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  • 1
    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.
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  • 2
    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.
    Additional Material: 5 Ill.
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  • 3
    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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  • 4
    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′.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 783-791 
    ISSN: 0749-1581
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR spin-lattice relaxation times (T1) have been measured for a series of meta- and para-substituted phenylbicyclo[2.2.2]octanes in CDCl3 solution. The non-equivalence of NT1 values (N = number of attached hydrogens) for the various protonated carbons in these molecules indicates that motion is highly anisotropic. Analysis of the T1 data using the Woessner formalism for axially symmetric ellipsoids yields a set of diffusion coefficients for overall and internal motion. In para-substituted derivatives, motion about the symmetry axis is 3-12 times faster than motion about the perpendicular axes, depending on the substituent. Both the size (inertia) and the interacting properties of the substituent are important in determining the motional anisotropy, as indicated by the following observed order: H 〈 NH2 〈 CH3 〈 NO2 〈 CH2OH 〈 Br 〈 NH3+ 〈 CO2H. The change in anisotropy is a result of the anchoring effect of the substituent (via either its inertia or its hydrogen-bonding ability), which restricts motion about axes perpendicular to the long axis of the molecule. In meta derivatives, a similar model of motional anisotropy is observed, although the absolute magnitudes of diffusion coefficients are smaller than for the para series. In both series, the bicyclooctane ring undergoes fast internal motion relative to the phenyl ring. This reflects the fact that the bicyclooctane ring is able to rotate essentially in its own volume, with minimum disturbance to neighbouring solvent molecules. On the other hand, the planar phenyl ring must displace solvent molecules as it rotates.
    Additional Material: 6 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 26 (1988), S. 275-280 
    ISSN: 0749-1581
    Keywords: Thyroxine ; Triiodothyronine ; Variable-temperature ; 1H NMR ; Activation barriers ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H NMR spectra at 300 and 400 MHz have been recorded for the thyroid hormones thyroxine (T4) and triiodothyronine (T3) over a range of temperatures from 175 to 298 K in MeOH-d4. Above 200 K the aromatic region of the NMR spectrum of T4 consists of two peaks, one for the H-2′, H-6′ protons and one for H-2,H-6. As the temperature is lowered each of these resonances first broadens and then splits into two peaks of equal intensity at low temperature. This is consistent with slowed exchange between two equally populated conformers. Similar behaviour is noted for T3, although in this case the spectrum is complicated by the presence of spin-spin splitting. Consideration of coalescence temperatures and a line-shape analysis yielded activation barriers in the range 35-38 kJ mol-1. It is concluded that the observed spectral changes are due to dynamic interconversion between proximal and distal forms of the hormones, and that the interconversion takes place by cooperative rotations around the bonds between each phenyl ring and the linking oxygen atom.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 862-871 
    ISSN: 0749-1581
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aromatic 13C chemical shifts are reported for an extensive set (15 common substituents) of 1,3-disubstituted benzenes measured at low concentration in deuteriochloroform. The substituent chemical shift data show systematic non-additivity. Data for the para- and two meta-positions to the variable substituent were analysed using the recently developed non-linear resonance (DSP-NLR) and standard (DSP) dual substituent parameter equations. It is shown for these positions that mutual substituent interaction is responsible for the non-additive shifts and that (a) this interaction has both an inductive (polar) and a resonance component, even for meta-oriented substituents, and (b) the shift-charge ratio term extends past the ipso-position. These results are discussed in terms of local paramagnetic shielding contributions to 13C shifts.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 27 (1989), S. 852-862 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Bovine and porcine zinc insulin ; Spectral assignments ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Natural abundance 75 MHz 13C NMR spectral assignments are reported for bovine and porcine zinc insulin in solution. A large number of protein resonances are well resolved, and approximately 80% of these have been assigned to either residue types or to specific sites within the protein. Assignment techniques included consideration of free amino acid or peptide shifts pH studies and comparison of sequence and spectral differences between bovine and porcine insulin, in addition to the use of NMR relaxation times. The DEPT spectral editing technique was also found to be particularly valuable as an assignment aid. This technique allows subspectra containing only CH, CH2 or CH3 carbon types to be generated. The method also produces signal enhancement relative to broad band decoupled 13C NMR spectra of large proteins which generally have reduced nuclear Overhauser enhancements.
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  • 9
    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.
    Additional Material: 4 Ill.
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  • 10
    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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