Synthesis, growth, optical, mechanical, thermal, dielectric and third order nonlinear optical properties of
K Senthil1, K Elangovan1, A Senthil1
1Department of Physics, SRM Institute of Science and Technology, Ramapuram Campus, Chennai 600089, India.
Abstract:
The materials of Cyclohexylamine with 1,5-naphthalenedisulfonic acid and 3,5-dinitrosalicylic acid were used to synthesize the bis(cyclohexylammonium)-1,5-naphthalenedisulfonate (CA15NS) and bis(cyclohexylammonium)-3,5-dinitrosalicylate (CA35NS) compounds and single crystals of these compounds were grown successfully by low temperature solution growth technique. Crystal systems of the samples were identified for both the samples of CA15NS and CA35NS by the obtained unit cell parameters of the grown crystals which is determined by single crystal X-ray diffraction (SCXRD) analysis, the crystals of CA15NS and CA35NS are crystallized in monoclinic crystal structures. The powder X-ray diffraction (PXRD) analysis also was carried out for the title samples. The formations of the charge-transfer functional groups and the modes of vibrations of CA15NS and CA35NS have been confirmed by FT-IR and FT-Raman spectral analyses. The UV-Vis-NIR spectrum was carried out to find the optical behavior of the prepared crystals. The crystal of CA15NS has 232 nm and CA35NS has 207 nm as cut-off wavelength. The influences of mechanical and dielectric behavior in the crystals of CA15NS and CA35NS were investigated by means of Vickers microhardness test and dielectric study, respectively. By the thermo gravimetric analyses, the stability of the materials have been estimated for the title samples. Third order nonlinear optical study has also been studied by Z-scan technique.
Related Concept Videos
Stability of Substituted Cyclohexanes
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
Disubstituted Cyclohexanes: cis-trans Isomerism
In cyclohexane, the substituents can occupy different positions generating distinct isomers....
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Cycloaddition Reactions: MO Requirements for Thermal Activation
Structure of Amines
Nomenclature of Primary Amines


