18210-11-2Relevant academic research and scientific papers
Comparative studies of structural, thermal, optical, and electrochemical properties of azines with different end groups with their azomethine analogues toward application in (opto)electronics
Sek, Danuta,Siwy, Mariola,Bijak, Katarzyna,Grucela-Zajac, Marzena,Malecki, Grzegorz,Smolarek, Karolina,Bujak, Lukasz,Mackowski, Sebastian,Schab-Balcerzak, Ewa
, p. 10320 - 10332 (2013)
Two series of azines and their azomethine analogues were prepared via condensation reaction of benzaldehyde, 2-hydroxybenzaldehyde, 4-pyridinecarboxaldehyde, 2-thiophenecarboxaldehyde, and 4-(diphenylamino) benzaldehyde with hydrazine monohydrate and 1,4-phenylenediamine, respectively. The structures of given compounds were characterized by FTIR, 1H NMR, and 13C NMR spectroscopy as well as elemental analysis. Optical, electrochemical, and thermal properties of all compounds were investigated by means of differential scanning calorimetry (DSC), UV-vis spectroscopy, stationary and time-resolved photoluminescence spectroscopy, and cycling voltammetry (CV). Additionally, the electronic properties, that is, orbital energies and resulting energy gap were calculated theoretically by density functional theory (DFT). Influence of chemical structure of the compounds on their properties was analyzed.
Computer-aided design, synthesis, and biological studies of anticological nitrogen-containing tetraphosphonic acids against melanoma
Bekheit, Mohamed S.,Barghash, Reham F.,Abdou, Wafaa M.
, p. 1481 - 1491 (2018/07/02)
Abstract: As a part of our quest to develop new bioactive bisphosphonic acids, we synthesized a series of bis(α-aminobisphosphonic acids) in good yields (66–78%) as new entities for treating malignant melanoma. The reaction of the Schiff bases, 1,4-pheney
Optoelectronic property tailoring of conjugated heterocyclic azomethines - The effect of pyrrole, thiophene and furans
Dufresne, Stephane,Skene
experimental part, p. 211 - 221 (2012/07/01)
A series of de novo symmetric heterocyclic azomethine dyads and triads consisting uniquely of furans, thiophenes, pyrroles and methyl-pyrroles were prepared. These were prepared to investigate the effect of various heterocycles and the degree of conjugati
