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Beryllium electronic structure

The L shell can accommodate a total of 8 electrons, and as further electrons are added to form the sequence of elements beryllium, boron, carbon, etc., these electrons take their place in the second shell until finally, at the end of the second period, neon (Z = 10) is reached, with both the first and second shells fully occupied and with an electronic structure which can be symbolized as (2, 8). The addition of further electrons to form the sequence of elements sodium, magnesium, etc., of the third period requires the formation of a new shell, and in sodium (Z = 11) a single electron occupies the M shell of principal quantum number 3 again the ionization energies reflect the difference in energy between this electron and those more tightly bound in the L and K shells. [Pg.14]

The Electronic Structures of Lithium, Beryllium, Boron, and Silicon... [Pg.589]

The beryllium atom has the valence electronic structure 2/. The electronic configuration of Be2 would be This configura-... [Pg.56]

There is a slight decrease in AHjj between beryllium and boron. Although boron has one more proton than beryllium, there is a slight decrease in AH. on removal of the outer electron. Beryllium has the electronic structure Is 2s and boron has the electronic structure Is 2s 2pL The fifth electron in boron must be in the 2p subshell, which is slightly further away from the nucleus than the 2s subshell. There is less attraction between the fifth electron in boron and the nucleus because ... [Pg.52]

The hydrides of beryllium and magnesium are both largely covalent, magnesium hydride having a rutile (p. 36) structure, while beryllium hydride forms an electron-deficient chain structure. The bonding in these metal hydrides is not simple and requires an explanation which goes beyond the scope of this book. [Pg.127]

Staeking faults and sometimes proper polytypism are found in many inorganic compounds - to pick out just a few, zinc sulphide, zinc oxide, beryllium oxide. Interest in these faults arises from the present-day focus on electron theory of phase stability, and on eomputer simulation of lattice faults of all kinds investigators are attempting to relate staeking-fault concentration on various measurable character-isties of the compounds in question, such as ionicity , and thereby to cast light on the eleetronic strueture and phase stability of the two rival structures that give rise to the faults. [Pg.121]

There are a few species in which the central atom violates the octet rule in the sense that it is surrounded by two or three electron pairs rather than four. Examples include the fluorides of beryllium and boron, BeF2 and BF3. Although one could write multiple bonded structures for these molecules in accordance with the octet rule (liable 7.2), experimental evidence suggests the structures... [Pg.173]

Beryl. 385 Beryllium atomic size, 379 boiling point, 374 bonding capacity, 285 chemistry of, 382 electron configuration. 378 heat of vaporization, 374 ionization energies, 379 occurrence, 384 preparation, 385 properties, 381 structure, 381... [Pg.456]

It was concluded by Zachariasen [Norsk geol. Tidsskrift, 8, 189 (1925) Z. physik. Chem., 119, 201 (1926)] from the intensities of reflection of x-rays that beryllium oxide does not contain Be++ and O" ions. However, it has since been shown by Claassen [ibid., 124, 139 (1926)] and Zachariasen himself [Z. Physik, 40, 637 (1926)] that if the electron distribution of the ions is taken into account, the x-ray measurements are compatible with an ionic structure. [Pg.279]

It is also shown that theoretically a binary compound should have the sphalerite or wurzite structure instead of the sodium chloride structure if the radius ratio is less than 0.33. The oxide, sulfide, selenide and telluride of beryllium conform to this requirement, and are to be considered as ionic crystals. It is found, however, that such tetrahedral crystals are particularly apt to show deformation, and it is suggested that this is a tendency of the anion to share an electron pair with each cation. [Pg.281]

A polymeric structure is exhibited by "beryllium dimethyl," which is actually [Be(CH3)2] (see the structure of (BeCl2) shown earlier), and LiCH3 exists as a tetramer, (LiCH3)4. The structure of the tet-ramer involves a tetrahedron of Li atoms with a methyl group residing above each face of the tetrahedron. An orbital on the CH3 group forms multicentered bonds to four Li atoms. There are numerous compounds for which the electron-deficient nature of the molecules leads to aggregation. [Pg.127]

The structure of dimethylberyllium is similar to that of trimethylaluminum except for the fact that the beryllium compound forms chains, whereas the aluminum compound forms dimers. Dimethylberyllium has the structure shown in Figure 12.3. The bridges involve an orbital on the methyl groups overlapping an orbital (probably best regarded as sp3) on the beryllium atoms to give two-electron three-center bonds. Note, however, that the bond angle Be-C-Be is unusually small. Because beryllium is a Lewis acid, the polymeric [Be(CH3)2] is separated when a Lewis base is added and adducts form. For example, with phosphine the reaction is... [Pg.402]

Therefore beryllium can have two half filled orbitals and two (unpaired electrons) in its excited state and form the BeH2 molecule with hydrogen. The bond structure of BeH2 is given below ... [Pg.28]

Some atoms are able to form compounds even though the resulting structure doesn t provide eight valence electrons. For example beryllium and boron do not complete their octet in their covalent compounds because these atoms have less than four valence electrons. For example, in BeF2 (F - Be - F) beryllium shares its two valance electrons but it doesn t complete its octet, it is only surrounded by four electrons. In BF3, the boron atom shares its three valence electrons but does not complete its octet as it has just three electron pairs (six electrons) surrounding it. [Pg.42]

Figure 12.20 shows the structure of the side-window circular cage type and linear focused head-on type of photomultiplier which are both preeminent in fluorescence studies. The lower cost of side-window tubes tends to favor their use for steady-state studies, whereas the ultimate performance for lifetime studies is probably at present provided by linear focused devices. In both types internal current amplification is achieved by virtue of secondary electron emission from discrete dynode stages, usually constructed of copper-beryllium (CuBe) alloy, though gallium-phosphide (GaP) first dynodes have been used to obtain higher gains. [Pg.402]


See other pages where Beryllium electronic structure is mentioned: [Pg.138]    [Pg.129]    [Pg.296]    [Pg.251]    [Pg.1235]    [Pg.162]    [Pg.99]    [Pg.7]    [Pg.186]    [Pg.119]    [Pg.121]    [Pg.112]    [Pg.1234]    [Pg.5185]    [Pg.63]    [Pg.72]    [Pg.90]    [Pg.177]    [Pg.227]    [Pg.475]    [Pg.27]    [Pg.131]    [Pg.127]    [Pg.29]    [Pg.71]    [Pg.551]    [Pg.556]    [Pg.67]    [Pg.227]   
See also in sourсe #XX -- [ Pg.33 ]




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Beryllium: electrons

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