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In quantum mechanics, the term symbol is an abbreviated description of the (total) angular momentum quantum numbers in a multi-electron atom (however, even a single electron can be described by a term symbol). Each energy level of an atom with a given electron configuration is described by not only the electron configuration but also its own term symbol, as the energy level also depends on the total angular momentum including spin. The usual atomic term symbols assume LS coupling (also known as Russell-Saunders coupling or spin-orbit coupling). The ground state term symbol is predicted by Hund's rules.

The use of the word term for an energy level is based on the Rydberg-Ritz combination principle, an empirical observation that the wavenumbers of spectral lines can be expressed as the difference of two terms. This was later explained by the Bohr quantum theory, which identified the terms (multiplied by hc, where h is the Planck constant and c the speed of light) with quantized energy levels and the spectral wavenumbers (again multiplied by hc) with photon energies.

Tables of atomic energy levels identified by their term symbols have been compiled by the National Institute of Standards and Technology. In this database, neutral atoms are identified as I, singly ionized atoms as II, etc.[1] Neutral atoms of the chemical elements have the same term symbol for each column in the s-block and p-block elements, but may differ in d-block and f-block elements, if the ground state electron configuration changes within a column. Ground state term symbols for chemical elements are given below.

Contents

LS coupling and symbolEdit

For light atoms, the spin-orbit interaction (or coupling) is small so that the total orbital angular momentum L and total spin S are good quantum numbers. The interaction between L and S is known as LS coupling, Russell-Saunders coupling or Spin-Orbit coupling. Atomic states are then well described by term symbols of the form

2S+1LJ

where

S is the total spin quantum number. 2S + 1 is the spin multiplicity, which represents the number of possible states of J for a given L and S, provided that L ≥ S. (If L < S, the maximum number of possible J is 2L + 1).[2] This is easily proved by using Jmax = L + S and Jmin = |L - S|, so that the number of possible J with given L and S is simply Jmax - Jmin + 1 as J varies in unit steps.
J is the total angular momentum quantum number.
L is the total orbital quantum number in spectroscopic notation. The first 17 symbols of L are:
L = 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 ...
S P D F G H I K L M N O Q R T U V (continued alphabetically)[note 1]

The nomenclature (S, P, D, F) is derived from the characteristics of the spectroscopic lines corresponding to (s, p, d, f) orbitals: sharp, principal, diffuse, and fundamental; the rest being named in alphabetical order, except that J is omitted. When used to describe electron states in an atom, the term symbol usually follows the electron configuration. For example, one low-lying energy level of the carbon atom state is written as 1s22s22p2 3P2. The superscript 3 indicates that the spin state is a triplet, and therefore S = 1 (2S + 1 = 3), the P is spectroscopic notation for L = 1, and the subscript 2 is the value of J. Using the same notation, the ground state of carbon is 1s22s22p2 3P0.[1]

Terms, levels, and statesEdit

The term symbol is also used to describe compound systems such as mesons or atomic nuclei, or molecules (see molecular term symbol). For molecules, Greek letters are used to designate the component of orbital angular momenta along the molecular axis.

For a given electron configuration

  • The combination of an S value and an L value is called a term, and has a statistical weight (i.e., number of possible microstates) equal to (2S+1)(2L+1);
  • A combination of S, L and J is called a level. A given level has a statistical weight of (2J+1), which is the number of possible microstates associated with this level in the corresponding term;
  • A combination of S, L, J and MJ determines a single state.

The product (2S+1)(2L+1) as a number of possible microstates   with given S and L is also a number of basis states in the uncoupled representation, where S, mS, L, mL (mS and mL are z-axis components of total spin and total orbital angular momentum respectively) are good quantum numbers whose corresponding operators mutually commute. With given S and L, the eigenstates   in this representation span function space of dimension (2S+1)(2L+1), as   and  . In the coupled representation where total angular momentum (spin + orbital) is treated, the associated microstates (or eigenstates) are   and these states span the function space with dimension of   as  . Obviously the dimension of function space in both representation must be the same.

As an example, for S = 1, L = 2, there are (2×1+1)(2×2+1) = 15 different microstates (= eigenstates in the uncoupled representation) corresponding to the 3D term, of which (2×3+1) = 7 belong to the 3D3 (J = 3) level. The sum of (2J+1) for all levels in the same term equals (2S+1)(2L+1) as the dimensions of both representations must be equal as described above. In this case, J can be 1, 2, or 3, so 3 + 5 + 7 = 15.

Term symbol parityEdit

The parity of a term symbol is calculated as

 

where li is the orbital quantum number for each electron.   means even parity while   is for odd parity. In fact, only electrons in odd orbitals (with l odd) contribute to the total parity: an odd number of electrons in odd orbitals (those with an odd l such as in p, f,...) correspond to an odd term symbol, while an even number of electrons in odd orbitals correspond to an even term symbol. The number of electrons in even orbitals is irrelevant as any sum of even numbers is even. For any closed subshell, the number of electron is 2(2l+1) which is even, so the summation of li in closed subshell is always an even number. The summation of quantum numbers   over open (unfilled) subshells of odd orbitals (l odd) determines the parity of the term symbol. If the number of electrons in this reduced summation is odd (even) then the parity is also odd (even).

When it is odd, the parity of the term symbol is indicated by a superscript letter "o", otherwise it is omitted:

2Po
½
has odd parity, but 3P0 has even parity.

Alternatively, parity may be indicated with a subscript letter "g" or "u", standing for gerade (German for "even") or ungerade ("odd"):

2P½,u for odd parity, and 3P0,g for even.

Ground state term symbolEdit

It is relatively easy to calculate the term symbol for the ground state of an atom using Hund's rules. It corresponds with a state with maximum S and L.

  1. Start with the most stable electron configuration. Full shells and subshells do not contribute to the overall angular momentum, so they are discarded.
    • If all shells and subshells are full then the term symbol is 1S0.
  2. Distribute the electrons in the available orbitals, following the Pauli exclusion principle. First, fill the orbitals with highest ml value with one electron each, and assign a maximal ms to them (i.e. +½). Once all orbitals in a subshell have one electron, add a second one (following the same order), assigning ms = −½ to them.
  3. The overall S is calculated by adding the ms values for each electron. According to Hund's first rule, the ground state has all unpaired electron spins parallel with the same value of ms, conventionally chosen as +½. The overall S is then ½ times the number of unpaired electrons. The overall L is calculated by adding the ml values for each electron (so if there are two electrons in the same orbital, add twice that orbital's ml).
  4. Calculate J as
    • if less than half of the subshell is occupied, take the minimum value J = |LS|;
    • if more than half-filled, take the maximum value J = L + S;
    • if the subshell is half-filled, then L will be 0, so J = S.

As an example, in the case of fluorine, the electronic configuration is 1s22s22p5.

1. Discard the full subshells and keep the 2p5 part. So there are five electrons to place in subshell p (l = 1).

2. There are three orbitals (ml = 1, 0, −1) that can hold up to 2(2l + 1) = 6 electrons. The first three electrons can take ms = ½ (↑) but the Pauli exclusion principle forces the next two to have ms = −½ (↓) because they go to already occupied orbitals.

ml
+1 0 −1
ms: ↑↓ ↑↓

3. S = ½ + ½ + ½ − ½ − ½ = ½; and L = 1 + 0 − 1 + 1 + 0 = 1, which is "P" in spectroscopic notation.

4. As fluorine 2p subshell is more than half filled, J = L + S = 32. Its ground state term symbol is then 2S+1LJ = 2P32.

Atomic term symbols of the chemical elementsEdit

In the periodic table, because atoms of elements in a column usually have the same outer electron structure, and always have the same electron structure in the "s-block" and "p-block" elements (see block (periodic table)), all elements may share the same ground state term symbol for the column. Thus, hydrogen and the alkali metals are all 2S12, the alkali earth metals are 1S0, the boron column elements are 2P12, the carbon column elements are 3P0, the pnictogens are 4S32, the chalcogens are 3P2, the halogens are 2P32, and the inert gases are 1S0, per the rule for full shells and subshells stated above.

Term symbols for the ground states of all chemical elements are given in the collapsed table below (with citations here). In the d-block and f-block, the term symbols are not always the same for elements in the same column of the periodic table.

Element Group Electron configuration Term symbol note
  1, 2, S, P,
1 H hydrogen 1 1s1 2S12 S2S12
2 He helium 18 1s2 1S0 S1S0
3 Li lithium 1 [He] 2s1 2S12 S2S12
4 Be beryllium 2 [He] 2s2 1S0 S1S0
5 B boron 13 [He] 2s2 2p1 2P12 P2P12
6 C carbon 14 [He] 2s2 2p2 3P0 P3P0
7 N nitrogen 15 [He] 2s2 2p3 4S32 S4S32
8 O oxygen 16 [He] 2s2 2p4 3P2 P3P2
9 F fluorine 17 [He] 2s2 2p5[3] 2P32 P2P32
10 Ne neon 18 [He] 2s2 2p6 1S0 S1S0
11 Na sodium 1 [Ne] 3s1 2S12 S2S12
12 Mg magnesium 2 [Ne] 3s2 1S0 S1S0
13 Al aluminium 13 [Ne] 3s2 3p1 2P12 P2P12
14 Si silicon 14 [Ne] 3s2 3p2 3P0 P3P0
15 P phosphorus 15 [Ne] 3s2 3p3 4S32 S4S32
16 S sulfur 16 [Ne] 3s2 3p4 3P2 P3P2
17 Cl chlorine 17 [Ne] 3s2 3p5 2P32 P2P32
18 Ar argon 18 [Ne] 3s2 3p6 1S0 S1S0
19 K potassium 1 [Ar] 4s1 2S12 S2S12
20 Ca calcium 2 [Ar] 4s2 1S0 S1S0
21 Sc scandium 3 [Ar] 3d1 4s2 2D3/2 D2D3/2
22 Ti titanium 4 [Ar] 3d2 4s2 3F2 F3F2
23 V vanadium 5 [Ar] 3d3 4s2 4F3/2 F4F3/2
24 Cr chromium 6 [Ar] 3d5 4s1 7S3 S7S3
25 Mn manganese 7 [Ar] 3d5 4s2 6S5/2 S6S5/2
26 Fe iron 8 [Ar] 3d6 4s2 5D4 D5D4
27 Co cobalt 9 [Ar] 3d7 4s2 4F9/2 F4F9/2
28 Ni nickel 10 [Ar] 3d8 4s2 or [Ar] 3d9 4s1 3F4 F3F4
29 Cu copper 11 [Ar] 3d10 4s1 2D1/2 D2D1/2
30 Zn zinc 12 [Ar] 3d10 4s2 1S0 S1S0
31 Ga gallium 13 [Ar] 3d10 4s2 4p1 2P12 P2P12
32 Ge germanium 14 [Ar] 3d10 4s2 4p2 3P0 P3P0
33 As arsenic 15 [Ar] 3d10 4s2 4p3 4S32 S4S32
34 Se selenium 16 [Ar] 3d10 4s2 4p4 3P2 P3P2
35 Br bromine 17 [Ar] 3d10 4s2 4p5 2P32 P2P32
36 Kr krypton 18 [Ar] 3d10 4s2 4p6 1S0 S1S0
37 Rb rubidium 1 [Kr] 5s1 2S12 S2S12
38 Sr strontium 2 [Kr] 5s2 1S0 S1S0
39 Y yttrium 3 [Kr] 4d1 5s2 2D3/2 D2D3/2
40 Zr zirconium 4 [Kr] 4d2 5s2 3F2 F3F2
41 Nb niobium 5 [Kr] 4d4 5s1 6D1/2 D6D1/2
42 Mo molybdenum 6 [Kr] 4d5 5s1 7S3 S7S3
43 Tc technetium 7 [Kr] 4d5 5s2 6S5/2 S6S5/2
44 Ru ruthenium 8 [Kr] 4d7 5s1 5F5 F5F5
45 Rh rhodium 9 [Kr] 4d8 5s1 4F9/2 F4F9/2
46 Pd palladium 10 [Kr] 4d10 1S0 S1S0
47 Ag silver 11 [Kr] 4d10 5s1 2D1/2 D2D1/2
48 Cd cadmium 12 [Kr] 4d10 5s2 1S0 S1S0
49 In indium 13 [Kr] 4d10 5s2 5p1 2P12 P2P12
50 Sn tin 14 [Kr] 4d10 5s2 5p2 3P0 P3P0
51 Sb antimony 15 [Kr] 4d10 5s2 5p3 4S32 S4S32
52 Te tellurium 16 [Kr] 4d10 5s2 5p4 3P2 P3P2
53 I iodine 17 [Kr] 4d10 5s2 5p5 2P32 P2P32
54 Xe xenon 18 [Kr] 4d10 5s2 5p6 1S0 S1S0
55 Cs caesium 1 [Xe] 6s1 2S12 S2S12
56 Ba barium 2 [Xe] 6s2 1S0 S1S0
57 La lanthanum 3 [Xe] 5d1 6s2 2D3/2 D2D3/2
58 Ce cerium n/a [Xe] 4f1 5d1 6s2[4] 1G4 G1G4
59 Pr praseodymium n/a [Xe] 4f3 6s2 4I9/2 I4I9/2
60 Nd neodymium n/a [Xe] 4f4 6s2 5I4 I5I4
61 Pm promethium n/a [Xe] 4f5 6s2 6H5/2 H6H5/2
62 Sm samarium n/a [Xe] 4f6 6s2 7F0 F7F0
63 Eu europium n/a [Xe] 4f7 6s2 8S7/2 S8S7/2
64 Gd gadolinium n/a [Xe] 4f7 5d1 6s2 9D2 D9D2
65 Tb terbium n/a [Xe] 4f9 6s2 6H15/2 H6H15/2
66 Dy dysprosium n/a [Xe] 4f10 6s2 5I8 I5I8
67 Ho holmium n/a [Xe] 4f11 6s2 4I15/2 I4I15/2
68 Er erbium n/a [Xe] 4f12 6s2 3H6 H3H6
69 Tm thulium n/a [Xe] 4f13 6s2 2F7/2 F2F7/2
70 Yb ytterbium n/a [Xe] 4f14 6s2 1S0 S1S0
71 Lu lutetium n/a [Xe] 4f14 5d1 6s2 2D3/2 D2D3/2
72 Hf hafnium 4 [Xe] 4f14 5d2 6s2 3F2 F3F2
73 Ta tantalum 5 [Xe] 4f14 5d3 6s2 4F3/2 F4F3/2
74 W tungsten 6 [Xe] 4f14 5d4 6s2[5] 5D0 D5D0
75 Re rhenium 7 [Xe] 4f14 5d5 6s2 6S5/2 S6S5/2
76 Os osmium 8 [Xe] 4f14 5d6 6s2 5D4 D5D4
77 Ir iridium 9 [Xe] 4f14 5d7 6s2 4F9/2 F4F9/2
78 Pt platinum 10 [Xe] 4f14 5d9 6s1 3D3 D3D3
79 Au gold 11 [Xe] 4f14 5d10 6s1 2D1/2 D2D1/2
80 Hg mercury 12 [Xe] 4f14 5d10 6s2 1S0 S1S0
81 Tl thallium 13 [Xe] 4f14 5d10 6s2 6p1 2P12 P2P12
82 Pb lead 14 [Xe] 4f14 5d10 6s2 6p2 3P0 P3P0
83 Bi bismuth 15 [Xe] 4f14 5d10 6s2 6p3 4S32 S4S32
84 Po polonium 16 [Xe] 4f14 5d10 6s2 6p4 3P2 P3P2
85 At astatine 17 [Xe] 4f14 5d10 6s2 6p5 2P32 P2P32
86 Rn radon 18 [Xe] 4f14 5d10 6s2 6p6 1S0 S1S0
87 Fr francium 1 [Rn] 7s1 2S12 S2S12
88 Ra radium 2 [Rn] 7s2 1S0 S1S0
89 Ac actinium 3 [Rn] 6d1 7s2 2D3/2 D2D3/2
90 Th thorium n/a [Rn] 6d2 7s2 3F2 F3F2
91 Pa protactinium n/a [Rn] 5f2 6d1 7s2 4K11/2 K4K11/2
92 U uranium n/a [Rn] 5f3 6d1 7s2 5L6 L5L6
93 Np neptunium n/a [Rn] 5f4 6d1 7s2 6L11/2 L6L11/2
94 Pu plutonium n/a [Rn] 5f6 7s2 7F0 F7F0
95 Am americium n/a [Rn] 5f7 7s2 8S7/2 S8S7/2
96 Cm curium n/a [Rn] 5f7 6d1 7s2 9D2 D9D2
97 Bk berkelium n/a [Rn] 5f9 7s2 6H15/2 H6H15/2
98 Cf californium n/a [Rn] 5f10 7s2[6] 5I8 I5I8
99 Es einsteinium n/a [Rn] 5f11 7s2 5I15/2 I5I15/2
100 Fm fermium n/a [Rn] 5f12 7s2 3H6 H3H6
101 Md mendelevium n/a [Rn] 5f13 7s2 2F7/2 F2F7/2
102 No nobelium n/a [Rn] 5f14 7s2 1S0 S1S0
103 Lr lawrencium n/a [Rn] 5f14 7s2 7p1 2P1/2? P2P1/2?
104 Rf rutherfordium 4 [Rn] 5f14 6d2 7s2[7][8] 3F2 F3F2
105 Db dubnium 5 [Rn] 5f14 6d3 7s2[8] 4F3/2? F4F3/2?
106 Sg seaborgium 6 [Rn] 5f14 6d4 7s2[8] 5D0? D5D0?
107 Bh bohrium 7 [Rn] 5f14 6d5 7s2[9][8] 6S5/2? S6S5/2?
108 Hs hassium 8 [Rn] 5f14 6d6 7s2[8]
109 Mt meitnerium 9 [Rn] 5f14 6d7 7s2 (calculated)[8][10]
110 Ds darmstadtium 10 [Rn] 5f14 6d8 7s2 (predicted)[8]
111 Rg roentgenium 11 [Rn] 5f14 6d9 7s2 (predicted)[11][8]
112 Cn copernicium 12 [Rn] 5f14 6d10 7s2 (predicted)[8]
113 Nh nihonium 13 [Rn] 5f14 6d10 7s2 7p1 (predicted)[8]
114 Fl flerovium 14 [Rn] 5f14 6d10 7s2 7p2 (predicted)[8]
115 Mc moscovium 15 [Rn] 5f14 6d10 7s2 7p3 (predicted)[8]
116 Lv livermorium 16 [Rn] 5f14 6d10 7s2 7p4 (predicted)[8]
117 Ts tennessine 17 [Rn] 5f14 6d10 7s2 7p5 (predicted)[8]
118 Og oganesson 18 [Rn] 5f14 6d10 7s2 7p6 (predicted)[12][8]
119 Uue ununennium 1 [Og] 8s1 (predicted)[8]
120 Ubn unbinilium 2 [Og] 8s2 (predicted)[8]
121 Ubu unbiunium 3 [Og] 8s2 8p1 (predicted)[8]

Term symbols for an electron configurationEdit

The process to calculate all possible term symbols for a given electron configuration is a bit longer.

  • First, calculate the total number of possible microstates N for a given electron configuration. As before, we discard the filled (sub)shells, and keep only the partially filled ones. For a given orbital quantum number l, t is the maximum allowed number of electrons, t = 2(2l+1). If there are e electrons in a given subshell, the number of possible microstates is
 
As an example, let's take the carbon electron structure: 1s22s22p2. After removing full subshells, there are 2 electrons in a p-level (l = 1), so we have
 
different microstates.
  • Second, draw all possible microstates. Calculate ML and MS for each microstate, with   where mi is either ml or ms for the i-th electron, and M represents the resulting ML or MS respectively:
  ml  
  +1 0 −1 ML MS
all up 1 1
0 1
−1 1
all down 1 −1
0 −1
−1 −1
one up
one down
↑↓ 2 0
1 0
0 0
1 0
↑↓ 0 0
−1 0
0 0
−1 0
↑↓ −2 0
  • Third, count the number of microstates for each MLMS possible combination
  MS
  +1 0 −1
ML +2 1
+1 1 2 1
0 1 3 1
−1 1 2 1
−2 1
  • Fourth, extract smaller tables representing each possible term. Each table will have the size (2L+1) by (2S+1), and will contain only "1"s as entries. The first table extracted corresponds to ML ranging from −2 to +2 (so L = 2), with a single value for MS (implying S = 0). This corresponds to a 1D term. The remaining terms fit inside the middle 3×3 portion of the table above. Then we extract a second table, removing the entries for ML and MS both ranging from −1 to +1 (and so S = L = 1, a 3P term). The remaining table is a 1×1 table, with L = S = 0, i.e., a 1S term.

S = 0, L = 2, J = 2
1D2

  Ms
  0
Ml +2 1
+1 1
0 1
−1 1
−2 1

S=1, L=1, J=2,1,0
3P2, 3P1, 3P0

  Ms
  +1 0 −1
Ml +1 1 1 1
0 1 1 1
−1 1 1 1

S=0, L=0, J=0
1S0

  Ms
  0
Ml 0 1
  • Fifth, applying Hund's rules, deduce which is the ground state (or the lowest state for the configuration of interest.) Hund's rules should not be used to predict the order of states other than the lowest for a given configuration. (See examples at Hund's rules#Excited states.)
  • If only two equivalent electrons are involved, there is an "Even Rule" which states
For two equivalent electrons the only states that are allowed are those for which the sum (L + S) is even.

Case of three equivalent electronsEdit

  • For three equivalent electrons (with the same orbital quantum number l), there is also a general formula (denoted by X(L,S,l) below) to count the number of any allowed terms with total orbital quantum number "L" and total spin quantum number "S".

 

where the floor function   denotes the greatest integer not exceeding x.

The detailed proof could be found in Renjun Xu's original paper.[13]

  • For a general electronic configuration of lk, namely k equivalent electrons occupying one subshell, the general treatment and computer code could also be found in this paper.[13]

Alternative method using group theoryEdit

For configurations with at most two electrons (or holes) per subshell, an alternative and much quicker method of arriving at the same result can be obtained from group theory. The configuration 2p2 has the symmetry of the following direct product in the full rotation group:

Γ(1) × Γ(1) = Γ(0) + [Γ(1)] + Γ(2),

which, using the familiar labels Γ(0) = S, Γ(1) = P and Γ(2) = D, can be written as

P × P = S + [P] + D.

The square brackets enclose the anti-symmetric square. Hence the 2p2 configuration has components with the following symmetries:

S + D (from the symmetric square and hence having symmetric spatial wavefunctions);
P (from the anti-symmetric square and hence having an anti-symmetric spatial wavefunction).

The Pauli principle and the requirement for electrons to be described by anti-symmetric wavefunctions imply that only the following combinations of spatial and spin symmetry are allowed:

1S + 1D (spatially symmetric, spin anti-symmetric)
3P (spatially anti-symmetric, spin symmetric).

Then one can move to step five in the procedure above, applying Hund's rules.

The group theory method can be carried out for other such configurations, like 3d2, using the general formula

Γ(j) × Γ(j) = Γ(2j) + Γ(2j-2) + ... + Γ(0) + [Γ(2j-1) + ... + Γ(1)].

The symmetric square will give rise to singlets (such as 1S, 1D, & 1G), while the anti-symmetric square gives rise to triplets (such as 3P & 3F).

More generally, one can use

Γ(j) × Γ(k) = Γ(j+k) + Γ(j+k−1) + ... + Γ(|jk|)

where, since the product is not a square, it is not split into symmetric and anti-symmetric parts. Where two electrons come from inequivalent orbitals, both a singlet and a triplet are allowed in each case. [14]

Summary of various coupling schemes and corresponding term symbolsEdit

Basic concepts for all coupling schemes:

  •  : individual orbital angular momentum vector for an electron,  : individual spin vector for an electron,  : individual total angular momentum vector for an electron,  .
  •  : Total orbital angular momentum vector for all electrons in an atom ( ).
  •  : total spin vector for all electrons ( ).
  •  : total angular momentum vector for all electrons. The way the angular momenta are combined to form   depends on the coupling scheme:   for LS coupling,   for jj coupling, etc.
  • A quantum number corresponding to the magnitude of a vector is a letter without an arrow (ex: l is the orbital angular momentum quantum number for   and  )
  • The parameter called multiplicity represents the number of possible values of the total angular momentum quantum number J for certain conditions.
  • For a single electron, the term symbol is not written as S is always 1/2 and L is obvious from the orbital type.
  • For two electron groups A and B with their own terms, each term may represent S, L and J which are quantum numbers corresponding to the  ,  and   vectors for each group. "Coupling" of terms A and B to form a new term C means finding quantum numbers for new vectors  ,   and  . This example is for LS coupling and which vectors are summed in a coupling is depending on which scheme of coupling is taken. Of course, the angular momentum addition rule is that  where X can be s, l, j, S, L, J or any other angular momentum-magnitude-related quantum number.

LS coupling (Russell-Saunders coupling)Edit

  • Coupling scheme:   and   are calculated first then   is obtained. In practical point of view, it means L, S and J are obtained by using addition rule of angular momentums with given electronics groups that are to be coupled.
  • Electronic configuration + Term symbol:  .   is a Term which is from coupling of electrons in  group. n,l are principle quantum number, orbital quantum number and  means there are N (equivalent) electrons in nl subshell. For  , (2S+1) is equal to multiplicity, a number of possible values in J (final total angular momentum quantum number) from given S and L. For  , multiplicity is (2L+1) but (2S+1) is still written in the Term symbol. Strictly speaking,   is called Level and   is called Term. Sometimes superscript o is attached to the Term, means the parity  of group is odd (P = -1).
  • Example:
    1.  :   is Level of 3d7 group in which are equivalent 7 electrons are in 3d subshell.
    2.  : Terms are assigned for each group (with different principal quantum number n) and rightmost Level   is from coupling of Terms of these groups so   represents final total spin quantum number S, total orbital angular momentum quantum number L and total angular momentum quantum number J in this atomic energy level.
    3.  : There is a space between 5d and  . It means   and 5d are coupled to get  . Final level   is from coupling of   and 6p.
    4.  : There is only one Term   which is isolated in the left of the leftmost space. It means   is coupled lastly;   and 6s are coupled to get   then   and   are coupled to get final Term  .

jj CouplingEdit

  • Coupling scheme:  .
  • Electronic configuration + Term symbol:  
  • Example:
    1.  : There are two groups. One is   and the other is  . In  , there are 2 electrons having   in 6p subshell while there is an electron having   in the same subshell in  .Coupling of these two groups results in J = 3/2 (coupling of j of three electrons).
    2.  : 9/2 in () is   for 1st group   and 2 in () is J2 for 2nd group  . Subscript 11/2 of Term symbol is final J of  .

J1L2 couplingEdit

  • Coupling scheme:   and  .
  • Electronic configuration + Term symbol:  . For K > S2, (2S2+1) is equal to multiplicity, a number of possible values in J (final total angular momentum quantum number) from given S2 and K. For S2 > K, multiplicity is (2K + 1) but (2S2 + 1) is still written in the Term symbol.
  • Example:
    1.  :  . 9/2 is K, which comes from coupling of J1 and l2. Subscript 5 in Term symbol is J which is from coupling of K and s2.
    2.  :  . 7/2 is K, which comes from coupling of J1 and L2. Subscript 7/2 in Term symbol is J which is from coupling of K and S2.

LS1 couplingEdit

  • Coupling scheme: ,  .
  • Electronic configuration + Term symbol:  . For K > S2, (2S2 + 1) is equal to multiplicity, a number of possible values in J (final total angular momentum quantum number) from given S2 and K. For S2 > K, multiplicity is (2K+1) but (2S2 + 1) is still written in the Term symbol.
  • Example:
    1.  :  .  .

Most famous coupling schemes are introduced here but these schemes can be mixed together to express energy state of atom. This summary is based on [1].

Racah notation and Paschen notationEdit

These are notations for describing states of singly excited atoms, especially noble gas atoms. Racah notation is basically a combination of LS or Russell-Saunder coupling and J1L2 coupling. LS coupling is for a parent ion and J1L2 coupling is for an coupling of the parent ion and the excited electron. The parent ion is an unexcited part of the atom. For example, in Ar atom excited from a ground state …3p6 to an excited state …3p54p in electronic configuration, 3p5 is for the parent ion while 4p is for the excited electron.[15]

In Racah notation, states of excited atoms are denoted as  . Quantities with a subscript 1 are for the parent ion, n and l are principal and orbital quantum numbers for the excited electron, K and J are quantum numbers for   and   where   and   are orbital angular momentum and spin for the excited electron respectively. “o” represents a parity of excited atom. For an inert (noble) gas atom, usual excited states are Np5nl where N = 2, 3, 4, 5, 6 for Ne, Ar, Kr, Xe, Rn, respectively in order. Since the parent ion can only be 2P1/2 or 2P3/2, the notation can be shortened to   or  , where nl means the parent ion is in 2P3/2 while nl′ is for the parent ion in 2P1/2 state.

Paschen notation is a somewhat odd notation; it is an old notation made to attempt to fit an emission spectrum of neon to a hydrogen-like theory. It has a rather simple structure to indicate energy levels of an excited atom. The energy levels are denoted as n’l#. l is just an orbital quantum number of the excited electron. n'l is written in a way that 1s for (n = N + 1, l = 0), 2p for (n = N + 1, l = 1), 2s for (n = N + 2, l = 0), 3p for (n = N + 2, l = 1), 3s for (n = N + 3, l = 0), etc. Rules of writing n'l from the lowest electronic configuration of the excited electron are: (1) l is written first, (2) n' is consecutively written from 1 and the relation of l = n' - 1, n' - 2, ... , 0 (like a relation between n and l) is kept. n'l is an attempt to describe electronic configuration of the excited electron in a way of describing electronic configuration of hydrogen atom. # is an additional number denoted to each energy level of given n'l (there can be multiple energy levels of given electronic configuration, denoted by the term symbol). # denotes each level in order, for example, # = 10 is for a lower energy level than # = 9 level and # = 1 is for the highest level in a given n’l. An example of Paschen notation is below.

Electronic configuration of Neon n’l Electronic configuration of Argon n’l
1s22s22p6 Ground state [Ne]3s23p6 Ground state
1s22s22p53s1 1s [Ne]3s23p54s1 1s
1s22s22p53p1 2p [Ne]3s23p54p1 2p
1s22s22p54s1 2s [Ne]3s23p55s1 2s
1s22s22p54p1 3p [Ne]3s23p55p1 3p
1s22s22p55s1 3s [Ne]3s23p56s1 3s

See alsoEdit

NotesEdit

  1. ^ There is no official convention for naming angular momentum values greater than 20 (symbol Z). Many authors begin using Greek letters at this point (  ...). The occasions for which such notation is necessary are few and far between, however.

ReferencesEdit

  1. ^ a b NIST Atomic Spectrum Database To read neutral carbon atom levels for example, type "C I" in the Spectrum box and click on Retrieve data.
  2. ^ Levine, Ira N., Quantum Chemistry (4th ed., Prentice-Hall 1991), ISBN 0-205-12770-3
  3. ^ Jaccaud et al. 2000, p. 381.
  4. ^ Ground levels and ionization energies for the neutral atoms, NIST
  5. ^ Berger, Dan. "Why does Tungsten not 'Kick' up an electron from the s sublevel ?". Bluffton College, USA. 
  6. ^ CRC 2006, p. 1.14.
  7. ^ Cite error: The named reference rsc was invoked but never defined (see the help page).
  8. ^ a b c d e f g h i j k l m n o p q r Hoffman, Darleane C.; Lee, Diana M.; Pershina, Valeria (2006). "Transactinides and the future elements". In Morss; Edelstein, Norman M.; Fuger, Jean. The Chemistry of the Actinide and Transactinide Elements (3rd ed.). Dordrecht, The Netherlands: Springer Science+Business Media. ISBN 1-4020-3555-1. 
  9. ^ Johnson, E.; Fricke, B.; Jacob, T.; Dong, C. Z.; Fritzsche, S.; Pershina, V. (2002). "Ionization potentials and radii of neutral and ionized species of elements 107 (bohrium) and 108 (hassium) from extended multiconfiguration Dirac–Fock calculations". The Journal of Chemical Physics. 116: 1862. Bibcode:2002JChPh.116.1862J. doi:10.1063/1.1430256. 
  10. ^ Thierfelder, C.; Schwerdtfeger, P.; Heßberger, F. P.; Hofmann, S. (2008). "Dirac-Hartree-Fock studies of X-ray transitions in meitnerium". The European Physical Journal A. 36 (2): 227. Bibcode:2008EPJA...36..227T. doi:10.1140/epja/i2008-10584-7. 
  11. ^ Turler, A. (2004). "Gas Phase Chemistry of Superheavy Elements" (PDF). Journal of Nuclear and Radiochemical Sciences. 5 (2): R19–R25. 
  12. ^ Nash, Clinton S. (2005). "Atomic and Molecular Properties of Elements 112, 114, and 118". Journal of Physical Chemistry A. 109 (15): 3493–3500. Bibcode:2005JPCA..109.3493N. doi:10.1021/jp050736o. PMID 16833687. 
  13. ^ a b Xu, Renjun; Zhenwen, Dai (2006). "Alternative mathematical technique to determine LS spectral terms". Journal of Physics B: Atomic, Molecular and Optical Physics. 39 (16): 3221–3239. arXiv:physics/0510267 . Bibcode:2006JPhB...39.3221X. doi:10.1088/0953-4075/39/16/007. 
  14. ^ McDaniel, Darl H. (1977). "Spin factoring as an aid in the determination of spectroscopic terms". Journal of Chemical Education. 54 (3): 147. Bibcode:1977JChEd..54..147M. doi:10.1021/ed054p147. 
  15. ^ "APPENDIX 1 - Coupling Schemes and Notation" (PDF). University of Toronto: Advanced Physics Laboratory - Course Homepage. Retrieved 5 Nov 2017.