Relativistic quantum chemistry

Relativistic quantum chemistry invokes quantum chemical and relativistic mechanical arguments to explain elemental properties and structure, especially for the heavier elements of the periodic table. A prominent example of such an explanation is the color of gold; due to relativistic effects, it is not silvery like most other metals.

The term "relativistic effects" was developed in light of the history of quantum mechanics. Initially quantum mechanics was developed without considering the theory of relativity.^[1] By convention, "relativistic effects" are those discrepancies between values calculated by models considering and not considering relativity.^[2] Relativistic effects are important for the heavier elements with high atomic numbers. In the most common layout of the periodic table, these elements are shown in the lower area. Examples are the lanthanides and actinides.^[3]

Relativistic effects in chemistry can be considered to be perturbations, or small corrections, to the non-relativistic theory of chemistry, which is developed from the solutions of the Schrödinger equation. These corrections affect the electrons differently depending on the electron speed relative to the speed of light. Relativistic effects are more prominent in heavy elements because only in these elements do electrons attain relativistic speeds.

History

Beginning in 1935, Bertha Swirles described a relativistic treatment of a many-electron system,^[4] in spite of Paul Dirac's 1929 assertion that the only imperfections remaining in quantum mechanics "...give rise to difficulties only when high-speed particles are involved, and are therefore of no importance in the consideration of atomic and molecular structure and ordinary chemical reactions in which it is, indeed, usually sufficiently accurate if one neglects relativity variation of mass and velocity and assumes only Coulomb forces between the various electrons and atomic nuclei."^[5]

Theoretical chemists by and large agreed with Dirac's sentiment until the 1970s, when relativistic effects began to become realized in heavy elements.^[6] The Schrödinger equation had been developed without considering relativity in Schrödinger's 1926 paper.^[7] Relativistic corrections were made to the Schrödinger equation (see Klein–Gordon equation) in order to explain the fine structure of atomic spectra, but this development and others did not immediately trickle into the chemical community. Since atomic spectral lines were largely in the realm of physics and not in that of chemistry, most chemists were unfamiliar with relativistic quantum mechanics, and their attention was on lighter elements typical for the organic chemistry focus of the time.^[8]

Dirac's opinion on the role relativistic quantum mechanics would play for chemical systems is wrong for two reasons: the first being that electrons in s and p atomic orbitals travel at a significant fraction of the speed of light and the second being that there are indirect consequences of relativistic effects which are especially evident for d and f atomic orbitals.^[6]

Qualitative treatment

Relativistic mass as a function of velocity. For a small velocity, the

m_{rel}

(ordinate) is equal to

m_0

but as

v_e\to c

the

m_{rel}

goes to infinity.

One of the most important and familiar results of relativity is that the relativistic mass of the electron increases by

m_{rel}=\frac{m_{e}}{\sqrt{1-(v_e/c)^2}}

where $\displaystyle m_e, v_e, c$ are the electron rest mass, velocity of the electron, and speed of light respectively. The figure at the right illustrates the relativistic effects on the mass of an electron as a function of its velocity.

This has an immediate implication on the Bohr radius ( $\displaystyle a_0$ ) which is given by

a_0=\frac{\hbar}{m_e c \alpha}

where $\hbar$ is the reduced Planck's constant and α is the fine-structure constant (a relativistic correction for the Bohr model).

Arnold Sommerfeld calculated that, for a 1s electron of a hydrogen atom with an orbiting radius of 0.0529 nm, α ≈ 1/137. That is to say, the fine-structure constant shows the electron traveling at nearly 1/137 the speed of light.^[9] One can extend this to a larger element by using the expression v ≈ Zc/137 for a 1s electron where v is its radial velocity. For gold with (Z = 79) the 1s electron will be going (α = 0.58c) 58% of the speed of light. Plugging this in for v/c for the relativistic mass one finds that m_rel = 1.22m_e and in turn putting this in for the Bohr radius above one finds that the radius shrinks by 22%.

If one substitutes in the relativistic mass into the equation for the Bohr radius it can be written

a_{rel}=\frac{\hbar \sqrt{1-(v_e/c)^2}}{m_e c \alpha}

Ratio of relativistic and nonrelativistic Bohr radii, as a function of electron velocity

It follows that

\frac{a_{rel}}{a_0} =\sqrt{1-(v_e/c)^2}

At right, the above ratio of the relativistic and nonrelativistic Bohr radii has been plotted as a function of the electron velocity. Notice how the relativistic model shows the radius decreasing with increasing velocity.

The same result is obtained when the relativistic effect of length contraction is applied to the radius of the 6s orbital. The length contraction is expressed as

L' = L \, \sqrt{1-v^2/c^2}

so the radius of the 6s orbital shrinks to

a_{rel} = a_0 \, \sqrt{1-v^2/c^2}

which is consistent with the result obtained by incorporating the increase of mass.

When the Bohr treatment is extended to hydrogenic-like atoms using the Quantum Rule, the Bohr radius becomes

r=\frac{n^2\hbar^2 4 \pi \epsilon_0}{m_eZe^2}

where $n$ is the principal quantum number and Z is an integer for the atomic number. From quantum mechanics the angular momentum is given as $mv_{e}r=n\hbar$ . Substituting into the equation above and solving for $v$ gives

r=\frac{mv_ern\hbar 4 \pi \epsilon_0}{mZe^2}

1=\frac{v_en\hbar 4 \pi \epsilon_0}{Ze^2}

v_e=\frac{Ze^2}{n\hbar 4 \pi \epsilon_0}

From this point atomic units can be used to simplify the expression into

v_e=\frac{Z}{n}

Substituting this into the expression for the Bohr ratio mentioned above gives

\frac{a_{rel}}{a_0}=\sqrt{1-\left(\frac{Z}{nc}\right)^2}

At this point one can see that for a low value of $n$ and a high value of $Z$ that $\frac{a_{rel}}{a_0} < 1$ . This fits with intuition: electrons with lower principal quantum numbers will have a higher probability density of being nearer to the nucleus. A nucleus with a large charge will cause an electron to have a high velocity. A higher electron velocity means an increased electron relativistic mass, as a result the electrons will be near the nucleus more of the time and thereby contract the radius for small principal quantum numbers.^[10]

Periodic table deviations

The periodic table was constructed by scientists who noticed periodic trends in known elements of the time. Indeed, the patterns found in it is what gives the periodic table its power. Many of the chemical and physical differences between the 6th period (Cs–Rn) and the 5th period (Rb–Xe) arise from the larger relativistic effects for the former. These relativistic effects are particularly large for gold and its neighbors, platinum and mercury.

Mercury

Mercury (Hg) is a liquid down to −39 °C (see m.p.). Bonding forces are weaker for Hg–Hg bonds than for its immediate neighbors such as cadmium (m.p. 321 °C) and gold (m.p. 1064 °C). The lanthanide contraction is a partial explanation; however, it does not entirely account for this anomaly.^[9] In the gas phase mercury is alone in metals in that it is quite typically found in a monomeric form as Hg(g). Hg₂²⁺(g) also forms and it is a stable species due to the relativistic shortening of the bond.

Hg₂(g) does not form because the 6s² orbital is contracted by relativistic effects and may therefore only weakly contribute to any bonding; in fact Hg–Hg bonding must be mostly the result of van der Waals forces, which explains why the bonding for Hg–Hg is weak enough to allow for Hg to be a liquid at room temperature.^[9]

Au₂(g) and Hg(g) are analogous, at the least in having the same nature of difference, to H₂(g) and He(g). It is for the relativistic contraction of the 6s² orbital that gaseous mercury can be called a pseudo noble gas.^[9]

Color of gold and caesium

Spectral reflectance curves for aluminum (Al), silver (Ag), and gold (Au) metal mirrors

The reflectivity of Au, Ag, Al is shown on the figure to the right. The human eye sees electromagnetic radiation with a wavelength near 600 nm as yellow. As is clear from its reflectance spectrum, gold appears yellow because it absorbs blue light more than it absorbs other visible wavelengths of light; the reflected light (which is what we see) is therefore lacking in blue compared to the incident light. Since yellow is complementary to blue, this makes a piece of gold appear yellow (under white light) to human eyes.

The electronic transition responsible for this absorption is a transition from the 5d to the 6s level. An analogous transition occurs in Ag but the relativistic effects are lower in Ag so while the 4d experiences some expansion and the 5s some contraction, the 4d-5s distance in Ag is still much greater than the 5d-6s distance in Au because the relativistic effects in Ag are smaller than those in Au. Thus, non-relativistic gold would be white. The relativistic effects are raising the 5d orbital and lowering the 6s orbital.^[11]

A similar effect occurs in caesium metal, the heaviest of the alkali metals which can be collected in quantities sufficient to allow viewing. Whereas the other alkali metals are silver-white, caesium metal has a distinctly golden hue.

Inert pair effect

Main article: inert pair effect

In Tl(I) (thallium), Pb(II) (lead), and Bi(III) (bismuth) complexes there is a 6s² electron pair. The 'inert pair effect' refers to the tendency for this pair of electrons to resist oxidation due to a relativistic contraction of the 6s orbital.^[6]

Others

Some of the phenomena commonly attributed to relativistic effects are:

The existence of mercury(IV) fluoride
Aurophilicity
The stability of the gold anion, Au⁻, in compounds such as CsAu
The crystal structure of lead, which is face-centered cubic instead of diamond-like
The striking similarity between zirconium and hafnium
The stability of the uranyl cation, as well as other high oxidation states in the early actinides (Pa-Am)
The small atomic radii of francium and radium
About 10% of the lanthanide contraction is attributed to the relativistic mass of high velocity electrons and the smaller Bohr radius that results.
In the case of gold, a lot more than 10% of its contraction is due to relativistically heavy electrons, and gold #79 is almost twice as dense as lead #82.

References

↑ Kleppner, Daniel (1999). "A short history of atomic physics in the twentieth century" (PDF). Reviews of Modern Physics 71 (2): S78. Bibcode:1999RvMPS..71...78K. doi:10.1103/RevModPhys.71.S78.
↑ Kaldor, U.; Wilson, Stephen (2003). Theoretical Chemistry and Physics of Heavy and Superheavy Elements. Dordrecht, Netherlands: Kluwer Academic Publishers. p. 4. ISBN 1-4020-1371-X.
↑ Kaldor & Wilson 2003, p. 2.
↑ Swirles, B. (1935). "The Relativistic Self-Consistent Field". Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 152 (877): 625. Bibcode:1935RSPSA.152..625S. doi:10.1098/rspa.1935.0211.
↑ Dirac, P. A. M. (1929). "Quantum Mechanics of Many-Electron Systems" (free download pdf). Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 123 (792): 714. Bibcode:1929RSPSA.123..714D. doi:10.1098/rspa.1929.0094. JSTOR 95222.
1 2 3 Pyykko, Pekka (1988). "Relativistic effects in structural chemistry". Chemical Reviews 88 (3): 563. doi:10.1021/cr00085a006.
↑ Erwin Schrödinger, Annalen der Physik, (Leipzig) (1926), Main paper
↑ Kaldor, U.; Wilson, Stephen, eds. (2003). Theoretical Chemistry and Physics of Heavy and Superheavy Elements. Dordrecht, Netherlands: Kluwer Academic Publishers. ISBN 1-4020-1371-X.
1 2 3 4 Norrby, Lars J. (1991). "Why is mercury liquid? Or, why do relativistic effects not get into chemistry textbooks?". Journal of Chemical Education 68 (2): 110. Bibcode:1991JChEd..68..110N. doi:10.1021/ed068p110.
↑ Pitzer, Kenneth S. (1979). "Relativistic effects on chemical properties". Accounts of Chemical Research 12 (8): 271. doi:10.1021/ar50140a001.
↑ Pyykko, Pekka; Desclaux, Jean Paul (1979). "Relativity and the periodic system of elements". Accounts of Chemical Research 12 (8): 276. doi:10.1021/ar50140a002.