chromatic aberration that increases the beam divergence much beyond that of the symmetric Bragg geometry. Measurements from a recent experiment at the ESRF are presented to compare Si(220) (symmetric Bragg), diamond(111) (asymmetric Laue), and diamond(111) (symmetric Bragg inclined) geometries. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.1145892
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  • 8
    Electronic Resource
    Electronic Resource
    The influence of tall fescue on the germination, seedling growth and yield of birdsfoot trefoil (1988)
    Oxford, UK : Blackwell Publishing Ltd
    Grass and forage science 43 (1988), S. 0 
    Details
    ISSN: 1365-2494
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: The influence of tall fescue (Festuca arundinacea Schreb.) on germination and seedling growth of birdsfoot trefoil (Lotus corniculatus L.) was evaluated during 1983-85 at Manhattan, Kansas. Studies were designed to evaluate tall fescue cv. Kentucky-31 for possible allelopathic compounds, determine the effects of tall fescue on the germination, seedling growth and yield of birdsfoot trefoil, and to characterize the chemical properties of tall fescue. Fescue produced allelopathic compounds, particularly during the spring and autumn months when it was actively growing. The greatest trefoil inhibition occurred with fescue plant extracts prepared during the autumn (September and October). The concentration of fescue extracts influenced trefoil germination, with greater inhibition as fescue concentration increased. In a sand medium under greenhouse conditions, fescue extracts prepared in spring and autumn reduced trefoil growth by 50 and 56%, respectively, with no inhibition during the summer months. Under field conditions, full strength fescue extracts reduced trefoil plant populations by 14 and 57% with spring and autumn prepared extracts, respectively. Fescue competition reduced sod-seeded trefoil plants per unit area by 17 and 31% for spring and autumn seeding, respectively. Full strength fescue extracts reduced trefoil seedling growth by an average of 37%, and trefoil dry matter yields by 53%.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1365-2494.1988.tb02152.x
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  • 9
    Electronic Resource
    Electronic Resource
    Scanning tunneling microscope investigation of the growth morphology of titanium silicide on Si(111) substrates (1995)
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 78 (1995), S. 5143-5154 
    Details
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A scanning tunneling microscope in ultrahigh vacuum has been used to investigate the growth, morphology, and surface atomic structure of ultrathin titanium silicide films on Si(111) substrates. Microstructural considerations have been used to identify various stages of the silicide growth. Atomic resolution images of a titanium silicide crystallite facet, formed at 850 °C, have been identified as a 2×2 silicon termination of a C54-TiSi2(010) surface. Possible epitaxial silicide/silicon relationships are provided. Theoretical consideration has been given to the interatomic bonding in the C54-TiSi2 lattice and the dangling bond density of ideally terminated silicide planes has been calculated. The highly reconstructed atomically flat surface of a large crystallite, formed at 1200 °C, has been assigned as a C54-TiSi2(311) plane giving the epitaxial relation C54-TiSi2(311)(parallel)Si(111). The presence of pairs and linear chains of defects, with common orientations, is attributed to the decomposition of a diatomic gas on the facet, producing sites of preferential adsorption on the silicide surface. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.359747
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  • 10
    Electronic Resource
    Electronic Resource
    Scanning tunneling microscope crystallography of titanium silicide on Si(100) substrates (1995)
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 77 (1995), S. 563-571 
    Details
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A scanning tunneling microscope (STM) in ultrahigh vacuum has been used to investigate the growth, morphology, and surface atomic structure of ultrathin titanium silicide films on Si(100) substrates. Microstructural considerations have been used to identify various stages of the silicide growth. Methods for STM crystallography have been developed and used to identify possible epitaxial silicide/silicon relationships based on morphological considerations. Atomic resolution images of a titanium silicide crystallite have identified a 2×2 silicon termination of a C54-TiSi2(111) surface. It is shown that unambiguous identification of epitaxial relationships requires images of the atomic structure of the silicide crystallite surfaces in addition to morphological information. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1063/1.359040
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