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Isolobal Analogy

The document discusses the isolobal analogy in inorganic chemistry. The isolobal analogy shows that fragments with similar numbers, symmetry, and energies of frontier orbitals can substitute for each other, even if composed of different elements. For example, the methyl (CH3) fragment is isolobal to the transition metal fragment Mn(CO)5. This allows prediction of new compounds by substituting isolobal fragments. Applications of the isolobal analogy generate compounds like ferrocene, which can be viewed as metallocyclopropane or ethylene complex.

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633 views4 pages

Isolobal Analogy

The document discusses the isolobal analogy in inorganic chemistry. The isolobal analogy shows that fragments with similar numbers, symmetry, and energies of frontier orbitals can substitute for each other, even if composed of different elements. For example, the methyl (CH3) fragment is isolobal to the transition metal fragment Mn(CO)5. This allows prediction of new compounds by substituting isolobal fragments. Applications of the isolobal analogy generate compounds like ferrocene, which can be viewed as metallocyclopropane or ethylene complex.

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indu priya
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We take content rights seriously. If you suspect this is your content, claim it here.
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Department of Chemistry Modern Approaches to Inorganic Bonding

6 The isolobal analogy


C
6.1 Introduction
O
The outline of Wade's rule given above showed how quite different groups of atoms can give rise to similar
N shaped clusters. For example, the C-H group and the P atom have 5 electrons and can contribute 3 electrons
to a cluster,

T C-H has 4+1 electrons and uses 2 electrons for the C-H bond

E P has 5 electrons and uses 2 electrons for a lone pair

N Both fragments are 3 electrons short of making maximum use of their 4 valence orbitals (s and 3 p) by
achieving an octet. The clusters C4H 4 or (CH)4 (tetrahedrane) and P 4 have the same number of cluster
T electrons and therefore adopt the same shape:

The organometallic fragment Co(CO)3 has 15 electrons,

Co has 9 valence electrons and each CO donates 2e to the metal

The fragment is 3 electrons short of the stable electron count for an organometallic fragment of eighteen
Eighteen electrons corresponds to making maximum use of the 9 valence orbitals of the transition metal (s +
3 p and 5 d). It can achieve 18 electrons by sharing 3 electrons to make 3 covalent bonds. The Co(CO)3
fragment thus has the same requirements as the C-H unit and the P atom. The cluster [Co(CO)3]4 thus also
has the same tetrahedral shape as that shown by C 4H 4 and P 4. It is also possible to swap the three
fragments around:

B and C are more conventionally thought of as (m 3-P)[CoCO) 3]3 and (h 3-C3H 3)Co(CO)3 respectively but this
hides the structural and electronic links between all these clusters.

The similarity between these fragments and between other groups of fragments has been investigated in
detail by Roald Hoffmann. Fragments are deemed to be isolobal if

"the number, symmetry properties, approximate energy and shape of the frontier
orbitals and the number of electrons in them are similar"

The isolobal relationship is symbolized by a double-headed arrow with a tear-drop,

The isolobal analogy relates the orbitals and bonding in inorganic, organometallic and cluster chemistry to that
in organic and main group chemistry. The utility of the isolobal analogy is that one should be able to replace
a (transition metal) MLn fragment in a molecule with the isolobal (main group) AHn fragment, and vice versa,
to produce new molecules with very similar bonding.

6.2 Generating isolobal fragments


Main group fragments can be generated by starting from methane, 1 (or any molecule obeying the octet
rule). Homolytic cleavage of a CH bond generates the methyl radical, 1 a,, which has one frontier orbital
pointing towards the missing hydrogen with one electron in it. Homolytic cleavage of a second CH gives
methylene, 1b, which has too singly occupied hybrids pointing towards the two vacant hydrogen positions.
Removal of a third hydrogen gives methine, 1c, with three singly occupied hybrids.

The transition metal fragments are generated in an analogous way. For example, from the starting point of
CrL 6, 2, where L is a two electron donor such as CO, (or any molecule obeying the eighteen electron rule
such as 3), the fragments 2a, 2b and 2c are generated by successive homolytic cleavage of ML bonds on one
octahedral face. As L is a two-electron donor, homolytic cleavage of CrL 6 gives CrL 5- and L + . To remove the
charge, the metal is then replaced by Mn (the element one to the right in the 3d series):

6.3 Isolobal scheme


The isolobal scheme generated by this approach is shown below.

8electron 18-electron 16-


electron

1 2 3 4

1a 2a 3a 4a
1b 2b 3b 4b

1c 2c 3c 4c

As long as the electron count is maintained or consistent changes are made, the metal or main group element
can be substituted. Thus,

CH3 Me3Sn Mn(CO) 5 Fe(PPh3) 5+ Mo(CO) 5

CH3+ BH3 Mn(CO) 5+ Cr(CO)5 Rh(PPh3)3+

CH3 NH 3 Mn(CO) 5 Fe(CO) 5 Rh(CO)5+

It should be noted that the main use of the isolobal analogy is in generating alternative fragments in
molecules. The geometry of the fragment in a molecule not as an isolated species is important. Thus, CH3 and
BH3 are considered as pyramidal (not planar) species and Cr(CO)5 is considered as a square-based pyramid
(not trigonal bipyramid).

6.4 Applications

The isolobal analogy between CH3 and d7 MnL 5 implies similar bonding in the following compounds:

The isolobal relationship of CH2, with Fe(CO) 4 generates the compounds illustrated below. The transition
metal molecule has been drawn as a metallocyclopropane. A more common description is to consider it as an
ethene complexes, (h2C2H 4)Fe(CO) 4. The isolobal relationship shows that cyclopropane itself can be consider
as (h2C 2H 4)CH2.

Other known compounds generated using this relationship include:

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