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  • 1
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The nature of internal and overall motions in native (double-stranded) and denatured (single-stranded) DNA fragments 120-160 base pairs (bp) long is examined by molecular-dynamics modeling using 13C-nmr spin-relaxation data obtained over the frequency range of 37-125 MHz. The broad range of 13C frequencies is required to differentiate among various models. Relatively narrow linewidths, large nuclear Overhauser enhancements (NOEs), and short T1 values all vary significantly with frequency and indicate the presence of rapid, restricted internal motions on the nanosecond time scale. For double-stranded DNA monomer fragments (147 bp, 24 Å diam at 32°C), the overall motion is that of an axially symmetric cylinder (τx = ∼10-6 s;τZ = ∼1.8 × 10-8s), which is in good agreement with values calculated from hydrodynamic theory (τx = ∼1.8 × 10-6 s; τZ = ∼2.7 × 10-8 s). The DNA internal motion can be modeled as restricted amplitude internal diffusion of individual C—H vectors of deoxyribose methine carbons C1′, C3′, and C4′, either with conic boundary conditions (τw = ∼4 × 10-9 s, θcone = ∼21°) or as a bistable jump (τA = τB = ∼2 × 10-9 s, θ = ∼15°). We discuss the critical role in molecular-dynamics modeling played by the angle (β) that individual C—H vectors make with the long axis of the DNA helix. Heat denaturation brings about increases in both the rate and amplitude of the internal motion (described by the wobble model with τW = ∼0.2 × 10-9 s, θcone = ∼50°), and overall motion is affected by becoming essentially isotropic (τx = τZ = ∼5 × 10-8 s) for the single-stranded molecules. Since 13C-nmr data obtained at various DNA concentrations for C2′ of the deoxyribose ring is not described well by the above models, a new model incorporating an additional internal motion is proposed to take into account the rapid, extensive, and weakly coupled motion of C2′.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 21 (1983), S. 616-620 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 17O NMR chemical shifts and calculated (ab initio MO theory) electron densities are reported for a series of para-substituted acetophenones, X—C4H6—COCH3, where X = NH2, OCH3, F, Cl, CH3, H, COCH3, CN, NO2. The 17O shifts are very sensitive to the para substituent and cover a range of some 51 ppm. Donors induce upfield shifts and acceptors downfield shifts. The substituent chemical shifts (SCS) correlate precisely with σI and σR+ using the Dual Substituent Parameter (DSP) method. The derived transmission coefficients ρI and ρR indicate that polar and resonance mechanisms contribute approximately equally to the observed substituent effects. The shifts also correlate well with calculated π-electron densities (slope = 1500 ppm per electron) confirming their electronic origin. λmsxn→π* values are also reported, and the role of the average excitation energy, ΔE, in determining 17O SCS values is discussed. It is concluded that variations in ΔE are minor and that the local Δ-electron density is the dominant feature controlling 17O SCS values.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 14 (1980), S. 186-191 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 19F substituent chemical shifts (SCS) of meta- and para-benzoyl fluorides are found to correlate well with substituent parameters using the dual substituent parameter (DSP) equation, indicating that they reflect electronic perturbations induced by the substituent. The direction of the SCS values is such that donating substituents cause upfield shifts whilst acceptors cause downfield shifts. STO-3G calculations indicate that substituents induce only very small changes in π-electron density about the fluorine atom, but that these changes correlate reasonably well with the observed SCS values. For the para series, the slope of the relationship between δqπF and 19F SCS is 5000 ppm/electron, indicating the great sensitivity of the flourine atom to small changes in electron density.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 15 (1981), S. 248-256 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 19F substituent chemical shifts (SCS) of a series of para-phenylacetyl fluorides (X—Ph—CH2—COF) are reported and compared with the related benzoyl fluoride series (X—Ph—COF). A dual substituent parameter analysis of the results for the new series shows that both inductive and resonance effects are reduced by one third when compared with the benzoyl fluorides. 13C shifts for the side chain carbonyl were also measured and found to follow a reversed trend in substituent effects, consistent with a pi polarization mechanism. SCS values for the fluorine and its adjacent carbon are not directly related. Ab initio (STO-3G) calculations of the carbon and fluorine electron density for this series have been compared with the appropriate SCS values. From the electron densities and the observation that the fluorine SCS values follow a normal direction, whilst those for electron densities and the observation that the fluorine SCS values follow a normal direction, whilst those for the adjacent carbon are reversed, it is concluded that fluorine SCS values (and Δqπ values) result from polarization of the C—F pi bond and do not merely monitor changes in electron density of the adjacent carbon.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 28 (1990), S. 533-540 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Spin-lattice relaxation times ; Nuclear Overhauser enhancement ; Tricyclic antidepressants ; Solution molecular dynamics ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR spin-lattice relaxation times (T1s) and nuclear Overhauser enhancements (NOE's) were measured for a series of clinically used tricyclic antidepressants (TCAs), imipramine (1), amitriptyline (2), doxepin (3) and dothiepin (4), at two magnetic field strengths (corresponding to 13C frequencies of 75 and 100 MHz). The measurements were carried out at a range of solution concentrations in CDCI3 and D2O in order to determine the factors that influence overall and internal molecular dynamics in these systems. Both the hydrochloride salts and free bases were examined. For solutions in CDCI3 over a range of concentrations, or for low-concentration (0.03 M) solutions in D2O, T1 and NOE measurements were independent of magnetic field strength, indicating that motion of the TCAs was in the ‘extreme narrowing limit.’ In contrast, for 0.3 M solutions of the hydrochloride salts in D2O, T1 and NOE measurements were field dependent, indicating the presence of significantly slower molecular mobility. It is proposed that micelles are present at this concentration and are responsible for reduced overall tumbling of the TCAs. Several degrees of internal motion were detected by the relaxation and T1 measurements, viz. rapid flexing motion of the benzylic bridging carbons in the central seven-membered ring and segmental motion of the side-chain. From an examination of the effect of solvent, concentration and protonation state of the side-chain on the latter motion, it was possible to derive information on side-chain conformations and interactions.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 335-342 
    ISSN: 0749-1581
    Keywords: NMR ; 1H NMR ; 13C NMR ; Conformational analysis ; Coupling constants ; NOE ; Non-steroidal anti-inflammatory drugs ; Mefenamic acid ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H and 13C NMR spectra of the non-steroidal anti-inflammatory drugs mefenamic acid, meclofenamic acid and flufenamic acid were assigned and the solution dynamics and conformations of the compounds were probed by the analysis of NMR chemical shifts, temperature coefficients, 3J(C,H) coupled constants, nuclear Overhauser enhancement (NOE) effects and saturation transfer experiments. At low concentrations the anthranilic acid derivatives (the fenamates) exist as monomer units with intramolecular hydrogen bonding between the amine proton and the carboxylic acid group. At concentrations of 10 mM and above, solution aggregates exist. The intermolecular association does not disrupt the intramolecular N—H…O=C hydrogen bonding, resulting in a similar conformation for mefenamic and flufenamic acids at both low and high concentrations. Meclofenamic acid has an additional intramolecular hydrogen bond, resulting in a slightly different conformation to the other two fenamates. The results from this conformational study are of potential value in molecular and pharmacophore modelling studies on the bioactive conformations of these drugs.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 509-516 
    ISSN: 0749-1581
    Keywords: NMR ; 1H NMR ; 13C NMR ; Hoechst 32985 ; Dynamics of piperazine rings ; pKa ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H NMR spectra of the dipiperazine-based DNA minor groove binding compound Hoechst 32985 indicate that at room temperature and low pH (2.90) a single conformation is detected. This is attributed to the form in which both piperazine rings are protonated at the N-methyl and the bulky methyl and aromatic groups are in an equatorial arrangement. The aliphatic regions of the spectra broaden considerably with an increase in either temperature or pH, indicating the presence of a dynamic exchange process. This process results in interchange of axial and equatorial environments of the piperazine ring protons and is attributed to combined ring and nitrogen inversions. Analysis of the variable-temperature spectra for a solution at pH 2.90 allowed a Gibb's free energy of activation (ΔG
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 33 (1995), S. 367-374 
    ISSN: 0749-1581
    Keywords: NMR ; 1H NMR ; 13C NMR ; antidepressants ; trimipramine maleate ; nitrogen inversion ; molecular dynamics ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The solution conformations and dynamics of the antidepressant drug trimipramine maleate were investigated by 1H and 13C NMR spectroscopy. Of particular interest was an observed non-equivalence of the N-methyl groups in the aliphatic side-chain of the drug, which is present in both 1H and 13C spectra under a range of aqueous and non-aqueous solvent conditions when the terminal nitrogen is protonated. Although the inequivalence was first observed for the maleate salt, the nature of the counter ion is not a determining factor. The solution concentration of the drug does, however, modulate the observed inequivalence, with the two peaks coalescing at higher drug concentrations. The diastereotopic environments of the two methyl groups arise because of a chiral centre in the aliphatic side-chain. Inversion of the terminal nitrogen produces exchange between the two environments, thereby destroying the inequivalence and leading to a single averaged resonance for the two methyl groups. The energy barrier for the exchange process was determined from variable-temperature NMR experiments to be 16.3 kcal ml-1 (1 kcal = 4.184 kJ). This is higher than would be expected for simple inversion of a tertiary nitrogen, but reflects the fact that inversion can only occur for the small fraction of molecules which are not protonated. The barrier determined from the variable-temperature experiments was in agreement with rates of interchange between the two methyl environments determined from saturation transfer experiments. These rates were measured for a series of different protonation states of the nitrogen, with the rate contant for interchange of environments decreasing with an increasing degree of nitrogen protonation. 13C spin-lattice relaxation times and nuclear Overhauser enhancement effects were also measured to determine the degree of mobility in the aliphatic side-chain of trimipramine maleate.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 28 (1990), S. 824-829 
    ISSN: 0749-1581
    Keywords: 13C NMR chemical shifts ; oxazine derivatives ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR chemical shifts are reported for six pyridoxal-derived and fourteen salicylaldehyde-derived oxazines and their immediate precursors. Similar data for seven vitamin B6-related compounds are also reported.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 31 (1993), S. 222-230 
    ISSN: 0749-1581
    Keywords: Amphetamines ; NMR ; Relaxation times ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of phenylethylamine and amphetamine derivatives were synthesized in order to determine the nature of the internal and overall molecular dynamics in these systems. 13C and 2H NMR relaxation times were measured. For the latter measurements, compounds specifically deuteriated in the side-chains were synthesized. The relaxation data were analysed via a computer model incorporating the spectral density function for axially symmetric anisotropic motion. The motion of these molecules was found to be substantially anisotropic, with rotation about the symmetry axis of the molecule being at least twice as fast as rotation normal to the symmetry axis. The results of more complex models of axially symmetric anisotropic molecular motion, involving internal rotation or conic diffusion of the side-chains, were found to be sensitive to variation of the input data, but the correlation times for internal rotation of the ring - C-β bond were longer than might have been expected. Similarly, owing to its flexibility, the effective correlation times of atoms in the side-chain were found to be faster than those of the ring carbons, but did not always decrease along the side chain. Intermolecular interactions or aggregation states in CDCl3 may reduce segmental motion of side-chains. A particular feature of the current study is that it was demonstrated that deuteriation of the side-chain gives a unique opportunity to determine independently side-chain correlation times via the quadrupolar relaxation times of the 2H nucleus, and to compare these results with those of the carbon atoms. These correlation times were found to be in very good agreement with those obtained from the 13C data.
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