SYNTHESIS, STRUCTURE AND BIOLOGICAL ACTIVITY OF N(4)-ALLYL-3-THIOSEMICARBAZONES AND THEIR COORDINATION COMPOUNDS WITH SOME 3D METALS

<p>The paper presents a review of different N(4)-allyl-3-thiosemicarbazones and their coordination compounds described in literature. N(4)-allyl-3-thiosemicarbazide can form corresponding thiosemicarbazones with aliphatic, aromatic and heteroaromatic carbonyl compounds. In the presence of tran...

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Main Author: Vasilii GRAUR
Format: Article
Language:English
Published: Moldova State University 2016-02-01
Series:Studia Universitatis Moldaviae: Stiinte reale si ale naturii
Subjects:
Online Access:http://ojs.studiamsu.eu/index.php/real-nature/article/view/305
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author Vasilii GRAUR
author_facet Vasilii GRAUR
author_sort Vasilii GRAUR
collection DOAJ
description <p>The paper presents a review of different N(4)-allyl-3-thiosemicarbazones and their coordination compounds described in literature. N(4)-allyl-3-thiosemicarbazide can form corresponding thiosemicarbazones with aliphatic, aromatic and heteroaromatic carbonyl compounds. In the presence of transitional metal ions they can form coordination compounds of different structures. Both coordination compounds and proligands manifest antitumor, antibacterial, antiviral, and antimalarial activities. Copper(II) coordination compounds with these ligands manifest better antitumor activity than corresponding proligands.</p><p> </p><p><strong>SINTEZA, STRUCTURA ŞI ACTIVITATEA BIOLOGICĂ A N(4)-ALIL-3-TIOSEMICARBAZONELOR ŞI A COMPUŞILOR COORDINATIVI AI UNOR METALE 3D CU ACEŞTI LIGANZI</strong></p><p>Lucrarea prezintă o revistă a N(4)-alil-3-tiosemicarbazonelor şi a compuşilor coordinativi cu aceşti liganzi descrise în literatura de specialitate. N(4)-alil-3-tiosemicarbazida formează tiosemicarbazone cu aldehide şi cetone alifatice, aro­matice şi heteroaromatice. În prezenţa ionilor de metale de tranziţie acestea pot forma compuşi coordinativi cu diferite structuri. N(4)-alil-3-tiosemicarbazonele şi compuşii coordinativi manifestă activitate antitumorală, antibacterială, antivirală şi antimalarică. Compuşii coordinativi ai cuprului cu aceşti liganzi manifestă activitate antitumorală sporită în comparaţie cu N(4)-alil-3-tiosemicarbazonele corespunzătoare.</p><p> </p>
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spelling doaj.art-a8a9eb169fb34262ae77605234a652962022-12-22T03:51:55ZengMoldova State UniversityStudia Universitatis Moldaviae: Stiinte reale si ale naturii1814-32371857-498X2016-02-0106 (86)255SYNTHESIS, STRUCTURE AND BIOLOGICAL ACTIVITY OF N(4)-ALLYL-3-THIOSEMICARBAZONES AND THEIR COORDINATION COMPOUNDS WITH SOME 3D METALSVasilii GRAUR0State University of Moldova<p>The paper presents a review of different N(4)-allyl-3-thiosemicarbazones and their coordination compounds described in literature. N(4)-allyl-3-thiosemicarbazide can form corresponding thiosemicarbazones with aliphatic, aromatic and heteroaromatic carbonyl compounds. In the presence of transitional metal ions they can form coordination compounds of different structures. Both coordination compounds and proligands manifest antitumor, antibacterial, antiviral, and antimalarial activities. Copper(II) coordination compounds with these ligands manifest better antitumor activity than corresponding proligands.</p><p> </p><p><strong>SINTEZA, STRUCTURA ŞI ACTIVITATEA BIOLOGICĂ A N(4)-ALIL-3-TIOSEMICARBAZONELOR ŞI A COMPUŞILOR COORDINATIVI AI UNOR METALE 3D CU ACEŞTI LIGANZI</strong></p><p>Lucrarea prezintă o revistă a N(4)-alil-3-tiosemicarbazonelor şi a compuşilor coordinativi cu aceşti liganzi descrise în literatura de specialitate. N(4)-alil-3-tiosemicarbazida formează tiosemicarbazone cu aldehide şi cetone alifatice, aro­matice şi heteroaromatice. În prezenţa ionilor de metale de tranziţie acestea pot forma compuşi coordinativi cu diferite structuri. N(4)-alil-3-tiosemicarbazonele şi compuşii coordinativi manifestă activitate antitumorală, antibacterială, antivirală şi antimalarică. Compuşii coordinativi ai cuprului cu aceşti liganzi manifestă activitate antitumorală sporită în comparaţie cu N(4)-alil-3-tiosemicarbazonele corespunzătoare.</p><p> </p>http://ojs.studiamsu.eu/index.php/real-nature/article/view/305N(4)-allyl-3-thiosemicarbazone, complexes, biological activity
spellingShingle Vasilii GRAUR
SYNTHESIS, STRUCTURE AND BIOLOGICAL ACTIVITY OF N(4)-ALLYL-3-THIOSEMICARBAZONES AND THEIR COORDINATION COMPOUNDS WITH SOME 3D METALS
Studia Universitatis Moldaviae: Stiinte reale si ale naturii
N(4)-allyl-3-thiosemicarbazone, complexes, biological activity
title SYNTHESIS, STRUCTURE AND BIOLOGICAL ACTIVITY OF N(4)-ALLYL-3-THIOSEMICARBAZONES AND THEIR COORDINATION COMPOUNDS WITH SOME 3D METALS
title_full SYNTHESIS, STRUCTURE AND BIOLOGICAL ACTIVITY OF N(4)-ALLYL-3-THIOSEMICARBAZONES AND THEIR COORDINATION COMPOUNDS WITH SOME 3D METALS
title_fullStr SYNTHESIS, STRUCTURE AND BIOLOGICAL ACTIVITY OF N(4)-ALLYL-3-THIOSEMICARBAZONES AND THEIR COORDINATION COMPOUNDS WITH SOME 3D METALS
title_full_unstemmed SYNTHESIS, STRUCTURE AND BIOLOGICAL ACTIVITY OF N(4)-ALLYL-3-THIOSEMICARBAZONES AND THEIR COORDINATION COMPOUNDS WITH SOME 3D METALS
title_short SYNTHESIS, STRUCTURE AND BIOLOGICAL ACTIVITY OF N(4)-ALLYL-3-THIOSEMICARBAZONES AND THEIR COORDINATION COMPOUNDS WITH SOME 3D METALS
title_sort synthesis structure and biological activity of n 4 allyl 3 thiosemicarbazones and their coordination compounds with some 3d metals
topic N(4)-allyl-3-thiosemicarbazone, complexes, biological activity
url http://ojs.studiamsu.eu/index.php/real-nature/article/view/305
work_keys_str_mv AT vasiliigraur synthesisstructureandbiologicalactivityofn4allyl3thiosemicarbazonesandtheircoordinationcompoundswithsome3dmetals