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排序方式: 共有436条查询结果,搜索用时 15 毫秒
71.
Feng PL Beedle CC Koo C Wernsdorfer W Nakano M Hill S Hendrickson DN 《Inorganic chemistry》2008,47(8):3188-3204
A family of distorted heterometallic cubanes, [Mn (III) 3Ni (II)(hmp) 3O(N 3) 3(O 2CR) 3], where O 2CR (-) is benzoate ( 1), 3-phenylpropionate ( 2), 1-adamantanecarboxylate ( 3), or acetate ( 4) and hmp (-) is the anion of 2-pyridinemethanol, was synthesized and structurally as well as magnetically characterized. These complexes have a distorted-cubane core structure similar to that found in the S = 9/2 Mn 4 cubane family of complexes. Complexes 1, 3, and 4 crystallize in rhombohedral, hexagonal, and cubic space groups, respectively, and have C 3 molecular symmetry, while complex 2 crystallizes in the monoclinic space group Cc with local C 1 symmetry. Magnetic susceptibility and magnetization hysteresis measurements and high-frequency electron paramagnetic resonance (HFEPR) spectroscopy established that complexes 1-4 have S = 5 spin ground states with axial zero-field splitting (ZFS) parameters ( D) ranging from -0.20 to -0.33 cm (-1). Magnetization versus direct-current field sweeps below 1.1 K revealed hysteresis loops with magnetization relaxation, definitely indicating that complexes 1-4 are single-molecule magnets that exhibit quantum tunneling of magnetization (QTM) through an anisotropy barrier. Complex 2 exhibits the smallest coercive field and fastest magnetization tunneling rate, suggesting a significant rhombic ZFS parameter ( E), as expected from the low C 1 symmetry. This was confirmed by HFEPR spectroscopy studies on single crystals that gave the following parameter values for complex 2: gz = 1.98, gx = gy = 1.95, D = -0.17 cm (-1), B 4 (0) = -6.68 x 10 (-5) cm (-1), E = 6.68 x 10 (-3) cm (-1), and B 4 (2) = -1.00 x 10 (-4) cm (-1). Single-crystal HFEPR data for complex 1 gave g z = 2.02, gx = gy = 1.95, D = -0.23 cm (-1), and B 4 (0) = -5.68 x 10 (-5) cm (-1), in keeping with the C 3 site symmetry of this Mn 3Ni complex. The combined results highlight the importance of spin-parity effects and molecular symmetry, which determine the QTM rates. 相似文献
72.
Prof. Dr. Mingoo Jin Satsuki Matsuura Hikaru Yamamoto Prof. Dr. Motohiro Mizuno Prof. Dr. Hajime Ito 《European journal of organic chemistry》2023,26(12):e202201468
We report multidynamic molecular rotations in crystals using a concave-shape N-heterocyclic carbene (NHC) binuclear Au(I) complex rotor bearing pyrazine and tetrahydrofuran (THF) molecules as multicomponent rotators. Single-crystal X-ray diffraction (XRD) measurements revealed that two THF molecules are located near the central pyrazine encapsulated by two bulky NHC ligands. From 2H solid-state NMR analysis, it was observed that the pyrazine rotated in a 2-fold site exchange with a 180° rotational angle and a 31 kJ mol−1 energy barrier, while the THF molecules showed a 23°-38° libration with a lower energy barrier (14 kJ mol−1). Interestingly, the pyrazine rotation was accelerated when the THF molecules rotated in fast site exchange with a large angle of libration, suggesting that the rotators exhibit multidynamics in a correlated manner. 相似文献
73.
Unraveling Inter‐ and Intrachain Electronics in Polythiophene Assemblies Mediated by Coordination Nanospaces 下载免费PDF全文
Michael W. A. MacLean Takashi Kitao Dr. Takeo Suga Prof. Dr. Motohiro Mizuno Prof. Dr. Shu Seki Dr. Takashi Uemura Prof. Susumu Kitagawa 《Angewandte Chemie (International ed. in English)》2016,55(2):708-713
Strong interchain interactions render unsubstituted polythiophene un‐fusible, non‐melting, and insoluble. Therefore, control of the packing structure, which has a profound effect on the optical and electronic properties of the polymer, has never been achieved. Unsubstituted polythiophene was prepared in the one‐dimensional channels of [La(1,3,5‐benzenetrisbenzoate)]n, where polymer chains form unprecedented assembly structures mediated by the host framework. It is noteworthy that the emission and carrier transport properties were drastically changed by varying the number of chains within a particular assembly. The response of the composite to additional guests is also examined as a method to use the composites as low‐concentration sensors. Our findings show that the encapsulation of polymer chains in host materials is a facile method for understanding the intrinsic properties of conjugated polymers, along with controlling and enhancing their functions. 相似文献
74.
Ken-ichi Kasuya Nariaki Ishii Koji Yazawa Taro Yotsumoto Daisuke Nagai 《Polymer Degradation and Stability》2009,94(8):1190-1196
We isolated 5 mesophilic microorganisms that form clear zones around the colony on an opaque medium containing the aliphatic-aromatic copolyester poly(60 mol% butylene adipate-co-40 mol% butylene terephthalate) (PBAT). Among all strains, the fungal strain NKCM1712 degraded PBAT at the fastest rate (3.5 ± 0.3 μg cm−2 h−1). Genetic and morphological analyses revealed that this strain was closely related to Isaria fumosorosea (phylum Ascomycota). Mass spectroscopic analysis revealed that the degradation products were T, AB, TB, BAB, and ABT (T, terephthalic acid unit; A, adipic acid unit; B, 1,4-butanediol unit)] in the culture of the strain that used PBAT as the sole carbon source. Furthermore, the PBAT degradation ability of this strain in terms of BOD suggested that it could utilize the PBAT degradation products as growth substrates. This is the first report of a mesophilic strain that can mineralize an aliphatic-aromatic polyester into carbon dioxide on its own. 相似文献
75.
Tatsuo Taniguchi Masakatsu Kasuya Yusuke Kunisada Tomohiro Miyai Hiroshi Nagasawa Takayuki Nakahira 《Colloids and surfaces. B, Biointerfaces》2009,71(2):194-199
Grafting of a styrene derivative bearing a lactose residue, i.e., N-2-4-(vinylbenzenesulfonamido)ethyl lactobionamide (VBSAELA), onto polymer latex particles was carried out in aqueous media by activator generated electron transfer atom transfer radical polymerization (AGET ATRP). The core polymer latex particles having α-chloroester groups as ATRP-initiating groups were prepared by miniemulsion polymerization of styrene and 2-chloropropionyloxyethyl methacrylate (CPEM) in the presence of a polymerizable surfactant, i.e., N,N-dimethyl-N-dodecyl-N-2-methacryloyloxyethylammonium bromide (C12Br). AGET ATRP was initiated with tris[(2-pyridylmethyl)amine] copper (II) dichloride and l-ascorbic acid. Dynamic light scattering (DLS) revealed that the P(St-CPEM)-g-P(VBSAELA) particles possess graft layers of 10 nm in thickness on the core particles of 91 nm in diameter. Critical coagulation concentration measurement revealed that the dispersion stability of the particles in water increased due to hydrated P(VBSAELA) shell layers. Adsorption of bovine serum albumin (BSA) onto the particles was considerably suppressed by the hydrated shell layers. 相似文献
76.
First-principles fully relaxed tensile and shear test simulations were performed on Σ10(1124)/[1100] tilt Mg grain boundary (GB) models, with and without H segregation, to investigate mechanisms of H embrittlement of Mg. Strengthening as a result of covalent-like characteristics of Mg-H bonds prevailed over weakening of Mg-Mg bonds resulting from charge transfer; as a result, an H atom strengthened the GB. In addition, because the strong Mg-H bonds suppressed macroscopic GB fracture, elongation to failure was not reduced by H segregation. However, the resistance to GB shearing was increased by H segregation. It is therefore suggested that H segregation enhances crack growth at the GB, because dislocation emission from the crack tip is suppressed, resulting in H embrittlement of Mg. 相似文献
77.
Suzuki M Kawamura N Miyagawa H Garitaonandia JS Yamamoto Y Hori H 《Physical review letters》2012,108(4):047201
We show that bulk gold (Au) exhibits temperature-independent paramagnetism in an external magnetic field by x-ray magnetic circular dichroism spectroscopy at the Au L(2) and L(3) edges. Using the sum-rule analysis, we obtained a magnetic moment of 1.3 × 10(-4) μB/atom in an external magnetic field of 10 T and a paramagnetic susceptibility of 8.9 × 10(-6) for the 5d orbit. The induced paramagnetism in bulk Au is characterized by a large (≈ 30%) orbital contribution. This orbital component was retained even when Au atoms formed nanoparticles, playing an important role in stabilizing the spontaneous spin polarization in the Au nanoparticles. 相似文献
78.
The local structure of phosphorus and silicon in the molten CaO–SiO2–PO2.5 slag system was investigated by magic angle spinning nuclear magnetic resonance (MAS-NMR). The 31P MAS-NMR spectra revealed that phosphorus was present primarily as the monophosphate complex ion PO43?, with a small amount of diphosphate ion also present. Their relative ratio to total phosphorus was independent of the phosphate concentration of the sample. In the case of the 29Si MAS-NMR, the mean number of the non-bridging oxygen atoms associated with tetrahedrally coordinated silicon decreased as the phosphate concentration increased at a fixed CaO/SiO2 ratio. This indicates that the nonbridging oxygen atoms around the silicon were replaced by bridging oxygen atoms around the phosphorus as the phosphate concentration in the samples increased.To elucidate the basicity dependence of the structure of slag, the relationship between the structure and optical basicity was also investigated. The relative ratio of Qn (Qn means the silicon atoms tetrahedrally bonded with “n” number of bridging oxygen atoms) strongly depends on the optical basicity. These optical basicity dependencies of the structures of phosphorus and silicon can be explained clearly by the basicity equalization concept (Duffy and Ingram, 1976) [12]. 相似文献
79.
F. Kokai K. Takahashi D. Kasuya M. Yudasaka S. Iijima 《Applied Physics A: Materials Science & Processing》2001,73(4):401-407
Single-wall carbon nanotubes (SWNTs) were synthesized by the irradiation of 20-ms CO2 laser pulses onto a graphite–Co/Ni target at room temperature. We investigated the effect of laser power density (10–150 kW/cm2) and ambient Ar gas pressure (150–760 Torr) on the abundance of SWNTs with lengths of up to about 200 nm in soot-like carbonaceous
deposits. For a constant power density (30 kW/cm2), depending on the Ar gas pressure, SWNTs with diameters of 1.2–1.4 nm were synthesized. Expansion behavior and temperature-fall
rates of clusters and/or particles in laser plumes were also analyzed by high-speed video imaging and temporally and spatially
resolved emission spectroscopy. The temperature-fall rates were estimated to be 171–427 K/ms. The SWNT growth on the time
scale of a few milliseconds appeared to be related to some features of condensing clusters and/or particles, including resident
densities, collision frequencies and temperatures.
Received: 16 July 2001 / Accepted: 23 July 2001 / Published online: 30 August 2001 相似文献
80.
Dr. Kuirun Zhang Dr. Soonchul Kang Dr. Zi‐shuo Yao Kazusa Nakamura Dr. Takashi Yamamoto Prof. Dr. Yasuaki Einaga Nobuaki Azuma Dr. Yuji Miyazaki Prof. Dr. Motohiro Nakano Dr. Shinji Kanegawa Prof. Dr. Osamu Sato 《Angewandte Chemie (International ed. in English)》2016,55(20):6047-6050
Heterometallic Prussian blue analogues are known to exhibit thermally induced charge transfer, resulting in switching of optical and magnetic properties. However, charge‐transfer phase transitions have not been reported for the simplest FeFe cyanide‐bridged systems. A mixed‐valence FeII/FeIII cyanide‐bridged coordination polymer, {[Fe(Tp)(CN)3]2Fe(bpe)?5 H2O}n, which demonstrates a thermally induced charge‐transfer phase transition, is described. As a result of the charge transfer during this phase transition, the high‐spin state of the whole system does not change to a low‐spin state. This result is in contrast to FeCo cyanide‐bridged systems that exhibit charge‐transfer‐induced spin transitions. 相似文献