Metallic Solids

Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms.  The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties. All exhibit high thermal and electrical conductivity, metallic luster, and malleability. Many are very hard and quite strong. Because of their malleability (the ability to deform under pressure or hammering), they do not shatter and, therefore, make useful construction materials.

Metals are characterized by their ability to reflect light, called luster, their high electrical and thermal conductivity, their high heat capacity, and their malleability and ductility. Every lattice point in a pure metallic element is occupied by an atom of the same metal. The packing efficiency in metallic crystals tends to be high, so the resulting metallic solids are dense, with each atom having as many as 12 nearest neighbors.

Figure 11.8.5

: Copper is a metallic solid. Image used with permission of OpenStax.

Bonding in metallic solids is quite different from the bonding in the other kinds of solids we have discussed. Because all the atoms are the same, there can be no ionic bonding, yet metals always contain too few electrons or valence orbitals to form covalent bonds with each of their neighbors. Instead, the valence electrons are delocalized throughout the crystal, providing a strong cohesive force that holds the metal atoms together.  Valence electrons in a metallic solid are delocalized, providing a strong cohesive force that holds the atoms together.

The strength of metallic bonds varies dramatically. For example, cesium melts at 28.4°C, and mercury is a liquid at room temperature, whereas tungsten melts at 3680°C. Metallic bonds tend to be weakest for elements that have nearly empty (as in Cs) or nearly full (Hg) valence subshells, and strongest for elements with approximately half-filled valence shells (as in W). As a result, the melting points of the metals increase to a maximum around group 6 and then decrease again from left to right across the d block. Other properties related to the strength of metallic bonds, such as enthalpies of fusion, boiling points, and hardness, have similar periodic trends.

Figure 1.1 : The Electron-Sea Model of Bonding in Metals. Fixed, positively charged metal nuclei from group 1 (a) or group 2 (b) are surrounded by a “sea” of mobile valence electrons. Because a group 2 metal has twice the number of valence electrons as a group 1 metal, it should have a higher melting point.

A somewhat oversimplified way to describe the bonding in a metallic crystal is to depict the crystal as consisting of positively charged nuclei in an electron sea (Figure 1.1). In this model, the valence electrons are not tightly bound to any one atom but are distributed uniformly throughout the structure. Very little energy is needed to remove electrons from a solid metal because they are not bound to a single nucleus. When an electrical potential is applied, the electrons can migrate through the solid toward the positive electrode, thus producing high electrical conductivity. The ease with which metals can be deformed under pressure is attributed to the ability of the metal ions to change positions within the electron sea without breaking any specific bonds. The transfer of energy through the solid by successive collisions between the metal ions also explains the high thermal conductivity of metals. This model does not, however, explain many of the other properties of metals, such as their metallic luster and the observed trends in bond strength as reflected in melting points or enthalpies of fusion. Some general properties of the four major classes of solids are summarized in Table 1.1.

مواضيع ذات صلة

التفاعل مع اصباغ الازو

تفاعل الجالكونات مع البروم

تفاعل الجالكونات مع الهكسانون الحلقي

تفاعل الجالكونات مع اليوريا ومعوضاته

تفاعل الجالكونات مع البيروكسيدات

تفاعل الجالكون مع الهيدرازين والفنيل هيدرازين

مركبات الجالكون Chalcone Compounds

تفاعل إضافة مايكل

الاضافة الالكتروفيلية الى مركبات الكاربونيل ألفا – بيتا غير المشبعة

تفاعلات تكاثف مركبات الكاربونيل

تحضير مركبات الكاربونيل ألفا – بيتا غيرالمشبعة

مركبات الكاربونيل ألفا – بيتا غير المشبعة