Synthesis, characterization, computational calculation and biological studies of some 2,6-diaryl-1-(prop-2-yn-1-yl)piperidin-4-one oxime derivatives

Sundararajan, G.; Rajaraman, D.; Srinivasan, T.; Velmurugan, D.; Krishnasamy, K.

doi:10.1016/j.saa.2014.12.014

Cited by 5 publications

(4 citation statements)

References 29 publications

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“…Compounds 2-2 and 3-2 were obtained by slow evaporation in absolute ethanol/acetone and acetone/n-hexane at room temperature, respectively. [8][9][10][11][12] Crystals suitable for XRD were mounted on a glass fiber for determination, and the data was collected by a Bruker D8 ADVANCE diffractometer with graphite monochromatic Cu Kα radiation at 296 K. The single crystal of compound 2-2 is shown in Figure 1 [13]. The analytical software was SAINT v8.37A (Bruker, 2015), SHELXL (Sheldrick, 2015), and Olex2 (Dolomanov).…”

Section: Chemicalsmentioning

confidence: 99%

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Synthesis and Characterization of Compounds Based on Carbazole and Sulfone Groups

jia¹,

Feng

Han³

et al. 2021

Preprint

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Two compounds containing carbazole and sulfone groups with different alkyl chain lengths have been designed and synthesized. The sulfone group has strong absorption characteristics and the alkoxy chain and carbazole group are electron-rich, forming D-δ-A-type symmetrical molecules. The molecules have the characteristics of charge transfer and high thermal stability, and the molecules stack to form a layered staggered stack, reducing the intermolecular π–π interactions. The target compounds also exhibit strong ultraviolet-fluorescent emission in the solid state at room temperature, and they are expected to be good luminescent materials.

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Section: Chemicalsmentioning

confidence: 99%

“…Compound 3-2 was obtained as white crystals and 3-1 was a white solid and their yields were 65%. The structures of the target compounds were characterized by 1 H and 13 NMR spectroscopy, mass spectroscopy, Fourier transform IR (FT-IR) spectroscopy, and elemental analysis.…”

Section: Introductionmentioning

confidence: 99%

Synthesis and Characterization of Compounds Based on Carbazole and Sulfone Groups

jia¹,

Feng

Han³

et al. 2021

Preprint

View full text Add to dashboard Cite

show abstract

Section: Chemicalsmentioning

confidence: 99%

Synthesis and Characterization of Compounds Based on Carbazole and Sulfone Groups

Jia

Feng

Han³

et al. 2021

J Fluoresc

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“…Because of the significance of oxime ethers as cited above, there is a continuous interest amidst the researchers to study the theoretical properties of the former [16][17][18][19][20][21][22]. All the above studies explored the features of the compounds associated with their reactivity, structure and advanced applications.…”

Section: Introductionmentioning

confidence: 99%

Computational Aspects of (E)-O-Carbomethoxy Methyl Oxime Ether of 1,3-Dimethyl-2,6-Diphenylpiperidin-4-One

2019

IJITEE

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Density Functional Theoretical (DFT) studies on the biologically active oxime ether derived from 1,3-dimethyl-2,6-diphenylpiperidin-4-one has been carried out. Various quantum chemical parameters of the molecule viz. molecular geometry, Highest Occupied Molecular Orbital – Lowest Unoccupied Molecular Orbital (HOMO–LUMO) energies, Non-Linear Optical (NLO) properties, Mulliken atomic charge distribution were obtained theoretically and compared with the single crystal data. An insight into the structure and property correlation revealed the probable behavior of the molecule studied

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Synthesis, characterization, computational calculation and biological studies of some 2,6-diaryl-1-(prop-2-yn-1-yl)piperidin-4-one oxime derivatives

Cited by 5 publications

References 29 publications

Synthesis and Characterization of Compounds Based on Carbazole and Sulfone Groups

Synthesis and Characterization of Compounds Based on Carbazole and Sulfone Groups

Synthesis and Characterization of Compounds Based on Carbazole and Sulfone Groups

Computational Aspects of (E)-O-Carbomethoxy Methyl Oxime Ether of 1,3-Dimethyl-2,6-Diphenylpiperidin-4-One

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