Crystal structure, synthesis, growth and characterization of a non-linear chalcone crystal: (2E)-1-(4-chlorophenyl)-3-(4-diethylaminophenyl)-prop-2-en-1-one

Jebapriya, J. Christina; Jonathan, D. Reuben; Maidur, Shivaraj R.; Nallamuthu, Prabhu; Patil, P. S.; Prasana, Johanan Christian

doi:10.1016/j.molstruc.2021.131184

Cited by 11 publications

(1 citation statement)

References 41 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…compounds described in the literature [39][40][41]. When compared to other known NLO materials stimulated under the same conditions utilizing DPSS continuous wave (CW) laser excitation (637 nm), all of the current works exhibit higher nonlinear susceptibilities due to bigger conjugated molecules (Table 2).…”

Section: Third Order Susceptibilities Calculationsmentioning

confidence: 94%

An experimental and DFT investigations of fused ring anthracenyl chalcones with effective modification in acceptor moiety: Nonlinear optical and optical limiting response

Zainuri

Abdullah

Bakar

et al. 2023

Int J of Quantum Chemistry

View full text Add to dashboard Cite

The significance of the anthracene moiety on nonlinear optical (NLO) characteristics is thoroughly examined. The presence of strong electron donor and acceptor groups, large and prolonged conjugation transfer axis, amplifies the push–pull action and increases NLO responses. The values of χ3 obtained for AC derivatives are considerably larger (10−3 esu), indicating that they accurately reflect NLO reactions. According to the optical limiting (OL) investigation, AC has a strong limiting behavior with action beginning at 1.6 KW/cm2. The relationship between transmittance and intensity has demonstrated their potential use in OL applications. Nonlinear optical studies show that all conjugated anthracene chalcones are potential materials for OL devices.

show abstract

Section: Third Order Susceptibilities Calculationsmentioning

confidence: 94%