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981.
Andrew Burritt Mariusz Krawiec Alan P. Marchand Duoli Sun William H. Watson 《Journal of chemical crystallography》1995,25(2):63-68
In the solid state the 21 Diels-Alder adduct between spiro[4.2]hepta-1,3-diene and p-benzoquinone has a planar cyclohexadione ring with a center of symmetry. Both planar and boat conformations have been observed in similar systems, and the relative stability of the two conformers is of interest. The adduct in the gas phase should contain a mirror plane perpendicular to the cyclohexadione ring; however, a data set collected on a crystal in a capillary resulted in a structure where some bond lengths related by this mirror plane differed by more than 4 in the solid state. Molecular mechanics, MOPAC, and the Cambridge Structural Data Base were used to investigate the factors influencing the conformation of the cyclohexadione ring and the asymmetry across the noncrystallographic mirror plane. The energy differences between the planar and nonplanar ring system is small, and the conformation is determined by crystal packing. No reason for the bond length asymmetry could be found, and a recollection of data on a crystal exposed to the environment led to a structure with statistically equivalent bond lengths. 相似文献
982.
Philip J. Cox Neil S. Stewart Alan B. Turner R. Alan Howie 《Journal of chemical crystallography》1990,20(6):577-581
The crystal and molecular structure of the product from the solvolysis of dehydroepiandrosterone (DHEA) tosylate has been determined by X-ray analysis,1H-NMR, IR, UV, and mass spectrometry. The compound was obtained from DHEA via the 3-tosyl derivative by refluxing in benzyl alcohol (containing dried potassium acetate) for 12 hr. X-ray analysis shows a planar cyclopropane ring at C(3), C(4), C(5), a-orientated benzylozy group attached to C(6) and a benzylidene group attached to C(16). Spectroscopic evidence for the presence of these features in the steroid nucleus are presented and details of the synthesis and possible mechanisms of formation are also discussed. 相似文献
983.
Xinyue Li Sergey Semin Leandro A. Estrada Chunqing Yuan Yulong Duan Jonathan Cremers Paul Tinnemans Paul Kouwer Alan E. Rowan Theo Rasing Jialiang Xu 《中国化学快报》2018,29(2):297-300
The polymorphs of a phenylethynyl functionalized fluorenone derivative, and their controlled self-assembly for microstructures with different morphologies have been studied. These polymorphic microcrystals exhibit very distinctive NLO properties, which are highly correlated to their electronic and supramolecular structures. 相似文献
984.
Controllable Synthesis of Few‐Layer Bismuth Subcarbonate by Electrochemical Exfoliation for Enhanced CO2 Reduction Performance
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Ying Zhang Xiaolong Zhang Yunzhi Ling Fengwang Li Prof. Alan M. Bond Dr. Jie Zhang 《Angewandte Chemie (International ed. in English)》2018,57(40):13283-13287
Two‐dimensional (2D) engineering of materials has been recently explored to enhance the performance of electrocatalysts by reducing their dimensionality and introducing more catalytically active ones. In this work, controllable synthesis of few‐layer bismuth subcarbonate nanosheets has been achieved via an electrochemical exfoliation method. These nanosheets catalyse CO2 reduction to formate with high faradaic efficiency and high current density at a low overpotential owing to the 2D structure and co‐existence of bismuth subcarbonate and bismuth metal under catalytic turnover conditions. Two underlying fast electron transfer processes revealed by Fourier‐transformed alternating current voltammetry (FTacV) are attributed to CO2 reduction at bismuth subcarbonate and bismuth metal. FTacV results also suggest that protonation of CO2.? is the rate determining step for bismuth catalysed CO2 reduction. 相似文献
985.
Tia Jarvis Carl Jacky Saint-Louis Alexander R. Fisch Korry L. Barnes Dolan Dean Luis A. Flores Thomas F. Hunt Lyndsay Munro Tyler J. Simmons Vincent J. Catalano Lei Zhu Alan K. Schrock Michael T. Huggins 《Tetrahedron》2018,74(14):1698-1704
Pyrrole β-amides are useful building blocks for the preparation of novel molecular architectures that can be used in supramolecular chemistry and sensor development. Under basic conditions, pyrrole β-amides with an α-aldehyde produce different condensation products when reacted with pyrrolinones depending on the amide substitution. Secondary amides form the expected dipyrrinones, but unexpectedly undergo a subsequent trans-amidation with the pyrrolinone nitrogen to produce an unsymmetrical imide (an N-confused fluorescent dipyrrinone). Under the same conditions, tertiary amides produce the expected dipyrrinone carboxylic acids, which have been shown to have strong self-association properties as determined by vapor pressure osmometry measurements, NMR studies, and X-ray crystal structure determination. Furthermore, an N-confused fluorescent dipyrrinone was produced from the same trans-amidation reaction during attempts to decarboxylate a dipyrrinone amide with a 9-carboxylic moiety. 相似文献
986.
We prove that theq-state Potts antiferromagnet on a lattice of maximum coordination numberr exhibits exponential decay of correlations uniformly at all temperatures (including zero temperature) wheneverq>2r. We also prove slightly better bounds for several two-dimensional lattices: square lattice (exponential decay forq7), triangular lattice (q11), hexagonal lattice (q4), and Kagomé lattice (q6). The proofs are based on the Dobrushin uniqueness theorem. 相似文献
987.
It is well known that the ability to fibrillate is intrinsic to a normal ventricle that exceeds a critical mass. The questions we address are how is ventricular fibrillation (VF) initiated and perpetuated in normal myocardium, and why is VF not seen more often in the general population if all ventricles have the ability to fibrillate. To study the mechanisms of VF, we used computerized mapping techniques with up to 512 channels of simultaneous multisite recordings for data acquisition. The data were then processed for dynamic display of the activation patterns and for mathematical analyses of the activation intervals. The results show that in normal ventricles, VF can be initiated by a single strong premature stimulus given during the vulnerable period of the cardiac cycle. The initial activations form a figure-eight pattern. Afterward, VF will perpetuate itself without any outside help. The self-perpetuation itself is due to at least two factors. One is that single wave fronts spontaneously break up into two or more wavelets. The second is that when two wavelets intersect perpendicular to each other, the second wavelet is broken by the residual refractoriness left over from the first wavelet. Mathematical analyses of the patterns of activation during VF revealed that VF is a form of chaos, and that transition from ventricular tachycardia (VT) to VF occurs via the quasiperiodic route. In separate experiments, we found that we can convert VF to VT by tissue size reduction. The physiological mechanism associated with the latter transition appears to be the reduction of the number of reentrant wave fronts and wandering wavelets. Based on these findings, we propose that the reentrant wave fronts and the wandering wavelets serve as the physiological equivalent of coupled oscillators. A minimal number of oscillators is needed for VF to perpetuate itself, and to generate chaotic dynamics; hence a critical mass is required to perpetuate VF. We conclude that VF in normal myocardium is a form of reentrant cardiac arrhythmia. A strong electrical stimulus initiates single or dual reentrant wave fronts that break up into multiple wavelets. Sometimes short-lived reentry is also generated during the course of VF. These organized reentrant and broken wavelets serve as coupled oscillators that perpetuate VF and maintain chaos. Although the ability to support these oscillators exists in a normal ventricle, the triggers required to generate them are nonexistent in the normal heart. Therefore, VF and sudden death do not happen to most people with normal ventricular myocardium. (c) 1998 American Institute of Physics. 相似文献
988.
The point code of a Steiner triple system uniquely determines the system when the number of vectors whose weight equals the replication number agrees with the number of points. The existence of a Steiner triple system with this minimum point code property is established for all v 1,3 (mod 6) with v 15. 相似文献
989.
Jill E. Morris Philip J. Squattrito Kristin Kirschbaum A. Alan Pinkerton 《Journal of chemical crystallography》2003,33(4):307-321
Salts of 4-aminonaphthalene-1-sulfonate with divalent Mg, Mn, Co, and Ni cations have been crystallized and their structures determined by single crystal X-ray methods. The Mg and Mn salts are isostructural. Crystal data for hexa-aquamagnesium(II) 4-aminonaphthalene-1-sulfonate dihydrate, [Mg(H2O)6](H2NC10H6SO3)2 2H
2O: monoclinic, P21/c, Z = 2, a = 8.622(3), b = 7.043(3), c = 23.178(3) Å, =93.78(2)°, V = 1404.3(7) Å3; hexa-aquamanganese(II) 4-aminonaphthalene-1-sulfonate dihydrate, [Mn(H2O)6](H2NC10H6SO3)2 2H
2O: monoclinic, P21/c, Z = 2, a = 8.652(3), b = 7.031(4), c = 23.402(2) Å, =93.09(2)°, V = 1421.5(9) Å3. The structures are composed of alternating layers of octahedral metal–aqua complexes and sulfonate anions linked by an extensive network of hydrogen bonds. The extra water molecules of crystallization are located in the hexa-aquametal cation layers. The repeat unit along the c axis is a double layer. The Co and Ni compounds are isostructural with each other, but compared to the Mg and Mn compounds, have a strikingly different structure. Crystal data for hexa-aquacobalt(II) 4-aminonaphthalene-1-sulfonate trihydrate, [Co(H2O)6](H2NC10H6SO3)2 3H
2O: orthorhombic, Pbca, Z = 8, a = 8.518(1), b = 14.327(2), c = 45.367(6) Å, V = 5536(1) Å3; hexa-aquanickel(II) 4-aminonaphthalene-1-sulfonate trihydrate, [Ni(H2O)6](H2NC10H6SO3)2 3H
2O: orthorhombic, Pbca, Z = 8, a = 8.4976(6), b = 14.288(1), c = 45.076(3) Å, V = 5472.9(7) Å3. These structures also contain layers of octahedral hexa-aquametal complexes and additional water molecules of crystallization sandwiched by layers of sulfonate anions, however the stacking pattern is more complex with a quadruple layer repeat unit and two different types of anion layers. 相似文献
990.
Rasim Tanbug Kristin Kirschbaum A. Alan Pinkerton 《Journal of chemical crystallography》1999,29(1):45-55
Two energetic salts of the melaminium cation have been prepared and structurally characterized from room temperature X-ray single crystal diffraction data. Melaminium dinitramide (I), triclinic, P1¯, a = 6.6861(11), b = 6.9638(16), c = 10.447(2) Å , = 99.07(3), = 98.30(3), = 108.50(3)°, V = 445.6(2) Å3, and Z = 2. Melaminium nitrate (II), monoclinic, P21/c, a = 3.5789(7), b = 20.466(4), c = 10.060(2) Å, = 94.01(2)°, V = 735.0(3) Å3, and Z = 4. The crystal structures of both salts show distinct monoprotonated melaminium cations and dinitramide- or nitrate anions, respectively. Efficient packing in the solid state is achieved by extensive hydrogen bonding between two-dimensional zigzag ribbons of the melaminium cations and the respective anions resulting in high densities of the solid state structures of 1.74 (I) and 1.71 g/cm3 (II). 相似文献