ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Chemistry  (36)
Collection
Keywords
Publisher
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 1 (1987), S. 52-55 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 30 (1995), S. 52-56 
    ISSN: 1076-5174
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The optical emission spectra between 190 and 680 nm of 8 keV O2+· and CO2+· collisions with He and N2 target gases were obtained and analyzed on a modified commercial VG ZAB-2F mass spectrometer. Emissions observed were from O, O+, He, N2+· (B2∑+u → X2∑+g) and N2 (C3∏u → B3∏g) in the case of O2+· projectiles and C, CO2+· (B2∑+u, A 2∏u → X 2∏g), CO+· (B2∑+ → X2∑+), N2+· (B2 ∑+g → X2∑g) and N2 (C3∏u → B 3∏g) in the case of CO2+· projectiles. The results are discussed in relation to previous reports on N2+·-target collisions and the collision-induced dissociation mass spectral characteristics of O2+· and CO2+·.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 993-1007 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of o-nitrobenzoic acid, o-nitroanisole, o-nitrosobenzoic acid, o-nitrobenzamide, o-nitrobenzyl alcohol and o-nitrosobenzaldehyde have been studied. Fragmentation mechanisms are proposed for the above compounds; their elucidation was aided by isotopic labeling with D and O18. Two ‘ortho-effects’ are discussed; one involving H atom transfer between substituents and the other migration of an atom or group to a charge carrying vacant ortho position. The importance of nitro to nitrite conversion in molecular and fragment ions is discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1971), S. 1349-1362 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of norbornene, nortricyclene and deuterium labeled derivatives thereof have been studied. The appearance potentials of the ions [C7H10]+·, [C7H9]+, [C6H7]+ and [C5H6]+· have been determined for both compounds and heats of formation of the hydrocarbons have been estimated. Detailed fragmentation schemes are proposed for the molecular ions and it is concluded that they dissociate by essentially different mechanisms which do not involve common intermediates. The structures and energy contents of the primary fragment ions are discussed in detail by comparing energetics, labeling experiments and metastable ion abundances.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 4 (1970), S. 97-107 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of benzoic acid and its carboxyl-deuterated derivative have been studied in detail. Molecular and fragment ion structures are proposed and the role of ortho hydrogen atoms in rearrangements is discussed. The behaviour under electron-impact of phthalaldehydic acid and its carboxyl deuterated derivative provides evidence in support of ion structures in the benzoic acid fragmentation. From these results the fragmentation mechanism for phthalic acid is further elucidated. The mass spectrum and fragmentation mechanism of thiobenzoic acid is described and compared with that of benzoic acid.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1971), S. 1339-1341 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The position of deuterium in the products of the addition of HCL and DCI to exo 5, 6-d2 norbornene has been determined mass spectrometrically by measuring metastable ion abundances. The results show a stereo-selective hydrogen atom abstraction when the molecular ion of exo-2-norbornyl chloride fragements by loss of a chloroethyl radical.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 7 (1973), S. 335-339 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of maleic, fumaric, citraconic, mesaconic and itaconic diamides have been studied. In the molecular ions of the cis isomers, amide-amide interaction does take place, analogous to but less pronounced than, the carboxyl-carboxyl interaction of the corresponding acids.In spite of the weaker interaction a prominent loss of CONH from the molecular ion of a diamide would be strong evidence in support of a cis or similarly rigid geometrical arrangement of the amide groups. The mass spectra of maleic and fumaric nitriles are also reported.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1974), S. 618-621 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reverse activation energy, Erev, for the dissociation [C3H7]+ → [C3H5]+ + H2 has been determined as 0.24 ± 0.06 eV from measurements of the AP of [C3H5]+ produced by electron-impact from thermally generated sec-C3H7 radicals. The energy release observed in the corresponding metastable dissociation is 0.21 ± 0.01 eV, indicating that virtually all of Erev is partitioned as translational Kinetic energy of the fragmentation products. The metastable ion peak shape is also discussed with respect to the evaluation of the energy release.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The structures of the m/z 87, [C4H7O2]+, ions generated by dissociative ionization of CH3CGXCOOCH3 and XCH2CH2COOCH3 (X = CH3, Cl, Br, and I) have been investigated via their unimolecular and collisionally activated fragmentations and by apperance energy measurements. For both precursors loss of X = CH3 produced, via H atom transfer, ions of structure \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH_2 = CH}\mathop {\rm C}\limits^{\rm + } \left({{\rm OH}} \right){\rm OCH}_{\rm 3} $\end{document} (a), ΔHf = 386 kj mol-1. In marked contrast, loss of I· from ionized CH3CHICOOCH3 and ICH2CH2COOCH3 proceeded without rearrangement to yield respectively ions of structure \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm CH_3}\mathop {\rm C}\limits^{\rm + } {{\rm HCOOCH_3}} $\end{document} (b), ΔHf = 480 kJ mol-1 and (c), ΔHf = 450 kJ mol-1. These different fragmentation behaviours are explained via photoelectron spectra which show that the formal charge site in the precursor ion is at the carbonyl oxygen when X = CH3 but at the halogen atom when X = I. The precursor molecules X = Cl and Br display both of the above characteristics, CH3CHXCOOCH3 yielding mixtures of a and b and XCH2CH2COOCH3 producing a and c ions.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 23 (1988), S. 609-612 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By means of collisionally induced dissociative ionization mass spectrometry it was shown that the three isomeric aminopyridine molecular ions display ion chemistry similar to aniline molecular ions; i.e. metastable HNC loss, rather than losing the more stable neutral species HCN, behaviour typical of ionized pyridine. The molecular ions do not isomerize to a common intermediate prior to fragmentation and can readily be distinguished from their collisional activation and charge-stripping mass spectra.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...