Lanthanide Metal–Organic Frameworks Assembled from Unexplored Imidazolylcarboxylic Acid: Structure and Field-Induced Two-Step Magnetic Relaxation
A series of 3D homologous metal–organic frameworks, [M(H0.5L)2] [M = Dy (1), Ho (2), Yb (3), Sm (4), Gd (5), and Y (6); H2L = 5-(1H-imidazol-1-yl)isophthalic acid], were isolated. In these complexes, the metal centers behave as hexacoordinated environments with distorted octahedral geometries, whi...
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Veröffentlicht in: | Inorganic chemistry 2020-09, Vol.59 (17), p.11930-11934 |
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creator | Wu, Yuewei Zhou, Yuting Cao, Senni Cen, Peipei Zhang, Yi-Quan Yang, Jinhui Liu, Xiangyu |
description | A series of 3D homologous metal–organic frameworks, [M(H0.5L)2] [M = Dy (1), Ho (2), Yb (3), Sm (4), Gd (5), and Y (6); H2L = 5-(1H-imidazol-1-yl)isophthalic acid], were isolated. In these complexes, the metal centers behave as hexacoordinated environments with distorted octahedral geometries, which is unusual in the lanthanide series, linking to each other and producing a fascinating 3D architecture. Magnetically, 1 features a field-driven dual-magnetic relaxation, which is rarely observed in high-dimensional coordination polymers. Analysis on the dilution sample (1@Y) and ab initio calculation unveil that the thermally assisted slow relaxation is mostly caused by the single-ion magnetism of DyIII itself. |
doi_str_mv | 10.1021/acs.inorgchem.0c01855 |
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In these complexes, the metal centers behave as hexacoordinated environments with distorted octahedral geometries, which is unusual in the lanthanide series, linking to each other and producing a fascinating 3D architecture. Magnetically, 1 features a field-driven dual-magnetic relaxation, which is rarely observed in high-dimensional coordination polymers. 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Chem</addtitle><description>A series of 3D homologous metal–organic frameworks, [M(H0.5L)2] [M = Dy (1), Ho (2), Yb (3), Sm (4), Gd (5), and Y (6); H2L = 5-(1H-imidazol-1-yl)isophthalic acid], were isolated. In these complexes, the metal centers behave as hexacoordinated environments with distorted octahedral geometries, which is unusual in the lanthanide series, linking to each other and producing a fascinating 3D architecture. Magnetically, 1 features a field-driven dual-magnetic relaxation, which is rarely observed in high-dimensional coordination polymers. Analysis on the dilution sample (1@Y) and ab initio calculation unveil that the thermally assisted slow relaxation is mostly caused by the single-ion magnetism of DyIII itself.</description><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkc1uEzEQgC0EEqHwCEg-ctkw3rU3WW5RRSBSqkq0lbitZu3ZdIvXDrZXTTj1HfqGfRJcpeLKaX6_kUYfYx8FzAWU4jPqOB-cDzt9S-McNIilUq_YTKgSCiXg52s2A8i5qOvmLXsX4x0ANJWsZ-xxiy7dohsM8QtKaJ8eHi_DLjc0Xwcc6d6HX5GvYqSxs2R4H_zIbxwd9taHXG_GweAfb49WY-j84WgzudKD-cKvUph0mgJxdIavB7Km2Dgz6Yxd3_viKtGeX-DOUcrMD7J4wDR495696dFG-vASz9jN-uv1-fdie_ltc77aFliVy1RUC4lguqqRgiTV2EPXg9GgF6pvJKiFlqojMig1dhJKaqTWDRhR62ZZoqrO2KfT3X3wvyeKqR2HqMladOSn2JayUqIBWS7zqjqt6uBjDNS3-zCMGI6tgPZZQpsltP8ktC8SMidO3PP4zk_B5Yf-w_wF05aUiA</recordid><startdate>20200908</startdate><enddate>20200908</enddate><creator>Wu, Yuewei</creator><creator>Zhou, Yuting</creator><creator>Cao, Senni</creator><creator>Cen, Peipei</creator><creator>Zhang, Yi-Quan</creator><creator>Yang, Jinhui</creator><creator>Liu, Xiangyu</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1818-0612</orcidid><orcidid>https://orcid.org/0000-0001-8864-3411</orcidid></search><sort><creationdate>20200908</creationdate><title>Lanthanide Metal–Organic Frameworks Assembled from Unexplored Imidazolylcarboxylic Acid: Structure and Field-Induced Two-Step Magnetic Relaxation</title><author>Wu, Yuewei ; Zhou, Yuting ; Cao, Senni ; Cen, Peipei ; Zhang, Yi-Quan ; Yang, Jinhui ; Liu, Xiangyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a328t-374a0db3941e4e6af0bf0dc0c75f94057c45beeda4cab402e94cc90d16c982a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Yuewei</creatorcontrib><creatorcontrib>Zhou, Yuting</creatorcontrib><creatorcontrib>Cao, Senni</creatorcontrib><creatorcontrib>Cen, Peipei</creatorcontrib><creatorcontrib>Zhang, Yi-Quan</creatorcontrib><creatorcontrib>Yang, Jinhui</creatorcontrib><creatorcontrib>Liu, Xiangyu</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Yuewei</au><au>Zhou, Yuting</au><au>Cao, Senni</au><au>Cen, Peipei</au><au>Zhang, Yi-Quan</au><au>Yang, Jinhui</au><au>Liu, Xiangyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lanthanide Metal–Organic Frameworks Assembled from Unexplored Imidazolylcarboxylic Acid: Structure and Field-Induced Two-Step Magnetic Relaxation</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2020-09-08</date><risdate>2020</risdate><volume>59</volume><issue>17</issue><spage>11930</spage><epage>11934</epage><pages>11930-11934</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>A series of 3D homologous metal–organic frameworks, [M(H0.5L)2] [M = Dy (1), Ho (2), Yb (3), Sm (4), Gd (5), and Y (6); H2L = 5-(1H-imidazol-1-yl)isophthalic acid], were isolated. In these complexes, the metal centers behave as hexacoordinated environments with distorted octahedral geometries, which is unusual in the lanthanide series, linking to each other and producing a fascinating 3D architecture. Magnetically, 1 features a field-driven dual-magnetic relaxation, which is rarely observed in high-dimensional coordination polymers. Analysis on the dilution sample (1@Y) and ab initio calculation unveil that the thermally assisted slow relaxation is mostly caused by the single-ion magnetism of DyIII itself.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.inorgchem.0c01855</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-1818-0612</orcidid><orcidid>https://orcid.org/0000-0001-8864-3411</orcidid></addata></record> |
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title | Lanthanide Metal–Organic Frameworks Assembled from Unexplored Imidazolylcarboxylic Acid: Structure and Field-Induced Two-Step Magnetic Relaxation |
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