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 82 (1960), S. 3268-3271 
    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
    Journal of the American Chemical Society 84 (1962), S. 676-676 
    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 ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Immunogenetics 44 (1996), S. 86-96 
    ISSN: 1432-1211
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract  We identified four cDNA sequences encoding sheep homologues of the CD1 molecule. The sheep sequences were selected from λgt11 thymocyte cDNA libraries by hybridization with a human CD1C probe and a homologous sheep probe. The SCD1B-42 and SCD1A25 sequences encode complete CD1 molecules. The third sequence, SCD1B-52, which is closely related to SCD1B-42 and may be an allele, has the sequence encoding the α3 region precisely deleted. The fourth sequence, SCD1T10, is truncated at the 5′ end. All four sequences are related to the human CD1B and domestic rabbit CD1B-like sequences at both nucleotide and amino acid level. Comparison of the derived CD1 amino acid sequences with the sequence of major histocompatibility complex class I molecules showed that the sheep CD1 molecules, like human CD1 molecules, lack most of the conserved class I residues known to be involved in interaction with β2-microglobulin and the CD8 molecule. They do not contain the peptide docking residues involved in anchoring peptides in the peptide binding groove of class I molecules. Southern hybridization of sheep DNA with a sheep CD1 exon 4/α3 probe showed that the sheep genome encodes at least seven CD1 genes. The implications of these analyses for CD1 function are discussed.
    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 91 (1989), S. 4426-4427 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    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 90 (1989), S. 1648-1651 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The vibrational quenching rate constants for NO+(v), predominantly in the v=1 state, have been measured at 200 and 293 K in collisions with H2 and D2 and at 200, 293, and 458 K with O2. The rate constants are all very low, corresponding to quenching probabilities ∼10−4. The low rate constants reflect very shallow attractive potential wells. In the case of H2 and D2 this is a consequence of their low polarizabilities. In the case of O2, repulsive chemical interactions offset the electrostatic attraction to yield a shallow attractive well. This is a consequence of the singlet NO+ and triplet ground state O2 not approaching on the attractive NO+3 ground state potential surface, which is a singlet. The temperature dependences of the quenching rate constants are generally slight, indicating that the collision energies are in a range comparable to the attractive well depth and that the quenching is not strongly dominated by either the attractive forces, which would give a negative energy dependence, or by the repulsive forces which would give a positive energy dependence.
    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 88 (1988), S. 6335-6340 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The decay of (Ar+3)*→Ar+2+Ar is found to be metastable on a time scale longer than 40 μs. Theoretical considerations are presented for these slow metastable dissociation rates reported in this and other studies. From model calculations it is inferred that tunneling lifetimes from 10−10 to 10 s may be observed.
    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 89 (1988), S. 5692-5694 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The vibrational relaxation of NO+(v=1) ions in collisions with CH4 molecules has been measured in a flow drift tube experiment from thermal energy to 1.2 eV relative kinetic energy. The quenching rate constant has a broad minimum as a function of collision energy in the ∼0.5–0.6 eV range. These results are interpreted in terms of complex formation at low energies (KEcm (very-much-less-than)U) followed by vibrational predissociation in the complex and by a Landau–Teller nonadiabatic energy transfer at large relative kinetic energies (KEcm (very-much-greater-than)U), where U is the interaction well depth.
    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 89 (1988), S. 1445-1447 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The competitive charge–transfer and vibrational quenching of N+2 (X,v=1) ions in collision with O2 and NO molecules have been found to have comparable rate constants. The vibrational relaxation rate constants are rationalized in terms of a vibrational predissociation mechanism occurring in relatively long-lived complexes (τ∼10−10−10−11 s). The large magnitudes are attributed to unusually large attractive ion–neutral interaction potentials resulting from a charge–transfer stabilization interaction resulting from the near resonance of the N+2 +NO→NO+(a 3Σ+)+N2 and N+2 +O2→O+2 (a 4Πu) +N2 interactions. The more favorable orbital overlap of the O+2(a 4πu) with N2 relative to that for O+2(X 2Πg) with N2 may explain the slight preference for vibrational quenching over charge transfer and also the order of magnitude faster O+2(a 4πu) charge–transfer with N2 compared to N+2 charge–transfer with O2.
    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 85 (1986), S. 3851-3859 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In the gas phase O+2 reacts with methane at 300 K to produce a hydrogen atom and the CH3O+2 ion. The structure of this ion has recently been determined to be H2COOH+, methylene hydroperoxide ion. The reaction rate coefficients and product distributions have now been measured at 300 K for the CHnD4−n isotopes. The reaction shows both inter- and intramolecular isotope effects, e.g., CH2D2 reacts more slowly than methane and more rapidly than CD4, but loses hydrogen or deuterium with equal probability. The ion readily transfers HO+ to alkenes, CS2, and many other neutral molecules. The reaction with CS2 has been used to investigate the isotopic distribution within mixed isotope product ions. In addition, the reaction rate coefficients for both CH4 and CD4 have been measured as functions of temperature between 20 and 500 K; in both cases a clear minimum is observed in the reaction rate coefficient near room temperature. A mechanism for the reaction is proposed which allows us to model the temperature dependence of the reaction rate coefficient over the entire range for which there are data.
    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 91 (1989), S. 4037-4042 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The dependences on temperature of the rate coefficients for the endothermic proton transfer reactions of HBr+ with CO2 and CH4 have been obtained in a variable-temperature selected ion flow tube. The measurements have been used to determine the 300 K proton affinity of CO2, P.A.(CO2), =128.5±1.0 kcal mol−1, utilizing the literature value of P.A.(Br)=131.8 kcal mol−1, obtained from the dissociation energy of HBr+, as a primary standard. The proton affinity difference between CO2 and CH4 has been substantiated by equilibrium constant measurements as a function of temperature for proton transfer between CO2 and CH4. Similar equilibrium constant measurements have been used to determine the proton affinities of HCl, N2 O, HBr, and CO, giving a proton affinity ladder ordered (in kcal mol−1) as CO(141.4), HBr(138.8), N2 O(137.3), HCl(133.0), Br(131.8), CH4 (130.0), and CO2(128.5). Proton affinities have also been determined for Br2(140.0), NO(127.0), and CF4(126.5), the last two values being obtained from selected ion flow drift tube measurements. An upper limit to P.A.(SF6) of 127 kcal mol−1 has been inferred from the instability of SF6 H+ towards dissociation into SF+5 and HF.
    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...