Synthesis, growth and characterization of L-Phenylalaninium methanesulfonate nonlinear optical single crystal

被引:13
作者
Mangaiyarkarasi, K. [1 ]
Ravichandran, A. T. [1 ]
Anitha, K. [2 ]
Manivel, A. [3 ]
机构
[1] Natl Coll Autonomous, PG & Res Dept Phys, Tiruchirappalli 620001, Tamil Nadu, India
[2] Madurai Kamaraj Univ, Sch Phys, Dept Phys, Madurai 625021, Tamil Nadu, India
[3] Saraswathi Narayanan Coll Autonomous, PG & Res Dept Chem, Madurai 625022, Tamil Nadu, India
关键词
L-phenylalanine; Methane sulfonate; Single crystal; X-ray diffraction; NLO studies; LASER DAMAGE THRESHOLD; MECHANICAL-PROPERTIES; ACID;
D O I
10.1016/j.molstruc.2017.11.065
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The titled compound, L-Phenylalaninium methanesulfonate (LPA-MS) was synthesized and grown into single crystals by slow solvent evaporation solution growth technique in aqueous solution containing equimolar concentrations of t-phenylalanine and methanesulfonic acid at room temperature. The grown crystals were subjected to single crystal X-ray diffraction studies. It crystallizes in the monoclinic crystal structure with P-21 space group and the unit cell parameters are a = 5.312 (10) angstrom, b = 8.883 (2) angstrom and c = 25.830 (7) angstrom. The functional groups of the LPA-MS crystal were confirmed with FT-IR and FT-Raman analysis. The carbon-hydrogen skeleton was confirmed with H-1 NMR and C-13 NMR analysis. TG-DTG and DSC studies were carried out to determine the thermal stability of the crystals. The optical transparency ranges were studied through UV-vis-spectroscopy and the crystal was found to be transparent in the visible region. The second Harmonic generation (SHG) efficiency of the grown LPA-MS crystal was measured by the Kurtz Perry powder technique. The dipolar nature of the L-phenylalaninium methanesulfonate and the presence of the intermolecular hydrogen bonding between the molecules are the vital factors responsible for the existence of SHG activity in the crystal. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:758 / 764
页数:7
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