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Journal articles on the topic 'Molecular Magnets'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Wang, Bing-Wu, Xin-Yi Wang, Hao-Ling Sun, Shang-Da Jiang, and Song Gao. "Evolvement of molecular nanomagnets in China." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 371, no. 2000 (2013): 20120316. http://dx.doi.org/10.1098/rsta.2012.0316.

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Molecular nanomagnets have been undergoing development for 20 years since the first single-molecule magnet (SMM), Mn 12 Ac, was characterized as the molecule-behaved magnet. The multi-disciplinary scientists promoted the magnetic characteristics to be more suitable for use in information science and spintronics. The concept of molecular nanomagnets has also evolved to include single-chain magnets (SCMs), single-ion magnets (SIMs) and even magnetic molecules that showed only slow magnetic relaxation, in addition to the initial cluster-type SMMs. In this review, several aspects, including SMMs,

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2

Bałanda, Maria, and Magdalena Fitta. "Molecular Magnets." Crystals 9, no. 3 (2019): 132. http://dx.doi.org/10.3390/cryst9030132.

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Molecular magnetism is an interdisciplinary research area, which deals with design, synthesis and physical characterization as well as the theoretical modeling of molecular materials showing acquired properties [...]

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3

Blundell, Stephen J. "Molecular magnets." Contemporary Physics 48, no. 5 (2007): 275–90. http://dx.doi.org/10.1080/00107510801967415.

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4

Laget, V., C. Hornick, P. Rabu, M. Drillon, and R. Ziessel. "Molecular magnets." Coordination Chemistry Reviews 178-180 (December 1998): 1533–53. http://dx.doi.org/10.1016/s0010-8545(98)00166-0.

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5

Luneau, Dominique. "Molecular magnets." Current Opinion in Solid State and Materials Science 5, no. 2-3 (2001): 123–29. http://dx.doi.org/10.1016/s1359-0286(00)00043-7.

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6

SATO, Osamu. "Switchable molecular magnets." Proceedings of the Japan Academy, Series B 88, no. 6 (2012): 213–25. http://dx.doi.org/10.2183/pjab.88.213.

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7

Goswami, Soumyabrata, Amit Kumar Mondal, and Sanjit Konar. "Nanoscopic molecular magnets." Inorganic Chemistry Frontiers 2, no. 8 (2015): 687–712. http://dx.doi.org/10.1039/c5qi00059a.

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8

Inglis, Ross, Constantinos J. Milios, Leigh F. Jones, Stergios Piligkos, and Euan K. Brechin. "Twisted molecular magnets." Chem. Commun. 48, no. 2 (2012): 181–90. http://dx.doi.org/10.1039/c1cc13558a.

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9

Davidson, Ernest R., and Aurora E. Clark. "Model Molecular Magnets." Journal of Physical Chemistry A 106, no. 32 (2002): 7456–61. http://dx.doi.org/10.1021/jp026123i.

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10

Epstein, Arthur J., and Joel S. Miller. "Molecular/Polymeric Magnets." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 228, no. 1 (1993): 99–130. http://dx.doi.org/10.1080/10587259308032150.

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11

Linert, Wolfgang, and Michel Verdaguer. "Editorial: Molecular Magnets." Monatshefte f�r Chemie / Chemical Monthly 134, no. 2 (2003): 111–12. http://dx.doi.org/10.1007/s007060300000.

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12

Park, Joonho, Heok Yang, K. S. Park, and Eok-Kyun Lee. "Spin-Polarized Current of a Transistor in Single Mn12 Molecular Magnets." Journal of Nanoscience and Nanotechnology 7, no. 11 (2007): 4111–15. http://dx.doi.org/10.1166/jnn.2007.030.

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Focusing on the framework of how to realize the molecular spintronics in a single molecular magnet, we present theoretical studies on the spin-polarized quantum transport behavior through a single Mn12 molecular magnet. Our theoretical results were obtained by carrying out density functional theoretical calculation within the Keldysh nonequilibrium Green function formalism. The ultimate goal of the molecular spintronics is to develop single molecule transistors which generate spin-polarized currents through the molecular magnet. We obtained the densityof states, the transmission coefficients a

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13

Park, Joonho, Heok Yang, K. S. Park, and Eok-Kyun Lee. "Spin-Polarized Current of a Transistor in Single Mn12 Molecular Magnets." Journal of Nanoscience and Nanotechnology 7, no. 11 (2007): 4111–15. http://dx.doi.org/10.1166/jnn.2007.18087.

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Focusing on the framework of how to realize the molecular spintronics in a single molecular magnet, we present theoretical studies on the spin-polarized quantum transport behavior through a single Mn12 molecular magnet. Our theoretical results were obtained by carrying out density functional theoretical calculation within the Keldysh nonequilibrium Green function formalism. The ultimate goal of the molecular spintronics is to develop single molecule transistors which generate spin-polarized currents through the molecular magnet. We obtained the densityof states, the transmission coefficients a

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14

Yang, Mei, Fusan Chen, Xianjing Sun, Zhuo Zhang, Wen Kang, and Yingshun Zhu. "Development of the CEPC collider prototype magnets." International Journal of Modern Physics A 36, no. 22 (2021): 2142009. http://dx.doi.org/10.1142/s0217751x21420094.

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A Circular Electron Positron Collider (CEPC) with a circumference of about 100 km and a beam energy up to 120 GeV is proposed to be constructed in China. Over 80% of the collider ring is covered by conventional magnets. Most dipole and quadrupole magnets are twin aperture magnets with an inter-beam separation of 350 mm. Two 1-meter-long twin aperture prototype magnets are designed and manufactured. One is a combined dipole–sextupole magnet with aluminum bus bar coils, and the other one is a twin aperture quadrupole magnet with a DT4 compensation sheet to reduce the crosstalk effect between the

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15

Ren, Shenqiang. "(Invited) Switching Molecular Ionic Magnetism." ECS Meeting Abstracts MA2022-02, no. 59 (2022): 2211. http://dx.doi.org/10.1149/ma2022-02592211mtgabs.

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Magneto-ionics of molecular based magnets, the ionic control of magnetism, promise ultralow-power sensor technologies, while the extent of reversible ion intercalation in turn is also the key state-of-charge feature in rechargeable battery electrodes. Here we report the reversible ion intercalation in molecular magnetic electrode, which simultaneously monitors the state of charge in battery and enables dynamic switching of its room-temperature magnetic transition. Microwave excited spin wave reveals lithiation degree in molecular-magnetic anode, enabling magneto-ionics towards the real-time mo

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16

Blundell, S. J., and F. L. Pratt. "Organic and molecular magnets." Journal of Physics: Condensed Matter 16, no. 24 (2004): R771—R828. http://dx.doi.org/10.1088/0953-8984/16/24/r03.

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17

Day, P. "Molecular magnets: the prehistory." Notes and Records of the Royal Society of London 56, no. 1 (2002): 95–103. http://dx.doi.org/10.1098/rsnr.2002.0170.

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The circumstances leading to the present worldwide explosion of interest in molecule–based magnetic materials are summarized. Interactions between developments in inorganic coordination and solid–state chemistry with developments in condensed–matter physics are identified as key factors in the emergence of this new field.

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18

BUSHBY, R. J., and J. L. PAILLAUD. "ChemInform Abstract: Molecular Magnets." ChemInform 27, no. 15 (2010): no. http://dx.doi.org/10.1002/chin.199615327.

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19

Misiorny, Maciej, and Józef Barnaś. "Switching of molecular magnets." physica status solidi (b) 246, no. 4 (2009): 695–715. http://dx.doi.org/10.1002/pssb.200844442.

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20

Yakhmi, J. V. "Design of molecular magnets." Macromolecular Symposia 212, no. 1 (2004): 141–58. http://dx.doi.org/10.1002/masy.200450814.

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21

HU, DONG-SHENG, and SHI-JIE XIONG. "SPIN DYNAMICS OF MOLECULAR MAGNET INTERACTING WITH INJECTED ELECTRONS." International Journal of Modern Physics B 17, no. 07 (2003): 1117–25. http://dx.doi.org/10.1142/s0217979203015930.

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We investigate the time evolution of the local spin in a molecular magnet interacting with injected electrons. By solving the time-dependent Schrödinger equations, we find that the variation in the magnetization of the molecular magnet and the electron spin crucially depends on the strength of the exchange interaction. We calculate the time evolution of the entanglement between the injected electron and the molecular magnet. It is found that the entanglement oscillates in time and the oscillations are closely related to the changes in the spins. The study provides an estimation of the feasibil

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22

Florez, J. M., Álvaro S. Núñez, C. García, and P. Vargas. "Magnetocaloric features of complex molecular magnets: The (Cr7Ni)2Cu molecular magnet and beyond." Journal of Magnetism and Magnetic Materials 322, no. 19 (2010): 2810–18. http://dx.doi.org/10.1016/j.jmmm.2010.04.035.

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23

Veciana, Jaume, and Hiizu Iwamura. "Organic Magnets." MRS Bulletin 25, no. 11 (2000): 41–51. http://dx.doi.org/10.1557/mrs2000.223.

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The notion of organic molecular materials showing metallic properties, such as electric conductivity or ferromagnetism, started several decades ago as a mere dream of some members of the chemical community. The goal was to create an assembly of organic molecules or macromolecules containing only light elements (C, H, N, O, S, etc.) and yet possessing the electron/hole mobility or spin alignment that is inherent in typical metals or their oxides and different from the isolated molecular materials. Organic molecular conductors initially were developed during the 1960s, but the first examples of

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24

Blachowicz, Tomasz, and Andrea Ehrmann. "New Materials and Effects in Molecular Nanomagnets." Applied Sciences 11, no. 16 (2021): 7510. http://dx.doi.org/10.3390/app11167510.

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Molecular magnets are a relatively new class of purely organic or metallo-organic materials, showing magnetism even without an external magnetic field. This interdisciplinary field between chemistry and physics has been gaining increased interest since the 1990s. While bulk molecular magnets are usually hard to build because of their molecular structures, low-dimensional molecular magnets are often easier to construct, down to dot-like (zero-dimensional) structures, which are investigated by different scanning probe technologies. On these scales, new effects such as superparamagnetic behavior

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25

Laskowski, Lukasz, Iwan Kityk, Piotr Konieczny, Oleksandr Pastukh, Mateusz Schabikowski, and Magdalena Laskowska. "The Separation of the Mn12 Single-Molecule Magnets onto Spherical Silica Nanoparticles." Nanomaterials 9, no. 5 (2019): 764. http://dx.doi.org/10.3390/nano9050764.

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The Mn12 single-molecule magnets (SMMs) could be attached to the surface of spherical silica for the first time with a high probability. This allowed separation of the individual molecular magnets and direct microscopic observation of the SMMs. We described in detail how to fabricate such a composite material. The synthesis procedure proposed here is simple and efficient. We confirmed the efficiency of the method by transmission electron microscopy (TEM): single-molecule magnets were visible at the surface of a silica substrate. Based on TEM observation, we described how the molecules anchor t

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26

Pilawa, Bernd. "New concepts for molecular magnets." Annalen der Physik 511, no. 3 (1999): 191–254. http://dx.doi.org/10.1002/andp.19995110302.

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27

Leuenberger, Michael N., and Daniel Loss. "Quantum computing in molecular magnets." Nature 410, no. 6830 (2001): 789–93. http://dx.doi.org/10.1038/35071024.

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28

Enoki, T., T. Umeyama, M. Enomoto, et al. "Novel TTF-based molecular magnets." Synthetic Metals 103, no. 1-3 (1999): 2275–78. http://dx.doi.org/10.1016/s0379-6779(98)00238-0.

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29

Fleck, Michel. "Molecular magnets wired on gold." Materials Today 12, no. 4 (2009): 12. http://dx.doi.org/10.1016/s1369-7021(09)70105-1.

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30

Chudnovsky, Eugene M. "Quantum Hysteresis in Molecular Magnets." Science 274, no. 5289 (1996): 938–39. http://dx.doi.org/10.1126/science.274.5289.938.

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31

Hoshino, Norihisa, Ayuk M. Ako, Annie K. Powell, and Hiroki Oshio. "Molecular Magnets Containing Wheel Motifs." Inorganic Chemistry 48, no. 8 (2009): 3396–407. http://dx.doi.org/10.1021/ic801776w.

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32

Enoki, T., H. Yamazaki, K. Okabe, et al. "Unconventional TTF-based molecular magnets." Synthetic Metals 133-134 (March 2003): 501–3. http://dx.doi.org/10.1016/s0379-6779(02)00436-8.

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33

Yukalov, V. I., and E. P. Yukalova. "Coherent radiation by molecular magnets." Europhysics Letters (EPL) 70, no. 3 (2005): 306–12. http://dx.doi.org/10.1209/epl/i2004-10496-6.

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34

Miller, Joel S. "Molecular-based magnets: an epilogue." Philosophical Transactions of the Royal Society of London. Series A: Mathematical, Physical and Engineering Sciences 357, no. 1762 (1999): 3159–61. http://dx.doi.org/10.1098/rsta.1999.0486.

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35

Stepanenko, Dimitrije, Mircea Trif, and Daniel Loss. "Quantum computing with molecular magnets." Inorganica Chimica Acta 361, no. 14-15 (2008): 3740–45. http://dx.doi.org/10.1016/j.ica.2008.02.066.

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36

Inglis, Ross, Constantinos J. Milios, Leigh F. Jones, Stergios Piligkos, and Euan K. Brechin. "ChemInform Abstract: Twisted Molecular Magnets." ChemInform 43, no. 15 (2012): no. http://dx.doi.org/10.1002/chin.201215271.

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37

IBERS, JAMES A. "Porphyrinic molecular conductors and magnets." Journal of Porphyrins and Phthalocyanines 04, no. 04 (2000): 425. http://dx.doi.org/10.1002/(sici)1099-1409(200006/07)4:4<425::aid-jpp229>3.0.co;2-3.

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38

Ibers, James A. "Porphyrinic molecular conductors and magnets." Journal of Porphyrins and Phthalocyanines 4, no. 4 (2000): 425. http://dx.doi.org/10.1002/(sici)1099-1409(200006/07)4:4<425::aid-jpp229>3.3.co;2-v.

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39

Pilawa, Bernd. "New concepts for molecular magnets." Annalen der Physik 8, no. 3 (1999): 191–254. http://dx.doi.org/10.1002/(sici)1521-3889(199903)8:3<191::aid-andp191>3.0.co;2-d.

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40

Wang, Zhongxuan, Yulong Huang, Weiyi Gong, Qimin Yan, and Shenqiang Ren. "Lithiation bridged molecular conducting magnets." Applied Materials Today 38 (June 2024): 102188. http://dx.doi.org/10.1016/j.apmt.2024.102188.

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41

Brumfield, Amelia, and Jason Haraldsen. "Thermodynamics and Magnetic Excitations in Quantum Spin Trimers: Applications for the Understanding of Molecular Magnets." Crystals 9, no. 2 (2019): 93. http://dx.doi.org/10.3390/cryst9020093.

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Molecular magnets provide a playground of interesting phenomena and interactions that have direct applications for quantum computation and magnetic systems. A general understanding of the underlying geometries for molecular magnets therefore generates a consistent foundation for which further analysis and understanding can be established. Using a Heisenberg spin-spin exchange Hamiltonian, we investigate the evolution of magnetic excitations and thermodynamics of quantum spin isosceles trimers (two sides J and one side α J ) with increasing spin. For the thermodynamics, we produce exact general

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42

Phan, Tra Nguyen, Jesus Javier Aranda, Bengt Oelmann, and Sebastian Bader. "Design Optimization and Comparison of Cylindrical Electromagnetic Vibration Energy Harvesters." Sensors 21, no. 23 (2021): 7985. http://dx.doi.org/10.3390/s21237985.

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Investigating the coil–magnet structure plays a significant role in the design process of the electromagnetic energy harvester due to the effect on the harvester’s performance. In this paper, the performance of four different electromagnetic vibration energy harvesters with cylindrical shapes constrained in the same volume were under investigation. The utilized structures are (i) two opposite polarized magnets spaced by a mild steel; (ii) a Halbach array with three magnets and one coil; (iii) a Halbach array with five magnets and one coil; and (iv) a Halbach array with five magnets and three c

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43

Sirenko, Valentyna, Fernando Bartolomé Usieto, and Juan Bartolomé. "The paradigm of magnetic molecule in quantum matter: Slow molecular spin relaxation." Low Temperature Physics 50, no. 6 (2024): 431–45. http://dx.doi.org/10.1063/10.0026056.

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The quantum nature of single-ion magnets, single-molecule magnets, and single-chain magnets has been manifested among other phenomena by magnetic hysteresis due to slow spin relaxation, competing with fast quantum tunneling at low temperatures. Slow spin relaxation, described by Arrhenius-type law with the effective barrier energies Ueff = 50 cm–1, was discovered 3 decades ago in paramagnetic Mn12-acetate complex of oxy-bridged mixed-valence manganese ions, below the blocking temperature TB = 3 K. In contrast to common magnetic materials, it is governed primarily by magnetic anisotropy, set by

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44

Wilkinson, J. M., F. Lang, P. J. Baker, S. P. Cottrell, and S. J. Blundell. "Identifying muon sites “by eye” in KPF₆ and KBF₄." Journal of Physics: Conference Series 2462, no. 1 (2023): 012007. http://dx.doi.org/10.1088/1742-6596/2462/1/012007.

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Abstract Molecular magnets are one of the key research themes of µSR, but locating the muon stopping site in these compounds using density functional theory is often very challenging as their unit cells tend to contain a very large number of atoms. Nevertheless, many molecular magnets contain the [PF6]− and [BF4]− molecular ions, which, due to their fluorine nuclei, produce a distinctive µSR spectrum, which can give information about the muon stopping site. This paper details the calculation of the muon sites in the much simpler materials KPF6 and KBF4, providing insights which can be applied

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45

Moreno-Pineda, Eufemio, and Wolfgang Wernsdorfer. "Measuring molecular magnets for quantum technologies." Nature Reviews Physics 3, no. 9 (2021): 645–59. http://dx.doi.org/10.1038/s42254-021-00340-3.

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46

Wynn, C. M., A. S. Albrecht, C. P. Landee, C. Navas, and M. M. Turnbull. "Properties of Molecular-Based Frustrated Magnets." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 274, no. 1 (1995): 1–10. http://dx.doi.org/10.1080/10587259508031859.

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47

Casellas, H., D. de Caro, L. Valade, and L. Ariès. "Molecular magnets and conductors on surfaces." Le Journal de Physique IV 11, PR3 (2001): Pr3–271—Pr3–277. http://dx.doi.org/10.1051/jp4:2001334.

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48

Miyazaki, Akira, K. Okabe, K. Enomoto та ін. "π–d Interaction-based molecular magnets". Polyhedron 22, № 14-17 (2003): 2227–34. http://dx.doi.org/10.1016/s0277-5387(03)00178-5.

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49

Barbara, B., L. Thomas, F. Lionti, I. Chiorescu, and A. Sulpice. "Macroscopic quantum tunneling in molecular magnets." Journal of Magnetism and Magnetic Materials 200, no. 1-3 (1999): 167–81. http://dx.doi.org/10.1016/s0304-8853(99)00409-6.

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50

Miller, Joel S., and Arthur J. Epstein. "New higher-Tc molecular based magnets." Synthetic Metals 56, no. 2-3 (1993): 3291–98. http://dx.doi.org/10.1016/0379-6779(93)90117-f.

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