Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

1
6
0

Year Published

2019
2019
2021
2021

Publication Types

Select...
3

Relationship

1
2

Authors

Journals

citations
Cited by 8 publications
(8 citation statements)
references
References 15 publications
(8 reference statements)
1
6
0
Order By: Relevance
“…The spectra revealed the presence of -CH=N group around δ 158.01 ppm. The signal at δ 176.47 ppm due to C-OH [8]. These spectra data sports the structure of synthesized compound.…”
Section: Chemistrysupporting
confidence: 51%
“…The cross peak at δH/δC = 8.39/158 ppm due to azomethine group (CH=N). Thus, the correlation of protons and carbon in aromatic rings such as, δH/δC = 7.57/137, 7.48/129 ppm and other positions can be assigned to the protons and carbon atoms of the aromatic rings [8], while the cross peak at δH/δC = 3.73/54.7 and δH/δC = 2.93/37.4 ppm can be attributed to methylene groups, Figures 1 and 2.…”
Section: Chemistrymentioning
confidence: 95%
“…SBDTC Schiff bases can form cis-trans and trans-cis isomers due to the N–C and C–S bond and they have significant versatile coordination character and biological activities [ 6 , 7 , 8 , 9 ]. An imine group (–RC = N–) containing Schiff bases are also used as dyes, intermediate reactants in the synthesis of organic compounds, catalysts, stabilizing agent in polymeric products, chelating agents in analytical separation methods and inhibitor of corrosion [ 10 , 11 ]. Moreover, Schiff bases possess noteworthy applications in multifaceted areas such in the solar cell, optical ingredients [ 6 , 7 , 9 , 12 ] and medication area such as antiviral, antifungal, antibacterial, insecticidal, anti-HIV, anticancer, antiprotozoal, antimalarial, anti-inflammatory, antidiabetic and antitumor [ 2 , 3 , 5 , 7 , 10 , 11 , 12 , 13 , 14 , 15 ].…”
Section: Introductionmentioning
confidence: 99%
“…An imine group (–RC = N–) containing Schiff bases are also used as dyes, intermediate reactants in the synthesis of organic compounds, catalysts, stabilizing agent in polymeric products, chelating agents in analytical separation methods and inhibitor of corrosion [ 10 , 11 ]. Moreover, Schiff bases possess noteworthy applications in multifaceted areas such in the solar cell, optical ingredients [ 6 , 7 , 9 , 12 ] and medication area such as antiviral, antifungal, antibacterial, insecticidal, anti-HIV, anticancer, antiprotozoal, antimalarial, anti-inflammatory, antidiabetic and antitumor [ 2 , 3 , 5 , 7 , 10 , 11 , 12 , 13 , 14 , 15 ]. From the point of view, we report herein the synthesis, characterization as well as investigation of in silico quantum calculations of the entitled SBDTC Schiff base in particulars.…”
Section: Introductionmentioning
confidence: 99%
“…Symmetrical bis-azomethines (Ar-N=CH-Ar-CH=N-Ar) have a similar synthetic mono Schiff b e' p hw y bu by u ing he different molar ratio (Ozdemir Gungor, 2017). Schiff bases have broad variability applications in a medicinal field that possess a wide spectrum of biological activities such as antibacterial (Ziwar and Musheer), antioxidant (Hassan, 2019), antifungal (Noori et al, 2019), anti-inflammatory, ZANCO Journal of Pure and Applied Sciences 2021 analgesic, anticancer (Kajal et al, 2013), antitumor (Ibrahim, 2015), anticonvulsant antimalarial, anti-tubercular (Khdur and Zimam, 2018a), and antidiabetic (Al-Masoudi et al, 2016).…”
Section: Introductionmentioning
confidence: 99%