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Chapter I Brief Introduction...<br />

Organic NLO Materials:<br />

Organic materials are molecular materials that consist of chemically<br />

bonded molecular units interacting in the bulk media through weak van der<br />

Waal interactions. The organic molecules which contain both conjugated<br />

bonds and acceptor group on one side and a donor group on the other side<br />

are known as nonlinear optical (NLO) materials [12].<br />

A typical SHG active molecule can be represented as follows:<br />

Donor π – conjugated system acceptor<br />

The π – conjugated molecules with a donor and acceptor will not<br />

display SHG activity if they possess a centre of symmetry. This symmetry<br />

requirement eliminates several materials for consideration of SHG. The π<br />

conjugated systems would be benzene, azobenzene, stilbene, tolans,<br />

biphenyl, hetrocycle, polyens, benzylidene, etc. Some accepter groups are,<br />

for instance, NO2, NO, CN, NH3 + , CF3, COCH3, COOH, COO - , etc. Whereas,<br />

some donor groups are NH2, NHCH3, FCl, Br, CH3, COOCH3, NHCOCH3, O -<br />

etc.<br />

The trade off between optical transparency and SHG efficiency is an<br />

important issue while designing devices using NLO materials. Both the<br />

second order optical nonlinearity and optical transparency are affected by the<br />

nature of conjugated bonds, length of π - conjugation and strength of electron<br />

donor/ acceptor constituents[14,42].<br />

The second order NLO organic materials are most often based on π<br />

conjugated molecules (Chromophores) with strong electron donor and<br />

accepter group at the end of π – conjugate structure. Such molecules must be<br />

ordered in an acentric manner in a material to achieve a macroscopic second<br />

23

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