Diatomic molecule

All other diatomic molecules are chemical compounds of two different elements. Many elements can combine to form heteronuclear diatomic molecules, depending on temperature and pressure.

Examples are gases carbon monoxide (CO), nitric oxide (NO), and hydrogen chloride (HCl).

Many 1:1 binary compounds are not normally considered diatomic because they are polymeric at room temperature, but they form diatomic molecules when evaporated, for example gaseous MgO, SiO, and many others.

Hundreds of diatomic molecules have been identified[5] in the environment of the Earth, in the laboratory, and in interstellar space. About 99% of the Earth's atmosphere is composed of two species of diatomic molecules: nitrogen (78%) and oxygen (21%). The natural abundance of hydrogen (H₂) in the Earth's atmosphere is only of the order of parts per million, but H₂ is the most abundant diatomic molecule in the universe. The interstellar medium is dominated by hydrogen atoms.

All diatomic molecules are linear and characterized by a single parameter which is the bond length or distance between the two atoms. Diatomic nitrogen has a triple bond, diatomic oxygen has a double bond, and diatomic hydrogen, fluorine, chlorine, iodine, and bromine all have single bonds.[6]

Diatomic elements played an important role in the elucidation of the concepts of element, atom, and molecule in the 19th century, because some of the most common elements, such as hydrogen, oxygen, and nitrogen, occur as diatomic molecules. John Dalton's original atomic hypothesis assumed that all elements were monatomic and that the atoms in compounds would normally have the simplest atomic ratios with respect to one another. For example, Dalton assumed water's formula to be HO, giving the atomic weight of oxygen as eight times that of hydrogen,[7] instead of the modern value of about 16. As a consequence, confusion existed regarding atomic weights and molecular formulas for about half a century.

As early as 1805, Gay-Lussac and von Humboldt showed that water is formed of two volumes of hydrogen and one volume of oxygen, and by 1811 Amedeo Avogadro had arrived at the correct interpretation of water's composition, based on what is now called Avogadro's law and the assumption of diatomic elemental molecules. However, these results were mostly ignored until 1860, partly due to the belief that atoms of one element would have no chemical affinity toward atoms of the same element, and also partly due to apparent exceptions to Avogadro's law that were not explained until later in terms of dissociating molecules.

At the 1860 Karlsruhe Congress on atomic weights, Cannizzaro resurrected Avogadro's ideas and used them to produce a consistent table of atomic weights, which mostly agree with modern values. These weights were an important prerequisite for the discovery of the periodic law by Dmitri Mendeleev and Lothar Meyer.[8]

Diatomic molecules are normally in their lowest or ground state, which conventionally is also known as the ${\displaystyle X}$ state. When a gas of diatomic molecules is bombarded by energetic electrons, some of the molecules may be excited to higher electronic states, as occurs, for example, in the natural aurora; high-altitude nuclear explosions; and rocket-borne electron gun experiments.[9] Such excitation can also occur when the gas absorbs light or other electromagnetic radiation. The excited states are unstable and naturally relax back to the ground state. Over various short time scales after the excitation (typically a fraction of a second, or sometimes longer than a second if the excited state is metastable), transitions occur from higher to lower electronic states and ultimately to the ground state, and in each transition results a photon is emitted. This emission is known as fluorescence. Successively higher electronic states are conventionally named ${\displaystyle A}$, ${\displaystyle B}$, ${\displaystyle C}$, etc. (but this convention is not always followed, and sometimes lower case letters and alphabetically out-of-sequence letters are used, as in the example given below). The excitation energy must be greater than or equal to the energy of the electronic state in order for the excitation to occur.

In quantum theory, an electronic state of a diatomic molecule is represented by the molecular term symbol

${\displaystyle ^{2S+1}\Lambda (v)_{(g/u)}^{+/-}}$

where ${\displaystyle S}$ is the total electronic spin quantum number, ${\displaystyle \Lambda }$ is the total electronic angular momentum quantum number along the internuclear axis, and ${\displaystyle v}$ is the vibrational quantum number. ${\displaystyle \Lambda }$ takes on values 0, 1, 2, ..., which are represented by the electronic state symbols ${\displaystyle \Sigma }$, ${\displaystyle \Pi }$, ${\displaystyle \Delta }$,.... For example, the following table lists the common electronic states (without vibrational quantum numbers) along with the energy of the lowest vibrational level (${\displaystyle v=0}$) of diatomic nitrogen (N₂), the most abundant gas in the Earth's atmosphere.[10]

The subscripts and superscripts after ${\displaystyle \Lambda }$ give additional quantum mechanical details about the electronic state. The superscript ${\displaystyle +}$ or ${\displaystyle -}$ determines whether reflection in a plane containing the internuclear axis introduces a sign change in the wavefunction. The sub-script ${\displaystyle g}$ or ${\displaystyle u}$ applies to molecules of identical atoms, and when reflecting the state along a plane perpendicualr to the molecular axis, states that does not change are labelled ${\displaystyle g}$ (gerade), and states that change sign are labelled ${\displaystyle u}$ (ungerade).

State	Energy[lower-alpha 1] (${\displaystyle T_{0}}$, cm−1)
${\displaystyle X^{1}\Sigma _{g}^{+}}$	0.0
${\displaystyle A^{3}\Sigma _{u}^{+}}$	49754.8
${\displaystyle B^{3}\Pi _{g}}$	59306.8
${\displaystyle W^{3}\Delta _{u}}$	59380.2
${\displaystyle B'^{3}\Sigma _{u}^{-}}$	65851.3
${\displaystyle a'^{1}\Sigma _{u}^{-}}$	67739.3
${\displaystyle a^{1}\Pi _{g}}$	68951.2
${\displaystyle w^{1}\Delta _{u}}$	71698.4

The aforementioned fluorescence occurs in distinct regions of the electromagnetic spectrum, called "emission bands": each band corresponds to a particular transition from a higher electronic state and vibrational level to a lower electronic state and vibrational level (typically, many vibrational levels are involved in an excited gas of diatomic molecules). For example, N₂ ${\displaystyle A}$-${\displaystyle X}$ emission bands (a.k.a. Vegard-Kaplan bands) are present in the spectral range from 0.14 to 1.45 μm (micrometres).[9] A given band can be spread out over several nanometers in electromagnetic wavelength space, owing to the various transitions that occur in the molecule's rotational quantum number, ${\displaystyle J}$. These are classified into distinct sub-band branches, depending on the change in ${\displaystyle J}$.[11] The ${\displaystyle R}$ branch corresponds to ${\displaystyle \Delta J=+1}$, the ${\displaystyle P}$ branch to ${\displaystyle \Delta J=-1}$, and the ${\displaystyle Q}$ branch to ${\displaystyle \Delta J=0}$. Bands are spread out even further by the limited spectral resolution of the spectrometer that is used to measure the spectrum. The spectral resolution depends on the instrument's point spread function.

The molecular term symbol is a shorthand expression of the angular momenta that characterize the electronic quantum states of a diatomic molecule, which are also eigenstates of the electronic molecular Hamiltonian. It is also convenient, and common, to represent a diatomic molecule as two-point masses connected by a massless spring. The energies involved in the various motions of the molecule can then be broken down into three categories: the translational, rotational, and vibrational energies.The theoretical study of the rotational energy levels of the diatomic molecules can be described using the below description of the rotational energy levels. While the study of vibrational energy level of the diatomic molecules can be described using the harmonic oscillator approximation or using the quantum vibrational interaction potentials. [12][13] These potentials give more accurate energy levels because they take multiple vibrational effects into account.

Concerning history, the first treatment of diatomic molecules with quantum mechanics was made by Lucy Mensing in 1926.[14]

The good quantum numbers for a diatomic molecule, as well as good approximations of rotational energy levels, can be obtained by modeling the molecule using Hund's cases.

The mnemonics BrINClHOF, pronounced "Brinklehof",[15] HONClBrIF, pronounced "Honkelbrif",[16] “HOBrFINCl”, pronounced “Hoberfinkel”, and HOFBrINCl, pronounced "Hofbrinkle", have been coined to aid recall of the list of diatomic elements. Another method, for English-speakers, is the sentence: "Never Have Fear of Ice Cold Beer" as a representation of Nitrogen, Hydrogen, Fluorine, Oxygen, Iodine, Chlorine, Bromine.

• Symmetry of diatomic molecules
• AXE method
• Octatomic element
• Covalent bond
• Industrial gas

• Huber, K. P.; Herzberg, G. (1979). Molecular Spectra and Molecular Structure IV. Constants of Diatomic Molecules. New York: Van Nostrand: Reinhold.
• Tipler, Paul (1998). Physics For Scientists and Engineers: Vol. 1 (4th ed.). W. H. Freeman. ISBN 1-57259-491-8.

• Hyperphysics – Rotational Spectra of Rigid Rotor Molecules
• Hyperphysics – Quantum Harmonic Oscillator
• 3D Chem – Chemistry, Structures, and 3D Molecules
• IUMSC – Indiana University Molecular Structure Center