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Boron ionization energy

Elemental boron has a diverse and complex chemistry, primarily influenced by three circumstances. Eirst, boron has a high ionization energy, 8.296 eV, 23.98 eV, and 37.75 eV for first, second, and third ionization potentials, respectively. Second, boron has a small size. Third, the electronegativities of boron (2.0), carbon (2.5), and hydrogen (2.1) are all very similar resulting in extensive and unusual covalent chemistry. [Pg.183]

The electron-deficient character of boron also affects its aHotropic forms. The high ionization energies and small size prevent boron from adopting... [Pg.183]

Boron is unique among the elements in the structural complexity of its allotropic modifications this reflects the variety of ways in which boron seeks to solve the problem of having fewer electrons than atomic orbitals available for bonding. Elements in this situation usually adopt metallic bonding, but the small size and high ionization energies of B (p. 222) result in covalent rather than metallic bonding. The structural unit which dominates the various allotropes of B is the B 2 icosahedron (Fig. 6.1), and this also occurs in several metal boride structures and in certain boron hydride derivatives. Because of the fivefold rotation symmetry at the individual B atoms, the B)2 icosahedra pack rather inefficiently and there... [Pg.141]

The mles can readily be extended to isoelectronic anions and carbaboranes (BH=B =C) and also to metalloboranes (p. 174), metallocarbaboranes (p. 194) and even to metal clusters themselves, though they become less reliable the further one moves away from boron in atomic size, ionization energy, electronegativity, etc. [Pg.178]

If you look carefully at Figure 6.15, you will note a few exceptions to the general trends referred to above and illustrated in Example 6.11. For example, the ionization energy of B (801 kj/mol) is less than that of Be (900 kj/mol). This happens because the electron removed from the boron atom comes from the 2p as opposed to the 2s sublevel for beryllium. Because 2p is higher in energy than 2s, it is not too surprising that less energy is required to remove an electron from that sublevel. [Pg.156]

The first four ionization energies of boron atoms are as follows ... [Pg.273]

Self-Test 1.14A Account for the slight decrease in first ionization energy between beryllium and boron. [Pg.168]

Metallic elements with low ionization energies commonly form basic ionic oxides. Elements with intermediate ionization energies, such as beryllium, boron, aluminum, and the metalloids, form amphoteric oxides. These oxides do not react with or dissolve in water, but they do dissolve in both acidic and basic solutions. [Pg.704]

Boron forms perhaps the most extraordinary structures of all the elements. It has a high ionization energy and is a metalloid that forms covalent bonds, like its diagonal neighbor silicon. However, because it has only three electrons in its valence shell and has a small atomic radius, it tends to form compounds that have incomplete octets (Section 2.11) or are electron deficient (Section 3.8). These unusual bonding characteristics lead to the remarkable properties that have made boron an essential element of modern technology and, in particular, nan otechn ol ogy. [Pg.718]

Arrange the following atoms in order of increasing first ionization energy boron, thallium, gallium. [Pg.738]

The first ionization energy for boron is lower than what you would predict, based on the general trend for ionization energy across a period. Explain this exception to the trend. [Pg.215]

For implanted acceptor activation there have been several reviews during the last few years since Troffer et al. s often-cited paper on boron and aluminum from 1997 [88]. Aluminum is now the most-favored choice of acceptor ion despite the larger mass, which results in substantially more damage compared with implanted boron. Mainly it is the high ionization energy for boron that results in this choice, as well as its low solubility. In addition, boron has other drawbacks, such as an ability to form deep centers like the D-center [117] rather than shallow acceptor states and, as shown in Section 4.3.2, boron ions also diffuse easily at the annealing temperatures needed for activation. The diffusion properties may be used in a beneficial way, although it is normally more convenient if the implanted ion distribution is determined by the implant conditions alone. [Pg.146]

The formation of a metal structure from free atoms must be associated with ionization, from which it follows that a high ionization energy in an element prevents it. Metallic properties are therefore found in the alkali- and alkaline-earth elements. Boron, the first element in the third group, is hardly metallic in this group the element with the smallest ionic radius loses its metallic character. [Pg.239]

Metallic elements with low ionization energies commonly form ionic oxides. As remarked in Section 10.1, the oxide ion is a strong base, so the oxides of most of these metals form basic solutions in water. Magnesium is an exception because its oxide, MgO, is insoluble in water. However, even this oxide reacts with acids, so it is regarded as basic. Elements with intermediate ionization energies, such as beryllium, boron, aluminum, and the metalloids, form amphoteric oxides. These oxides do not react with water, but they do dissolve in both acidic and basic solutions. [Pg.802]

The addition of a trivalent atom (e.g. boron) to silicon leads to an empty electron state, or positive hole, which can be ionized from the effective single negative charge — e on the B atom. The ionization energy is again about 0.01 eV, as might be expected. Therefore the doping of silicon with boron leads to the... [Pg.33]

In Fig. 12.35 we see that there are some discontinuities in ionization energy in going across a period. For example, discontinuities occur in Period 2, in going from beryllium to boron and from nitrogen to oxygen. These exceptions to the normal trend can be explained in terms of how electron repulsions depend on the electron configuration. We will discuss the elements in Period 2 individually to further develop the concept of shielding. [Pg.562]

Rather different, and higher, values of the boron-boron bond energies were obtained by Dibeler and his co-workers from photoionization mass spectrometric studies of B2F4 and B2CI4 and the corresponding trihalides. Essentially, this work combines known heats of formation of the subhalides (106) with threshold energies for dissociative ionization processes such as... [Pg.248]


See other pages where Boron ionization energy is mentioned: [Pg.215]    [Pg.65]    [Pg.215]    [Pg.65]    [Pg.312]    [Pg.183]    [Pg.25]    [Pg.144]    [Pg.145]    [Pg.456]    [Pg.201]    [Pg.569]    [Pg.1522]    [Pg.643]    [Pg.146]    [Pg.68]    [Pg.183]    [Pg.223]    [Pg.251]    [Pg.312]    [Pg.659]    [Pg.659]    [Pg.11]    [Pg.131]    [Pg.133]    [Pg.562]    [Pg.563]    [Pg.43]    [Pg.49]    [Pg.244]   
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