Ionic Radii


Welcome to the database of ionic radii. The following web interface allows listing and comparison of ionic and crystal radii with different coordination and charge states. Suggestions as to how the scope and content of the database can be extended are gratefully received. Calculation of ionic radii - Pauling's Method, Slater rules Pauling has calculated the radii of the ions on the basis of the observed internuclear distances in four crystals namely NaF, KCl, RbBr and CsI. In each ionic crystal the cations and anions are isoelectronic with inert gas configuration. Calculation of ionic radii. Database of Ionic Radii: To view details for a particular element click on element in the table below.

The chemical, metallurgical, and physical behaviours of the rare earths are governed by the electron configuration of these elements. In general, these elements are trivalent, R3+, but several of them have other valences. The number of 4felectrons of each lanthanide is given in the table of the number of 4f electrons and ionic radii for the R3+ ion. The 4f electrons have lower energies than and radially lie inside the outer three valence electrons (i.e., 4f electrons are “localized” and part of the ion core), and thus they do not directly participate in the bonding with other elements when a compound is formed. This is why the lanthanides are chemically similar and difficult to separate and why they occur together in various minerals. The outer or valence electrons for the 14 lanthanides and lanthanum are the same, 5d6s2; for scandium, 3d4s2; and for yttrium, 4d5s2. There is some variation in the chemical properties of the lanthanides because of the lanthanide contraction and the hybridization, or mixing, of the 4f electrons with the valence electrons.

The systematic and smooth decrease from lanthanum to lutetium is known as the lanthanide contraction. It is due to the increase in the nuclear charge, which is not completely screened by the additional 4f electron as one goes from one lanthanide to the next. This increased effective charge draws the electrons (both the core and outer valence electrons) closer to the nucleus, thus accounting for the smaller radius of the higher-atomic-number lanthanides. The lanthanide contraction also accounts for the decreased basicity from lanthanum to lutetium and is the basis of various separation techniques.

As the 4f electrons are added when one moves across the lanthanide series from lanthanum to cerium to praseodymium and so on, the electrons, which have a magnetic moment due to the electron’s spin, maintain the same spin direction and the moments are aligned parallel with one another until the 4f level is half-filled—i.e., at seven 4f electrons in gadolinium. The next electron must align antiparallel in accordance with the Pauli exclusion principle, and thus two 4f electrons are paired. This continues until the 14th electron is added at lutetium, where all the 4f electron spins are paired up, and lutetium has no 4fmagnetic moment.

The 4f electron configuration is extremely important and determines the magnetic and optical behaviours for the lanthanide elements; e.g., the peculiar properties of strong Nd2Fe14B permanent magnets are due to the three 4f electrons in neodymium, and the red colour in optical displays that use cathode-ray tubes is provided by the europiumion in a host compound, while the green colour is provided by terbium.

As noted above, several lanthanides may exhibit another valence state, R4+ for R = cerium, praseodymium, and terbium and R2+ for R = samarium, europium, and ytterbium. These additional valence states are a striking example of Hund’s rule, which states that empty, half-filled, and completely filled electronic levels tend to be more stable states: Ce4+ and Tb4+ give up an f electron to have an empty and half-filled 4f level, respectively, and Eu2+ and Yb2+ gain an f electron to have a half-filled or completely filled 4f level, respectively. Pr4+ and Sm2+ can, by giving up or gaining an f electron, respectively, in rare instances gain extra stability. In these two cases they tend toward but do not reach the respective empty or half-filled level. By giving up a 4f electron to become an R4+ ion, the radii of cerium, praseodymium, and terbium become smaller, 0.80, 0.78, and 0.76 Å, respectively. Conversely, samarium, europium, and ytterbium gain a 4f electron from the valence electrons to become an R2+ ion, and their radii increase to 1.19, 1.17, and 1.00 Å, respectively. Chemists have made use of these valence changes to separate Ce4+, Eu2+, and Yb2+ from the other trivalent R3 ions by relatively cheap chemical methods. CeO2 (where Ce is tetravalent) is the normal stable oxide form, while the oxides of praseodymium and terbium have the Pr6O11 and Tb4O7stoichiometries containing both the tetra- and the trivalent states—i.e., 4PrO2∙Pr2O3 and 2TbO2∙Tb2O3, respectively. The divalent ions Sm2+, Eu2+, and Tb2+ form dihalides—e.g., SmCl2, EuCl2, and YbCl2. Several europium oxide stoichiometries are known: EuO (Eu2+), Eu2O3 (Eu3+), and Eu3O4 (i.e., EuO∙Eu2O3).

The ionic radius of scandium is much smaller than that of the smallest lanthanide, lutetium: 0.745 Å versus 0.861 Å. Scandium’s radius is slightly larger than those of the common metal ions—e.g., Fe3+, Nb5+, U5+, and W5+. This is the main reason why scandium is essentially absent from any of the normal rare-earth minerals, generally less than 0.01 percent by weight. However, scandium is obtained as a by-product of processing other ores (e.g, wolframite) and from mining tailings (e.g., uranium). On the other hand, the radius of yttrium, 0.9 Å, is nearly the same as that of holmium, 0.901 Å, and this accounts for the presence of yttrium in the heavy lanthanide minerals.

Most rare-earth metals have a valence of three; however, that of cerium is 3.2, and europium and ytterbium are divalent. This is quite evident when the metallic radii are plotted versus atomic number. The metallic radii of the trivalent metals exhibit the normal lanthanide contraction, but a noticeable deviation occurs for cerium, where its radius falls below the line established by the trivalent metals, and also for europium and ytterbium, where their radii lie well above this line.

The melting points for europium and ytterbium are significantly lower than those of the neighbouring trivalent lanthanides when they are plotted versus atomic number, and this is also consistent with the divalent nature of these two metals. Anomalies are also evident in other physical properties of europium and ytterbium compared with the trivalent lanthanide metals (see belowProperties of the metals).

The table presents the number of 4f electrons and the radius of the R3+ ion for the rare-earth elements.

Number of 4f electrons and
ionic radii for the R3+ ion
number of
4f electrons
number of
4f electrons
La00 1.045
Ce11 1.01
Pr22 0.997
Nd33 0.983
Pm44 0.97
Sm55 0.958
Eu66 0.947
Gd77 0.938
Tb86 0.923
Dy95 0.912
Ho104 0.901
Er113 0.890
Tm122 0.880
Yb131 0.868
Lu140 0.861
Sc00 0.745
Y00 0.900

Ionic Radii List

EENS 2110


Tulane University

Prof. Stephen A. Nelson

Coordination and Pauling's Rules

The arrangement of atoms in a crystal structure not only depends on the charge on the ion and type of bonding between atoms, but also on the size of the atoms or ions. In any given molecule or crystal structure each atom or ion will be surrounded by other atoms or ions. The number of ions or atoms that immediately surround an atom or ion of interest is called the coordination number, - C.N. As we shall see, the coordination number depends on the relative size of the atoms or ions. So, we must first discuss their sizes.

Atomic and Ionic Radii

The size of an atom or ion depends on the size of the nucleus and the number of electrons. Generally atoms with higher numbers of electrons have larger radii than those with smaller numbers of electrons. Thus ions will have radii different from the atoms because ions will have either gained or lost electrons. The number of positive charges in the nucleus determines both the number of electrons that surround an atom and the number of electrons that can be lost or gained to form ions.

  • Thus as the charge on the ion becomes more positive, there will be less electrons and the ion will have a smaller radius.
  • As the charge on the ion becomes more negative, there will be more electrons and the ion will have a larger radius.
  • As the atomic number increases in any given column of the Periodic Table, the number of protons and electrons increases and thus the size of the atom or ion increases.

Atomic and ionic radii also depend on the type of bonding that takes place between the constituents, and on the coordination number. Thus, atomic and ionic radii will vary somewhat as a function of the environment in which the atoms or ions are found.
A list of ionic radii of the more common elements for various coordination numbers is shown on page 67 of your text. First, let's examine the table looking at one column of the Periodic Table to see how the radii are affected by increasing atomic number.

Here we see the effect of increasing the atomic number (and total number of electrons) for ions of equal charge and the effect of changing the coordination number. The radii increase with increasing total number of electrons downward in table. Ionic radius also increases with increasing coordination number, the electron cloud is drawn out by the presence of more surrounding ions.
C.N. = 6
R (Å)
C.N. = 8

Next, we examine one row of the Periodic Table to see how the radii are affected by charge of the ion.

Here we see that as the charge becomes more positive the radius of the cation decreases. This is because there are fewer electrons in the outer shells of the ions. The sizes of anions are relatively large because there are more electrons in their outermost shells.

C.N. = 4
R (Å)
C.N. = 6

Coordination of Ions

Coordination number, C.N. depends on the relative size of the ions. If all of the atoms in a crystal are the same size, then there are two ways to pack the atoms to form a crystal structure. In this case, the maximum number of atoms that be coordinated around any individual is 12. We call this 12-fold coordination. There are two ways that atoms can be packed in 12-fold coordination.

First, examine a single layer of atoms of equal size. Note that there are two kinds of voids between the atoms, those that have a sort of triangular shape with the triangles pointing up we'll call B voids, and those with the triangles pointing down we'll call C voids.

If we add the next layer of atoms so that they occupy the space above the B voids, and then add the next layer above the A atoms, this will result in a stacking sequence that runs AB AB AB ..etc. This type of closest packing is referred to as hexagonal closest packing. It results in a hexagonal lattice with the c-axis oriented perpendicular to the AB AB layers.

If after adding the layer of B atoms we place the next layer so that the atoms occupy positions over the C voids in the A layer, and continue the process upward, we get a stacking sequence that runs ABC ABC ABC.. etc. This type of packing is referred to as cubic closest packing. It results in a cubic or isometric lattice with the axis perpendicular to the layers.

To see what happens when one of the involved ions or atoms becomes smaller, we need to examine the relative sizes of the atoms. The relative sizes are indicated by the radius ratio of the coordinating atoms or ions. In crystal structures we usually look at cations surrounded by anions, so the radius ratio is defined as Rx/Rz, where Rx is the radius of the cation, and Rz is the radius of the surrounding anions. Since the anions are usually the larger ions, this results in decreasing values of Rx/Rz as the size of the cation decreases.

If we decrease the size of the cation in such an arrangement, still allowing for the surrounding anions to touch each other and touch the cation, with decreasing size of the cation, the coordination will first result in 8 anions surrounding the cation.

This is called 8-fold coordination or cubic coordination because the shape of the object constructed by drawing lines through the centers of the larger ions is a cube.

If the size of the coordinated cation becomes smaller, it will become too small to touch the surrounding anions. Thus, there is limiting radius ratio that will occur when the Rx/Rz becomes too small. To see what this limit is, we must look at the vertical plane running through the centers anions labeled A and B.

In this construction we can determine the radius ratio for the limiting condition, often called the 'no rattle limit' because if the radius ratio becomes smaller than this the cation will 'rattle' in its site. Using the Pythagorean theorem we can write:

(2Rz +2Rx)2 = (2Rz)2 + (2Ö2Rz)2

2Rz +2Rx = √(4Rz2 + 8Rz2)

2Rz +2Rx = (12Rz2)

2Rz +2Rx = 3.464Rz

2Rx = 1.464Rz

Giving Rx/Rz = 0.732 Samsung kies galaxy s3.

Thus, for Rx/Rz < 0.732 the cation will be too small or will rattle in its site and the structure will have to change to 6-fold coordination.

Six-fold coordination is also called octahedral coordination because the shape defined by drawing planes through the center of the larger ions is an octahedron. Octahedral coordination is stable when Rx/Rz , 0.732, but decreasing the radius of cation, Rx, will eventually reach a limit where again the smaller ion will rattle in its site.
The no rattle limit can be determined by looking at the horizontal plane running through the ions labeled C and D. In this case we can write:

(2Rz + 2Rx)2 = (2Rz)2 + (2Rz)2 = 2(4Rz2)

2Rz +2Rx = 2√2Rz

Rz + Rx = √2Rz

Rx = (√2 - 1)Rz

Rx/Rz = 0.414

For Rx/Rz < 0.414 the structure goes into 4-fold coordination. Planes through the centers of the larger atoms in this case will form a tetrahedron, so 4-fold coordination is also called tetrahedral coordination.
The calculation to determine the 'no rattle' limit for tetrahedral coordination is complex (see text by Klein and Dutrow, page 70). The result shows that the limit is reached when Rx/Rz = 0.225. As the radius ratio becomes smaller than this, triangular coordination becomes the stable configuration.
For triangular coordination, the coordination number is three, that is 3 anions surround the smaller cation. The 'no rattle' limit is reached for triangular coordination when Rx/Rz becomes less than 0.155.
At values of Rx/Rz < 0.155 the only way the smaller ion can be coordinated by the larger ions is to have 2 of the larger ions on either side. This 2-fold coordination is termed linear coordination.
Ionic radii na
The table here summarizes the cation to anion radius ratios, Rx/Rz, for various coordination numbers and gives the name of the coordination polyhedron for each coordination number.
1.012Hexagonal or Cubic
Closest Packing
1.0 - 0.7328Cubic
0.732 - 0.4146Octahedral
0.414 - 0.2254Tetrahedral
0.225 - 0.1553Triangular

In describing the structure of crystals and the locations of various ions or atoms within crystals, reference is often made to a crystallographic site on which an atom resides. Such sites are usually referred to in terms of the coordination number or coordination polyhedron that surrounds the ion. For example, in the silicate minerals Si is surrounded by 4 oxygens in tetrahedral coordination. Thus Si is often said to occupy the tetrahedral sites in silicate minerals. We will explore these concepts in more detail latter in the course.

Ionic Radii Size

These general relationships of coordination only apply if the bonding is dominantly ionic. In covalent structures the atoms overlap because they share electrons. It should also be noted that 5-, 7-, 9-, and 10-fold coordination are also possible in complex structures.

For the elements that occur in common minerals in the Earth's crust, the most common coordinating anion is Oxygen. The following table gives the ionic radius and coordination of these common metal cations coordinated with oxygen.

(with Oxygen)
Coord. PolyhedronIonic Radius, Å
K+8 - 12cubic to closest1.51 (8) - 1.64 (12)
Na+8 - 6cubic to octahedral1.18 (8) - 1.02 (6)
Ca+28 - 61.12 (8) - 1.00 (6)

Pauling's Rules

Linus Pauling studied crystal structures and the types of bonding and coordination that occurs within them. His studies found that crystal structures obey the following rules, now known as Pauling's Rules.

Rule 1

Around every cation, a coordination polyhedron of anions forms, in which the cation-anion distance is determined by the radius sums and the coordination number is determined by the radius ratio.

This rule simply sets out what we have discussed above, stating that the different types of coordination polyhedra are determined by the radius ratio, Rx/Rz, of the cation to the anion.

Rule 2, The Electrostatic Valency Principle

An ionic structure will be stable to the extent that the sum of the strengths of the electrostatic bonds that reach an ion equal the charge on that ion.

In order to understand this rule we must first define electrostatic valency, e.v.

e.v = Charge on the ion/C.N.

For example, in NaCl each Na+ is surrounded by 6 Cl- ions. The Na is thus in 6 fold coordination and C.N. = 6. Thus e.v. = 1/6. So 1/6 of a negative charge reaches the Na ion from each Cl. So the +1 charge on the Na ion is balanced by 6*1/6 =1 negative charge from the 6 Cl ions.
Similarly, in the CaF2 structure, each Ca+2 ion is surrounded by 8 F- ions in cubic or 8-fold coordination. The e.v. reaching the Ca ion from each of the F ions is thus 1/4. Since there are 8 F ions, the total charge reaching the Ca ion is 8*1/4 or 2. So, again the charge is balanced.
Notice that in NaCl, each Cl ion is also surrounded by 6 Na ions in octahedral coordination. So, again, the 1/6 of a positive charge from each Na reaches the Cl ion and thus the Cl ion sees 6*1/6 = 1 positive charge, which exactly balances the -1 charge on the Cl.

In the case of NaCl the charge is exactly balanced on both the cations and anions. In such a case, we say that the bonds are of equal strength from all directions. When this occurs the bonds are said to be isodesmic.

This is not the case for C+4 ion in triangular coordination with O-2. Here, e.v. = 4/3 (C has a charge of +4 and is coordinated by 3 oxygens). Thus, the 3 Oxygens each contribute 4/3 charge to the Carbon ion, and the charge on the carbon is balanced. But, each Oxygen still has 2/3 of a charge that it has not used. Thus, a carbonate structural group is formed - CO3-2.

In cases like this, where the electrostatic valency is greater than 1/2 the charge on the anion (4/3 > 1/2*2), the anion will be more strongly bound to the central coordinating cation than it can be bonded to other structural groups. When this occurs the bonding is said to be anisodesmic.

A third case arises when the e.v. reaching the cation is exactly 1/2 the charge on the anion. This is the case for Si+4 in tetrahedral coordination with O-2. Here, the e.v. reaching the Si is 4/4 =1. This leaves each Oxygen with a -1 charge that it has not shared. Since this -1 is exactly 1/2 the original charge on O-2, the Oxygens in the SiO4-4 group can be just as tightly bound to ions outside the group as to the centrally coordinated Si. In this case the bonding is said to be mesodesmic.

The SiO4-4 group is the basic building block of the most common minerals in the Earth's crust, the silicates.

Rule 3

Shared edges, and particularly faces of two anion polyhedra in a crystal structure decreases its stability.

The reason for this is that sharing of only corners of polyhedra places the positively charged cations at the greatest distance from each other. In the example shown here, for tetrahedral coordination, if the distance between the cations in the polyhedrons that share corners is taken as 1, then sharing edges reduces the distance to 0.58, and sharing of faces reduces the distance to 0.38.

Rule 4

In a crystal structure containing several cations, those of high valency and small coordination number tend not to share polyhedral elements.

Sharing of polyhedral elements for cations of high charge will place cations close enough together that they may repel one another. Thus, if they do not share polyhedral elements they can be better shielded from the effects of other positive charges in the crystal structure.

Rules 1 through 4 maximize the cation - anion attractions and minimize the anion-anion and cation-cation repulsions.

Rule 5, The Principle of Parsimony

The number of different kinds of constituents in a crystal tends to be small.

This means that there are only a few different types of cation and anion sites in a crystal. Even though a crystal may have tetrahedral sites, octahedral sites, and cubic sites, most crystals will be limited to this small number of sites, although different elements may occupy similar sites.

Next time we will see how these principles apply to the silicate minerals.

Examples of questions on this material that could be asked on an exam

  1. Define the following: (a) coordination number, (b) octahedral coordination, (c) tetrahedral coordination, (d) tringular coordination, (e) electrostatic valence, (f) isodesmic, (g) anisodesmic, (h) mesodesmic.
  2. Explain what factors control the size of ions and why.
  3. Why are anions in general larger than cations?
  4. Expalin Pauling's five rules in simple terms and explain why they are important.