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Chapter I Brief Introduction...<br />

Jagannathan, et al [49] have reported 141 times efficiency of SHG than that of<br />

urea for 4-Dimethylamino-N-methyl-4-stilbazolium tosylate (DAST) crystals.<br />

DAST has found application in continuously tunable THz and the far infrared<br />

generation system [50]. Azariah et al [51] have found that the SHG efficiency<br />

is 1.24 times that of KDP for n-nitro-4-methoxy benzylidene aniline. Urea has<br />

been studies for several years. It is difficult to grow crystals and the polished<br />

surfaces other than cleavage surfaces which are extremely hygroscopic [52].<br />

Devices based on urea must immerse the crystal in oil, which is usually<br />

absorbing in the UV region [53]. The efforts made to resolve the problems<br />

associated with urea are not very successful.<br />

Organic molecules with π-electron delocalization are currently of wide<br />

interest as NLO materials in optical switches and NLO devices [13]. A large<br />

amount of organic compounds have been studied as NLO materials [14].<br />

Historically, the optical SHG in an organic material was reported for the first<br />

time in 1964 by two research groups in 3, 4-benzopyrene by Rentzepis and<br />

Pao [54] and in hexamethylenetetramine single crystals by Heilmer et al<br />

[55].Two years later, Orlov [56] reported SHG from the hippuric acid. Further<br />

research in organic NLO was stimulated in 1970, when Davydov et al [57]<br />

reported strong SHG from organic compounds having electron donor and<br />

acceptor groups attached to a benzene ring while screening a large variety of<br />

organic compounds using the Kurtz and Perry powder method.<br />

Semi-organic Materials<br />

Semi-organic compounds share the properties of both organic and<br />

inorganic compounds. They are organic based materials in which the<br />

polarizable part is an organic molecule which is stoichiometrically bonded with<br />

25

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