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101.
The reaction of tert-butylamine, isoxazolidine and hydrazine with N-[(3-chloropropyl)oxy]phthalimide is investigated. A convenient synthesis of oxazolidine is described. 相似文献
102.
The phase diagram for the binary system K2CrO4CaCrO4 has been determined for CaCrO4 concentrations up to 60 mole%, using the techniques of differential thermal analysis, X-ray diffraction, and drop calorimetry. Essential features of the phase diagram are: the solid-solid phase transition for pure K2CrO4 at 670°C, β-K2CrO4 ? α-K2CrO4; a eutectoid reaction at 14 mole% CaCrO4 and 548°C, β-K2CrO4 ? α-K2CrO4 + K2CrO4 · CaCrO4; a peritectoid event at 50 mole% CaCrO4 and 640°C, β-K2CrO4 + CaCrO4 ? K2CrO4 · CaCrO4; and a eutectic reaction at 51 mole% CaCrO4 and 678°C, L ? β-K2CrO4 + CaCrO4. X-ray diffraction studies lead to the determination of the unit cell dimensions for the K2CrO4 · CaCrO4 double salt, a C-centered monoclinic form with a0 = 7.615(6) Å, b0 = 22.797(15) Å, c0 = 9.777(9) Å, β = 115.45(5)°. 相似文献
103.
K. Yabuta N. Kinomura M. Shimada F. Kanamaru M. Koizumi 《Journal of solid state chemistry》1980,33(2):253-256
The complete solid solutions of Cr1?xFexOOH with the InOOH-type structure were synthesized under high pressures. They were antiferromagnetic with Néel temperatures of 570 K for FeOOH, 454 K for Cr0.2Fe0.8OOH, 332 K for Cr0.4Fe0.6OOH, and 160 K for Cr0.6Fe0.4OOH as determined by the Mössbauer effect measurements. 相似文献
104.
Samples of head-to-head polypropylene have been prepared by the hydrogenation of two polydienes; 1,4-poly(2,4-hexadiene) and 1,4-poly(2,3-dimethyl-1,3-butadiene). Glass transition temperatures were found to be marginally lower than for conventional polypropylene suggesting that the head-to-head placements in the chain increased the polymer flexibility. 相似文献
105.
Thermal decomposition of bis(hexamethylbenzene)iron(0) in the presence of carbon monoxide yields a novel carbonyl iron complex, [C6(CH3)6]Fe(CO)2. The cyclohexadiene complex [C6(CH3)6]Fe(C6H8) is obtained from reaction of bis(hexamethylbenzene)iron(0) with either 1,3-cyclohexadiene or benzene, and the yield is much greater in the presence of hydrogen gas. Interaction of bis-(hexamethylbenzene)iron(0) with 2-butyne induces a catalytic cyclotrimerization to give more hexamethylbenzene. Kinetic and isotope distribution studies indicate that the primary step in these reactions is not a direct loss of one ring ligand, but rather an insertion of the iron center into one of the ligand methyl CH bonds, leading to a benzyl hydride complex species. Mechanisms for the subsequent reactions of this iron hydride species are proposed. 相似文献
106.
C.R. Leidner P. Denisevich K.W. Willman Royce W. Murray 《Journal of Electroanalytical Chemistry》1984,164(1):63-78
The cyclic voltammetric peaks for charging trapping and untrapping reactions between the inner and outer redox polymer films of five bilayer electrodes are compared to a theory for control of the rate of charge trapping by electron diffusion rates in the inner polymer film. The five bilayer electrodes use various different redox polymer films (electropolymerized poly-pyridine complexes of Fe, Ru, and Os, and polyvinylferrocene) arranged in different orders. The currents on the rising edge of the bilayer trapping and untrapping peaks follow the electron diffusion theory up to ca. 80% of the peak current; currents thereafter are controlled by another process(es). The analysis yields values for the electron diffusion constants in the inner bilayer polymer films, which agree with one another for different bilayers having the same inner film polymer films and which also agree with independent determinations by other methods. Two of the bilayers are made from the same two polymers, arranged in different inner-outer order. These bilayers also illustrate the occurrence of a “leak reaction”, in which charge trapped in the outer film is discharged via a thermodynamically unfavorable electron transfer reaction with the inner polymer film. 相似文献
107.
Tertiary phosphine oxides have been prepared in excellent yield from primary alkyl halides or aromatic halides and activated sodium phosphinates obtained by reaction of dialkyl phosphine oxides with complex bases (NaNH2/tBuONa). This reaction has been successfully applied to soluble and cross-linked bromopolystyrenes and to macroporous polystyrenes with bromooctyl substituents giving polymers which contain pendant phosphine oxide groups. 相似文献
108.
Horst P. Beck 《Journal of solid state chemistry》1983,47(3):328-332
A high pressure phase BaI2-II, which can be quenched and retained as a metastable form at ambient conditions, is reported. The structure has been determined by X-ray investigations using single crystals. BaI2-II crystallizes in an anti-Fe2P-type arrangement, space group Å, c = 5.173(3)Å, which is slightly denser than the PbCl2-type structure found at normal pressure. Structural features of the two phases are discussed in comparison. 相似文献
109.
U. Berg R. Isaksson J. Sandström U. Sjöstrand A. Eiglsperger A. Mannschreck 《Tetrahedron letters》1982,23(41):4237-4240
(+)- and (?)- as well as (+)- and (?)- were partially separated by liquid chromatography on triacetylcellulose; racemizations resulted in the barriers (Table 2) to rotation via planarized transition states. 相似文献
110.
The crystal structure of a second high-pressure copper vanadate phase, CuVO3(II), has been determined and refined by full-matrix least-squares procedures using automatic diffractometer data to a residual R = 0.042 (Rw = 0.051). The space group is rhombohedral, , with hexagonal unit cell a = 4.966(2) and c = 14.084(5) Å [aR = 5.501(2) Å and α = 53.66(3)°]. The structure is the fully ordered ilmenite-type and, on the basis of published magnetic data and the interatomic distances, the valence distribution Cu+V5+O3 is proposed. This represents a unique example of Cu+ in an octahedral environment. 相似文献