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J. Mercado 《Physics of Particles and Nuclei Letters》2011,8(9):885-887
ALICE is the experiment at the CERN Large Hadron Collider dedicated to study high-energy nuclear collisions which is also
carrying out a proton-proton physics program, thanks to its wide phase-space coverage and good momentum and spatial resolution.
We present first results on two-pion Bose-Einstein correlations in pp collisions at √s = 900 GeV measured with ALICE. An increase of the HBT radius with increasing event multiplicity is observed, in agreement
with previous measurements. However, a strong decrease of the radius with increasing transverse momentum, as observed at RHIC
and at Tevatron, is not evident in our analysis. 相似文献
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Yang H Mercado BQ Jin H Wang Z Jiang A Liu Z Beavers CM Olmstead MM Balch AL 《Chemical communications (Cambridge, England)》2011,47(7):2068-2070
Fullerenes are generally considered as highly symmetric, yet fullerene isomers with only C(1) symmetry, such as C(1)(30)-C(90) and C(1)(32)-C(90) whose structures are reported here, become increasingly numerous as fullerene size increases. 相似文献
3.
Forrest Nichols Dr. Jia En Lu Rene Mercado Ryan Dudschus Prof. Frank Bridges Prof. Shaowei Chen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(18):4136-4142
Electrochemical hydrogen generation is a rising prospect for future renewable energy storage and conversion. Platinum remains a leading choice of catalyst, but because of its high cost and low natural abundance, it is critical to optimize its use. In the present study, platinum oxide nanoparticles of approximately 2 nm in diameter are deposited on carbon nitride (C3N4) nanosheets by thermal refluxing of C3N4 and PtCl2 or PtCl4 in water. These nanoparticles exhibit apparent electrocatalytic activity toward the hydrogen evolution reaction (HER) in acid. Interestingly, the HER activity increases with increasing Pt4+ concentration in the nanoparticles, and the optimized catalyst even outperforms commercial Pt/C, exhibiting an overpotential of only −7.7 mV to reach the current density of 10 mA cm−2 and a Tafel slope of −26.3 mV dec−1. The results from this study suggest that the future design of platinum oxide catalysts should strive to maximize the Pt4+ sites and minimize the formation of the less active Pt2+ species. 相似文献
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Meenakshi Sharma Eileen Meehan Dr. Brandon Q. Mercado Prof. Dr. Christian Brückner 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(33):11706-11718
The reaction of β‐octaalkylporphyrins (octaethylporphyrin and etioporphyrin I) with ozone generated the corresponding heptaalkyloxazolochlorinhemiacetals in which a pyrrolic subunit of the porphyrins was replaced by an oxazoline moiety. Thus, a pyrrolic β‐carbon with its alkyl substituent was excised and replaced by an oxygen atom, and the neighboring β‐carbon was hydroxylated. This work clarifies the nature of the products first described by Fischer and De?eli?, in 1933, and verifies the work by Shulg′a and coworkers, from 1977. Furthermore, the chemistry of the oxazolochlorin hemiacetals was studied: They could be dehydroxylated or converted to alkyl acetals and gem‐dialkyl derivatives, all possessing chlorin‐type optical spectra. Their oxidative conversions generated a unique tetrahydrofuran‐linked oxazolochlorin dimer and a hexaethylporpholactone. The work expands on the knowledge of converting porphyrins to porphyrinoids of potential utility containing nonpyrrolic building heterocycles. 相似文献
5.
Zachary N. Vealey Brandon Q. Mercado Patrick H. Vaccaro 《Acta Crystallographica. Section C, Structural Chemistry》2016,72(10):730-737
Tropolone long has served as a model system for unraveling the ubiquitous phenomena of proton transfer and hydrogen bonding. This molecule, which juxtaposes ketonic, hydroxylic, and aromatic functionalities in a framework of minimal complexity, also has provided a versatile platform for investigating the synergism among competing intermolecular forces, including those generated by hydrogen bonding and aryl coupling. Small members of the troponoid family typically produce crystals that are stabilized strongly by pervasive π–π, C—H…π, or ion–π interactions. The organic salt (TrOH·iBA) formed by a facile proton‐transfer reaction between tropolone (TrOH) and isobutylamine (iBA), namely isobutylammonium 7‐oxocyclohepta‐1,3,5‐trien‐1‐olate, C4H12N+·C7H5O2−, has been investigated by X‐ray crystallography, with complementary quantum‐chemical and statistical‐database analyses serving to elucidate the nature of attendant intermolecular interactions and their synergistic effects upon lattice‐packing phenomena. The crystal structure deduced from low‐temperature diffraction measurements displays extensive hydrogen‐bonding networks, yet shows little evidence of the aryl forces (viz. π–π, C—H…π, and ion–π interactions) that typically dominate this class of compounds. Density functional calculations performed with and without the imposition of periodic boundary conditions (the latter entailing isolated subunits) documented the specificity and directionality of noncovalent interactions occurring between the proton‐donating and proton‐accepting sites of TrOH and iBA, as well as the absence of aromatic coupling mediated by the seven‐membered ring of TrOH. A statistical comparison of the structural parameters extracted for key hydrogen‐bond linkages to those reported for 44 previously known crystals that support similar binding motifs revealed TrOH·iBA to possess the shortest donor–acceptor distances of any troponoid‐based complex, combined with unambiguous signatures of enhanced proton‐delocalization processes that putatively stabilize the corresponding crystalline lattice and facilitate its surprisingly rapid formation under ambient conditions. 相似文献
6.
Ahmed Z Allada K Aniol KA Armstrong DS Arrington J Baturin P Bellini V Benesch J Beminiwattha R Benmokhtar F Canan M Camsonne A Cates GD Chen JP Chudakov E Cisbani E Dalton MM de Jager CW De Leo R Deconinck W Decowski P Deng X Deur A Dutta C Franklin GB Friend M Frullani S Garibaldi F Giusa A Glamazdin A Golge S Grimm K Hansen O Higinbotham DW Holmes R Holmstrom T Huang J Huang M Hyde CE Jen CM Jin G Jones D Kang H King P Kowalski S Kumar KS Lee JH LeRose JJ Liyanage N Long E McNulty D 《Physical review letters》2012,108(10):102001
The parity-violating cross-section asymmetry in the elastic scattering of polarized electrons from unpolarized protons has been measured at a four-momentum transfer squared Q2 = 0.624 GeV2 and beam energy E(b) = 3.48 GeV to be A(PV) = -23.80 ± 0.78(stat) ± 0.36(syst) parts per million. This result is consistent with zero contribution of strange quarks to the combination of electric and magnetic form factors G(E)(s) + 0.517G(M)(s) = 0.003 ± 0.010(stat) ± 0.004(syst) ± 0.009(ff), where the third error is due to the limits of precision on the electromagnetic form factors and radiative corrections. With this measurement, the world data on strange contributions to nucleon form factors are seen to be consistent with zero and not more than a few percent of the proton form factors. 相似文献
7.
Anniefer N. Magpusao Kelli Rutledge Dr. Trevor A. Hamlin Jean‐Marc Lawrence Dr. Brandon Q. Mercado Prof. Nicholas E. Leadbeater Prof. Mark W. Peczuh 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(17):6001-6011
Shape is an inherent trait of a molecule that dictates how it interacts with other molecules, either in binding events or intermolecular reactions. Large‐ring macrocyclic compounds in particular leverage their shape when they are selectively bound by biomolecules and also when they exhibit macrocyclic diastereoselectivity. Nonetheless, rules that link structural parameters to the conformation of a macrocycle are still rudimentary. Here we use a structural investigation of a family of [13]‐macrodilactones as a case study to develop rules that can be applied generally to macrocycles of different sizes and with a variety of functionality. A characteristic “ribbon” shape is adopted by the [13]‐macrodilactones in the absence of stereogenic centres, which exhibits planar chirality. When one stereogenic centre at key positions on the backbone is incorporated into the structure, the planar chirality is dictated by the configuration of the centre. In cases where two stereogenic centres are present, their relationships can either reinforce the characteristic ribbon shape or induce alternative shapes to be adopted. The rules established in the case study are then applied to the analysis of a structure of the natural product migrastatin. They lay the groundwork for the development of models to understand macrocycle‐biomolecule interactions and for the preparation of macrocycles with designed properties and activities. 相似文献
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L. A. Mercado G. Ribera M. Gali V. Cdiz 《Journal of polymer science. Part A, Polymer chemistry》2006,44(5):1676-1685
The curing system of diglycidyl ether of bisphenol A (DGEBA) with two phosphorus‐containing amine compounds—bis(3‐aminophenyl)methyl phosphine oxide and bis(4‐aminophenyl)‐bis(9,10‐dihydro‐9‐oxa‐10‐oxide‐10‐phosphaphenanthrene‐10‐yl)methane—was studied with differential scanning calorimetry under isothermal and nonisothermal conditions and compared with the DGEBA/diamino diphenyl methane system. The isoconversional method was used to evaluate the dependence of the effective activation energy on the extent of conversion. Modulated differential scanning calorimetry and dynamic mechanical thermal analysis were used to study the phenomena of vitrification and gelation. The thermal and flame‐retardant properties were evaluated, and the limiting oxygen index values of the phosphorylated resins, above 30, confirmed that phosphorus‐containing epoxy resins are effective flame retardants. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 1676–1685, 2006 相似文献