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- ItemHigh Blocking Temperature of Magnetization and Giant Coercivity in the Azafullerene Tb 2 @C 79 N with a Single-Electron Terbium–Terbium Bond(Weinheim : Wiley-VCH, 2019) Velkos, Georgios; Krylov, Denis S.; Kirkpatrick, Kyle; Spree, Lukas; Dubrovin, Vasilii; Büchner, Bernd; Avdoshenko, Stanislav M.; Bezmelnitsyn, Valeriy; Davis, Sean; Faust, Paul; Duchamp, James; Dorn, Harry C.; Popov, Alexey A.The azafullerene Tb 2 @C 79 N is found to be a single-molecule magnet with a high 100-s blocking temperature of magnetization of 24 K and large coercivity. Tb magnetic moments with an easy-axis single-ion magnetic anisotropy are strongly coupled by the unpaired spin of the single-electron Tb−Tb bond. Relaxation of magnetization in Tb 2 @C 79 N below 15 K proceeds via quantum tunneling of magnetization with the characteristic time τ QTM =16 462±1230 s. At higher temperature, relaxation follows the Orbach mechanism with a barrier of 757±4 K, corresponding to the excited states, in which one of the Tb spins is flipped. © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
- ItemRobust Single Molecule Magnet Monolayers on Graphene and Graphite with Magnetic Hysteresis up to 28 K(Weinheim : Wiley-VCH, 2021) Spree, Lukas; Liu, Fupin; Neu, Volker; Rosenkranz, Marco; Velkos, Georgios; Wang, Yaofeng; Schiemenz, Sandra; Dreiser, Jan; Gargiani, Pierluigi; Valvidares, Manuel; Chen, Chia-Hsiang; Büchner, Bernd; Avdoshenko, Stanislav M.; Popov, Alexey A.The chemical functionalization of fullerene single molecule magnet Tb2@C80(CH2Ph) enables the facile preparation of robust monolayers on graphene and highly oriented pyrolytic graphite from solution without impairing their magnetic properties. Monolayers of endohedral fullerene functionalized with pyrene exhibit magnetic bistability up to a temperature of 28 K. The use of pyrene terminated linker molecules opens the way to devise integration of spin carrying units encapsulated by fullerene cages on graphitic substrates, be it single-molecule magnets or qubit candidates. © 2021 The Authors. Advanced Functional Materials published by Wiley-VCH GmbH
- ItemSubstrate-Independent Magnetic Bistability in Monolayers of the Single-Molecule Magnet Dy2ScN@C80 on Metals and Insulators(Weinheim : Wiley-VCH, 2020) Krylov, Denis S.; Schimmel, Sebastian; Dubrovin, Vasilii; Liu, Fupin; Nguyen, T.T. Nhung; Spree, Lukas; Chen, Chia-Hsiang; Velkos, Georgios; Bulbucan, Claudiu; Westerström, Rasmus; Studniarek, Michał; Dreiser, Jan; Hess, Christian; Büchner, Bernd; Avdoshenko, Stanislav M.; Popov, Alexey A.Magnetic hysteresis is demonstrated for monolayers of the single-molecule magnet (SMM) Dy2ScN@C80 deposited on Au(111), Ag(100), and MgO|Ag(100) surfaces by vacuum sublimation. The topography and electronic structure of Dy2ScN@C80 adsorbed on Au(111) were studied by STM. X-ray magnetic CD studies show that the Dy2ScN@C80 monolayers exhibit similarly broad magnetic hysteresis independent on the substrate used, but the orientation of the Dy2ScN cluster depends strongly on the surface. DFT calculations show that the extent of the electronic interaction of the fullerene molecules with the surface is increasing dramatically from MgO to Au(111) and Ag(100). However, the charge redistribution at the fullerene-surface interface is fully absorbed by the carbon cage, leaving the state of the endohedral cluster intact. This Faraday cage effect of the fullerene preserves the magnetic bistability of fullerene-SMMs on conducting substrates and facilitates their application in molecular spintronics. © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
- ItemOn the Electrochemical Reduction of 4-(Thiazol-2-ylazo)-Substituted 1-Chloronaphthalenes: Formation and Characterization of Stable Radical Anions(Weinheim : Wiley-VCH, 2020) Dmitrieva, Evgenia; Popov, Alexey A.; Yu, Xiuling; Hartmann, HorstThe electrochemical reduction of two chloro-substituted 4-(thiazol-2-ylazo)has been studied by means of spectroelectrochemistry and simulated with the DFT method. Whereas the 1-chloro-4-(4-chlorothiazol-2-ylazo)forms both a stable radical anion and a dianion, the dianion of 1-chloro-4-(thiazol-2-ylazo)is instable. In the radical anion of both compounds, the spin densities are high not only at the azo moiety but also at C3 in the naphthalene and at C5 in the thiazole moiety. This is in agreement with former experimental results demonstrating the remarkable reactivity of these positions towards thiols which can act as nucleophiles as well as electron donors. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
- ItemSingle-Molecule Magnets DyM2N@C80 and Dy2MN@C80 (M=Sc, Lu): The Impact of Diamagnetic Metals on Dy3+ Magnetic Anisotropy, Dy⋅⋅⋅Dy Coupling, and Mixing of Molecular and Lattice Vibrations(Weinheim : Wiley-VCH, 2020) Spree, Lukas; Schlesier, Christin; Kostanyan, Aram; Westerström, Rasmus; Greber, Thomas; Büchner, Bernd; Avdoshenko, Stanislav M.; Popov, Alexey A.The substitution of scandium in fullerene single-molecule magnets (SMMs) DySc2N@C80 and Dy2ScN@C80 by lutetium has been studied to explore the influence of the diamagnetic metal on the SMM performance of dysprosium nitride clusterfullerenes. The use of lutetium led to an improved SMM performance of DyLu2N@C80, which shows a higher blocking temperature of magnetization (TB=9.5 K), longer relaxation times, and broader hysteresis than DySc2N@C80 (TB=6.9 K). At the same time, Dy2LuN@C80 was found to have a similar blocking temperature of magnetization to Dy2ScN@C80 (TB=8 K), but substantially different interactions between the magnetic moments of the dysprosium ions in the Dy2MN clusters. Surprisingly, although the intramolecular dipolar interactions in Dy2LuN@C80 and Dy2ScN@C80 are of similar strength, the exchange interactions in Dy2LuN@C80 are close to zero. Analysis of the low-frequency molecular and lattice vibrations showed strong mixing of the lattice modes and endohedral cluster librations in k-space. This mixing simplifies the spin–lattice relaxation by conserving the momentum during the spin flip and helping to distribute the moment and energy further into the lattice. © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
- ItemPAH/PAH(CF3)n Donor/Acceptor Charge-Transfer Complexes in Solution and in Solid-State Co-Crystals(Weinheim : Wiley-VCH, 2019) Castro, Karlee P.; Bukovsky, Eric V.; Kuvychko, Igor V.; DeWeerd, Nicholas J.; Chen, Yu-Sheng; Deng, Shihu H.M.; Wang, Xue-Bin; Popov, Alexey A.; Strauss, Steven H.; Boltalina, Olga V.A solution, solid-state, and computational study is reported of polycyclic aromatic hydrocarbon PAH/PAH(CF3)n donor/acceptor (D/A) charge-transfer complexes that involve six PAH(CF3)n acceptors with known gas-phase electron affinities that range from 2.11(2) to 2.805(15) eV and four PAH donors, including seven CT co-crystal X-ray structures that exhibit hexagonal arrays of mixed π-stacks with 1/1, 1/2, or 2/1 D/A stoichiometries (PAH=anthracene, azulene, coronene, perylene, pyrene, triphenylene; n=5, 6). These are the first D/A CT complexes with PAH(CF3)n acceptors to be studied in detail. The nine D/A combinations were chosen to allow several structural and electronic comparisons to be made, providing new insights about controlling D/A interactions and the structures of CT co-crystals. The comparisons include, among others, CT complexes of the same PAH(CF3)n acceptor with four PAH donors and CT complexes of the same donor with four PAH(CF3)n acceptors. All nine CT complexes exhibit charge-transfer bands in solution with λmax between 467 and 600 nm. A plot of E(λmax) versus [IE(donor)−EA(acceptor)] for the nine CT complexes studied is linear with a slope of 0.72±0.03 eV eV−1. This plot is the first of its kind for CT complexes with structurally related donors and acceptors for which precise experimental gas-phase IEs and EAs are known. It demonstrates that conclusions based on the common assumption that the slope of a CT E(λmax) versus [IE−EA] plot is unity may be incorrect in at least some cases and should be reconsidered. © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
- ItemTailoring Magnetic Features in Zigzag-Edged Nanographenes by Controlled Diels–Alder Reactions(Weinheim : Wiley-VCH, 2020) Ajayakumar, M.R.; Fu, Yubin; Liu, Fupin; Komber, Hartmut; Tkachova, Valeriya; Xu, Chi; Zhou, Shengqiang; Popov, Alexey A.; Liu, Junzhi; Feng, XinliangNanographenes (NGs) with tunable electronic and magnetic properties have attracted enormous attention in the realm of carbon-based nanoelectronics. In particular, NGs with biradical character at the ground state are promising building units for molecular spintronics. However, most of the biradicaloids are susceptible to oxidation under ambient conditions and photolytic degradation, which hamper their further applications. Herein, we demonstrated the feasibility of tuning the magnetic properties of zigzag-edged NGs in order to enhance their stability via the controlled Diels–Alder reactions of peri-tetracene (4-PA). The unstable 4-PA (y0=0.72; half-life, t1/2=3 h) was transformed into the unprecedented benzo-peri-tetracenes (BPTs) by a one-side Diels–Alder reaction, which featured a biradical character at the ground state (y0=0.60) and exhibited remarkable stability under ambient conditions for several months. In addition, the fully zigzag-edged circumanthracenes (CAs) were achieved by two-fold or stepwise Diels–Alder reactions of 4-PA, in which the magnetic properties could be controlled by employing the corresponding dienophiles. Our work reported herein opens avenues for the synthesis of novel zigzag-edged NGs with tailor-made magnetic properties. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
- ItemBetween Aromatic and Quinoid Structure: A Symmetrical UV to Vis/NIR Benzothiadiazole Redox Switch(Weinheim : Wiley-VCH, 2020) Rietsch, Philipp; Sobottka, Sebastian; Hoffmann, Katrin; Popov, Alexey A.; Hildebrandt, Pascal; Sarkar, Biprajit; Resch-Genger, Ute; Eigler, SiegfriedReversibly switching the light absorption of organic molecules by redox processes is of interest for applications in sensors, light harvesting, smart materials, and medical diagnostics. This work presents a symmetrical benzothiadiazole (BTD) derivative with a high fluorescence quantum yield in solution and in the crystalline state and shows by spectroelectrochemical analysis that reversible switching of UV absorption in the neutral state, to broadband Vis/NIR absorption in the 1st oxidized state, to sharp band Vis absorption in the 2nd oxidized state, is possible. For the one-electron oxidized species, formation of a delocalized radical is confirmed by electron paramagnetic resonance spectroelectrochemistry. Furthermore, our results reveal an increasing quinoidal distortion upon the 1st and 2nd oxidation, which can be used as the leitmotif for the development of BTD based redox switches. © 2020 The Authors. Published by Wiley-VCH GmbH
- ItemHierarchical Corannulene‐Based Materials: Energy Transfer and Solid‐State Photophysics(Weinheim : Wiley-VCH, 2017-3-23) Rice, Allison M.; Fellows, W. Brett; Dolgopolova, Ekaterina A.; Greytak, Andrew B.; Vannucci, Aaron K.; Smith, Mark D.; Karakalos, Stavros G.; Krause, Jeanette A.; Avdoshenko, Stanislav M.; Popov, Alexey A.; Shustova, Natalia B.We report the first example of a donor–acceptor corannulene-containing hybrid material with rapid ligand-to-ligand energy transfer (ET). Additionally, we provide the first time-resolved photoluminescence (PL) data for any corannulene-based compounds in the solid state. Comprehensive analysis of PL data in combination with theoretical calculations of donor–acceptor exciton coupling was employed to estimate ET rate and efficiency in the prepared material. The ligand-to-ligand ET rate calculated using two models is comparable with that observed in fullerene-containing materials, which are generally considered for molecular electronics development. Thus, the presented studies not only demonstrate the possibility of merging the intrinsic properties of π-bowls, specifically corannulene derivatives, with the versatility of crystalline hybrid scaffolds, but could also foreshadow the engineering of a novel class of hierarchical corannulene-based hybrid materials for optoelectronic devices.
- ItemThermally Activated Delayed Fluorescence in a Y3N@C80 Endohedral Fullerene: Time-Resolved Luminescence and EPR Studies(Weinheim : Wiley-VCH, 2017-12-8) Zalibera, Michal; Krylov, Denis S.; Karagiannis, Dimitrios; Will, Paul-Anton; Ziegs, Frank; Schiemenz, Sandra; Lubitz, Wolfgang; Reineke, Sebastian; Savitsky, Anton; Popov, Alexey A.The endohedral fullerene Y3N@C80 exhibits luminescence with reasonable quantum yield and extraordinary long lifetime. By variable-temperature steady-state and time-resolved luminescence spectroscopy, it is demonstrated that above 60 K the Y3N@C80 exhibits thermally activated delayed fluorescence with maximum emission at 120 K and a negligible prompt fluorescence. Below 60 K, a phosphorescence with a lifetime of 192±1 ms is observed. Spin distribution and dynamics in the triplet excited state is investigated with X- and W-band EPR and ENDOR spectroscopies and DFT computations. Finally, electroluminescence of the Y3N@C80/PFO film is demonstrated opening the possibility for red-emitting fullerene-based organic light-emitting diodes (OLEDs).