Group 1. Alkali Metals

These elements form two groups, often called the alkali (Group I) and alkaline earth (Group II) metals. Some of the physical properties usually associated with metals—hardness, high m.p. and b.p.—are noticeably lacking in these metals, but they all have a metallic appearance and are good electrical conductors. Table 6.1 gives some of the physical properties. 

The alkali metals of Group I are found chiefly as the chlorides (in the earth s crust and in sea water), and also as sulphates and carbonates. Lithium occurs as the aluminatesilicate minerals, spodimene and lepidolite. Of the Group II metals (beryllium to barium) beryllium, the rarest, occurs as the aluminatesilicate, beryl-magnesium is found as the carbonate and (with calcium) as the double carbonate dolomite-, calcium, strontium and barium all occur as carbonates, calcium carbonate being very plentiful as limestone. 

Unlike cadmium and mercury and, in fact, all metals of Group II, zinc dissolves readily in alkalis forming zincates. in which the zinc atom is contained in a complex hydroxo-anion, for example ... 

Sodium is present in fair abundance in the sun and stars. The D lines of sodium are among the most prominent in the solar spectrum. Sodium is the fourth most abundant element on earth, comprising about 2.6% of the earth s crust it is the most abundant of the alkali group of metals. 

As with other metals of the alkali group, it decomposes in water with the evolution of hydrogen. It catches fire spontaneously on water. Potassium and its salts impart a violet color to flames. 

Rubidium can be liquid at room temperature. It is a soft, silvery-white metallic element of the alkali group and is the second most electropositive and alkaline element. It ignites spontaneously in air and reacts violently in water, setting fire to the liberated hydrogen. As with other alkali metals, it forms amalgams with mercury and it alloys with gold, cesium, sodium, and potassium. It colors a flame yellowish violet. Rubidium metal can be prepared by reducing rubidium chloride with calcium, and by a number of other methods. It must be kept under a dry mineral oil or in a vacuum or inert atmosphere. 

Hydrogen can be prepared by the reaction of water or dilute acids on electropositive metals such as the alkali metals, alkaline earth metals, the metals of Groups 3, 4 and the lanthanoids. The reaction can be explosively violent. Convenient laboratory methods employ sodium amalgam or calcium with water, or zinc with hydrochloric acid. The reaction of aluminium or ferrosilicon with aqueous sodium hydroxide has also been used. For small-scale preparations the hydrolysis of metal hydrides is convenient, and this generates twice the amount of hydrogen as contained in the hydride, e.g. ... 

The performance of VASP for alloys and compounds has been illustrated at three examples The calculation of the properties of cobalt dislicide demonstrates that even for a transition-metal compound perfect agreement with all-electron calculations may be achieved at much lower computational effort, and that elastic and dynamic properties may be predicted accurately even for metallic systems with rather long-range interactions. Applications to surface-problems have been described at the example of the. 3C-SiC(100) surface. Surface physics and catalysis will be a. particularly important field for the application of VASP, recent work extends to processes as complex as the adsorption of thiopene molecules on the surface of transition-metal sulfides[55]. Finally, the efficiciency of VASP for studying complex melts has been illustrate for crystalline and molten Zintl-phases of alkali-group V alloys. 

Many liquid alloys, in particular, the alkali-group IV alloys, exhibit (Zintl) anion clustering and show strong effects of compound formation. A typical example of such Zintl systems are sodium-tin alloys. In the solid NaSn crystal the Zintl anions Sn appear [1]. An interesting question is the stability of these anions in the liquid. Furthermore, the electrical conductivity of these alloys shows a strong dependence on composition [2] For the limiting (sodium-rich or tin-rich) cases a metallic (small) conductivity appears, but for the nearly equimolar compositions a semi-metallic behavior - with a considerably smaller conductivity - is observed. 

Alkali metal A metal in Group 1 of the periodic table, 31 hydrogen reactions with, 542 oxygen reactions with, 543-544 reactions of, 541t, 552q water reactions with, 542... 

The element hydrogen has been placed by different authors in the alkali metals, in group 14 on top of carbon, among the halogens and sometimes simply allowed to float in an apparently unconnected manner above the main body of the periodic table. Citations for the first placement are unnecessary because this is a frequent choice. For the second, third, and fourth placements, see [36-40]. 

The first alkali metal-niobium-arsenic compounds were synthesized by accident while attempting the synthesis of alkali-metal main-group arsenides at relatively high temperature. It turns out that niobium and tantalum containers react readily... 

Although the comer atoms must move apart to convert a simple cube into a body-centered cube, the extra atom in the center of the stracture makes the body-centered cubic lattice more compact than the simple cubic structure. All the alkali metals, as well as iron and the transition metals from Groups 5 and 6, form ciystals with body-centered cubic structures. 

This article summarizes the chemistry of alkali metals with group 14, 15, and 16 ligands with specific emphasis on structure and bonding. With several excellent, recent review articles in the area, we focus specifically on newer developments, with already reviewed material only mentioned briefly to show trends and connections. 

Table 3.9. A comparison of Pauling (xa

The alkali metals in Group 1(a) have the lowest ionization energies, which is again expected since they always form cations with a +1 valence. There is little variation in I across the d-block and f-block elements, with a slight increase in / as the atomic number increases. 

An interesting related feature shown by several alloys of the more basic metals (alkali, alkaline earths) with many /5-block (13th, 14th, 15th groups) elements, and,... 

Because its outet valence electrons ate at a gteatet distance from its nuclei, potassium is more reactive than sodium or lithium. Even so, potassium and sodium are very similar in their chemical reactions. Due to potassiums high reactivity, it combines with many elements, particularly nonmetals. Like the other alkali metals in group 1, potassium is highly alkaline (caustic) with a relatively high pH value. When given the flame test, it produces a violet color. 

Francium s atoms are the largest and heaviest of the alkali metals in group 1 (lA). It is located just below cesium on the periodic table, and thus it is assumed to be an extremely reactive reducing agent even though it is the most scarce of the alkali metals. Its most stable isotope (Fr-223) exists for about 21 or 22 minutes. No one has figured out how to refine francium from natural minerals (ores) because the atoms of the most stable isotope found in nature (Fr-223) are scattered very thinly over the Earth s crust. All of the other 30 isotopes are produced for study by nuclear decay of other radioactive elements. 

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