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Cited by 45 publications
(24 citation statements)
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“…The band located at 3351 cm −1 in the free lapachol [31,32] assigned to OH, disappears upon coordination, as expected. The characteristic ν(C_O) stretching bands, found at ν(C 1 _O) 1664 and ν(C 4 _O) 1641 cm −1 in free lapachol [11] shifted to lower frequencies in complexes, 1561-1591 cm −1 and 1581-1533 cm −1 , respectively. This behavior was also observed for other complexes like Ru(II), Co(II), Ni(II) and Cu(II) containing the lapachol as ligand [5,11,12].…”
Section: Fragmentmentioning
confidence: 89%
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“…The band located at 3351 cm −1 in the free lapachol [31,32] assigned to OH, disappears upon coordination, as expected. The characteristic ν(C_O) stretching bands, found at ν(C 1 _O) 1664 and ν(C 4 _O) 1641 cm −1 in free lapachol [11] shifted to lower frequencies in complexes, 1561-1591 cm −1 and 1581-1533 cm −1 , respectively. This behavior was also observed for other complexes like Ru(II), Co(II), Ni(II) and Cu(II) containing the lapachol as ligand [5,11,12].…”
Section: Fragmentmentioning
confidence: 89%
“…The characteristic ν(C_O) stretching bands, found at ν(C 1 _O) 1664 and ν(C 4 _O) 1641 cm −1 in free lapachol [11] shifted to lower frequencies in complexes, 1561-1591 cm −1 and 1581-1533 cm −1 , respectively. This behavior was also observed for other complexes like Ru(II), Co(II), Ni(II) and Cu(II) containing the lapachol as ligand [5,11,12]. The characteristic ν(C 2 \O) stretching band found in 1028 cm −1 in the free lapachol shifted to higher frequencies in complexes (1065-1079 cm −1 ).…”
Section: Fragmentmentioning
confidence: 89%
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“…Thiosemicarbazones and their thiazole heterocyclic derivatives are of great importance in pharmacology due to their broad range of biological activities, such as anticonvulsant, antimicrobial, and antiparasitic activities (Gaikwad, Patil, Bobade, 2013;Souza et al, 2013;Bharti et al, 2010;Siddiqui et al, 2009;Oliveira et al, 2008a;Souza, 2005;Dimmock et al, 1991).…”
Section: Introductionmentioning
confidence: 99%
“…2-thiophene-thiosemicarbazone derivatives (5)(6)(7)(8)(9)(10)(11)(12)(13)(14) were prepared in two steps.…”
Section: Chemistrymentioning
confidence: 99%