Preparation of some lanthanide violurate complexes
Violurate complexes of Ce3+, Pr3+, Pr4+, Nd3+, Sm3+, Eu3+, Gd3+, Dy3+, Ho3+, Er3+, and Yb3+ were prepared. The prepared complexes are freely soluble in hot water and dilute mineral acids. Thermal analysis (DTA, DTG, and TGA) show that the solid complexes are characterized by endo‐ and exothermic ban...
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Veröffentlicht in: | Crystal research and technology (1979) 1989-02, Vol.24 (2), p.199-210 |
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creator | Farag, I. S. Ahmed Awadallah, R. M. Gad, A. A. M. |
description | Violurate complexes of Ce3+, Pr3+, Pr4+, Nd3+, Sm3+, Eu3+, Gd3+, Dy3+, Ho3+, Er3+, and Yb3+ were prepared. The prepared complexes are freely soluble in hot water and dilute mineral acids. Thermal analysis (DTA, DTG, and TGA) show that the solid complexes are characterized by endo‐ and exothermic bands, indicating that they are degradated at different temperature stages. The IR spectra of the ligand and its metal complexes reveal that bonding takes place through coordination bonds between the central metal ion and the oxygen atom of the oximino (C = NO) group and the oxygen of the phenolic (ketonic group . All the isomorphous complexes, detected by the X‐ray diffraction patterns, have similar IR spectra. |
doi_str_mv | 10.1002/crat.2170240215 |
format | Article |
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Ahmed</creatorcontrib><creatorcontrib>Awadallah, R. M.</creatorcontrib><creatorcontrib>Gad, A. A. M.</creatorcontrib><title>Preparation of some lanthanide violurate complexes</title><title>Crystal research and technology (1979)</title><addtitle>Cryst. Res. Technol</addtitle><description>Violurate complexes of Ce3+, Pr3+, Pr4+, Nd3+, Sm3+, Eu3+, Gd3+, Dy3+, Ho3+, Er3+, and Yb3+ were prepared. The prepared complexes are freely soluble in hot water and dilute mineral acids. Thermal analysis (DTA, DTG, and TGA) show that the solid complexes are characterized by endo‐ and exothermic bands, indicating that they are degradated at different temperature stages. The IR spectra of the ligand and its metal complexes reveal that bonding takes place through coordination bonds between the central metal ion and the oxygen atom of the oximino (C = NO) group and the oxygen of the phenolic (ketonic group . All the isomorphous complexes, detected by the X‐ray diffraction patterns, have similar IR spectra.</description><subject>Chemistry</subject><subject>Coordination compounds</subject><subject>Exact sciences and technology</subject><subject>Inorganic chemistry and origins of life</subject><subject>Preparations and properties</subject><issn>0232-1300</issn><issn>1521-4079</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><recordid>eNqFj0tPwkAUhSdGExFdu-3GZeXOs21cIQqY4CMGw3JyO8zEammbGVT495bUSFy5uotzvnPzEXJO4ZICsIHxuL5kNAEmgFF5QHpUMhoLSLJD0gPGWUw5wDE5CeENADIlWI-wJ28bbNGirqLaRaFe2ajEav2KVbG00WdRlx9tbCNTr5rSbmw4JUcOy2DPfm6fvIxv56NpPHuc3I2Gs9hwRWUslgnPhDLC5SBZTlWunMs5OqoyzDhKl1KV5jZByZxMWZpY6tKcZgytciB4nwy6XePrELx1uvHFCv1WU9A7Zb1T1nvllrjoiAaDwdJ5rEwR9lgmUxCKtb2rrvdVlHb736wePQ_nf77EHV2Etd380ujftUp4IvXiYaJvQIyvYTHV9_wbEyp3Dg</recordid><startdate>198902</startdate><enddate>198902</enddate><creator>Farag, I. S. 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M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3615-4d73946c4fb052b16b6ffb3af169a93a5f8168be7a52f58287e1f8b192ae6f043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Chemistry</topic><topic>Coordination compounds</topic><topic>Exact sciences and technology</topic><topic>Inorganic chemistry and origins of life</topic><topic>Preparations and properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Farag, I. S. Ahmed</creatorcontrib><creatorcontrib>Awadallah, R. M.</creatorcontrib><creatorcontrib>Gad, A. A. M.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Crystal research and technology (1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Farag, I. S. Ahmed</au><au>Awadallah, R. M.</au><au>Gad, A. A. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of some lanthanide violurate complexes</atitle><jtitle>Crystal research and technology (1979)</jtitle><addtitle>Cryst. Res. Technol</addtitle><date>1989-02</date><risdate>1989</risdate><volume>24</volume><issue>2</issue><spage>199</spage><epage>210</epage><pages>199-210</pages><issn>0232-1300</issn><eissn>1521-4079</eissn><coden>CRTEDF</coden><abstract>Violurate complexes of Ce3+, Pr3+, Pr4+, Nd3+, Sm3+, Eu3+, Gd3+, Dy3+, Ho3+, Er3+, and Yb3+ were prepared. The prepared complexes are freely soluble in hot water and dilute mineral acids. Thermal analysis (DTA, DTG, and TGA) show that the solid complexes are characterized by endo‐ and exothermic bands, indicating that they are degradated at different temperature stages. The IR spectra of the ligand and its metal complexes reveal that bonding takes place through coordination bonds between the central metal ion and the oxygen atom of the oximino (C = NO) group and the oxygen of the phenolic (ketonic group . All the isomorphous complexes, detected by the X‐ray diffraction patterns, have similar IR spectra.</abstract><cop>Berlin</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/crat.2170240215</doi><tpages>12</tpages></addata></record> |
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subjects | Chemistry Coordination compounds Exact sciences and technology Inorganic chemistry and origins of life Preparations and properties |
title | Preparation of some lanthanide violurate complexes |
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