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1 anides exhibit similar, but distinguishable, hyperfine coupling constants.
2 gely a type 1 copper protein at low pH (with hyperfine coupling constant A( parallel) = 54 x 10(-4) c
3  indicate that electron spin resonance (ESR) hyperfine coupling constants (aH values) computed at the
4  spectra and < 8 gauss changes in the copper hyperfine coupling constants (AII) in the X-band electro
5 in the ligand moiety and the (13)C isotropic hyperfine coupling constants, Aiso((13)C), for the indiv
6                                    The (13)C hyperfine coupling constants also provide an independent
7                                 The measured hyperfine coupling constant and associated bond length s
8                                          The hyperfine coupling constants and geometry of the NH(2) m
9 ons of molecular spin-orbitals (MSOs) to the hyperfine coupling constants and the spatial distributio
10 agreement with the observed g values, ligand hyperfine coupling constants, and FTIR stretching freque
11 ance for predicting NMR chemical shifts, EPR hyperfine coupling constants, and low-energy transitions
12 ble-temperature magnetic susceptibility, EPR hyperfine coupling constants, and the results of X-ray c
13  = 1.9887, g(y) = 1.9957, g(z) = 1.9775, and hyperfine coupling constants are A(III)(x) = |171| G, A(
14                                          The hyperfine coupling constants are consistent with a struc
15 et constraints on the relative amplitudes of hyperfine coupling constants, both for protons at chemic
16  addition to electron paramagnetic resonance hyperfine coupling constants, can now be calculated for
17                            Moreover, the 19F hyperfine coupling constants computed with the MP2 metho
18  three new nitrogen resonances appear having hyperfine coupling constants consistent with histidine l
19                                        These hyperfine coupling constants correlate well with those r
20 MDL 101,002 yielded a six-line spectrum with hyperfine coupling constants distinct from that of PBN.
21                                    Isotropic hyperfine coupling constants for the ligand nitrogen ato
22 5F10*-) are reported and their isotropic 19F hyperfine coupling constants (hfcc) of 198.6 +/- 0.4 G,
23                                          The hyperfine coupling constants (HFCs) determined from the
24                The magnitude of the nitrogen hyperfine coupling constant in the latter species unambi
25  shifts, and electron paramagnetic resonance hyperfine coupling constants in a model Fe(II)(NO)(imida
26 urately estimated by correlation with proton hyperfine coupling constants in antecedent monoradicals,
27 C isotope shifts in the IR spectra and (13)C hyperfine coupling constants in the EPR spectra exhibit
28 pectroscopy revealed a 9-line spectrum, with hyperfine coupling constants indicative of four almost m
29                                          The hyperfine coupling constant is determined for each compo
30 rongly coupled nonexchangeable proton with a hyperfine coupling constant of 50 MHz.
31 isotropic signal with a g value of 2.003 and hyperfine coupling constant of 8 x 10(-4) cm(-1) to the
32                                      The 17O hyperfine coupling constant of H2(17)O is determined as
33                                          The hyperfine coupling constant of the g = 2 signal in the E
34 t polarity constant E(T)(N) and the nitrogen hyperfine coupling constant of the released nitroxide a(
35  different pictures of the dependence of the hyperfine coupling constant of the trapped H atom upon t
36 ) gave rise to a distinct (13)C signal, with hyperfine coupling constants of 4.9 MHz for (13)C(a), 1.
37 n of the cluster is highly anisotropic, with hyperfine coupling constants of 9.1 and 2 x 33.3 G for t
38 igned to a thiyl radical adduct based on its hyperfine coupling constants of aN = 14.7 G and abetaH =
39 ild-type ESEEM modulation (denoted N1) has a hyperfine-coupling constant of Aiso = 1.05 MHz and nucle
40 stretching frequency and the imidazole (14)N hyperfine coupling constants show a good correlation wit
41  The Sc-based hyperfine structure with large hyperfine coupling constants shows that both oxidation a
42 duced two radical species in urine, one with hyperfine coupling constants similar to the 4-POBN/methy
43     Assuming a free-ion value for the Pu(4+) hyperfine coupling constant, we estimated a bare (239)ga
44    Following DFT calculations, the predicted hyperfine coupling constants were used to simulate the E

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