2017
DOI: 10.1016/j.molstruc.2017.03.113
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Synthesis, structural characterization and quantum chemical calculations on 1-(isomeric methylbenzoyl)-3-(4-trifluoromethylphenyl)thioureas

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Cited by 30 publications
(7 citation statements)
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“…Many reports have documented the ability of thioureas to coordinate transition metals such as Ni(II), Cu(II), Co(II), Fe(III) [5,6], Zn(II) [7], Pd(II) [8], and Ru(II) [9]. Their diversified use has received attention by various scientific communities including medical [10], analytical chemistry and metallurgy fields [11]. To name a few, they have been used in antiviral [12,13], anti-HIV [14], antimicrobial, antitumor, anti-inflammatory [15], and insecticidal substances [16].…”
Section: Discussionmentioning
confidence: 99%
“…Many reports have documented the ability of thioureas to coordinate transition metals such as Ni(II), Cu(II), Co(II), Fe(III) [5,6], Zn(II) [7], Pd(II) [8], and Ru(II) [9]. Their diversified use has received attention by various scientific communities including medical [10], analytical chemistry and metallurgy fields [11]. To name a few, they have been used in antiviral [12,13], anti-HIV [14], antimicrobial, antitumor, anti-inflammatory [15], and insecticidal substances [16].…”
Section: Discussionmentioning
confidence: 99%
“…Several regions of the FTIR spectra, recorded in KBr discs, are of interest for supporting the coordination via the sulfur atom: 3200-3400 cm −1 for ] N-H frequencies, 1500-1700 cm −1 for strong ] C�O and ] C-N frequencies, and finally, 1100-1250 cm −1 where strong absorption bands assigned to a combination of ] C-N and ] phenyl stretching frequencies can be found [54][55][56][57][58]. For example, the intensity and the position of the carbonyl stretching ] C�O at ∼1665 cm −1 are essentially the same in the IR spectra of 2a and 2b as in the free ligand 1. e medium intense band at 1350 cm −1 in the IR of ligand 1, assigned to ] C�S , is absent in the IR spectra of copper(I) complexes [34].…”
Section: Synthesismentioning
confidence: 99%
“…On the other hand, acyl thiourea derivatives are widely applied in recent decades, such as heterocyclic synthesis intermediate, non‐ionic surfactants, organocatalysts, etc. Further, due to the unique structure of CONHCSNH in the structure of the acyl thiourea compound, it has a wide range of biological activities, such as antiviral, antimicrobial, herbicidal, antitumor, anti‐inflammatory, and fungicidal properties . However, an increasing number of people are engaged in researching anticancer drugs as cancer cases have become more diverse and complex.…”
Section: Introductionmentioning
confidence: 99%