Synthesis, growth, XRD, NLO, CHNSO, computational-structural, dielectric, photoconductivity, hardness and biostudies of diethyl 2-amino-5-{4-[bis (4-methyl phenyl) amino] benzamido} thiophene-3,4-dicarboxylate (DABMPABTD) macro-, nano crystals for device fabrication, pharma, electronic uses

The organic materials are predominant over their pair offs based on their intense applications and vital utilities. The DABMPABTD crystal is synthesized by solution growth method under reduced pressure. The yield of 85% is obtained with crystal of yellowish color is attained, and the yield is better...

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Veröffentlicht in:Journal of materials science. Materials in electronics 2021-06, Vol.32 (11), p.15498-15508
Hauptverfasser: Ganesan, H., SenthilKannan, K., Christy, S., Maalmarugan, J., Flora, G., Joy, Juliet Josephine, Mohamed, M. Gulam, Patel, R. P., Gunasekaran, S., Vijayalakshmi, B., Murugananthan, K.
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Sprache:eng
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Zusammenfassung:The organic materials are predominant over their pair offs based on their intense applications and vital utilities. The DABMPABTD crystal is synthesized by solution growth method under reduced pressure. The yield of 85% is obtained with crystal of yellowish color is attained, and the yield is better than the earlier cases. The crystals belong to triclinic system with the formula of C 31 H 31 N 3 O 5 S. The elemental analyses are carried out using CHNSO, theoretical method to resolve the components. The crystal is a NLO type of second order and is of 1.45 times highly efficient and proficient than the standard crystals of KDP. The hardness profile shows the reverse indentation (RISE) effect for applied enrichment in tribological endeavors. The dielectric studies carried out and shows better utility in device fabrication and the DABMPABTD crystal shows the negative photoconductivity. The computational elucidation of the present crystal shows the impact of the structural data with experimental data and the anti-diabetic (AD) nature of the titled crystal is also analyzed and reported.
ISSN:0957-4522
1573-482X
DOI:10.1007/s10854-021-06100-4