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41.
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James N. Little James L. Waters Karl J. Bombaugh William J. Pauplis 《Journal of Polymer Science.Polymer Physics》1969,7(10):1775-1783
A systematic study of factors affecting the GPC separation showed that peak spreading with increasing flow rate was much less than predicted from the Van Deemter equation. Viscous fingering decreased and peak symmetry improved at increased flow rates. As a result, fast GPC analysis was shown to be readily attainable through optimization of operating parameters. 相似文献
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In a reaction-diffusion system, diffusion can induce the instability of a uniform equilibrium which is stable with respect to a constant perturbation, as shown by Turing in 1950s. We show that cross-diffusion can destabilize a uniform equilibrium which is stable for the kinetic and self-diffusion reaction systems; on the other hand, cross-diffusion can also stabilize a uniform equilibrium which is stable for the kinetic system but unstable for the self-diffusion reaction system. Application is given to predator-prey system with preytaxis and vegetation pattern formation in a water-limited ecosystem. 相似文献
45.
Vanessa Renee Little Hilary Jenkins Keith Vaughan 《Journal of chemical crystallography》2008,38(6):447-452
Abstract The crystal structures of methyl 4-{(E)-2-(4-methylpiperazino)-1-diazenyl}benzoate (2a) and 1,4-di[(E)-2-(2-nitrophenyl)-1-diazenyl]piperazine (3a) have been determined by single crystal X-ray diffraction analysis. The bis-triazene (3a) adopts an unusual pseudo-boat conformation in the piperazine ring, with a dihedral angle of 52.20(0.06)° between the two
planes defined within the piperazine ring. The crystal structures of 2a and 3a are compared with the structure of the triazene (4) and the closely related bis-triazene (5). The piperazine ring of 2a adopts a typical chair conformation, whereas the piperazine ring of 3a adopts an unusual boat conformation. Crystal data: 2a C13H18N4O2, monoclinic, space group P21
/n, a = 13.849(3) ?, b = 6.577(1) ?, c = 14.904(3) ?, α = 90°, β = 96.098(3)°, γ = 90° and V = 1,349.8(4) ?3, for Z = 4. 3a C16H16N8O4, triclinic, space group P-1, a = 7.6066(6) ?, b = 8.3741(7) ?, c = 14.507(1) ?, α = 78.673(1)°, β = 81.877(1)°, γ = 73.445(1)° and V = 865.0(1) ?3, for Z = 2.
Index abstract
The crystal structures of methyl 4-{(E)-2-(4-methylpiperazino)-1-diazenyl}benzoate (2a) and 1,4-di[(E)-2-(2-nitrophenyl)-1-diazenyl]piperazine (3a) have been determined by single crystal X-ray diffraction analysis. 相似文献
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Caitlin E. Shields Dr. Xue Wang Dr. Thomas Fellowes Rob Clowes Dr. Linjiang Chen Prof. Graeme M. Day Prof. Anna G. Slater Dr. John W. Ward Dr. Marc A. Little Prof. Andrew I. Cooper 《Angewandte Chemie (International ed. in English)》2023,62(34):e202303167
Hydrogen-bonded organic frameworks (HOFs) with low densities and high porosities are rare and challenging to design because most molecules have a strong energetic preference for close packing. Crystal structure prediction (CSP) can rank the crystal packings available to an organic molecule based on their relative lattice energies. This has become a powerful tool for the a priori design of porous molecular crystals. Previously, we combined CSP with structure-property predictions to generate energy-structure-function (ESF) maps for a series of triptycene-based molecules with quinoxaline groups. From these ESF maps, triptycene trisquinoxalinedione (TH5) was predicted to form a previously unknown low-energy HOF (TH5-A) with a remarkably low density of 0.374 g cm−3 and three-dimensional (3D) pores. Here, we demonstrate the reliability of those ESF maps by discovering this TH5-A polymorph experimentally. This material has a high accessible surface area of 3,284 m2 g−1, as measured by nitrogen adsorption, making it one of the most porous HOFs reported to date. 相似文献
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Raghavendra Kumar P. Ajai K. Singh J. E. Drake M. B. Hursthouse M. E. Little 《Structural chemistry》2007,18(2):203-207
A non-Schiff base (Te, N, O) ligand MeOC6 H4TeCH2CH2NHCH(CH3)C6H4–2–OH (LH) having a chiral center and its palladium(II) complex [PdClL]·CH2Cl2 (1) have been synthesized. Both have characteristic 1H and 13C NMR spectra. The single crystal structure of the complex 1 has been determined by X-ray diffraction methods. The monoclinic crystals of 1 (space group P21/n) have a=14.581(5) Å, b=13.160(5) Å and c=20.249(5) Å, β=99.398(5)°. The Te $\cdots A non-Schiff base (Te, N, O) ligand MeOC6 H4TeCH2CH2NHCH(CH3)C6H4–2–OH (LH) having a chiral center and its palladium(II) complex [PdClL]·CH2Cl2 (1) have been synthesized. Both have characteristic 1H and 13C NMR spectra. The single crystal structure of the complex 1 has been determined by X-ray diffraction methods. The monoclinic crystals of 1 (space group P21/n) have a=14.581(5) ?, b=13.160(5) ? and c=20.249(5) ?, β=99.398(5)°. The TeCl secondary interactions [3.303(2)–3.352(2) ?] between two nearly square planar palladium complex molecules results in a
bimolecular aggregate having a PdPd distance 3.203(1) ?. The Pd–Te, Pd–N and Pd–O bond lengths are 2.5005(7)/2.4914(7), 2.060(4)/2.061(4) and 2.054(3)/2.044(3) ?,
respectively. 相似文献
50.