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S. A. Basaif, T. R. Sobahi, A. Kh. Khalil and M. A. Has- san, “Stereoselective Crossed-Aldol Condesation of Hetarylmethyl Ketones with Aromatic Aldehydes in Water: Synthesis of (2E)-3-Aryl-1-hetarylprop-2-en-1-ones,” Bulletin of the Korean Chemical Society, Vol. 26, No. 11, 2005, pp. 1677-168.

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.