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991.
Ohno M Hayashi H Suzuki K Kose T Asada T Kawata K 《Journal of colloid and interface science》2011,364(2):407-412
When diluted solutions of giant micelles are under turbulent flow, large attenuations of the turbulence can be observed due to the action of the micelles on the dissipative vortices formed within the flow. This particular property is rapidly lost when the solution is heated due breakup of the giant micelles. Based on this property, we present a thermal-flow study of a mixed giant micelle formed by the combination of two surfactants and sodium salicylate. One of the surfactants, cetyltrimethylammonium bromide (C(16)TAB) was kept fixed, and the others were dodecyltrimethylammonium bromide (C(12)TAB), tetradecyltrimethylammonium bromide (C(14)TAB), octadecyltrimethylammonium bromide (C(18)TAB), polyoxyethylene (10) oleyl ether (Brij 97) or sodium dodecyl sulfate (SDS). Thermal diagrams for the combinations of the surfactants reveal deviations of the ideality. For the cationic surfactants, a synergistic effect was only observed when C(16)TAB was combined with the shorter surfactants. 相似文献
992.
Lim JM Inoue M Sung YM Suzuki M Higashino T Osuka A Kim D 《Chemical communications (Cambridge, England)》2011,47(13):3960-3962
Conformational flexibility and balance between M?bius aromatic and Hückel antiaromatic conformers in [28]hexaphyrins depend on N-fused structure and meso-aryl substituents, revealed by various spectroscopic methods. In particular, the existence of the two conformers has been confirmed for singly-N-fused [28]hexaphyrins by femtosecond time-resolved transient absorption spectroscopy. 相似文献
993.
Fujioka H Goto A Otake K Kubo O Sawama Y Maegawa T 《Chemical communications (Cambridge, England)》2011,47(35):9894-9896
An unusual and novel reaction of α-alkoxyphosphonium salts, generated from O,O-acetals and Ph(3)P, with Grignard reagents under an O(2) atmosphere afforded alcohols in moderate to high yields. It was clarified by isotopic labelling experiments that the reaction proceeded via a novel radical pathway. 相似文献
994.
Asahi Tomitaka Tomohiro KoshiShinsuke Hatsugai Tsutomu YamadaYasushi Takemura 《Journal of magnetism and magnetic materials》2011,323(10):1398-1403
The influence of the oleic acid surface coating on Fe3O4 and NiFe2O4 nanoparticles on their magnetic and calorimetric characterization was investigated. Fe3O4 nanoparticles (particle sizes of 15-20 and 20-30 nm) and NiFe2O4 nanoparticles (particle sizes of 20-30 nm) were dispersed in oleic acid. The surface coating resulted in a decrease in the dipole-dipole interaction between the particles, which in turn affected the coercivity and heat dissipation of the nanoparticles. The coercivity of the oleic-acid-coated nanoparticles was found to be lower than that of the uncoated nanoparticles. The temperature rise in the oleic-acid-coated nanoparticles was greater than that of the uncoated nanoparticles; this temperature rise was associated with the relaxation losses. The viscosity dependence on the self-heating temperature of Fe3O4 nanoparticles (15-20 and 20-30 nm) under an ac magnetic field was measured. The temperature rise for both the Fe3O4 nanoparticles (15-20 and 20-30 nm) exhibited a strong dependence on viscosity at each magnetic field frequency, and the contribution of Brownian relaxation loss to the temperature rise was revealed. Moreover, an in vitro cytotoxicity test of Fe3O4 and NiFe2O4 was performed using human cervical carcinoma cells (HeLa), and the cytotoxicity of NiFe2O4 nanoparticles was compared to that of Fe3O4 nanoparticles. 相似文献
995.
Kwee TC Takahara T Niwa T Yamashita T Van Cauteren M Nievelstein RA Luijten PR 《Magnetic resonance imaging》2011,29(6):877-880
Bowel contents and peripheral nerves often show high signal intensity at diffusion-weighted imaging (DWI) of the abdomen and pelvis, obscuring or mimicking pathology. This study introduced and compared short tau inversion recovery (STIR) with single-axis DWI to the usual combination of spectral fat suppression (SFS) with trace DWI in the suppression of bowel contents and peripheral nerves. Five volunteers underwent both STIR with single-axis DWI and SFS with trace DWI of the abdomen and pelvis. Images were evaluated by two observers with respect to the suppression of signal of bowel contents and peripheral nerves using four-point grading scales (4=poor suppression; 3=moderate suppression; 2=good suppression; 1=excellent suppression). Mean scores (±S.D.) regarding the suppression of bowel contents were 1.60±0.55 and 1.40±0.89 for STIR with single-axis DWI and 3.40±0.55 and 3.00±1.00 for SFS with trace DWI for observers 1 and 2, respectively. Mean scores regarding the suppression of peripheral nerves were 1.20±0.45 and 1.20±0.45 for STIR with single-axis DWI and 2.40±0.89 and 2.80±0.84 for SFS with trace DWI for observers 1 and 2, respectively. In conclusion, STIR with single-axis DWI is superior to SFS with trace DWI in the suppression of bowel signal and peripheral nerves. 相似文献
996.
In this paper, a novel numerical algorithm for solving quasi penta-diagonal linear systems is presented. The computational costs of the algorithm is less than those of three successful algorithms given by El-Mikkawy and Rahmo (Comput Math Appl 59:1386–1396, 2010), by Lv and Le (Appl Math Comput 204:707–712, 2008), and by Jia et al. (Int J Comput Math 89:851–860, 2012). In addition, a new recursive method for inverting the quasi penta-diagonal matrices is also discussed. The implementation of the algorithm using Computer Algebra Systems (CASs) such as MATLAB and MAPLE is straightforward. Two numerical examples are given in order to demonstrate the performance and efficiency of our algorithm. 相似文献
997.
After preparing a homologous series of tetrameric mesogenic compounds in which two U-shaped molecules were connected via a rigid benzene derivative or a flexible alkyl chain, we investigated their phase transition behaviour using optical microscopy, differential scanning calorimetry and X-ray diffraction analysis. The compounds possessing an alkyl spacer as the central group exhibited nematic and smectic A phases just as the corresponding U-shaped molecule did. The compound possessing a 1,2-benzene unit as the connecting group showed nematic and smectic A phases, although the compound possessing a 1,3-benzene unit exhibited only an anticlinic smectic C phase. Structure–property relations of the liquid crystalline tetramers are interpreted in terms of preorganised effects of the four mesogenic units. 相似文献
998.
Dr. Tomohiro Seki Sayaka Kurenuma Prof. Dr. Hajime Ito 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(48):16214-16220
We report the luminescent color tuning of a new complex, 2‐benzothiophenyl(4‐methoxyphenyl isocyanide)gold(I) ( 1 ), by using a new “polymorph doping” approach. The slow crystallization of the complex 1 afforded three different pure polymorphic crystals with blue, green, and orange emission under UV‐light irradiation. The crystal structures of pure polymorphs of 1 were investigated in detail by means of single‐crystal X‐ray analyses. Theoretical calculations based on the single‐crystal structures provided qualitative explanation of the difference in the excited energy‐levels of the three polymorphs of 1 . In sharp contrast, the rapid precipitation of 1 , with the optimized conditions reproducibly afforded homogeneous powder materials showing solid‐state white‐emission with Commission Internationale de l’Éclairage (CIE) 1931 chromaticity coordinates of (0.33, 0.35), which is similar to pure white. New “polymorphic doping” has been revealed to be critical to this white emission through spectroscopic and X‐ray diffraction analyses. The coexistence of the multiple polymorphs of 1 within the homogeneous powder materials and the ideal mixing of multiple luminescent colors gave its white emission accompanied with energy transfer from the predominant green‐emitting polymorph to the minor orange‐emitting polymorph. 相似文献
999.
Dr. Shinsuke Nishida Dr. Junya Kawai Miki Moriguchi Tomohiro Ohba Naoki Haneda Dr. Kozo Fukui Prof. Akira Fuyuhiro Prof. Daisuke Shiomi Prof. Kazunobu Sato Prof. Takeji Takui Prof. Kazuhiro Nakasuji Prof. Yasushi Morita 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(36):11904-11915
The tri‐tert‐butylphenalenyl (TBPLY) radical exists as a π dimer in the crystal form with perfect overlapping of the singly occupied molecular orbitals (SOMOs) causing strong antiferromagnetic exchange interactions. 2,5‐Di‐tert‐butyl‐6‐oxophenalenoxyl (6OPO) is a phenalenyl‐based air‐stable neutral π radical with extensive spin delocalization and is a counter analogue of phenalenyl in terms of the topological symmetry of the spin density distribution. X‐ray crystal structure analyses showed that 8‐tert‐butyl‐ and 8‐(p‐XC6H4)‐6OPOs (X=I, Br) also form π dimers in the crystalline state. The π‐dimeric structure of 8‐tert‐butyl‐6OPO is seemingly similar to that of TBPLY even though its SOMO–SOMO overlap is small compared with that of TBPLY. The 8‐(p‐XC6H4) derivatives form slipped stacking π dimers in which the SOMO–SOMO overlaps are greater than in 8‐tert‐butyl‐6OPO, but still smaller than in TBPLY. The solid‐state electronic spectra of the 6OPO derivatives show much weaker intradimer charge‐transfer bands, and SQUID measurements for 8‐(p‐BrC6H4)‐6OPO show a weak antiferromagnetic exchange interaction in the π dimer. These results demonstrate that the control of the spin distribution patterns of the phenalenyl skeleton switches the mode of exchange interaction within the phenalenyl‐based π dimer. The formation of the relevant multicenter–two‐electron bonds is discussed. 相似文献
1000.
1‐(Triisopropylsilyl)‐3,4‐dichloropyrrole and 1‐(triisopropylsilyl)‐3,4‐difluoropyrrole were conveniently prepared from the corresponding 3,4‐dibromopyrrole by lithiation followed by halogenation. 2,3,17,18‐Tetrahalogeno [26]‐ and [28]hexaphyrins have been prepared by condensation of 3,4‐dihalopyrroles and a dipyrromethane‐dicarbinol. 2,3,17,18‐Tetrahalogenated hexaphyrins display variable structural and electronic properties depending upon the halogen atom and the number of π‐electrons. Tetrabromo[28]hexaphyrin and tetrachloro[28]hexaphyrin were further reduced with excess NaBH4 to furnish meso‐reduced hexaphyrins as the first example of phlorin‐type meso‐aryl‐substituted hexaphyrins. 相似文献