Synthesis, growth, experimental, and theoretical characterization of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide single crystal

The single crystals of nonlinear optical organic compounds are essential for their use in optical devices. With this purpose, this research presents the formation of good quality single crystals of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide from an aqueous solution at room temperature by foll...

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Main Authors: Mugeshini, S., Santhakumari, R., Rajeshwari, N., Amudha, G., Chandrika, D., Sagadevan, Suresh
Format: Article
Published: Elsevier 2022
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Online Access:http://eprints.um.edu.my/43080/
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spelling my.um.eprints.430802023-09-04T07:28:47Z http://eprints.um.edu.my/43080/ Synthesis, growth, experimental, and theoretical characterization of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide single crystal Mugeshini, S. Santhakumari, R. Rajeshwari, N. Amudha, G. Chandrika, D. Sagadevan, Suresh QC Physics The single crystals of nonlinear optical organic compounds are essential for their use in optical devices. With this purpose, this research presents the formation of good quality single crystals of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide from an aqueous solution at room temperature by following the slow evaporation solution growth technique. While single crystal X-Ray Diffraction (SXRD) analysis was used to examine the structural properties of the grown crystal, Powder X-Ray Diffraction (PXRD) was employed toconfirm its crystalline nature and phase purity. The presence of the various functional groups was verified using Fourier Transform Infrared (FTIR) spectral analysis. The UV-vis-NIR spectrum was recorded to investigate the optical transparency of the grown crystal.Hirshfeld surface analysis was carried out to further examine the possibly present intermolecular interactions. Finally, the structure of the crystal was optimized using the DFT/B3LYP/3-21G(d,p)level combined with the DFT/B3LYP/6-311++G(d,p) level to study the molecular properties of the grown crystal such as stable configuration, dipole moment, polarizability, hyperpolarizability Nuclear Magnetic Resonance (NMR), Natural Bond Orbital (NBO) theory, and Mulliken's atomic charges in the gaseous state. Elsevier 2022-03 Article PeerReviewed Mugeshini, S. and Santhakumari, R. and Rajeshwari, N. and Amudha, G. and Chandrika, D. and Sagadevan, Suresh (2022) Synthesis, growth, experimental, and theoretical characterization of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide single crystal. Chinese Journal of Physics, 76. pp. 14-23. ISSN 0577-9073, DOI https://doi.org/10.1016/j.cjph.2021.10.037 <https://doi.org/10.1016/j.cjph.2021.10.037>. 10.1016/j.cjph.2021.10.037
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic QC Physics
spellingShingle QC Physics
Mugeshini, S.
Santhakumari, R.
Rajeshwari, N.
Amudha, G.
Chandrika, D.
Sagadevan, Suresh
Synthesis, growth, experimental, and theoretical characterization of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide single crystal
description The single crystals of nonlinear optical organic compounds are essential for their use in optical devices. With this purpose, this research presents the formation of good quality single crystals of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide from an aqueous solution at room temperature by following the slow evaporation solution growth technique. While single crystal X-Ray Diffraction (SXRD) analysis was used to examine the structural properties of the grown crystal, Powder X-Ray Diffraction (PXRD) was employed toconfirm its crystalline nature and phase purity. The presence of the various functional groups was verified using Fourier Transform Infrared (FTIR) spectral analysis. The UV-vis-NIR spectrum was recorded to investigate the optical transparency of the grown crystal.Hirshfeld surface analysis was carried out to further examine the possibly present intermolecular interactions. Finally, the structure of the crystal was optimized using the DFT/B3LYP/3-21G(d,p)level combined with the DFT/B3LYP/6-311++G(d,p) level to study the molecular properties of the grown crystal such as stable configuration, dipole moment, polarizability, hyperpolarizability Nuclear Magnetic Resonance (NMR), Natural Bond Orbital (NBO) theory, and Mulliken's atomic charges in the gaseous state.
format Article
author Mugeshini, S.
Santhakumari, R.
Rajeshwari, N.
Amudha, G.
Chandrika, D.
Sagadevan, Suresh
author_facet Mugeshini, S.
Santhakumari, R.
Rajeshwari, N.
Amudha, G.
Chandrika, D.
Sagadevan, Suresh
author_sort Mugeshini, S.
title Synthesis, growth, experimental, and theoretical characterization of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide single crystal
title_short Synthesis, growth, experimental, and theoretical characterization of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide single crystal
title_full Synthesis, growth, experimental, and theoretical characterization of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide single crystal
title_fullStr Synthesis, growth, experimental, and theoretical characterization of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide single crystal
title_full_unstemmed Synthesis, growth, experimental, and theoretical characterization of 6-amino-1H-pyrimidine-2,4-dione dimethylacetamide single crystal
title_sort synthesis, growth, experimental, and theoretical characterization of 6-amino-1h-pyrimidine-2,4-dione dimethylacetamide single crystal
publisher Elsevier
publishDate 2022
url http://eprints.um.edu.my/43080/
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