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Borazine WPS

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BORAZINE

AND
PHOSPHAZENE
BORAZINE

RAJAT BHATTACHARYA
BORAZINE
CONTENTS
• HISTORY
• ABOUT
• COMPARISION WITH BENZENE
• STRUCTURE
• PHYSICAL PROPERTIES
• CHEMICAL PROPERTIES
• USES
HISTORY
The compound was reported in 1926
by the chemists Alfred Stock and
Erich Pohland by a reaction of
diborane with ammonia.
He was the first to study compounds
such as the boranes, silanes, and
other similar nonmetal compounds
THE NAME
1. Borazine
2. Cyclotriborazaneborazol
3. Inorganic benzene
4. Borazole
5. Triboron Nitride 1,3,5,2,4,6-
Triazatriborinane
6. Borazane
WHAT ARE THE SIMILARITIES
BETWEEN BORAZINE AND BENZENE?

• Isoelectronic to benzene. - 42 electrons


• Isostreric to benzene (same no of atoms). - 12 atoms
• Similar structure to benzene
• Both are cyclic structures.
• Both have a six-membered ring.
• Have similar bond lengths between the atoms of the ring.
• Both are colourless liquids at room temperature.
The similarity of the
physical properties of
the alkyl-substituted
derivatives of benzene
and borazine is even
more remarkable.
DIFFERENCE BETWEEN BORAZINE AND
BENZENE
• Borazine is inorganic.
• Alternate bonds between Boron amd
Nitrogen.
• Comparatively more reactive.
• Not a perfect hexagon.
• Synthetic in nature.
INORGANIC BENZENE IS A MISNOMER
• This is a misnomer because the chemical properties of
borazine and benzene are quite different.
• Both compounds have aromatic π clouds of electron
density with potential for delocalization over all of the
ring atoms.
• Due to the difference in electronegativity between boron
and nitrogen, the cloud in borazine is “lumpy” because
more electron density is localized on the nitrogen atoms.
• This partial localization weakens the π-bonding in the
ring. Each nitrogen receives more σ-electron density
from neighbouring boron than it gives away as a π-donor.
• The net effect is that the charge density on nitrogen
increases. In addition, nitrogen retains its basicity and
boron its acidity.
Polar species
such as HCI can,
therefore, attack
the double bond
between
nitrogen and
boron. Thus, in
contrast to
benzene,
borazine readily
undergoes
addition
reactions:
STRUCTURE
OF
BORAZINE

B3H6N3
STRUCTURE OF BORAZINE
• It has a planar structure.
• It is an aromatic ring.
• Both Boron and Nitrogen are sp2 hybridized.
• B- N bond in Borazine is a dative bond that arises from
the sidewise overlap between the filled p orbitals of N
atom and empty p orbitals of B atom.
• N atom contains a lone pair.
• B atom is electron deficient.
• There
• Is a partial delocalization of electrons in the ring.
PHYSICAL PROPERTIES OF
BORAZINE
Compound: Borazole
Formula: B3N3H6
Molecular Formula: B3H6N3
Molecular Weight: 81
Properties: inorganic analog of benzene
Physical state. Colourless liquid
Solubility. Hydrolyzes
Density, g/cm3: 0.824 (0°C)
Melting Point, °C: −58
Boiling Point, °C: 53
CHEMICAL PROPERTIES OF BORAZINE
At ordinary temperatures, both air and oxygen have no action on
borazine.
Hydrolyses in excess of water

Addition reaction.
SUBSTITUTION REACTIONS.

Borazine undergo polymerization when strongly heated


under vacuum and yield biborazonyl and naphthazine
whose structure are similar to biphenyl and naphthalene.

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