Synthesis and structure of nonacoordinated tris-chelate lanthanide (III) complexes with tridentate 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one ligands

A series of new nonacoordinated tris-chelate lanthanide (III) complexes was prepared by the reaction of the reduced form of the tricyclic 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one ligand with Ln(III) acetates (Ln=La, Pr, Sm, Eu, Gd, Tb, Dy, Yb). The coordination polyhedron in all comple...

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Veröffentlicht in:Inorganica Chimica Acta 2017-03, Vol.458, p.116-121
Hauptverfasser: Ivakhnenko, Eugeny P., Romanenko, Galina V., Simakov, Vladimir I., Knyazev, Pavel A., Bogomyakov, Artyom S., Lyssenko, Konstantin A., Minkin, Vladimir I.
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container_title Inorganica Chimica Acta
container_volume 458
creator Ivakhnenko, Eugeny P.
Romanenko, Galina V.
Simakov, Vladimir I.
Knyazev, Pavel A.
Bogomyakov, Artyom S.
Lyssenko, Konstantin A.
Minkin, Vladimir I.
description A series of new nonacoordinated tris-chelate lanthanide (III) complexes was prepared by the reaction of the reduced form of the tricyclic 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one ligand with Ln(III) acetates (Ln=La, Pr, Sm, Eu, Gd, Tb, Dy, Yb). The coordination polyhedron in all complexes, the molecular structures of which were established by X-ray diffraction studies, is the tricapped trigonal prism composed by six oxygen and three nitrogen atoms of the deprotonated ligand. Electronic absorption spectra of the deeply colored complexes contain a broad long wavelength absorption band ranging from 600 to 900nm. The values of effective magnetic moments μeff (at 300K) were found to be equal to 1.78, 3.41, 3.50, 4.35, 7.85, 9.22 and 10.32 μB for the Sm(III), Pr(III), Eu(III), Yb(III), Gd(III), Tb(III) and Dy(III) complexes, respectively. [Display omitted] •The use of the rationally designed tridentate chelating ligand, 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one containing the rigid tricyclic molecular framework with the ONO donor centers suitably arranged for the complexation with trivalent metal ions having sufficiently big ionic radii allowed preparation of new nonacoordinated Ln(III) complexes (Ln=La, Pr, Sm, Eu, Gd, Tb, Dy, Yb).•The study of luminescent and redox properties of the prepared complexes, in particular their radical-anions the formation and stability of which is ensured by the redox-active hydroxyphenoxazinone ligands is currently underway. A series of new nonacoordinated tris-chelate lanthanide (III) complexes was prepared by the reaction of the reduced form of the tricyclic 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one ligand with Ln(III) acetates (Ln=La, Pr, Sm, Eu, Gd, Tb, Dy, Yb). The coordination polyhedron in all complexes, the molecular structures of which were established by X-ray diffraction studies, is the tricapped trigonal prism composed by six oxygen and three nitrogen atoms of the deprotonated ligand. Electronic absorption spectra of the deeply colored complexes contain a broad long wavelength absorption band ranging from 600 to 900nm. The values of effective magnetic moments μeff (at 300K) were found to be equal to 1.78, 3.41, 3.50, 4.35, 7.85, 9.22 and 10.32 μB for the Sm(III), Pr(III), Eu(III), Yb(III), Gd(III), Tb(III) and Dy(III) complexes, respectively.
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The coordination polyhedron in all complexes, the molecular structures of which were established by X-ray diffraction studies, is the tricapped trigonal prism composed by six oxygen and three nitrogen atoms of the deprotonated ligand. Electronic absorption spectra of the deeply colored complexes contain a broad long wavelength absorption band ranging from 600 to 900nm. The values of effective magnetic moments μeff (at 300K) were found to be equal to 1.78, 3.41, 3.50, 4.35, 7.85, 9.22 and 10.32 μB for the Sm(III), Pr(III), Eu(III), Yb(III), Gd(III), Tb(III) and Dy(III) complexes, respectively. [Display omitted] •The use of the rationally designed tridentate chelating ligand, 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one containing the rigid tricyclic molecular framework with the ONO donor centers suitably arranged for the complexation with trivalent metal ions having sufficiently big ionic radii allowed preparation of new nonacoordinated Ln(III) complexes (Ln=La, Pr, Sm, Eu, Gd, Tb, Dy, Yb).•The study of luminescent and redox properties of the prepared complexes, in particular their radical-anions the formation and stability of which is ensured by the redox-active hydroxyphenoxazinone ligands is currently underway. A series of new nonacoordinated tris-chelate lanthanide (III) complexes was prepared by the reaction of the reduced form of the tricyclic 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one ligand with Ln(III) acetates (Ln=La, Pr, Sm, Eu, Gd, Tb, Dy, Yb). The coordination polyhedron in all complexes, the molecular structures of which were established by X-ray diffraction studies, is the tricapped trigonal prism composed by six oxygen and three nitrogen atoms of the deprotonated ligand. Electronic absorption spectra of the deeply colored complexes contain a broad long wavelength absorption band ranging from 600 to 900nm. The values of effective magnetic moments μeff (at 300K) were found to be equal to 1.78, 3.41, 3.50, 4.35, 7.85, 9.22 and 10.32 μB for the Sm(III), Pr(III), Eu(III), Yb(III), Gd(III), Tb(III) and Dy(III) complexes, respectively.</description><identifier>ISSN: 0020-1693</identifier><identifier>EISSN: 1873-3255</identifier><identifier>DOI: 10.1016/j.ica.2017.01.001</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adsorption ; Antiferromagnetism ; Chelates ; Chemical compounds ; Chemical reactions ; Coordination compounds ; Coordination polymers ; Copper ; Copper compounds ; Coupling ; Diffraction ; Ferromagnetism ; Hydrothermal reactions ; Lanthanides ; Ligands ; Magnetic properties ; Molecular structures ; Nonacoordinated complexes ; Tethers ; Tetrazoles</subject><ispartof>Inorganica Chimica Acta, 2017-03, Vol.458, p.116-121</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright Elsevier Science Ltd. 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The coordination polyhedron in all complexes, the molecular structures of which were established by X-ray diffraction studies, is the tricapped trigonal prism composed by six oxygen and three nitrogen atoms of the deprotonated ligand. Electronic absorption spectra of the deeply colored complexes contain a broad long wavelength absorption band ranging from 600 to 900nm. The values of effective magnetic moments μeff (at 300K) were found to be equal to 1.78, 3.41, 3.50, 4.35, 7.85, 9.22 and 10.32 μB for the Sm(III), Pr(III), Eu(III), Yb(III), Gd(III), Tb(III) and Dy(III) complexes, respectively. [Display omitted] •The use of the rationally designed tridentate chelating ligand, 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one containing the rigid tricyclic molecular framework with the ONO donor centers suitably arranged for the complexation with trivalent metal ions having sufficiently big ionic radii allowed preparation of new nonacoordinated Ln(III) complexes (Ln=La, Pr, Sm, Eu, Gd, Tb, Dy, Yb).•The study of luminescent and redox properties of the prepared complexes, in particular their radical-anions the formation and stability of which is ensured by the redox-active hydroxyphenoxazinone ligands is currently underway. A series of new nonacoordinated tris-chelate lanthanide (III) complexes was prepared by the reaction of the reduced form of the tricyclic 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one ligand with Ln(III) acetates (Ln=La, Pr, Sm, Eu, Gd, Tb, Dy, Yb). The coordination polyhedron in all complexes, the molecular structures of which were established by X-ray diffraction studies, is the tricapped trigonal prism composed by six oxygen and three nitrogen atoms of the deprotonated ligand. Electronic absorption spectra of the deeply colored complexes contain a broad long wavelength absorption band ranging from 600 to 900nm. The values of effective magnetic moments μeff (at 300K) were found to be equal to 1.78, 3.41, 3.50, 4.35, 7.85, 9.22 and 10.32 μB for the Sm(III), Pr(III), Eu(III), Yb(III), Gd(III), Tb(III) and Dy(III) complexes, respectively.</description><subject>Adsorption</subject><subject>Antiferromagnetism</subject><subject>Chelates</subject><subject>Chemical compounds</subject><subject>Chemical reactions</subject><subject>Coordination compounds</subject><subject>Coordination polymers</subject><subject>Copper</subject><subject>Copper compounds</subject><subject>Coupling</subject><subject>Diffraction</subject><subject>Ferromagnetism</subject><subject>Hydrothermal reactions</subject><subject>Lanthanides</subject><subject>Ligands</subject><subject>Magnetic properties</subject><subject>Molecular structures</subject><subject>Nonacoordinated complexes</subject><subject>Tethers</subject><subject>Tetrazoles</subject><issn>0020-1693</issn><issn>1873-3255</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kU-r1DAUxYMoOI5-AHcFN-_BpN4kbdriSh7-GXjgQl2HNLljM_YlY5Lq1G_jNzXDuPZuLhd-554Dh5CXDGoGTL4-1s7omgPramA1AHtENqzvBBW8bR-TDQAHyuQgnpJnKR0BBEjRbsifz6vPEyaXKu1tlXJcTF4iVuFQ-eC1CSFa53VGW-XoEjUTzuWqZl102juL1c1-v7-tTHg4zXjGVP1yebrAFn2-oHzX7OSupxlz1N9duskYMx2XvM63dKDTamM4r6cJfTjr385TRoMvDu5biZSekycHPSd88W9vydf3777cfaT3nz7s797eU8MbyHQYQYsyWhs-9oxx1nXCtI00chgkl2BHaXCQg7UtYweJoHtoeiEOZjTQj2JLXl3_nmL4sWDK6hiW6Iul4tB0nPei0FvCrpSJIaWIB3WK7kHHVTFQlybUUZUm1KUJBUyVJormzVWDJf5Ph1El49AbtC6iycoG9x_1X3T0kp8</recordid><startdate>20170324</startdate><enddate>20170324</enddate><creator>Ivakhnenko, Eugeny P.</creator><creator>Romanenko, Galina V.</creator><creator>Simakov, Vladimir I.</creator><creator>Knyazev, Pavel A.</creator><creator>Bogomyakov, Artyom S.</creator><creator>Lyssenko, Konstantin A.</creator><creator>Minkin, Vladimir I.</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20170324</creationdate><title>Synthesis and structure of nonacoordinated tris-chelate lanthanide (III) complexes with tridentate 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one ligands</title><author>Ivakhnenko, Eugeny P. ; 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The coordination polyhedron in all complexes, the molecular structures of which were established by X-ray diffraction studies, is the tricapped trigonal prism composed by six oxygen and three nitrogen atoms of the deprotonated ligand. Electronic absorption spectra of the deeply colored complexes contain a broad long wavelength absorption band ranging from 600 to 900nm. The values of effective magnetic moments μeff (at 300K) were found to be equal to 1.78, 3.41, 3.50, 4.35, 7.85, 9.22 and 10.32 μB for the Sm(III), Pr(III), Eu(III), Yb(III), Gd(III), Tb(III) and Dy(III) complexes, respectively. [Display omitted] •The use of the rationally designed tridentate chelating ligand, 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one containing the rigid tricyclic molecular framework with the ONO donor centers suitably arranged for the complexation with trivalent metal ions having sufficiently big ionic radii allowed preparation of new nonacoordinated Ln(III) complexes (Ln=La, Pr, Sm, Eu, Gd, Tb, Dy, Yb).•The study of luminescent and redox properties of the prepared complexes, in particular their radical-anions the formation and stability of which is ensured by the redox-active hydroxyphenoxazinone ligands is currently underway. A series of new nonacoordinated tris-chelate lanthanide (III) complexes was prepared by the reaction of the reduced form of the tricyclic 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one ligand with Ln(III) acetates (Ln=La, Pr, Sm, Eu, Gd, Tb, Dy, Yb). The coordination polyhedron in all complexes, the molecular structures of which were established by X-ray diffraction studies, is the tricapped trigonal prism composed by six oxygen and three nitrogen atoms of the deprotonated ligand. Electronic absorption spectra of the deeply colored complexes contain a broad long wavelength absorption band ranging from 600 to 900nm. The values of effective magnetic moments μeff (at 300K) were found to be equal to 1.78, 3.41, 3.50, 4.35, 7.85, 9.22 and 10.32 μB for the Sm(III), Pr(III), Eu(III), Yb(III), Gd(III), Tb(III) and Dy(III) complexes, respectively.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.ica.2017.01.001</doi><tpages>6</tpages></addata></record>
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source Elsevier ScienceDirect Journals
subjects Adsorption
Antiferromagnetism
Chelates
Chemical compounds
Chemical reactions
Coordination compounds
Coordination polymers
Copper
Copper compounds
Coupling
Diffraction
Ferromagnetism
Hydrothermal reactions
Lanthanides
Ligands
Magnetic properties
Molecular structures
Nonacoordinated complexes
Tethers
Tetrazoles
title Synthesis and structure of nonacoordinated tris-chelate lanthanide (III) complexes with tridentate 2,4,6,8-tetrakis(tert-butyl)-9-hydroxyphenoxazin-1-one ligands
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