What is sigmatropic rearrangement ?
Many thermal or photo chemical rearrangements involve the
shifting of a σ-bond , flanked by one or more π-electron systems, to a new
position [ i , j ] within the molecule in an uncatalyzed intra molecular process .
Since it is rearrangement of a σ-bond , these reactions are called sigmatropic rearrangements of order [ i, j ].
Since it is rearrangement of a σ-bond , these reactions are called sigmatropic rearrangements of order [ i, j ].
FMO method:
The terms sigmatropic rearrangement is used to describe a chemical change in which a sigma bond along with the group attached to this, flanked by one or more π-electron system, migrates in an uncatalysed process to a new position in the molecule.
Sigmatropic rearrangements are given the order [ I,j ] which express the number of atoms , i and j across which the σ-bond migrates.
In sigmatropic rearrangement the migrating group usually H-atom is σ-bonded through the same atomic centre then such rearrangements are also referred to as [ I,j ] order of sigmatropic rearrangement .
When the value of [ i+j ] even then it is also represent the number of electrons delocalized in the transition state.
What is suprafacial and antarafacial process ?
Sigmatropic reaction involves the migration of a σ-bond across the π electronic system. When the migrating σ-bond moves across the same face of the conjugated system , it is called a suprafacial process.
On the other hand, when the migrating σ-bond is reformed on the opposite π electron face of the conjugated system, then it is called antarafacial process.
The following example of [ 1,5 ] sigmatropic shift exhibits both these process and their stereo chemical consequences.
Due to steric reasons, suprafacial migration are more common
than antarafacial shifts. However, with
lengthening of the conjugated system. Sometimes it is possible for a σ-bond
to migrate to the opposite π electron face.
Explanation of sigmatropic rearrangements :
One of the ways to explain the sigmatropic rearrangements is to assume that the migrating bond undergoes hemolytic cleavage resulting in the formation of a pair of radicals.
As bonding characters are to be maintained throughout the course of the rearrangement , the most important bonding interaction will be between the HOMO’s of the two species produced by this cleavage.
This is to be expected as it is these orbitals that contain the unpaired electrons. We shall illustrate this explanation by examining a suprafacial [1,5] sigmatropic shift of hydrogen in which the hemolytic cleavage results in the production of a hydrogen atom and pentadienyl radical.
The ground state electronic configuration of pentadienyl radical is Ѱ12Ѱ22
Ѱ3.
Since HOMO ( Ѱ3 ) of this radical has similar sign on the
terminal lobes, [ 1,5 ] suprafacial migration will be a thermally allowed
process.
The first excited state of the pentadienyl radical has the
configuration Ѱ12Ѱ22 Ѱ4
and the symmetry characteristics of HOMO
( Ѱ4
) are thus reversed ( C2 symmetry).
[ 1,5 ] suprafacial migration is no longer possible and the
shift has to be an antarafacial process.
A similar analysis of such systems has led the formation of selection rules which state that if a sigmatropic reaction of the order [i ,j ] has i+j =4n+2 , then thermal reaction is suprafacial and photo chemical reaction will be antarafacial.
However for those cases in which i+j=4n the rules are reversed and the thermal reactions are antarafacial while the photo chemical reaction will be suprafacial. These rules are summarized as,
Application of PMO method to sigmatropic reactions:
Sigmatropic reactions can be treated in the same fashion as above and similar conclusions are arrived at as by other approaches.
For instance, the [ 1,3 ] suprafacial shift occurs via an transition state with zero node and 4 electrons ( antiaromatic ) and thus is an photo chemical allowed process, whereas the [ 1,3 ]
antarafacial shift can occur via a transition state with one node, 4 electrons ( aromatic ) and is thus thermally allowed process . This two process are as follow,
The selection rules for sigmatropic reactions of order [1,j
] by this method are shown below.
Selection rules for sigmatropic change by PMO method.
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