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  • 1990-1994  (11)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 95 (1991), S. 1167-1177 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 6926-6927 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The ultraviolet photoelectron spectrum (hν=3.531 eV) of SO− shows transitions to the three lowest lying electronic states of SO neutral. The electron affinity of SO was determined to be 1.125(5) eV. The harmonic vibrational frequency and the spin-orbit splitting of the SO− electronic ground state (2Π) were also determined. Franck–Condon analyses of the SO vibrational progressions were used in conjunction with the molecular constants of the well-characterized SO neutral molecule to determine the equilibrium bond length of SO− [re=1.570(5) A(ring)].
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 4845-4853 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The ultraviolet negative ion photoelectron spectrum of Pd−2 is presented for electron binding energies up to 3.35 eV. The anion is prepared by sputtering in a flowing afterglow ion source. Multiple low-lying electronic states of Pd2, all unidentified previously, are observed with resolved vibrational structure. The spectrum shows two strong electronic bands, each with similar vibrational progressions. Franck–Condon analyses are carried out on the two transitions and molecular constants are extracted for the anion and the two neutral electronic states. With the help of simple molecular orbital arguments and ab initio calculations, these two electronic bands are assigned as the triplet ground state (3Σ+u) and a singlet excited state (1Σ+u). The adiabatic electron affinity is E.A.(Pd2)=1.685±0.008 eV and the singlet excitation energy T0(1Σ+u) is 0.497±0.008 eV (4008±65 cm−1 ). The bonding in the palladium dimers is discussed and we find that the anion bond strength is 1.123±0.013 eV stronger than that of the neutral. Related studies of Pd− yield an improved electron affinity of E.A.(Pd)=0.562±0.005 eV.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 6987-7002 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Negative ion photoelectron spectra of Cu−n, Ag−n(n=1–10), and Au−n (n=1–5) are presented for electron binding energies up to 3.35 eV at an instrumental resolution of 6–9 meV. The metal cluster anions are prepared in a flowing afterglow ion source with a cold cathode dc discharge. In the spectra of Cu−2, Ag−2, and Au−2, the M2 X 1Σ+g←M−2 X 2Σ+u transitions are vibrationally resolved. We analyze these spectra to yield the adiabatic electron affinities, vibrational frequencies, bond length changes, and dissociation energies. The a 3Σ+u triplet states of Cu2 and Ag2 are also observed. Using experimental and theoretical data, we assign the major features in the Cu−3 and Ag−3 spectra to the transition from the linear ground state of the anion (M−31Σ+g) to an excited linear state of the neutral (M3 2Σ+u). The Au−3 spectrum is attributed to a two-photon process, photodissociation followed by photodetachment of the Au− or Au−2 fragment. For larger clusters, we measure the threshold and vertical detachment energies as a function of size. Trends in the electron affinities and excited state energy levels as a function of cluster size and composition are discussed in terms of simple models.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 8542-8551 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Negative ion photoelectron spectra of Ni−2, Pd−2, and Pt−2 are presented for electron binding energies up to 3.35 eV at an instrumental resolution of 8–10 meV. The metal cluster anions are prepared in a flowing afterglow ion source. Each dimer exhibits multiple low-lying electronic states and a vibrationally resolved ground state transition. Franck–Condon analyses yield the anion and neutral vibrational frequencies and the bond length changes between anion and neutral. The electron affinities are determined to be EA(Ni2)=0.926±0.010 eV, EA(Pd2)=1.685±0.008 eV, and EA(Pt2)=1.898±0.008 eV. The electronic configurations of the ground states are tentatively assigned. Comparison of the nickel group dimers to the coinage metal dimers sheds light on the d orbital contribution to the metal bonding in the nickel group dimers.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 3575-3587 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Reactions of platinum cluster anions with carbon monoxide are investigated using a flow tube reactor (flowing afterglow) instrument. The platinum cluster anions are prepared with a cathodic discharge source. The cluster anions, Pt n−(n≤7), react with carbon monoxide in a flowing helium/argon buffer gas at 0.5 Torr total pressure and at 300 K. Clusters with four or more platinum metal atoms react by addition of CO with an effective bimolecular reaction rate of greater than 70% of the calculated collision rate, while for n=3 the reaction rate is 16% of the collision rate. At high CO concentrations, additional CO molecules attach to the clusters to form platinum carbonyl anion intermediates, with little loss of metal atoms. Saturation limits were found, above which no further CO addition occurred. The saturated cluster species are Pt3(CO)6−, Pt4(CO)8−, Pt5(CO)9−, and Pt6(CO)10−. The application of simple geometry arguments and electron counting rules to infer possible skeletal structures of the metal clusters is discussed.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 5715-5725 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Reactions of Ni−n(n=3–10), Pd−n(n=3–8), and Pt−n(n=3–7) with CO are studied in a flow tube reactor. Bimolecular rate coefficients are measured for the association reaction of CO adsorbing on the cluster surface. The rate coefficients range from about 10% of the collision rate for the trimer anions to near the collision rate for clusters larger than four atoms. The maximum number of CO molecules that bind to each cluster is determined. Whereas the saturation limits for nickel are typical for an 18 electron transition metal, the limits for platinum are lower, reflecting the electron deficient structures observed in condensed phase chemistry. The CO saturated palladium clusters represent the first examples of saturated binary palladium carbonyl compounds. Comparisons are made to similar studies on metal cation and neutral clusters and also to surface scattering studies of nickel group metals.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 96 (1992), S. 1130-1141 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 10023-10031 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 112 (1990), S. 5750-5759 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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