A phenomenological treatment of the absolute signs of spin-spin coupling constants.
Spin-spin coupling constants from perturbation- variation and first order perturbed trial function assumptions
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Spin-spin coupling constants from perturbation- variation and first order perturbed trial function assumptions
The N hyperfine coupling constant has been computed using multireference configuration interaction (MRCI) and averaged coupled pair functional (ACPF) treatments in very large one-particle basis sets. Unlike previous calculations, no selection of configurations has been performed. The calculations again illustrate the difficulty of computing the N hyperfine coupling constant accurately. The best MRCI result of 10.7 MHz is larger than the accurate experimental value of 10.4509 MHz, while the best ACPF result (10.3 MHz) is smaller than experiment. The difference between this work and previous calculations is discussed.
The FP-INDO (finite perturbation-intermediate neglect of differential overlap) method is used to calculate the H-H, C-H, and C-C coupling constants in hertz for molecules of six different benzenoid hydrocarbons: benzene, naphthalene, biphenyl, anthracene, phenanthrene, and pyrene. The calculations are based on both the actual and the average molecular geometries. It is found that only the actual molecular geometries can always yield the correct relative order of values for the H-H coupling constants. For the calculated C-C coupling constants, as for the calculated C-H coupling constants, the signs are positive (negative) for an odd (even) number of bonds connecting the two nuclei. Agreements between the calculated and experimental values of the coupling constants for all six molecules are comparable to those reported previously for other molecules.
The possibility of a Brans-Dicke scalar-tensor gravitation theory with a negative coupling constant is considered. The admissibility of a negative-coupling theory is investigated, and a simplified cosmological solution is obtained which allows a negative derivative of the gravitation constant. It is concluded that a Brans-Dicke theory with a negative coupling constant can be a viable alternative to general relativity and that a large negative value for the coupling constant seems to bring the original scalar-tensor theory into close agreement with perihelion-precession results in view of recent observations of small solar oblateness.
The nitrogen-atom isotropic hyperfine coupling constant A(iso) is studied as a function of improvements in both the one-particle and n-particle basis sets. The study underscores the importance of diffuse basis functions. For example, the (9s 5p) primitive set of Huzinaga (1965) augmented with an even-tempered diffuse s function yields values for A(iso) that are virtually identical to an energy-optimized (23s 12p) even-tempered set. The A(iso) constant is found to converge relatively quickly with increasing l quantum numbers: d, f, and g functions are estimated to contribute 2.5 + or - 0.2, 0.4 + or - 0.1, and 0.05 + or - 0.05 MHz, respectively. Full CI calibration calculations indicate that very high levels of correlation treatment are required for quantitative results. In addition, a strong coupling is observed between the one-particle and n-particle requirements. The best result, 10.4 MHz, is in excellent agreement with the accurate experimental value of 10.4509 MHz.
Relative signs and magnitudes of proton nuclear magnetic resonance coupling constants in phosphorus compounds
Phosphorous-proton nuclear magnetic resonance coupling constants - sign determination
The letter reports resolved measurements of the quadrupole hyperfine structure of HNC (hydrogen isocyanide). These measurements were made in the direction of the cool interstellar dust cloud L134, and were used to make an experimental determination of a fundamental spectroscopic constant of HNC, its quadrupole coupling constant.
Signs of phosphorus-fluorine nuclear resonance spin-spin coupling constants
Input and output coupling constants of spin-2 mesons with two pseudo-scalar mesons obtained by producing resonances at experimentally observed positions
Spin-two meson coupling constants with two pseudoscalar mesons with appropriate quantum number
Relative signs of nuclear magnetic resonance proton-proton coupling constants in styrene sulfide and styrenimine
Boron 11 nuclear quadrupole coupling constants in solid boron halides, finding fine structure on nuclear magnetic resonance in boron fluoride
The Na-23 nuclear quadrupole coupling constant in Rochelle salt is found to have a linear dependence on temperature which extends through both the higher- and lower-temperature nonferroelectric phases. This result necessitates a reinterpretation of some earlier data, but is in perfect agreement with the recent calculations of Zeks, Shulka, and Blinc.
Distinguishing the enantiomers of small organic molecules is an industrially relevant problem with important implications for the health of the population. In a recent publication, Bouchard and co-workers have suggested that large differences in indirect spin-spin (J) coupling constants between enantiomers are possible. A close inspection of their work revealed significant flaws in their density functional theory (DFT) calculations and that the reported effects disappear with appropriate care. We thus conclude that enantiospecificity in spin-spin coupling constants has not be demonstrated either experimentally or theoretically.
Hyperfine coupling constants of positive divalent Mn ion in calcium and barium fluorides, measuring temperature dependence by analyzing electron spin resonance spectrum
Relative signs of nuclear spin coupling constants in propylene oxide and indene oxide obtained from iterative analysis of NMR spectra
Fluorine-19-fluorine-19 and hydrogen-1-fluorine-19 nuclear magnetic resonance coupling constants