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51.
We investigate the quantum fluctuations of a single atom in a weakly driven cavity, where the center of mass motion of the atom is quantized in one dimension. We present analytic results for the second order intensity correlation function g((2))(tau) and the intensity-field correlation function h(theta)(tau), for transmitted light in the weak driving field limit. We find that the coupling of the center of mass motion to the intracavity field mode can be deleterious to nonclassical effects in photon statistics and field-intensity correlations, and compare the use of trapped atoms in a cavity to atomic beams. 相似文献
52.
Hashimoto A Przybyl AK Linders JT Kodato S Tian X Deschamps JR George C Flippen-Anderson JL Jacobson AE Rice KC 《The Journal of organic chemistry》2004,69(16):5322-5327
The synthesis of the ortho- and para-e isomers in the oxide-bridged 5-phenylmorphan series of rigid tetracyclic compounds was accomplished via rac-5-(2-fluoro-5-nitrophenyl)-2-methyl-2-azabicyclo[3.3.1]nonan-9beta-ol ((+/-)-10), an intermediate containing an aromatic nitro-activated fluorine atom. The fluorine atom was used as the leaving group for the formation of the strained tetracyclic trans-fused 5,6-ring system in rac-(1alpha,4aalpha,9aalpha)-1,3,4,9a-tetrahydro-2-methyl-6-nitro-2H-1,4a-propanobenzofuro[2,3-c]pyridine ((+/-)-11), although preference for cis ring fusion during the formation of tricyclic tetra- and hexahydrodibenzofurans has been well-documented. Single-crystal X-ray crystallographic study of the desired para-e isomer ((+/-)-2), as well as of two intermediates in its synthesis, provided assurance of the correct structures. The e-isomers are among the last of the 12 oxide-bridged 5-phenylmorphans to be synthesized. We envisioned the syntheses of these rigid, tetracyclic compounds in order to determine the three-dimensional pattern of a ligand that would enable interaction with opioid receptors as agonists or antagonists. 相似文献
53.
Harding LP Jeffery JC Riis-Johannessen T Rice CR Zeng Z 《Dalton transactions (Cambridge, England : 2003)》2004,(16):2396-2397
The amide-substituted unsymmetrical ligand L(1) upon coordination to Co(2+) forms the dinuclear triple helicate [Co(2)(L(1))(3)](4+) which exists as both possible C(1) and C(3) symmetric geometric isomers in solution, however, upon addition of nitrate ions, the formation of an anion binding cavity is favoured and hence the sole product is the C(3) symmetric isomer in which all three amide substituents are hydrogen bonded to the nitrate anion. 相似文献
54.
We report results from molecular dynamics simulations of cooperative motion in a quasi-two-dimensional system of colloid particles. We find that the onset of the deviation of the single-particle displacement distribution from Gaussian form starts in the liquid phase and extends, with increasing magnitude, through the hexatic phase into the crystalline phase. The time for which the deviation is maximum increases exponentially with the density. As the density increases toward the hexatic phase a third dynamical relaxation mode emerges. We argue that the collective motion is generated by superpositions of instantaneous normal mode vibrations, with lifetimes that increase with the density, along paths with strong bond-orientation correlation. 相似文献
55.
Zangi R Rice SA 《Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics》2000,61(1):671-681
We report the results of extensive molecular dynamics simulations of the reconstructive hexagonal to square lattice conversion in bilayer colloid systems. Two types of interparticle potential were used to represent the colloid-colloid interactions in the suspension. One potential, due to Marcus and Rice, is designed to describe the interaction of sterically stabilized colloid particles. This potential has a term that represents the attraction between colloid particles when there is incipient overlap between the stabilizing brushes on their surfaces, a (soft repulsion) term that represents the entropy cost associated with interpenetration of the stabilizing brushes, and a term that represents core-core repulsion. The other potential we used is an almost hard core repulsion with continuous derivatives. Our results clearly show that the character of the reconstructive hexagonal to square lattice conversion in bilayer colloid systems is potential dependent. For a system with colloid-colloid interactions of the Marcus-Rice type, the packing of particles in the square array exhibits a large interlayer lattice spacing, with the particles located at the minima of the attractive well. In this case the hexagonal to square lattice transition is first order. For a system with hard core colloid-colloid interactions there are two degenerate stable intermediate phases, linear and zigzag rhombic, that are separated from the square lattice by strong first order transitions, and from the hexagonal lattice by either weak first or second order transitions. 相似文献
56.
Simon M. Vornholt Caroline G. Elliott Cameron M. Rice Dr. Samantha E. Russell Peter J. Kerr Daniel N. Rainer Michal Mazur Dr. Mark R. Warren Dr. Paul S. Wheatley Prof. Russell E. Morris 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(33):8537-8546
The size of single crystals of the metal-organic framework CPO-27-Ni was incrementally increased through a series of modulated syntheses. A novel linker modulated synthesis using 2,5-dihydroxyterephthalic acid and the isomeric ligand 4,6-dihydroxyisophthalic acid yielded large single crystals of CPO-27-Ni (∼70 μm). All materials were shown to have high crystallinity and phase purity through powder X-ray diffraction, electron microscopy methods, thermogravimetry, and compositional analysis. For the first time single-crystal structure analyses were carried out on CPO-27-Ni. High BET surface areas and nitric oxide (NO) release efficiencies were recorded for all materials. Large single crystals of CPO-27-Ni showed a prolonged NO release and proved suitable for in situ single-crystal diffraction experiments to follow the NO adsorption. An efficient activation protocol was developed, leading to a dehydrated structure after just 4 h, which subsequently was NO-loaded, leading to a first NO loaded single-crystal structural model of CPO-27-Ni. 相似文献
57.
Joannie Chin Amanda Forster Lipiin Sung Kirk Rice 《Polymer Degradation and Stability》2007,92(7):1234-1246
In recent years, poly(p-phenylene-2,6-benzobisoxazole) (PBO) fibers have become prominent in high strength applications such as body armor, ropes and cables, and recreational equipment. The objectives of this study were to expose woven PBO body armor panels to elevated temperature and moisture, and to analyze the chemical, morphological and mechanical changes in PBO yarns extracted from the panels. A 30% decrease in yarn tensile strength, which was correlated to changes in the infrared peak absorbance of key functional groups in the PBO structure, was observed during the 26 week elevated temperature/elevated moisture aging period. Substantial changes in chemical structure were observed via infrared spectroscopy, as well as changes in polymer morphology using microscopy and neutron scattering. When the panels were removed to an ultra-dry environment for storage for 47 weeks, no further decreases in tensile strength degradation were observed. In a follow-on study, fibers were sealed in argon-filled glass tubes and exposed to elevated temperature; less than a 4% decrease in tensile strength was observed after 30 weeks, demonstrating that moisture is a key factor in the degradation of these fibers. 相似文献
58.
Appel EA Lee VY Nguyen TT McNeil M Nederberg F Hedrick JL Swope WC Rice JE Miller RD Sly J 《Chemical communications (Cambridge, England)》2012,48(49):6163-6165
Organocatalytic ring opening polymerization (OROP) is used to effect the rapid, scalable, room temperature formation of size-controlled, highly uniform, polyvalent, nanogel star polymer nanoparticles of biodegradable composition. 相似文献
59.
60.
Rice JE Cziegler I Diamond PH Duval BP Podpaly YA Reinke ML Ennever PC Greenwald MJ Hughes JW Ma Y Marmar ES Porkolab M Tsujii N Wolfe SM 《Physical review letters》2011,107(26):265001
Direction reversals of intrinsic toroidal rotation have been observed in diverted Alcator C-Mod Ohmic L-mode plasmas following electron density ramps. For low density discharges, the core rotation is directed cocurrent, and reverses to countercurrent following an increase in the density above a certain threshold. Such reversals occur together with a decrease in density fluctuations with 2 cm(-1)≤k(θ)≤11 cm(-1) and frequencies above 70 kHz. There is a strong correlation between the reversal density and the density at which the Ohmic L-mode energy confinement changes from the linear to the saturated regime. 相似文献