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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    The chemical educator 4 (1999), S. 128-130 
    ISSN: 1430-4171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The problem of the units associated with equilibrium constants is revisited. A brief survey of the arguments for and against using units with equilibrium constants is presented and the compromise solution that we have adopted in our teaching, both at the university and school level, is presented and justified.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 76 (1989), S. 291-293 
    ISSN: 1432-2234
    Keywords: NMR ; C-H coupling ; s-Character ; Delocalization effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Following earlier theoretical studies of orbital delocalization effects on one-bond 13C-H coupling constants (1 J CH) an approximate proportionality of (1 J CH) to ϱ 3/2, where ϱ is the s-character of the carbon hybrid orbital appropriate to the construction of the best localized molecular orbitals, is predicted and verified by using published data. It is proposed that this proportionality should replace the previous linear correlations of (1 J CH) with ϱ, which involve large additive constants.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The complexation of molybdenum(VI) by L-aspartate in dilute aqueous solutions, at pH 6, was studied using u.v. spectrophotometry,1H and13C n.m.r. spectroscopy. A single complex anion, [MoO3(C4H5NO4)]2−, is observed in solution. The conformation of the aspartate ion in the complex was determined and shown to be consistent with it acting as a terdentate ligand. The formation constant of the complex was determined at different ionic strengths. Job's method has been employed, here and elsewhere, to study the stoichiometry of the complex. However, the result is strongly affected by polymerization of molybdenum(VI): this effect is discussed.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Complex formation between molybdate ions and R,R-(+)-tartaric acid has been studied in aqueous solution, and to a limited extent in DMSO, over a range of concentrations and pH at 298K, using1H and13C n.m.r. techniques. Only four main species are evident; two, which have Mo: L ratios of 1∶1 and 1∶2, are bondedvia a carboxylic oxygen atom and an adjacent hydroxyl oxygen atom. The 1∶2 species forms stereospecifically. The other two main species contain bridging tartaric acid molecules, and a 2∶2 species, also formed stereo-specifically in solution, have been isolated and characterised in the solid state. A limited number of experiments with racemic acid and meso-tartaric acid indicate that only a few species are formed in these systems and with a good deal of stereospecificity also.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary [Ru(TPT)2]2+ undergoes nucleophilic attack at the ligand in aqueous solutions of HO−. The reaction is reversible and the equilibrium can be followed spectrophotometrically. In acid solution, the free nitrogen atoms of the uncoordinated pyridine residues are protonated to form a new species. Two reactions of [Fe(TPT)2]2+ take place in H2O over extended periods. The first is the well-known dissociative process, but the second appears to involve reaction at the ligand. The results are used to reinterpret some of the chemistry of complexes of TPT and related ligands.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 15 (1981), S. 96-98 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vicinal and geminal 13CO2H—1H coupling constants are reported for malic and thiomalic acids at various pH values and related, in a comparative manner, to the known conformational information obtained by 1H NMR.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 25 (1987), S. 203-207 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1H NMR ; Ranitidine ; E/Z isomerization ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The E/Z configurational equilibrium of the nitroethylenic moiety of the antiulcer agent ranitidine was studied in aqueous solution and in DMSO-d6 and CDCl3 using 1H and 13C NMR spectroscopy. In aqueous solution the room temperature E/Z isomerization of the unprotonated nitroketenediamine moiety is fast on the NMR time scale, but becomes slow for the species protonated at this moiety owing to intramolecular hydrogen bonding between the nitro group and a neighbouring NH2R+ group. In DMSO-d6 a free energy of activation of the order of 70 kJ mol-1 was estimated for the E/Z isomerization of the unprotonated moiety of ranitidine, in good agreement with values previously found for 2,2-disubstituted nitroethylene model compounds.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 27 (1989), S. 409-430 
    ISSN: 0749-1581
    Keywords: NMR ; Multinuclear spin coupling ; Lone-pair effects ; Substituent effects ; Stereochemistry ; MO ; Sum-over-states models ; Electron delocalization ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The nature and types of lone-pair effects on nuclear spin coupling constants are reviewed in the context of a localized bond description of molecular electronic structure. Emphasis is placed on the importance of residual delocalization involving the otherwise lone-pair orbital, in terms of which the effect of an X lone-pair, when compared with an isoelectronic Y—H or X—H+ group or with an X—R group, and its orientational dependence can be interpreted. One-, two- and three-bond coupling constants are considered and the importance of lone-pair effects for configurational and conformational information is stressed and illustrated. They also serve for a better understanding of substituent inductive effects on coupling constants.A large collection of illustrative examples are presented, with particular attention paid to couplings involving H, C, N, F and P nuclei, organized in a systematic manner into nine categories. The signs of the lone-pair effects on the reduced coupling constants are found to be independent of the actual nuclei under study in the same category. This is taken as an indication that the electron lone-pairs mainly affect the Fermi contact contribution to the coupling and, accordingly, an interpretation is given in terms of simple sum-over-states models. In addition, symmetry-based relationships are established involving the sign of lone-pair effects in coupling constants between nuclei which are a different number of bonds apart.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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