Alkaline earth metals strontium

Consider the alkaline earth metal strontium and the transition metal manganese. 

The alkali metals have one outermost electron in an s orbital. This is a very unstable electron configuration, so the alkali metals are very reactive. The alkaline earth metals have two outermost electrons in an s orbital, making them somewhat reactive because an arrangement with eight outermost electrons is the most stable. The larger alkaline earth metals, strontium (Sr) and barium (Ba), are very reactive because those two outermost electrons are far from the nucleus. 

Strontium belongs to group 2 of the periodic table and is mie of the alkaline earth metals. Strontium, with atomic number 38, lies between calcium and barium in this group. The discovery of strontium carbonate, which was originally thought to be barium carbonate, is associated with a lead mine located in Strontian, Scotland, hence the name strontium. 

Group IIB and know that this means the group of elements zine. cadmium and mercury, whilst Group IIA refers to the alkaline earth metals beryllium, magnesium, calcium, barium and strontium. 

The elements in Group II of the Periodic Table (alkaline earth metals) are. in alphabetical order, barium (Ba). beryllium (Be), calcium (Ca). magnesium (Mg), radium (Ra) and strontium (Sr). 

Strontium [7440-24-6] Sr, is in Group 2 (IIA) of the Periodic Table, between calcium and barium. These three elements are called alkaline-earth metals because the chemical properties of the oxides fall between the hydroxides of alkaU metals, ie, sodium and potassium, and the oxides of earth metals, ie, magnesium, aluminum, and iron. Strontium was identified in the 1790s (1). The metal was first produced in 1808 in the form of a mercury amalgam. A few grams of the metal was produced in 1860—1861 by electrolysis of strontium chloride [10476-85-4]. 

Strontium has a valence of +2 and forms compounds that resemble the compounds of the other alkaline-earth metals (see Barium compounds Calcium compounds). Although many strontium compounds are known, there are only a few that have commercial importance and, of these, strontium carbonate [1633-05-2] SrCO, and strontium nitrate [10042-76-9], Sr(N03)2, are made in the largest quantities. The mineral celestite [7759-02-6], SrSO, is the raw material from which the carbonate or the nitrate is made. 

Other. Insoluble alkaline-earth metal and heavy metal stannates are prepared by the metathetic reaction of a soluble salt of the metal with a soluble alkah—metal stannate. They are used as additives to ceramic dielectric bodies (32). The use of bismuth stannate [12777-45-6] Bi2(Sn02)3 5H20, with barium titanate produces a ceramic capacitor body of uniform dielectric constant over a substantial temperature range (33). Ceramic and dielectric properties of individual stannates are given in Reference 34. Other typical commercially available stannates are barium stannate [12009-18-6] BaSnO calcium stannate [12013 6-6] CaSnO magnesium stannate [12032-29-0], MgSnO and strontium stannate [12143-34-9], SrSnO. ... 

The properties of hydrated titanium dioxide as an ion-exchange (qv) medium have been widely studied (51—55). Separations include those of alkaH and alkaline-earth metals, zinc, copper, cobalt, cesium, strontium, and barium. The use of hydrated titanium dioxide to separate uranium from seawater and also for the treatment of radioactive wastes from nuclear-reactor installations has been proposed (56). 

Barium [7440-39-3] Ba, is a member of Group 2 (IIA) of the periodic table where it Hes between strontium and radium. Along with calcium and strontium, barium is classed as an alkaline earth metal, and is the densest of the three. Barium metal does not occur free in nature however, its compounds occur in small but widely distributed amounts in the earth s cmst, especially in igneous rocks, sandstone, and shale. The principal barium minerals are barytes [13462-86-7] (barium sulfate) and witherite [14941-39-0] (barium carbonate) which is also known as heavy spar. The latter mineral can be readily decomposed via calcination to form barium oxide [1304-28-5] BaO, which is the ore used commercially for the preparation of barium metal. 

Alkaline-earth metals are often deterruined volumetricaHy by complexometric titration at pH 10, using Eriochrome Black T as indicator. The most suitable complexing titrant for barium ion is a solution of diethylenetriaminepentaacetic acid (DTPA). Other alkaline earths, if present, are simultaneously titrated, and in the favored analytical procedure calcium and strontium are deterruined separately by atomic absorption spectrophotometry, and their values subtracted from the total to obtain the barium value. 

The stereochemistry of Mg and the heavier alkaline earth metals is more flexible than that of Be and, in addition to occasional compounds which feature low coordination numbers (2, 3 and 4), there are many examples of 6, 8 and 12 coordination, some with 7, 9 or 10 coordination, and even some with coordination numbers as high as 22 or 24, as in SrCdn, BaCdn and (Ca, Sr or Ba)Zni3. " Strontium is 5-coordinate on the hemisolvate [Sr(OC6H2Bu3)2(thf)3]. jthf which features a distorted trigonal bipyramidal structure with the two aryloxides in equatorial positions. ... 

Heating with the following solids, their fusions, or vapours (a) oxides, peroxides, hydroxides, nitrates, nitrites, sulphides, cyanides, hexacyano-ferrate(III), and hexacyanoferrate(II) of the alkali and alkaline-earth metals (except oxides and hydroxides of calcium and strontium) (b) molten lead, silver, copper, zinc, bismuth, tin, or gold, or mixtures which form these metals upon reduction (c) phosphorus, arsenic, antimony, or silicon, or mixtures which form these elements upon reduction, particularly phosphates, arsenates,... 

Slag modifiers raise the fusion point or sintering temperature of the ash and directly neutralize any S03 formed. They are based on alkaline-earth metals such as magnesium, calcium, and strontium, or rare-earth metals such as cerium they are available as oxides, salts, or soaps. 

Calcium, strontium, and barium are called the alkaline earth metals, because their earths —the old name for oxides—are basic (alkaline). The name alkaline earth metals is often extended to all the members of Group 2 (Table 14.4). 

The true alkaline earth metals—calcium, strontium, and barium—are obtained either by electrolysis or by reduction with aluminum in a version of the thermite process (see Fig. 6.8) ... 

The alkaline earth metals can be detected in burning compounds by the colors that they give to flames. Calcium burns orange-red, strontium crimson, and barium yellow-green. Fireworks are often made from their salts (typically nitrates and chlorates, because the anions then provide an additional supply of oxygen) together with magnesium powder. 

Most monochalcogenides of the Group 3 metals adopt the rock salt (NaCl) structure. Note that the crystal chemistry of divalent europium is very similar to that of the alkaline earths, particularly strontium, as the radius of Eu is almost the same as that of Sr ". For the Yb compounds, the cell dimensions are practically identical with those of the Ca compounds. 

Although the first report of an organometallic compound of the heavier alkaline earth metals appeared near the beginning of the twentieth century,291 the RMX Grignard analogs of Ca, Sr, and Ba never fulfilled their promise as general-purpose synthetic reagents. More difficult to form, less thermally stable, and less selective in their reactions than their Mg counterparts, the literature data of the compounds was often contradictory, and many syntheses were irreproducible (see Calcium, Strontium, and Barium in COMC (1982)). 

It is also possible to isolate bis(carbene) complexes involving the heavier alkaline earth metals. Thus, the reaction of two equivalents of 4 (R = Me or (Bu, R = H) with calcium, strontium and barium bis(trimethylsilyl)amides [M N(SiMe3)2 2(thf)2] (M = Ca, Sr, Ba) resulted in the displacement of two thf molecules to afford the corresponding biscarbene species, 19 (19). The solubilities and stabilities of these complexes were found to decrease from calcium to barium. 

The metalation of trialkylsilylphosphane and -arsane with the alkaline earth metal bis[bis(trimethylsilyl)amides] of calcium, strontium, and barium yields the mixed phosphanides and phosphanediides as well as arsanides and arsanediides depending on the stoichiometry and the demand of the trialkylsily] substituents according to Scheme 3.6-11. The main feature is the M2E3 bipyramid with the metal atoms in apical positions. These cages are often interconnected via common faces (61, 63, 64, 65, 67, and 69). A substitution of the phosphanide substituents by other Lewis bases such as THF or benzonitrile is not possible for these compounds and, consequently, homoleptic phosphanediides and arsanediides with inner M4E4 heterocubane moieties are so far unknown for M = Ca, Sr, and Ba. In all these cases a further metalation to obtain homoleptic phosphanediides failed. 

Homoleptic alkaline earth metal phosphanediides and arsanediides of calcium, strontium, and barium are unknown thus far, a consequence of the use of rather mild metalating reagents, because dialkylcalcium, -strontium, and -barium are at present not easily accessible [73]. 

The synthesis of heterobimetallic cages which contain alkaline-earth metals and tin(+2) atoms succeeds by the metalation of trialkylsilyl substituted phosphanes with the bis(trimethylsilyl)amides of tin(+2) and of calcium, strontium, or barium according to Scheme 3.6-13. Heterobimetallic cages of tin and magnesium are unknown, instead their formation mixtures of the homometallic phosphanides are observed [75],... 

Calcium, strontium, barium and radium, the alkaline earth metals proper, are the typical elements of the 2nd column (the 2nd group) of the Periodic Table. 

Polymers with extremely high molecular weights result from the polymerization of ethylene oxide initiated by the carbonates of the alkaline earth metals, e.g., strontium carbonate, which must, however, be very pure. Poly(ethylene oxides) having molecular weights up to about 600 are viscous liquids above that they are wax-like or solid, crystalline products that are readily soluble not only... 

This chapter discusses the coordination chemistry of selected main group and transition metal complexes with dipicolinic acid, its analogues, and derivatives as ligands. Selected elements will be presented in terms of increasing atomic number. Out of all of the alkali metals, there has been a report of the crystal structure of sodium coordinated to dipicolinic acid. Calcium, magnesium, and strontium, three alkaline earth metals, are popular metal centers, which have been reported in the literature to be coordinated to dipicolinic acid or its analogues. ... 

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