Concept

Irreducible representations — where it appears

One of the indivisible ways a group can act, labelled by its characters. Every degeneracy a symmetry requires is the dimension of one, and every selection rule is a statement about a product of them.

Named by 53 essays across 6 fields — each of them below, with the objects they name alongside it.

A d shell in an octahedral field. The five d energies in octahedral coordination, computed and drawn in units of the octahedral splitting. The dashed line is the barycentre, which the five levels sum to whatever the arrangement.

The splitting is a symmetry statement

Put six ligands round a metal and the five d orbitals stop being degenerate. Which of them stay together, and how many sets there are, follows from the point group alone — before any account of what the ligands are made of, and before any number is computed.

applied · Ligand field
The Td character table. The irreducible representations of the molecule's point group. The class headings carry the number of operations found by generating the group from the coordinates, and those counts were produced before this table was opened.

Character tables and reduction

A molecule's point group is a list of matrices, not a label. Generating them, sorting them into classes, and dividing by the group order turns any set of orbitals into a statement about how many energies there can be.

symmetry · Representation
Eighteen electrons, from a reduction. The ligand σ orbitals of an octahedral complex reduced in Oh (A₁g ⊕ Eg ⊕ T₁u), matched against the metal's nine valence orbitals by species, and counted. 6 bonding and 3 non-bonding orbitals hold 18 electrons.

Eighteen is a count

The eighteen-electron rule is usually justified by adding up an s, three p and five d orbitals. That is a restatement rather than a reason. Reduce the ligand orbitals in the complex's own point group, match them against the metal's by symmetry, and the number that comes out is the count of orbitals lying below a gap — which is eighteen for an octahedron, sixteen for a square plane, and eighteen again for a tetrahedron for a different reason.

applied · Electron count
6 molecules, counted. How many vibrations each molecule has, how many symmetry species they fall into, and how many frequencies are infrared active, Raman active, both, or neither. Every column after the first counts frequencies rather than modes, because a degenerate pair is one line in a spectrum. The molecules with a centre of inversion are the ones with nothing in the both column — mutual exclusion as a computed count. Nothing here uses a force constant.

How many frequencies, not how many modes

Benzene has thirty vibrations. It has twenty distinct frequencies, and of those, eleven can be seen — four in the infrared and seven in the Raman, with no band in common. The other nine are invisible to both experiments, exactly.

spectra · Spectrum
4 molecules, counted. How many vibrations each molecule has, how many symmetry species they fall into, and how many frequencies are infrared active, Raman active, both, or neither. Every column after the first counts frequencies rather than modes, because a degenerate pair is one line in a spectrum. The molecules with a centre of inversion are the ones with nothing in the both column — mutual exclusion as a computed count. Nothing here uses a force constant.

Two structures, two spectra

A linear XY₂ gives two infrared bands, one Raman band and no band in common. A bent XY₂ gives three of each and three in common. Counting settles the shape, without a force constant, an assignment or a single measured frequency.

spectra · Spectrum
benzene: 30 vibrations. The vibrational representation, obtained by subtracting the translations and rotations from the full set of Cartesian displacements, with the infrared and Raman activity of each species read off the same character table.

What an absence proves

A band that symmetry forbids is not weak. Its intensity is zero, exactly, by a theorem — while a band that is merely too faint to see is absent for reasons no theorem covers. The two look identical in a spectrum and support completely different conclusions.

spectra · Spectrum
The Td character table. The irreducible representations of the molecule's point group. The class headings carry the number of operations found by generating the group from the coordinates, and those counts were produced before this table was opened.

Degeneracy is a group theorem

How many orbitals can share an energy is decided before any energy is computed. The dimensions of a group's irreducible representations are the only degeneracies it permits, and a molecule with no representation larger than one cannot have a degenerate level at all.

symmetry · Representation
cyclobutadiene: what alternation costs and gains. The π energy of cyclobutadiene as its bonds are alternated by β(1 ± δ), the elastic cost of alternating them at a stated stiffness, and the sum. The π curve falls linearly in δ, which is measured here and is the whole difference between a molecule that distorts and one that does not. The stiffness is a stated parameter, so where the minimum falls is not a claim; which power of δ each curve goes as is.

The vibration that lowers the symmetry

A molecule in a degenerate electronic state distorts until the degeneracy is gone. Which distortion it needs is a direct product; whether it wins is a race between a π energy falling linearly and a σ frame resisting quadratically, and both powers are measured here.

beyond · Aromaticity
Oh descending to D4h. Every irreducible representation of Oh restricted to D4h and reduced there — A1g, A2g, Eg, T1g, T2g, A1u, A2u, Eu, T1u, T2u. A representation that arrives in more than one piece is a degeneracy the lower symmetry cannot hold, so a level carrying it must split when the molecule distorts.

Descent in symmetry

Lower a molecule's symmetry and its labels stop being available. Which of them survive, which split, and into what, is decided by restricting characters to the operations that are left — arithmetic, not a table to be looked up.

symmetry · Point group
carbon dioxide: D∞h worked in D2h. The vibrations of carbon dioxide, computed in D2h because D∞h has infinitely many operations and the reduction formula divides by the order of the group. Each constructed operation is checked against the molecule before use. The count must come out at 3N−5 rather than 3N−6 — 4 for 3 atoms — because rotation about the molecular axis moves no atom and is not a motion of the molecule at all.

An infinite group, worked in a finite one

A linear molecule has infinitely many symmetry operations, and every formula in character theory divides by the number of them. The standard device is to work in a finite subgroup — and it is worth computing what that trade costs rather than putting it in a footnote.

symmetry · Point group
F s on sulfur hexafluoride: a₁g ⊕ eg ⊕ t₁u. The character of the basis under each class of operations, which is a count of what did not move, and the multiplicities that come out of the reduction formula. The multiplicities must be whole numbers, and that is the check.

Six bonds and four orbitals

The six fluorine σ functions of sulfur hexafluoride span a₁g ⊕ eg ⊕ t₁u. Sulfur's 3s and 3p supply a₁g and t₁u and nothing else, so four bonding orbitals hold twelve electrons across six bonds — a bond order of two thirds, computed from characters with no energy anywhere in it.

symmetry · Hypervalency
Dipole selection rules in Oh. For every pair of symmetry species, whether an electric dipole transition between them is allowed and along which polarisation. An entry is allowed exactly when the triple product of representations contains the totally symmetric one.

Why a d–d band is weak

In a centrosymmetric complex the transition between the two halves of a split d shell is forbidden — exactly, by parity, with no small quantity anywhere. What makes it visible at all is that the molecule is never quite centrosymmetric, and the computation says which vibrations do the work.

spectra · Representation
Sixteen electrons, from a reduction. The ligand σ orbitals of a square planar complex reduced in D4h (A₁g ⊕ B₁g ⊕ Eu), matched against the metal's nine valence orbitals by species, and counted. 4 bonding and 4 non-bonding orbitals hold 16 electrons.

Sixteen is also a count

A transition metal brings nine valence orbitals, and nine filled orbitals is eighteen electrons. A square plane leaves more of those nine unmatched than an octahedron does and still holds fewer electrons, because one of the leftovers is out of reach.

applied · Electron count
Why a character table has the rows it has. All 20 groups this site defines, with the two counts that fix the shape of every character table: the number of representations equals the number of classes, and the sum of the squares of their dimensions equals the order of the group. Neither column pair differs anywhere in the table, and there is no room for another row in any of them.

Why a character table stops where it stops

A character table is square, and both of its dimensions are forced. The number of representations equals the number of classes, the squares of their dimensions sum to the order of the group, and between them there is no room for another row.

symmetry · Representation
ammonia: 3 valence bands. The measured valence photoelectron bands of ammonia, each labelled with the symmetry species of the orbital it comes from, and beside them the species the valence basis spans — the central atom's s and p functions and one s on each ligand, reduced in the molecule's own group. A band carrying a species the reduction does not produce would stop this figure being drawn.

Fewer bands than electrons

Methane has eight valence electrons and two photoelectron bands. Ammonia has eight and three; water has eight and four. The count is not of electrons, not of bonds and not of orbitals — it is of the symmetry species the occupied orbitals fall into, and it falls as the symmetry rises.

spectra · Photoelectron
Two answers from one projector: E1g. The E1g projection operator of benzene, applied to the pz function on one atom and then to the one on its neighbour. Both results belong to the same two-dimensional representation and span the same subspace; neither is more correct than the other; and they are different pictures, overlapping by 0.500. The circle areas are the coefficients and the two colours are their signs.

The projector is unique, the basis is not

A reduction says how many times each representation appears. It cannot say which combinations of orbitals they are — that takes a projection operator, and for a degenerate representation the operator returns a different pair of orbitals depending on which function it is handed first. Both pairs are correct, they span the same space, and every energy computed from either is identical.

symmetry · Representation
Mutual exclusion across every group here. The 20 groups with tables here, each with its highest rotation order, whether it has a centre of inversion, which of its representations carry a coordinate, which carry a product of coordinates, and whether any carries both. Every group with a centre excludes, which is a theorem. 1 group without a centre excludes as well — D5h — so the rule does not run backwards, and the counterexample needs a fivefold axis.

Mutual exclusion does not prove a centre

A centrosymmetric molecule shows no band in both its infrared and its Raman spectrum. The rule is a theorem and its converse is read off as though it were part of it — but ferrocene in the gas phase has no centre of inversion and no coincidence either, and the reason is that a fivefold axis separates the coordinates from their products where a threefold or fourfold axis cannot.

spectra · Spectrum
Every set of point groups here that shares a table. Found by comparing character matrices rather than named: five sets among the tabulated groups, at orders 2, 4, 6, 8, 20. The smallest is the most startling — a mirror plane, a centre of inversion and a twofold axis all have the two-row table with entries 1, 1 and 1, −1, and one of the three describes a chiral molecule. The largest is the eclipsed and staggered conformers of ferrocene, which are one molecule at two temperatures.

One table, three groups

A mirror plane, a centre of inversion and a twofold axis have the same character table — two rows, entries 1, 1 and 1, −1 — and one of the three describes a chiral molecule. A character table is a property of an abstract group; a point group is that plus an action on space, and the action is what a molecule has.

symmetry · Representation
The characters of C6, and the levels they are. The 6 representations of the ring's rotation group, drawn as points on the unit circle at 2πk/6. Each level is twice the horizontal coordinate: a representation and its complex conjugate have the same real part, so they are degenerate, and the levels pair up automatically. Only k = 0 — and k = n/2 when n is even — lands on the real axis, so one level is unpaired at the bottom and the shell closes at 4n + 2. Nothing here has been diagonalised.

The ring's levels are its group's characters

The Hückel energies of a cyclic system are twice the real part of the characters of its own rotation group, so the level pattern — one level, then pairs, then one more if the ring is even — is a group theorem rather than a calculation. Hückel's 4n+2 rule is a statement about the representations of a cyclic group and about nothing else.

symmetry · Aromaticity
Two moments of the n = 2 shell, and only one of them agrees. ⟨1/r⟩ and ⟨1/r²⟩ for each orbital of the n = 2 shell of hydrogen, computed from the radial functions and checked against their closed forms. The first is the same number for every member — which is why they share an energy — and the second differs by a factor of 3 across the shell.

The degeneracy no group predicts

How many orbitals can share an energy is decided by a group before any energy is computed, and the rotation group of a central potential permits one, three, five and seven. Hydrogen's second shell has four orbitals at one energy and its third has nine. The extra degeneracy is not an accident of the arithmetic — it is the signature of a symmetry that has not been named, and it survives only for a potential that goes exactly as one over r.

symmetry · Representation
The dipole moment, and how many bands there are. For each of five molecules: the dipole moment of the point-charge model, the number of modes whose dipole derivative does not vanish, and the largest derivative. The molecules with no dipole at all have the most active bands, which is the whole of the argument.

A dipole is not what an infrared spectrum sees

Carbon dioxide has no dipole moment at all and three of its four modes are infrared active. Methane has none and six of nine; boron trifluoride none and five of six. Water, which has the largest dipole of the five, has three modes and three bands — and its dipole predicted neither number.

shape · Dipole
A field splits the n = 2 shell into whole numbers. The eigenvalues of z inside the shell, which are the shifts a uniform field produces to first order. There are three distinct ones and each is a whole number times (3/2)n, so the splitting is proportional to the field itself rather than to its square — which is what no other atom does.

The symmetry that is not a rotation

Hydrogen's n = 2 shell holds four states at one energy and its rotation group accounts for at most three. The operator that accounts for the fourth is built here out of computed integrals: three matrices whose commutators close into the rotations, whose product with the angular momentum vanishes, and whose Casimir comes out at exactly n² − 1.

symmetry · Representation
The total energy against the distortion, at several gaps. The elastic cost plus the second-order lowering, for five gaps between the ground state and the excited state it mixes with. The critical gap is 1.00: above it the symmetric structure is the minimum, below it the minimum has moved off zero, and nothing about the molecule is degenerate in either case.

A distortion needs two states

A degenerate electronic state cannot survive — that is the Jahn–Teller theorem, and it can be computed. A closed shell can fail to survive too, and the condition is a number: the symmetric structure holds only while the nearest excited state of the right symmetry lies above 2λ²/k, and one of ten symmetry species in an octahedron is the right one.

applied · Peierls distortion
One distortion, resolved into the species of the group it left. An arbitrary displacement of benzene, projected onto each symmetry species of D6h. The weights add to 1, which is the check that the projectors resolve the whole of it: the largest is E2g at 35.0 per cent, and the totally symmetric part — 3.4 per cent here — is the part that changes every distance and no symmetry at all.

How far, and along which coordinate

A continuous symmetry measure returns one number: how far a structure is from a shape. Projecting the same displacement onto the twelve symmetry species of benzene's group turns it into a list that sums to 1.000000000000, says which coordinates the structure left along, and shows that the totally symmetric part — 3.4 per cent of this one — moves every atom by 0.0200 ångström and lowers the symmetry measure by nothing at all.

symmetry · Point group
Four, however many ligands there are. For each molecule, the number of ligand σ combinations that find a partner among the central atom's four s and p orbitals, against the number of ligands and lone pairs it has. The matched count rises along the diagonal and then stops at four, because there are four orbitals; everything above the ceiling is a pair with nowhere on the central atom to go, and that is what the word hypervalent names.

Four is all that s and p can match

Reduce the ligand σ set of ten molecules in each one's own point group and ask how many of its components transform as one of the central atom's four valence orbitals. The answer is never more than four — not by arrangement, in every geometry from linear to octahedral — and what is left over is n + L − 4, with exactly twice that many electrons in excess of an octet.

beyond · Hypervalency
Two kinds of answer to a flux, and only one of them is a curve. The π binding of three rings against the magnetic flux through them, in units of beta and of the flux quantum, measured from each ring's own value at zero flux. Beta is negative, so a binding that FALLS is an energy that rises: benzene's does, which is what a diamagnetic ring current is. Cyclobutadiene's rises in both directions from a corner — its energy has no second derivative at zero field at all, and the two one-sided slopes differ by 12.57.

Two rules that share no arithmetic

Hückel's rule is a statement about a gap. Put a magnetic flux through the same rings instead and ask which of them push the field out, and the answer is the same set — eighty cases, no exceptions — although the second calculation counts nothing and has no shells in it. And the rings the rule excludes turn out to have no magnetic susceptibility at all: their energy has a corner at zero field.

symmetry · Aromaticity
A photoelectron band is a filter, and the group chooses the filter. The Huang–Rhys factor of every vibration of five molecules under a change of geometry that lengthens every bond alike — which is what removing an electron from a non-degenerate orbital does. On a logarithmic scale spanning sixteen decades, eight modes carry the whole of it and the rest sit on the floor at arithmetic noise. Which ones is decided by the point group: only a totally symmetric vibration can appear, whatever the size of the change.

A band is a filter on the modes

A photoelectron band's vibrational structure reports the frequencies of a few of the ion's vibrations and is silent about the rest, and which few is decided by the point group before any geometry is known. Under a change of shape that lengthens every bond alike, methane's totally symmetric stretch gets a Huang–Rhys factor of 0.905 and its other eight modes get between 10⁻²⁸ and 10⁻³⁵.

spectra · Photoelectron
An effect that cannot distort a molecule, deciding how far it distorts. The energy along one distortion coordinate, three times. With only the first-order term the minimum is at 0.6; with only the second-order term there is no minimum away from zero at all, because the gap of 1.5 is above the critical 1 for a closed shell on its own. With both, the molecule distorts to 1.06 — well past the first-order answer — and gains 0.09 more than the two separate stabilisations add up to.

Two distortions in one coordinate

A second-order Jahn–Teller effect that cannot distort a molecule by itself — its gap is half again above the critical value — nearly doubles the distortion when a first-order effect is already acting. The molecule goes to 1.075 instead of 0.600 and gains twice the energy, and it does it while the gap the second-order term divides by is opening rather than closing.

shape · Peierls distortion
Three quarters, exactly, for every mode that is not totally symmetric. The depolarisation ratio of every Raman-active mode of five molecules, computed from a bond-polarisability model. 18 of the 26 sit on three quarters to better than a millionth, and they are exactly the modes that are not totally symmetric: the mean polarisability derivative is a trace, a trace is invariant, and an invariant has no derivative along any other species. The polarised ones below the line are the totally symmetric modes, and where they sit is a property of the model rather than of the group.

The one intensity symmetry does fix

Symmetry says which bands exist and declines to say how strong they are. It makes exactly one exception, and it is a ratio: every Raman band that is not totally symmetric is depolarised by exactly three quarters, whatever the molecule and whatever the model — and methane's symmetric stretch is polarised by exactly zero, because its group is cubic.

symmetry · Spectrum
The shallowest slope, and the steepest. For three molecules, the softest and stiffest vibrations, the species each belongs to, and what a unit distortion along each costs. The cost is not taken from the frequency: it is computed by resolving the distortion onto the normal coordinates in the mass-weighted metric and adding up ω²q². That it comes back as the frequency is the identity the whole comparison rests on — the species decomposition uses only the coordinates and the group, and the cost uses only the masses and the force constants, and the two have to agree on this case before they can be asked to disagree on any other.

The coordinate it was already soft along

A distorted structure can be resolved into the symmetry species of its ideal group, and that resolution cannot say which coordinate a molecule fell down by itself and which one something outside pushed it along. The force field answers that, and the two halves agree on the case where they must — a unit distortion along a normal mode costs exactly that mode's frequency, to a part in a million, computed from masses and force constants by one side and from coordinates and characters by the other.

symmetry · Point group
Where the orphan pair actually sits. A σ-only Hückel model of each molecule, built from its own coordinates: the central atom's four valence orbitals, one σ orbital on each ligand, and the coupling between them the direction cosine of that ligand. Lone pairs need no special handling — they come out of the diagonalisation as the central orbitals no ligand combination transforms like. The charge is measured rather than assigned, and PF₅ comes out with two kinds of fluorine at 3 at -0.13 and 2 at -0.3, the more charged pair being the axial one that carries the orphan.

The count is the population

The census counted how many ligand combinations have no partner on the central atom and called the count n + L − 4. A σ-only model built from each molecule's own coordinates says what that count is worth: with no electronegativity difference anywhere, the mean charge on a ligand is minus the orphan count divided by the ligand count, exactly, in all ten cases. And the prediction the census made — that the charge grows with the orphan count — is refused by the divisor.

beyond · Hypervalency
A ratio that measures a distortion, and squares it first. How far ammonia's depolarised bands come off three quarters against how far one of its bonds has been stretched. Undistorted the departure is 3.1e-8, which is the rounding in the stored coordinates rather than a physical effect; at 0.1 Å it is 0.04239, and the slope is 1.999 — the departure goes as the square of the distortion, so a ratio measured to three decimals fixes a length to one and a half.

A ratio that squares what it measures

A depolarised Raman band sits at exactly three quarters because symmetry says its mean polarisability derivative is zero. Distort the molecule and it comes off — by 4.5 × 10⁻⁴ for a hundredth of an ångström and 0.042 for a tenth, going as the square of the distortion, which makes a ratio measured to three decimals a length known to one and a half.

spectra · Spectrum
A species label is ambiguous for every one of 17. For each molecule, the share of its vibrations belonging to a symmetry species that appears more than once — the distortions a species label cannot price, because the label picks a space rather than a mode. Every molecule in the census has at least one such species, the share averages 71.4 per cent, and for 9 of 17 the repetition is not forced by the group's capacity — those molecules have fewer vibrations than their group could hold without repeating, and repeat anyway.

A label that prices nothing

Pricing a distortion by its symmetry species works when the species appears once. It appears more than once for every one of seventeen molecules — 71.4 per cent of their vibrations on average belong to a species that is not unique — and for nine of the seventeen nothing forces it: their groups have room to spare and they repeat anyway.

symmetry · Point group
However hard the π channel is driven, the counted orbital stays the metal's. The metal's share of the filled T₂g orbital against the π coupling, with the eighteen-electron count drawn beside it. The share falls from 1 to 0.5467 across a coupling range of 80,000 cm⁻¹ and approaches a half from above without reaching it: the lower eigenvector of a two-level problem always carries more of the lower basis function, whatever the coupling. The count is eighteen at every point.

The count that cannot be broken by strength

Back-donation puts electrons into orbitals that are not the metal's, and the eighteen-electron rule counts the metal's nine. Turning the π channel up as far as it will go never breaks it: the counted orbital's metal share falls from 100 per cent to 54.67 and approaches a half from above without reaching it. What does flip it is not strength but order.

applied · Electron count
Ten molecules, twenty-six arrangements, three disagreements. Every arrangement of every one of the ten molecules, with the point group recovered from the arrangement's own coordinates and the ligand σ set reduced in it. 27 of them can be worked in a tabulated group; the formula n + L − 4 is right for 23 and wrong for 4. Every failure is a planar arrangement of four or more ligands, and every one of them is a molecule that does not adopt that arrangement.

The square that wastes an orbital

The orphan count that prices hypervalency was treated as a property of a molecule's composition — ligands plus lone pairs minus four. Run on twenty-six arrangements of the same ten molecules it is right for twenty-three and wrong for three, and all three are flat. A planar arrangement gives a main-group centre three usable orbitals rather than four, so the count is a property of the shape.

beyond · Hypervalency
The gap that makes sixteen special does not move. The gap above the sixteen-electron closure of a square plane and above the eighteen-electron closure of an octahedron, against the π strength. The octahedron's is 3eσ − 4eπ and moves at every value; the square plane's is exactly 2eσ until the π strength reaches a quarter of the σ one, because the orbital that sets it is d(z²) and a square-planar ligand set has nothing of that symmetry to offer. Past the threshold the two are the same number, which is not a coincidence: beyond it the square plane's gap is set by d(xy) and the expression is the octahedron's.

The orbital a ligand cannot reach

The sixteen-electron count of a square plane is a statement about an energy rather than about symmetry matching, so it was the count that ought to be sensitive to a π channel where the eighteen-electron one is not. It is not sensitive either — and for a sharper reason. The orbital that sets its gap is d(z²), and a square-planar ligand set contains nothing of that symmetry, so the gap is exactly 2eσ until the π strength reaches a quarter of the σ one.

applied · Electron count
Where the explanation gives a negative number of vibrations. The usual formula against the answer, for the 15 molecules with internal coordinates here. It is right for 7 of them and wrong for 8, and for sulfur hexafluoride, benzene and both ferrocenes it predicts a negative number of totally symmetric vibrations — which is the clearest possible sign that the quantity being subtracted is not the one that should be.

A formula that predicts minus eleven vibrations

A molecule's count of totally symmetric vibrations is often explained as one per orbit of internal coordinates, less one per redundancy, with methane as the worked example. Computed for fifteen molecules it is right for seven and wrong for eight — and for sulfur hexafluoride, benzene and both ferrocenes it returns a negative number. Two independent corrections turn it into an identity.

symmetry · Point group
How fast the three quarters goes, along each coordinate. The coefficient of the square, for every non-symmetric mode of three molecules, against the mode's own frequency. A single measurement takes one of these — along a bond stretch — and reports the exponent rather than the size. The sizes span a factor of thirty within methane alone, and the coordinates a molecule is softest along are not systematically the most sensitive: ammonia's stiff pair is five times more sensitive than its soft one.

One number was one direction

The departure of a depolarisation ratio from three quarters goes as the square of a distortion, and the exponent was first measured along one bond stretch. Computed along every non-symmetric coordinate the exponent is always two and the coefficient is not: it spans a factor of thirty inside methane. And the ratio is not preferentially sensitive to the coordinates a molecule is soft along — in two molecules of three the stiffest coordinate is the most sensitive.

spectra · Spectrum
The repulsion against the count, and they do not sort together. Every arrangement of the census by how many ligand σ combinations are left without a central partner and by how far its ligand repulsion sits above the best arrangement of that many points. The three that break the formula are marked. They are not the expensive ones: they sit at 4.2, 6.3, 9.8 per cent while the arrangements the formula gets right run to 26.5.

Expensive is not the same as unadopted

A counting formula right for twenty-three arrangements and wrong for three invites a reading: the failures are the arrangements nothing adopts, so the formula is reliable because chemistry stays away from where it breaks. Put the repulsion energy on the same axis and the reading fails — the most expensive arrangement in the census is one the formula gets right.

beyond · Hypervalency
What a fifth ligand does to the gap above eight electrons. The gap between the fourth and fifth d levels as one axial σ donor is brought in, and as two are. It closes exactly linearly — 2eσ less one eσ for each unit of axial σ strength — and a full octahedron has none of it left. The rule of sixteen has a gap to be about only while the axial positions are empty, and how much of it survives is a number rather than a yes or no.

The ligand the rule was waiting for

A sixteen-electron complex is called reactive because it can add a ligand, and the gap that makes it sixteen points straight at where the ligand arrives. Bringing one in closes the gap exactly linearly — and leaves its exactness completely untouched, which is the opposite of what bending the same complex does.

applied · Electron count
Folding two ligands makes the gap bigger before it makes it smaller. The gap above eight electrons as two of the four ligands fold to the same side. It rises first, to 2.0938eσ at 20°, before falling. The four-ligand path only ever closes it, so the direction the gap moves is not a property of bending — it is a property of which ligands bend.

The distortion that opens the gap

Two distortions close the sixteen-electron gap — one by bending all four ligands, one by adding a fifth. Folding two of the four makes it larger, by five per cent, before it makes it smaller. And it costs the exactness at the first degree, while the gap is still growing, so the size of a gap and whether it is exact are not one measurement.

applied · Electron count
One steps, the other slides — and the step is at the far end. The repulsion energy and the orphan count along the path from a tetrahedron to a square plane. The energy rises smoothly and monotonically, lowest at the tetrahedron and highest at the plane. The count is zero everywhere — including at 89.99° — and becomes one only at 90° exactly. The step is not near the energy's minimum; it is at its maximum, and it is at a single point.

A count that changes at one point

Where does the orphan count step along a distortion, relative to where the energy's minimum sits? A rule that depends on an exact symmetry may have no answer for a real molecule. On the path from a tetrahedron to a square plane the count is the same at every angle up to 89.99° and changes only at 90° exactly — which is the energy's maximum, not its minimum, and a single geometry out of a continuum.

beyond · Hypervalency
The energy runs the whole way; the count exists at the two ends. The Coulomb repulsion of six ligands along the Bailar twist, from the trigonal prism at 0° to the octahedron at 60°, with the geometries that have an orphan count marked underneath. The energy is smooth and monotone, lowest at the octahedron. The count is defined at the two ends and at the handful of angles the symmetry finder rounds into them, and nowhere else — not because the geometry is unsymmetrical, but because its group is not tabulated.

The group nobody wrote a table for

The orphan count is predicted to be constant along the Bailar twist, because the twist keeps D3 the whole way. The premise is exactly right — at every angle strictly between the prism and the octahedron the symmetry finder assembles six operations that hold to four parts in 10¹⁶. The conclusion cannot be tested here, because a count is a reduction, and the calculation's nineteen character tables did not include D3.

beyond · Hypervalency
What happens to the level that was exact. The three levels of the trio as one of the two outer orbitals is raised. At zero detuning the middle one sits at -13.6 exactly — it is the antisymmetric combination, and nothing of its symmetry exists for it to mix with. The moment the two are made inequivalent that statement is gone: the level leaves linearly, and the other two barely move by comparison.

A symmetry holds or it does not

One level of a three-orbital trio sits at the free-atom energy exactly, at every third-orbital energy, because the antisymmetric combination of the pair has nothing of its own symmetry to mix with. Detuning one of the two by a twentieth of an electron volt moves it by half of that — first order, immediately, with no protected regime at all.

wrong · Overlap
The same number, in three different groups, all the way along. The orphan count along the Bailar twist once the D3 character table is written. It is 2 at every one of the 15 geometries the symmetry finder answers for, across D3h at the prism, D3 through the whole interior and Oh at the octahedron. The lower row shows what the same sweep gave before the table existed: two ends and nothing between. This constancy was predicted from the premise that the twist keeps D3 throughout, and the premise was right.

The count the table was hiding

The interior of the Bailar twist looks uncountable — exactly D3 at every angle, and D3 is a point group whose character table is rarely written out. Writing it takes nine lines and settles the prediction made for the path: the orphan count is two at every geometry on the path that can be answered, in three different groups, out of three different decompositions.

beyond · Hypervalency
The reading is a function of direction, with a sixty-degree period. The departure of a depolarised band from three quarters, for distortions of equal magnitude pointing all the way round the plane of stretches that sum to zero. It is not one number: it runs from 8.177e-6 to 1.617e-5, a factor of 1.978. The minima are at one bond against another and the maxima at two bonds against one, and the pattern repeats every sixty degrees.

One number was a direction too

The depolarisation probe is exactly blind to the totally symmetric direction, which suggests it reads the distortion's component outside that species. What is left is a plane, and over a circle in it the reading varies by a factor of 1.98 — smallest for one bond against another, largest for two bonds against one, repeating every sixty degrees.

spectra · Spectrum
One fold opens it, two close it, and the antisymmetric one does neither. The gap along three directions out of the square plane: folding one pair, folding both equally, and — from a symmetric point ten degrees out — folding one pair further while unfolding the other by as much. The first rises, the second falls, and the third leaves at zero slope. That third direction is the one the question asked for.

The direction the gap cannot see

A two-ligand fold opens the sixteen-electron gap and a four-ligand bend closes it, so a distortion mixing the two must pass through a direction the gap does not move along. It does, and the direction is the antisymmetric fold — one pair of trans ligands up, the other down. Its blindness is exact, because exchanging the two pairs is a symmetry of the arrangement.

applied · Electron count
The sum is flat and the maximum is not. Both readings round the circle, each divided by its own average so the two can be drawn together. The maximum varies by 98 per cent; the sum over all four depolarised bands varies by 0.038. A sum cannot be changed by reordering, so if each band's departure is an isotropic quadratic form the sum must be constant — and to four parts in ten thousand it is.

The sum was flat all along

The depolarisation reading varies by a factor of two round a circle in the non-symmetric plane, and the anisotropy may belong to taking a maximum over four bands rather than to the physics. Summing the four instead gives a reading constant to four parts in ten thousand, against a maximum that varies by ninety-eight per cent.

spectra · Spectrum
Which torsions a molecule's own operations turn backwards. Every torsion orbit of the molecules here that have torsions: how many operations carry the torsion onto itself, how many of those are proper, and which operations reverse it. 7 of 9 orbits are reversed, and in every one the operation doing it is improper — the plane of a planar molecule, a mirror bisecting the torsion's bond, or a centre of inversion at that bond. Proper operations fix torsions too, benzene's twofold axes and hydrogen peroxide's among them, and never reverse one. Staggered ferrocene gives the same rows as eclipsed.

Five coordinates for six vibrations

A torsion is reversed by every improper operation that carries it onto itself and by no proper one, so adding torsions tests the orbit rule on a second kind of signed coordinate — and the rule holds on every molecule. It also moves hydrogen peroxide's count of totally symmetric vibrations from three to four, which a property of a molecule cannot do. Its five coordinates never spanned its six vibrations, and three of fifteen coordinate sets had been counting vibrations they did not describe.

symmetry · Point group
Every exact fit lies on one closed curve. The one-parameter family of force fields that reproduce all six of boron trifluoride's frequencies exactly, drawn in the B–F stretch constant and the stretch–bend coupling. It is a closed curve: the stretch constant runs from 3.94 to 12.11 millidyne per ångström and the coupling from -0.36 to 6.71. The four fits from four starting points sit together in one small patch of it.

The residual was a loop

Projecting away boron trifluoride's flat direction left four fits disagreeing by a tenth in the B–F stretch constant, and the disagreement was put down to the search or to the arithmetic. It is neither. Two frequencies cannot fix three constants in one symmetry block, so the exact fits form a closed curve along which the stretch constant runs from 3.9 to 12.1, and the four fits are four points on a short arc of it.

spectra · Normal mode
The orbit identity holds on all nineteen, and the formula it replaced on eight. For each molecule in the census under the radius rule: its number of totally symmetric vibrations, the corrected count — symmetric orbits less symmetric redundancies — and the usual formula, orbits less redundancies. The corrected count lands on the molecule's own count every time. The usual formula is right for 8 of 19, and for ferrocene under the new bond list it predicts minus sixty-six.

The census a bond rule was hiding

Every internal coordinate, redundancy and totally symmetric count here is built on a bond list, and the bond list came from a length cutoff that gave five molecules no bonds. Rebuilt on the radius rule, the census reaches nineteen molecules instead of fifteen, the orbit identity holds on every newcomer, ferrocene's coordinates finally span all its vibrations — and a different gap appears: no bond rule can give a square-planar centre its two out-of-plane vibrations.

symmetry · Point group
Two centres, one path, and the leftover changes sides. The count of leftover orbitals along the Bailar twist, for a main-group centre and for a transition metal. At four valence orbitals against six ligand combinations, two combinations are left with no partner and the count is a count of orphans; at nine against six, every combination finds one and three metal orbitals are left instead. Both are constant along the whole path, in three different point groups, out of decompositions that share no species — which is the replacement rule holding in a case where the arithmetic runs the other way.

The leftover changes sides

A main-group centre brings four valence orbitals against six ligand combinations, so two are orphaned. A transition metal brings nine, so the arithmetic inverts and three metal orbitals are left instead — three at every geometry of the Bailar twist, out of decompositions that share no species. Run past the whole arrangement census, exactly one arrangement orphans anything at a metal, and it needs an f orbital to fix.

beyond · Hypervalency
Folding the ring off its plane never gives the orbital back. For rings of four to eight ligands round a centre with no lone pair, the orphan count minus the formula n + L − 4, at polar angles from 60° to 120°. The upper dot in each row is the bare ring and the lower the same ring with a ligand on the axis. The bare ring is one over the formula at every angle, including 90°, where the ring is flat and its group is D₄ₕ, D₅ₕ or D₆ₕ; there is no table here for D₇ₕ or D₈ₕ. The capped ring agrees with the formula at every angle, 90° included, where the ring is exactly flat and the apex alone keeps its group C₄ᵥ to C₈ᵥ.

Folding the ring does not give the orbital back

Three arrangements break the orphan count n + L − 4, all flat, and the reason given was flatness: the p orbital perpendicular to the ring has no ligand combination of its species. Fold the ring into an umbrella at any angle and that orbital becomes totally symmetric — and the count stays wrong by exactly one, for rings of four to eight. The ring offers one symmetric combination to a centre with two symmetric orbitals. Writing C₅ᵥ to see it also counts the pentagonal pyramid at last, and the formula holds there.

beyond · Hypervalency

Named alongside it

The objects these essays reach for when they reach for this one.

DegeneracyPoint groupModel limitReduction formulaSymmetry operationCharacter tableVibrational modesElectron countSelection rulesNormal modeConventionHypervalency

All concepts