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V. Crasta, V. Ravindrachary, R. F. Bhajantri and R. Gonsalves, “Growth and Characterization of an Organic NLO Crystal: 1-(4-Methylphenyl)-3-(4-ethoxyphenyl)-2-propen-1- one,” Journal of Crystal Growth, Vol. 267, No. 1-2, 2004, pp. 129-133. http://dx.doi.org/10.1016/j.jcrysgro.2004.03.037

has been cited by the following article:

• TITLE: Effect of Substituent Position on the Properties of Chalcone Isomer Single Crystals

  AUTHORS: R. Gandhimathi, G. Vinitha, R. Dhanasekaran

  KEYWORDS: Solution Growth; Characterization; Chalcones; Nonlinear Optical Materials

  JOURNAL NAME: Journal of Crystallization Process and Technology, Vol.3 No.4, October 21, 2013

  ABSTRACT: This paper summarizes the synthesis, growth and the effect of the position of the substituent in the thienyl ring and also the properties of the grown chalcone crystals, 2-CTP and 3-CTP. The formation of compound is confirmed by the re- corded H1NMR spectra. A FT-IR spectrum confirms the presence of all functional groups in both of the crystals. Single crystal XRD reports that even though these two compounds crystallize in monoclinic crystal system, 2-CTP has centro- symmetric P21/c space group and 3-CTP has non-centrosymmetric space group P21. Thermal properties of grown crys- tals analyzed by TG/DTA study explain that the 3-CTP compound is slightly more stable than 2-CTP. The transparency of these isomers in the vis-IR region has been studied. Second and third order nonlinear optical properties of 3-CTP and 2-CTP crystals have been investigated by powder SHG and Z-scan technique respectively.