Magnetic properties paramagnetic term

Electrical and magnetic properties of complexes of TMBP and TMBTP with HCNB are presented. If seems that the observed paramagnetism of TMBP HCNB complex can be separated into an extrinsic Curie term and the intrinsic component, the latter being only slightly temperature dependent. 

To study the magnetic properties of matter one would often like to be able to obtain information on the currents in the system and their coupling to possible external magnetic fields. Important classes of experiments for which this information is relevant are nuclear magnetic resonance and the quantum Hall effects. SDFT does not provide explicit information on the currents. RDFT in principle does, but standard implementations of it are formulated in a spin-only version, which prohibits extraction of information on the currents. Furthermore, the formalism of RDFT is considerably more complicated than that of SDFT. In this situation the formulation of nonrelativistic current-DFT (CDFT), accomplished by Vignale and Rasolt [140, 141], was a major step forward. CDFT is formulated explicitly in terms of the (spin) density and the nonrelativistic paramagnetic current density vector jp(r). Some recent applications of CDFT are Refs. [142, 143, 144, 145]. E. K. U. Gross and the author have shown that the existence of spin currents implies the existence of a link between the xc functionals of SDFT and those of CDFT [146], Conceptually, this link is similar to the one of Eq. (99) between functionals of DFT and SDFT, but the details are quite different. Some approximations for xc functionals of CDFT are discussed in Refs. [146, 147, 148]. 

Bertini et report a detailed study of the magnetic properties of myglobin, in which they determined the axial and orthorhombic terms of the paramagnetic susceptibility tensor using a combination of hyperfine chemical shift measurements and static suscetibility measurements (Evans Method). The determination of the magnetic anisotropy provided a measurement of the residual dipolar couplings and also permitted a separation of the contact and pseudocontact chemical shift contributions of resonances of the Fe(III) ligands. 

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