{"id":11826,"date":"2022-12-05T06:02:39","date_gmt":"2022-12-04T22:02:39","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11826"},"modified":"2022-12-05T06:02:39","modified_gmt":"2022-12-04T22:02:39","slug":"sathiyaraj-subbaiyans-team-published-research-in-synthesis-and-reactivity-in-inorganic-metal-organic-and-nano-metal-chemistry-in-44-cas-4551-69-3","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11826","title":{"rendered":"Sathiyaraj, Subbaiyan&#8217;s team published research in Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry  in 44 | CAS: 4551-69-3"},"content":{"rendered":"<p>Sathiyaraj, Subbaiyan published the artcile<b><i>Synthesis, Spectral Characterization, DNA Binding, DNA Cleavage, and Antioxidant Studies of Ruthenium(III) Heterocyclic Thiosemicarbazone Complexes<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/4551-69-3.html\">Application In Synthesis of  4551-69-3<\/a>,  the publication is  Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry (2014), 44(9), 1261-1271, database is CAplus.<\/p>\n<p>The reactions of benzothiazolyl thiosemicarbazone with [RuX<sub>3<\/sub>(PPh<sub>3<\/sub>)<sub>3<\/sub>] (X = Cl\/Br) in a 1:1 molar ratio gave stable solid complexes corresponding to [RuX(PPh<sub>3<\/sub>)<sub>2<\/sub>(L)]. Structural features were determined by anal. and spectral techniques. DNA binding properties of the ligands and its Ru(III) complexes were studied by electronic absorption spectroscopy. The complexes show good binding affinity to calf-thymus DNA. Gel electrophoresis of pBR322 DNA with complexes demonstrated that the complexes exhibit excellent cleavage activity via oxidative pathway. The antioxidant activity of the free ligands and its complexes was determined by DPPH and hydroxyl radicals. The complexes possess potent antioxidant activity.<\/p>\n<p>Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry published new progress about 4551-69-3. 4551-69-3 belongs to pyrazoles-derivatives, auxiliary class Benzenes, name is 4-Benzoyl-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, and the molecular formula is C17H14N2O2, <a href=\"https:\/\/www.ambeed.com\/products\/4551-69-3.html\">Application In Synthesis of  4551-69-3<\/a>.<\/p>\n<p>Referemce:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">https:\/\/en.wikipedia.org\/wiki\/Pyrazole<\/a>,<br \/><a href=\"Pyrazole - Wikipedia\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry published new progress about 4551-69-3. 4551-69-3 belongs to pyrazoles-derivatives, auxiliary class Benzenes, name is 4-Benzoyl-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, and the molecular formula is C17H14N2O2, <a href=\"https:\/\/www.ambeed.com\/products\/4551-69-3.html\">Application In Synthesis of  4551-69-3<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[808,131],"tags":[740],"class_list":["post-11826","post","type-post","status-publish","format-standard","hentry","category-4551-69-3","category-pyrazoles-derivatives","tag-m-w250-300"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - 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