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81.
A series of 1-(trans-4'-n-alkylcyclohexyl)-2-(4”-halobiphenyl-4'-yl)ethanes, which show nematic phases, was prepared. Their transition temperatures, enthalpies and entropies were measured. Their bulk viscosities, birefringences and dielectric constants were determined by extrapolation. 1-(trans-4'-n-propylcyclohexyl)-2-(4”-fluorobiphenyl-4'-yl)ethane has a high clearing of 125° C, a low viscosity of 25 c.p. at 20 °C, a relatively high birefringence of 0.166 at 25 °C, and a positive dielectric anisotropy of 4.9. The transition temperatures, the N-I transition entropies, the bulk viscosities and the birefringences for the 1-(trans-4'-n-alkylcyclohexyl)-2-(4”-fluorobiphenyl-4'-yl)ethanes exhibited odd-even effects in relation to the number of carbon atoms in the alkyl chain. The bulk viscosity as a function of the third power of the van der Waals radius of the halogeno group, the birefringence as a function of the van der Waals radius of the halogeno group, and the dielectric constants as a function of the dipole moment of the halogeno group are discussed for the 1-(trans-4'-n-propylcyclohexyl)-2-(4”-halobiphenyl-4'-yl)ethanes. 相似文献
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Low‐Symmetry Ω‐Shaped Zinc Phthalocyanine Sensitizers with Panchromatic Light‐Harvesting Properties for Dye‐Sensitized Solar Cells 下载免费PDF全文
Satoshi Yamamoto Angel Zhang Prof. Dr. Martin J. Stillman Prof. Dr. Nagao Kobayashi Prof. Dr. Mutsumi Kimura 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(52):18760-18768
Two low‐symmetry phthalocyanines (Pcs) substituted with thiophene units at the non‐peripheral (α) and peripheral (β) positions were synthesized and their optical, electronic‐structure, and electrochemical properties were investigated. The substitution of thiophene units at the α positions of the phthalocyanine skeleton resulted in a red shift of the Q band and significantly modified the molecular‐orbital electronic distributions just below the HOMO and just above the LUMO, with distortion of the typical Gouterman four‐orbital arrangement of MOs. Two amphiphilic Ω‐shaped ZnPcs ( αPcS1 and αPcS2 ) bearing a π‐conjugated side chain with an adsorption site at an α position of the Pc macrocycle were synthesized as sensitizers for dye‐sensitized solar cells (DSSCs). The absorption spectra of αPcS1 and αPcS2 showed red shifted Q bands and a broad band from 350 to 550 nm assignable to the intramolecular charge‐transfer transition from the ZnPc core to the side chains. Time‐dependent DFT calculations provided a clear interpretation of the effect of the thiophene conjugation on the typical phthalocyanine core π MOs. Compound αPcS1 was used as a light‐harvesting dye on a TiO2 electrode for a DSSC, which showed a panchromatic response in the range 400–800 nm with a power conversion efficiency of 5.5 % under one‐sun conditions. 相似文献
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Kenna L. Salvatore Diana M. Lutz Dr. Haoyue Guo Dr. Shiyu Yue Joceline Gan Dr. Xiao Tong Dr. Ping Liu Dr. Esther S. Takeuchi Dr. Kenneth J. Takeuchi Dr. Amy C. Marschilok Dr. Stanislaus S. Wong 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(42):9389-9402
Solution-based, anionic doping represents a convenient strategy with which to improve upon the conductivity of candidate anode materials such as Li4Ti5O12 (LTO). As such, novel synthetic hydrothermally-inspired protocols have primarily been devised herein, aimed at the large-scale production of unique halogen-doped, micron-scale, three-dimensional, hierarchical LTO flower-like motifs. Although fluorine (F) doping has been explored, the use of chlorine (Cl) dopants is the primary focus here. Several experimental variables, such as dopant amount, lithium hydroxide concentration, and titanium butoxide purity, were probed and perfected. Furthermore, the Cl doping process did not damage the intrinsic LTO morphology. The analysis, based on interpreting a compilation of SEM, XRD, XPS, and TEM-EDS results, was used to determine an optimized dopant concentration of Cl. Electrochemical tests demonstrated an increased capacity via cycling of 12 % for a Cl-doped sample as compared with pristine LTO. Moreover, the Cl-doped LTO sample described in this study exhibited the highest discharge capacity yet reported at an observed rate of 2C for this material at 143mAh g−1. Overall, these data suggest that the Cl dopant likely enhances not only the ion transport capabilities, but also the overall electrical conductivity of our as-prepared structures. To help explain these favorable findings, theoretical DFT calculations were used to postulate that the electronic conductivity and Li diffusion were likely improved by the presence of increased Ti3+ ion concentration coupled with widening of the Li migration channel. 相似文献
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The zero field cooled (ZFC) and field cooled (FC) low-field magnetic moment m of a dense frozen ferrofluid containing Fe55Co45 particles of size 4.6nm in hexane exhibits irreversibility at temperatures T?T b≈ 30?K. FC in μ 0 H ≤ 1?T gives rise to shifted minor hysteresis loops below T b. At T c≈ 10?K, sharp peaks of m ZFC and of the ac susceptibility χ ′, a kink of the thermoremanent magnetic moment m TRM, a sizeable reduction of the coercive field H c, and the appearance of a spontaneous moment m SFM indicate a phase transition with near mean-field critical behaviour of both m SFM and χ ′ . These features are explained within a core-shell model of nanoparticles, whose strongly disordered shells gradually become blocked below T b, while their soft ferromagnetic cores couple dipolarly and become superferromagnetic (SFM) below T c. 相似文献
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