Heterospin Single‐Molecule Magnets Based on Terbium Ions and TCNQF4 Radicals: Interplay between Single‐Molecule Magnet and Phonon Bottleneck Phenomena Investigated by Dilution Studies |
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Authors: | Nazario Lopez Andrey V. Prosvirin Dr. Hanhua Zhao Dr. Wolfgang Wernsdorfer Dr. Kim R. Dunbar Prof. |
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Affiliation: | 1. Department of Chemistry, Texas A&M University, College Station, TX 77842 (USA), Fax: (+1)?979‐845‐7177;2. Institut Néel, CNRS & Université J. Fourier, BP‐166, Grenoble, Cedex 9 (France) |
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Abstract: | A series of isostructural compounds with formula [M(TCNQF4)2(H2O)6]TCNQF4 ? 3 H2O (M=Tb ( 1 ), Y ( 2 ), Y:Tb (74:26) ( 3 ), and Y:Tb (97:3) ( 4 ); TCNQF4= tetrafluorotetracyanoquinodimethane) were prepared and their magnetic properties investigated. Compounds 1 , 3 , and 4 show the beginning of a frequency‐dependent out‐of‐phase ac signal, and decreasing intensity of the signal with decreased concentration of TbIII ions in the diluted samples is observed. No out‐of‐phase signal was observed for 2 , an indication that the behavior of 1 , 3 , and 4 is indicative of slow paramagnetic relaxation of TbIII ions in the samples. A more detailed micro‐SQUID study at low temperature revealed an interplay between single‐molecule magnetic (SMM) behavior and a phonon bottleneck (PB) effect, and that these properties depend on the concentration of diamagnetic yttrium ions. A combination of SMM and PB phenomena was found for 1 , whereby the PB effect increases with increasing dilution until eventually a pure PB effect is observed for 2 . The PB behavior is interpreted as being due to the presence of a “sea of organic S=1/2 radicals” from the TCNQF4 radicals in these compounds. The present data underscore the fact that the presence of an out‐of‐phase ac signal may not, in fact, be caused by SMM behavior, particularly when magnetic metal ions are combined with organic radical ligands such as those found in the organocyanide family. |
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Keywords: | magnetic properties quinodimethanes radicals rare earths single‐molecule magnets |
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