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A Redox‐Active Bridging Ligand to Promote Spin Delocalization,High‐Spin Complexes,and Magnetic Multi‐Switchability
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Xiaozhou Ma Dr. Elizaveta A. Suturina Dr. Siddhartha De Dr. Philippe Négrier Mathieu Rouzières Dr. Rodolphe Clérac Dr. Pierre Dechambenoit 《Angewandte Chemie (International ed. in English)》2018,57(26):7841-7845
A dinuclear CoII complex, [Co2(tphz)(tpy)2]n+ (n=4, 3 or 2; tphz: tetrapyridophenazine; tpy: terpyridine), has been assembled using the redox‐active and strongly complexing tphz bridging ligand. The magnetic properties of this complex can be tuned from spin‐crossover with T1/2≈470 K for the pristine compound (n=4) to single‐molecule magnet with an ST=5/2 spin ground state when once reduced (n=3) to finally a diamagnetic species when twice reduced (n=2). The two successive and reversible reductions are concomitant with an increase of the spin delocalization within the complex, promoting remarkably large magnetic exchange couplings and high‐spin species even at room temperature. 相似文献
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H. Mühe Mc. Candless E. Valenta Utz Wilh Vaubel B. Ahlström O. Aschan J. Kondakow J. Schindelmeiser R. Böhme H. Herzfeld J. E. Teeple R. Adan J. Marcusson Darmois H. Wolff C. Piest R. Marcille EA. Parry M. Adams H. W. Fosse K. Ihnatowzcz 《Analytical and bioanalytical chemistry》1917,56(10-11):541-560
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Anna G. Scott Diogo Alves Galico Isabel Bogacz Paul H. Oyala Junko Yano Elizaveta A. Suturina Muralee Murugesu Theodor Agapie 《Angewandte Chemie (International ed. in English)》2023,62(49):e202313880
Atomically defined large metal clusters have applications in new reaction development and preparation of materials with tailored properties. Expanding the synthetic toolbox for reactive high nuclearity metal complexes, we report a new class of Fe clusters, Tp*4W4Fe13S12 , displaying a Fe13 core with M−M bonds that has precedent only in main group and late metal chemistry. M13 clusters with closed shell electron configurations can show significant stability and have been classified as superatoms. In contrast, Tp*4W4Fe13S12 displays a large spin ground state of S=13. This compound performs small molecule activations involving the transfer of up to 12 electrons resulting in significant cluster rearrangements. 相似文献
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RD Harris WS Baker Van Stipdonk MJ RM Crooks EA Schweikert 《Rapid communications in mass spectrometry : RCM》1999,13(14):1374-1380
A suite of keV polyatomic or 'cluster' projectiles was used to bombard unoxidized and oxidized self-assembled monolayer surfaces. Negative secondary ion yields, collected at the limit of single ion impacts, were measured and compared for both molecular and fragment ions. In contrast to targets that are orders of magnitude thicker than the penetration range of the primary ions, secondary ion yields from polyatomic projectile impacts on self-assembled monolayers show little to no enhancement when compared with monatomic projectiles at the same velocity. This unusual trend is most likely due to the structural arrangement and bonding characteristics of the monolayer molecules with the Au(111). Copyright 1999 John Wiley & Sons, Ltd. 相似文献
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Aderholz M Aggarwal MM Akbari H Allport PP Badyal SK Ballagh HC Barth M Baton JP Bingham HH Brucker EB Burnstein RA Campbell JR Cence RJ Chatterjee TK Clayton EF Corrigan G Coutures C DeProspo D Devanand De Wolf EA Faulkner PJ Foeth H Fretter WB Gupta VK Hanlon J Harigel G Harris FA Jabiol MA Jacques P Jain V Jones GT Jones MD Kafka T Kalelkar M Kasper P Kohli JM Koller EL Krawiec RJ Lauko M Lys JE Marage P Milburn RH Miller DB Mittra IS Mobayyen MM Moreels J Morrison DR Myatt G Nailor P 《Physical review D: Particles and fields》1992,45(7):2232-2243
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