Modulating Magnetic Property of Phthalocyanine Supported MII–DyIII (M = Ni, Zn) Heterodinuclear Complexes

Three heterometallic dinuclear compounds, [MIIDyIII­(L)­(Pc)­(ROH)]·ROH (R = CH3, M = Ni (1), Zn (2); R = C2H5, M = Zn (3)), were stepwise synthesized based on phthalocyanine (H2Pc) and one tripodal Schiff-base ligand 1,1,1-tris­[(salicyli­dene­amino)­methyl]­ethane (H3L). All of them have been stud...

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Published inInorganic chemistry Vol. 58; no. 14; pp. 9387 - 9396
Main Authors Ge, Jing-Yuan, Chen, Zhongyan, Qiu, Ya-Ru, Huo, Dexuan, Zhang, Yi-Quan, Wang, Peng, Zuo, Jing-Lin
Format Journal Article
LanguageEnglish
Japanese
Published American Chemical Society 15.07.2019
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ISSN0020-1669
1520-510X
1520-510X
DOI10.1021/acs.inorgchem.9b01179

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Abstract Three heterometallic dinuclear compounds, [MIIDyIII­(L)­(Pc)­(ROH)]·ROH (R = CH3, M = Ni (1), Zn (2); R = C2H5, M = Zn (3)), were stepwise synthesized based on phthalocyanine (H2Pc) and one tripodal Schiff-base ligand 1,1,1-tris­[(salicyli­dene­amino)­methyl]­ethane (H3L). All of them have been studied structurally and magnetically. The six-coordinate MII ion and the seven-coordinate DyIII ion are bridged by two phenolic oxygen atoms to form an MII–LnIII heterodinuclear unit. Magnetic measurements indicate that the ferromagnetic NiII–DyIII interaction is operative in compound 1 and all three compounds exhibit the field-induced slow relaxation of magnetizations. In particular, compounds 2 and 3 have the improved magnetic performance. Ab initio calculations indicate that the weak NiII–DyIII interaction decreases the energy barrier, while the replacement of the paramagnetic NiII ion by the diamagnetic ZnII in compound 2 and 3 not only controls the magnetic interaction but also alters the local magnetic axes of DyIII ions to optimize the magnetic relaxation behavior.
AbstractList Three heterometallic dinuclear compounds, [MIIDyIII(L)(Pc)(ROH)]·ROH (R = CH3, M = Ni (1), Zn (2); R = C2H5, M = Zn (3)), were stepwise synthesized based on phthalocyanine (H2Pc) and one tripodal Schiff-base ligand 1,1,1-tris[(salicylideneamino)methyl]ethane (H3L). All of them have been studied structurally and magnetically. The six-coordinate MII ion and the seven-coordinate DyIII ion are bridged by two phenolic oxygen atoms to form an MII-LnIII heterodinuclear unit. Magnetic measurements indicate that the ferromagnetic NiII-DyIII interaction is operative in compound 1 and all three compounds exhibit the field-induced slow relaxation of magnetizations. In particular, compounds 2 and 3 have the improved magnetic performance. Ab initio calculations indicate that the weak NiII-DyIII interaction decreases the energy barrier, while the replacement of the paramagnetic NiII ion by the diamagnetic ZnII in compound 2 and 3 not only controls the magnetic interaction but also alters the local magnetic axes of DyIII ions to optimize the magnetic relaxation behavior.Three heterometallic dinuclear compounds, [MIIDyIII(L)(Pc)(ROH)]·ROH (R = CH3, M = Ni (1), Zn (2); R = C2H5, M = Zn (3)), were stepwise synthesized based on phthalocyanine (H2Pc) and one tripodal Schiff-base ligand 1,1,1-tris[(salicylideneamino)methyl]ethane (H3L). All of them have been studied structurally and magnetically. The six-coordinate MII ion and the seven-coordinate DyIII ion are bridged by two phenolic oxygen atoms to form an MII-LnIII heterodinuclear unit. Magnetic measurements indicate that the ferromagnetic NiII-DyIII interaction is operative in compound 1 and all three compounds exhibit the field-induced slow relaxation of magnetizations. In particular, compounds 2 and 3 have the improved magnetic performance. Ab initio calculations indicate that the weak NiII-DyIII interaction decreases the energy barrier, while the replacement of the paramagnetic NiII ion by the diamagnetic ZnII in compound 2 and 3 not only controls the magnetic interaction but also alters the local magnetic axes of DyIII ions to optimize the magnetic relaxation behavior.
Three heterometallic dinuclear compounds, [MIIDyIII­(L)­(Pc)­(ROH)]·ROH (R = CH3, M = Ni (1), Zn (2); R = C2H5, M = Zn (3)), were stepwise synthesized based on phthalocyanine (H2Pc) and one tripodal Schiff-base ligand 1,1,1-tris­[(salicyli­dene­amino)­methyl]­ethane (H3L). All of them have been studied structurally and magnetically. The six-coordinate MII ion and the seven-coordinate DyIII ion are bridged by two phenolic oxygen atoms to form an MII–LnIII heterodinuclear unit. Magnetic measurements indicate that the ferromagnetic NiII–DyIII interaction is operative in compound 1 and all three compounds exhibit the field-induced slow relaxation of magnetizations. In particular, compounds 2 and 3 have the improved magnetic performance. Ab initio calculations indicate that the weak NiII–DyIII interaction decreases the energy barrier, while the replacement of the paramagnetic NiII ion by the diamagnetic ZnII in compound 2 and 3 not only controls the magnetic interaction but also alters the local magnetic axes of DyIII ions to optimize the magnetic relaxation behavior.
Author Wang, Peng
Chen, Zhongyan
Zuo, Jing-Lin
Huo, Dexuan
Zhang, Yi-Quan
Ge, Jing-Yuan
Qiu, Ya-Ru
AuthorAffiliation Jiangsu Key Laboratory for NSLSCS, School of Physical Science and Technology
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering
College of Materials and Environmental Engineering
College of Chemical and Environmental Engineering
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Snippet Three heterometallic dinuclear compounds, [MIIDyIII­(L)­(Pc)­(ROH)]·ROH (R = CH3, M = Ni (1), Zn (2); R = C2H5, M = Zn (3)), were stepwise synthesized based on...
Three heterometallic dinuclear compounds, [MIIDyIII(L)(Pc)(ROH)]·ROH (R = CH3, M = Ni (1), Zn (2); R = C2H5, M = Zn (3)), were stepwise synthesized based on...
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Title Modulating Magnetic Property of Phthalocyanine Supported MII–DyIII (M = Ni, Zn) Heterodinuclear Complexes
URI http://dx.doi.org/10.1021/acs.inorgchem.9b01179
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