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  • 11
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 387-393 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A probability distribution of internal energies is derived for aromatic molecular ions which can decompose to give only a single product whose relative intensity and appearance potential are each a function of Hammett sigma constants, with certain simplifying assumptions.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 12
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acetylacetone (Hacac) admitted as a gas to an ion source containing CoCl2 adsorbed on a field ionization/field desorption emitter produces the ion [Co(acac)Cl]+. Similar ions arising from interaction of adsorbed salt and a ligand admitted as a gas were found for CoCl2 and trifluoroacetyl acetone, and for FeCl2 and acetylacetone. The chelation process represents a new kind of reaction of chemisorbed species in field ionization mass spectrometry.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 20 (1985), S. 445-453 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hydrogen chemical ionization (H2 CI) mass spectra of a range of metal(II) (Ni, Cu, Co, Pt), metal (III) (Al, Mn, Ga, Fe (bearing a single axial ligand)) and metal(IV) (Si, Ge, Sn (bearing two axial ligands) and V (as V=O2+)) porphyrins have been determined, The spectra are highly dependent on the coordinated metal, rather than the axial ligand(s) (where present). Ni(II), Cu(II), Mn(II or III), Ga(III), Ge(IV), Fe(III) and Sn(IV) porphyrins fragment via hydrogenation and demetallation, followed by cleavage of the resulting porphyrinogens at the meso(bridge) positions to give mono- and di-pyrrolic fragments. Tripyrrolic fragments are also observed in the case of Ni(II), Cu(II) and Sn(IV). Fragmentations of this type are similar to those observed for free-base porphyrins. In the case of Pt(II), Co(II), Al(III), Si(IV) and V(IV) (as vanadyl), the dipyrrolic fragment ions are either very weak or completely absent; hence their H2CI spectra contain limited structural information. This variable CI behaviour may be related to the relative stabilities of the metalloporphyrins together with the multiple stable valency states exhibited by several metals.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 17 (1986), S. 471-475 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Apparatus is described for the acquisition of Raman spectra with excitation at wavelengths as short as 184 nm. The H2 Raman-shifted output of an Nd:YAG laser is directed on to a free-flowing sample, and the Raman photons are collected and dispersed by a scanning 1.26 m single monochromator equipped with a 2400 groove holographic grating and a solar blind phototube with integrating electronics, or by a 0.5 m spectrograph with an 1800 groove holographic grating and a reticon multi-channel detector. Data for air-sensitive samples are obtained by enclosing the sample jet in an inert gas purged shroud equipped with a UV-transparent optical window. Raman spectra are reported for phenylalanine at a series of excitation wavelengths down to 184 nm. They show a sharp transition between 200 and 192 nm from vibronic to Franck-Condon scattering. At 200 nm, the intensities of the vibronically induced ν8a and ν8b modes, at 1606 and 1586 cm-1, are nearly the same as that of the 1000 cm-1 ν1 ring breathing mode, whereas at 192 nm the relative intensities of the former bands are dramatically dimished. In contrast, the ν8a and ν8b modes of tyrosine continue to show enhancement comparable to the ring breathing modes at 192 nm, the maximum of the strong 1Bα, b tyrosine absorption. The spectrum of insulin at 192 nm shows comparable contributions from tyrosine, phenylalanine and amide vibrations, whereas at 200 and 218 nm excitation the aromatic contributions are dominant.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 8 (1979), S. 323-325 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Raman spectra of thiocyanate at the surface of a silver electrode and in a series of aqueous test solutions were compared. The results indicate that spectral variations can be correlated with changes in bonding stoichiometry at the electrode surface as a function of potential.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 12 (1982), S. 76-81 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Raman spectra of three forms of dithizone are presented. Significant structural changes are indicated in the Raman spectra when a proton is added or lost from neutral dithizone (H2Dz) to form the corresponding conjugate acid of dithizone (H3Dz+) and the dithizone anion (HDz-), respectively. These spectral changes are correlated with the structures previously proposed for these species.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 15 (1984), S. 350-353 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Surface-enhanced resonance Raman (SERR) spectra of a series of highly fluorescent complexes of ruthenium(II), 2,2′-bipyridine and 1,10-phenanthroline are presented. The effect of applied potential on the SERR spectra is discussed. SERR spectra of mixed ligand complexes can be predicted from weighted averages of spectral features for the tris complexes.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 16 (1985), S. 171-173 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Comparison of Raman spectra of octahedral Ru(pyridine)6(BF4)2 with those of Ru(bipyridine)(pyridine)4(ClO4)2 provides an opportunity to analyse the orientation of Ru(pyridine)6 at silver over a wide potential range. At the more positive potentials, the Ru(pyridine)6 appears to be bonded through two pyridine ligands, while at more negative potentials, the orientation is probably C4ν, indicating bonding through one pyridine. Previously reported potential dependences of Raman scattering intensities show mobility of the complex on the electrode surface and probable conversion between these two orientations. Possibilities for further orientation changes at more positive and more negative potentials are obscured by electrode oxidation and complex desorption, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 15 (1984), S. 160-164 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Surface-enhanced Raman spectra of 2,2′-bipyridine, Ru(bpy)(py)4(CIO4)2, Ru(py)6(BF4)2 and Ru(bpy)-(PVP)(CIO4)2 at the surface of a copper electrode are presented [bpy = 2,2′-bipyridine; py=pyridine; and PVP =poly(4-vinylpyridine)]. The dependence of the spectra on potential is demonstrated through presentation of complete spectra at applied potentials from -0.2 to -1 V, as well as in plots of SER intensity vs electrode potential. The effect of excitation wavelength on the spectra is discussed. Significant differences between the potential dependences of these compounds at copper and silver electrode surfaces are shown. SER spectra from the surface-enhanced resonance Raman active ruthenium complexes could be obtained only with an excitation wavelength longer than 514.5 nm.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 13 (1982), S. 149-152 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman spectra of disordered Hg(NH3)2Cl2, Hg(ND3)2Cl2 and Hg(NH3)2Br2 are reported. The spectra consist of the internal vibrations of the mercuric complex with no lattice phonons being observed. The bending and the symmetric stretching mode for the complex (Hg(NH3)22+) occur at 110 cm-1 and 413 cm-1 in the chloride and at 85 cm-1 and 381 cm-1 in the bromide.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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