{"id":6842,"date":"2021-10-14T02:26:06","date_gmt":"2021-10-13T18:26:06","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=6842"},"modified":"2021-10-14T02:26:06","modified_gmt":"2021-10-13T18:26:06","slug":"brief-introduction-of-67-51-6-2","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=6842","title":{"rendered":"Brief introduction of 67-51-6"},"content":{"rendered":"<p>An article Cu(II) and Zn(II) Complexes with Dinitrobenzoates and Pyrazolyl Ligands: Structural and Thermal Stability Influence of N-H Moiety WOS:000470938700032 published article about TRINUCLEAR COPPER(II) COMPLEX; RING-OPENING POLYMERIZATION; CRYSTAL-STRUCTURE; NONCOVALENT INTERACTIONS; THERMOCHEMICAL KINETICS; DENSITY FUNCTIONALS; X-RAY; COORDINATION; 3,5-DIMETHYLPYRAZOLE; ACID in [Torres, Juan F.; Macias, Mario A.; Hurtado, John J.] Univ Los Andes, Dept Chem, Carrera 1 18A-12, Bogota 111711, Colombia; [Franco-Ulloa, Sebastian; Pietro Miscione, Gian] Univ Los Andes, Chem Dept, COBO Computat Bioorgan Chem Bogota, Cra 1 18A-12, Bogota 111711, Colombia; [Cobo, Justo] Univ Jaen, Dept Inorgan &#038; Organ Chem, Jaen 23071, Spain in 2019, Cited 53. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. <a href=\"https:\/\/www.ambeed.com\/products\/67-51-6.html\">SDS of cas: 67-51-6<\/a><\/p>\n<p>The synthesis and characterization of air-stable Cu(II) and Zn(II) complexes with 3,5-dinitrobenzoate (DNB) and 3,5-dimethylpyrazole (L1) or bis(3,5-dimethylpyrazol-1-yl)methane (L2) are described. Three of these complexes exhibit a monomeric structure, while the Cu(II) complex with L2 is a trinuclear complex. Density functional theory calculations were performed to understand the unexpected formation of the three-centered compound. In agreement with the X-ray crystal structure, the N-H moiety present in LI was identified as possible driving force to obtain monomeric structures, while L2, without it, can favor the trinuclear complex formation. Thermal studies were carried for the complexes, and it was observed that the presence of the azole ligand allows the decomposition of the complexes at lower temperatures due to the presence of acidic protons, being especially important for L1.<\/p>\n<p><a href=\"https:\/\/www.ambeed.com\/products\/67-51-6.html\">SDS of cas: 67-51-6<\/a>. About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Torres, JF; Macias, MA; Franco-Ulloa, S; Miscione, GP; Cobo, J; Hurtado, JJ or concate me.<\/p>\n<p>Reference:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">Pyrazole &#8211; Wikipedia<\/a>,<br \/>,<a href=\"https:\/\/www.sciencedirect.com\/topics\/chemistry\/pyrazoles\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p><a href=\"https:\/\/www.ambeed.com\/products\/67-51-6.html\">SDS of cas: 67-51-6<\/a>. About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Torres, JF; Macias, MA; Franco-Ulloa, S; Miscione, GP; Cobo, J; Hurtado, JJ or concate me.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[249,131],"tags":[145],"class_list":["post-6842","post","type-post","status-publish","format-standard","hentry","category-67-51-6","category-pyrazoles-derivatives","tag-m-w0-100"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Brief introduction of 67-51-6 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"An article Cu(II) and Zn(II) Complexes with Dinitrobenzoates and Pyrazolyl Ligands: Structural and Thermal Stability Influence of N-H Moiety WOS:000470938700032 published article about TRINUCLEAR COPPER(II) COMPLEX; RING-OPENING POLYMERIZATION; CRYSTAL-STRUCTURE; NONCOVALENT INTERACTIONS; THERMOCHEMICAL KINETICS; DENSITY FUNCTIONALS; X-RAY; COORDINATION; 3,5-DIMETHYLPYRAZOLE; ACID in [Torres, Juan F.; Macias, Mario A.; Hurtado, John J.] Univ Los Andes, Dept Chem, Carrera 1 18A-12, Bogota 111711, Colombia; [Franco-Ulloa, Sebastian; Pietro Miscione, Gian] Univ Los Andes, Chem Dept, COBO Computat Bioorgan Chem Bogota, Cra 1 18A-12, Bogota 111711, Colombia; [Cobo, Justo] Univ Jaen, Dept Inorgan &amp; Organ Chem, Jaen 23071, Spain in 2019, Cited 53. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. 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The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. 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The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. 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The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. 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The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. SDS of cas: 67-51-6","breadcrumb":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=6842#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.pyrazoles-derivatives.com\/?p=6842"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=6842#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"\u9996\u9875","item":"https:\/\/www.pyrazoles-derivatives.com\/"},{"@type":"ListItem","position":2,"name":"Brief introduction of 67-51-6"}]},{"@type":"WebSite","@id":"https:\/\/www.pyrazoles-derivatives.com\/#website","url":"https:\/\/www.pyrazoles-derivatives.com\/","name":"pyrazoles-derivatives","description":"Several pyrazole derivatives possess important pharmacological activities and they have been proved useful materials in drug research. 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