F-electrons

Because the neutron has a magnetic moment, it has a similar interaction with the clouds of impaired d or f electrons in magnetic ions and this interaction is important in studies of magnetic materials. The magnetic analogue of the atomic scattering factor is also tabulated in the International Tables [3]. Neutrons also have direct interactions with atomic nuclei, whose mass is concentrated in a volume whose radius is of the order of... 

Egerton, R. F., Electron Energy-Loss Spectroscopy in the Electron Microscope, 2nd edn.. Plenum Press, New York-London, 1996. 

According to this assignment the differentiating electron, that is, the final electron to enter the atom of lutetium, wss seen as an f electron. This suggested that lutetium should be the final element in the first row of the rare earth elements, in which f electrons are progressively filled, and not a transition element as had been believed by the chemists. As a result of more recent spectroscopic experiments the configuration of ytterbium has been altered to (27)... 

Mazda, F. F., Electronics Engineer s Reference Book, 6th Edition, Butterworths, 1989. 

Mixing of LS-states by spin orbit coupling will be stronger with an increasing number of f-electrons. As a consequence, intermediate values of Lande g factor and reduced crystal field matrix elements must be used. 

Thus the rather easily obtained atomic sizes are the best indicator of what the f-electrons are doing. It has been noted that for all metallic compounds in the literature where an f-band is believed not to occur, that the lanthanide and actinide lattice parameters appear to be identical within experimental error (12). This actually raises the question as to why the lanthanide and actinide contractions (no f-bands) for the pure elements are different. Analogies to the compounds and to the identical sizes of the 4d- and 5d- electron metals would suggest otherwise. The useful point here is that since the 4f- and 5f-compounds have the same lattice parameters when f-bands are not present, it simplifies following the systematics and clearly demonstrates that actinides are worthy of that name. 

Cox PA (1975) Fractional Parentage Methods for Ionisation of Open shells of d and f Electrons. 24 59-81... 

Rosenberg M, Farris F. Electronic systems and decision making. Curr Drug Discov 2003 3 1-4. 

Why do s electrons form a broad band in a metal, while d-electrons give rise to relatively narrow bands What do you expect for bands formed from f electrons ... 

B they may lose f electrons when forming ions... 

Figure 5.6. Diagram of a low-energy, high-angle electron-impact spectrometer. (A) Electron gun (B) monochromator (180° spherical electrostatic energy selector) (C) electron optics (D) scattering chamber (E) analyzer (180° spherical electrostatic energy selector) (F) electron multiplier (G) amplifier and pulse discriminator (H) count-rate meter (I) multichannel scaler (J) X Y recorder (K) digital recorder. (After Kupperman et a/.<42))...

Abstract Hazardous effects of various amines, produced in the environment from the partial degradation of azo dyes and amino acids, adversely affect the quality of human life through water, soil and air pollution and therefore needed to be degraded. A number of such studies are already available in the literature, with or without the use of ultrasound, which have been summarized briefly. The sono-chemical degradation of amines and in the combination with a photocatalyst, TiC>2 has also been discussed. Similar such degradation studies for ethylamine (EA), aniline (A), diphenylamine (DPA) and naphthylamine (NA) in the presence of ultrasound, Ti02 and rare earths (REs) La, Pr, Nd, Sm and Gd, in aqueous solutions at 20 kHz and 250 W power have been carried out and reported, to examine the combinatorial efficacy of ultrasound in the presence of a photocatalyst and rare earth ions with reactive f-electrons. 

Although the role of rare earth ions on the surface of TiC>2 or close to them is important from the point of electron exchange, still more important is the number of f-electrons present in the valence shell of a particular rare earth. As in case of transition metal doped semiconductor catalysts, which produce n-type WO3 semiconductor [133] or p-type NiO semiconductor [134] catalysts and affect the overall kinetics of the reaction, the rare earth ions with just less than half filled (f5 6) shell produce p-type semiconductor catalysts and with slightly more than half filled electronic configuration (f8 10) would act as n-type of semiconductor catalyst. Since the half filled (f7) state is most stable, ions with f5 6 electrons would accept electrons from the surface of TiC>2 and get reduced and rare earth ions with f8-9 electrons would tend to lose electrons to go to stabler electronic configuration of f7. The tendency of rare earths with f1 3 electrons would be to lose electrons and thus behave as n-type of semiconductor catalyst to attain completely vacant f°- shell state [135]. The valence electrons of rare earths are rather embedded deep into their inner shells (n-2), hence not available easily for chemical reactions, but the cavitational energy of ultrasound activates them to participate in the chemical reactions, therefore some of the unknown oxidation states (as Dy+4) may also be seen [136,137]. 

As to the first route, we started in 1969 (1) in investigating unconventional transition metal complexes of the 5 and 4f block elements of periodic table, e.g., actinides and lanthanides as catalysts for the polymerization of dienes (butadiene and isoprene) with an extremely high cis content. Even a small increase of cistacticity in the vicinity of 100% has an important effect on crystallization and consequently on elastomer processability and properties (2). The f-block elements have unique electronic and stereochemical characteristics and give the possibility of a participation of the f-electrons in the metal ligand bond. 

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