1,213 research outputs found
A Pyrrole-Based Triazolium-Phane with Nh and Cationic Ch Donor Groups as a Receptor for Tetrahedral Oxyanions that Functions in Polar Media
The pyrrole-based triazolium-phane 1(4+)center dot 4BF(4)(-) has been prepared via the tetraalkylation of a macrocycle originally prepared via click chemistry. It displays a high selectivity for tetrahedral oxyanions relative to various test monoanions and trigonal planar anions in mixed polar organic-aqueous media. This selectivity is solvent dependent and is less pronounced in acetonitrile. Theoretical calculations were carried out in with the chloride anion in an effort to understand the influence of solvent on the intrinsic hydrogen bonding ability of the donor groups (pyrrole N-H, benzene C-H and triazolium C-H). The host-guest interactions between receptor 1(4+)center dot 4BF(4)(-) and representative tetrahedral oxyanions were further analysed by H-1 NMR spectroscopy, and the findings proved consistent with the differences in the intrinsic strength of the various H-bond donor groups inferred from the electronic structure calculations carried out in methanol, namely that (CH)(+)-anion interactions are less important in an energetic sense than neutral CH-anion interactions in polar media. Single crystal X-ray diffraction analyses of the mixed salts 1(4+)center dot HP2O73-center dot BF4- and 31(4+)center dot 4H(2)PO(4)(-)center dot 8BF(4)(-) confirmed that receptor 1(4+) can bind the pyrophosphate and phosphate anions in the solid state.Cai, Jiajia, Benjamin P. Hay, Neil J. Young, Xiaoping Yang, and Jonathan L. Sessler. "A pyrrole-based triazolium-phane with NH and cationic CH donor groups as a receptor for tetrahedral oxyanions that functions in polar media." Chemical Science 4, no. 4 (Jan., 2013): 1560-1567.Chemistr
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On The Performance Characteristics Of Electron Ring accelerators
On the basis of our present understanding of the physical phenomena involved in an electron ring accelerator (ERA), a theoretical study is made of the performance which might be expected for an ERA. Rigorous upper bounds are obtained on the rate of energy gain, from which it is shown that, in order to prevent azimuthal instability, parameters must be selected such that (for reasonable fields, injector properties, etc., but with no safety factors) the proton energy gain is less than 80 MeV/m. Numerical examples and approximate formulas are given for the properties of rings satisfying the stability conditions for both azimuthal oscillations and ion-electron oscillations. It is found that for reasonable fields and injector properties, but without safety factors, the useable proton energy gain is less than 45 MeV/m
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Rubyrin macrocycles
The present invention is directed to the synthesis and use of novel macrocyclic compounds, based upon a new class of expanded porphyrins, termed rubyrins. Disclosed herein is the structure and synthesis of a prototypical rubyrin and various substituted rubyrin analogues, conjugates and compositions. Rubyrin itself is characterized by the presence of six pyrrolic subunits contained within a fully aromatic 26 .pi.-electron macrocyclic framework and by UV/VIS absorption bands that are very red-shifted as compared to those of other porphyrins or pentapyrrolic expanded porphyrins. The rubyrin-type class of compounds is further characterized by an ability to undergo facile protonation at the pyrrolic nitrogens and, once protonated, by an ability to form complexes with anions such as nucleotide-containing compounds. Rubyrin-based compounds are useful as, for example, anion chelators and receptors and as transporters for various anionic compounds including antiviral agents. In addition to the 26 .pi.-electron target system, the present invention concerns other oxidation states bearing the same connectivity and the same total number of non-hydrogen atoms, and various analogues in which different substituents are present at the various meso and/or .beta.-pyrrolic positions or in which furan and/or thiophene moieties replace one or more of the six pyrrolic subunits.Board of Regents, University of Texas Syste
Photodissociation of Non-Covalent Peptide-Crown Ether Complexes
Highly chromogenic 18-crown-6-dipyrrolylquinoxaline coordinates primary amines of peptides, forming non-covalent complexes that can be transferred to the gas-phase by electrospray ionization. The appended chromogenic crown ether facilitates efficient energy transfer to the peptide upon ultraviolet irradiation in the gas phase, resulting in diagnostic peptide fragmentation. Collisional-activated dissociation and infrared multiphoton dissociation of these non-covalent complexes result only in their disassembly with the charge retained on either the peptide or crown ether, yielding no sequence ions. Upon UV photon absorption the intermolecular energy transfer is facilitated by the fast activation timescale of ultraviolet photodissociation (<10 ns) and by the collectively strong hydrogen bonding between the crown ether and peptide, thus allowing effective transfer of energy to the peptide moiety before disruption of the intermolecular hydrogen bonds
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Coherent Electromagnetic Effects in High-Current Particle Accelerators: [Part] 3. Electromagnetic-Coupling Instabilities in a Coasting Beam
The electromagnetic interaction of an intense relativistic coasting beam with itself, including the effect of a confining nonperfect vacuum tank, or a quiescent rf cavity, is investigated theoretically. It is shown that the resonances that may occur between harmonics of the particle circulation frequencies and the electromagnetic modes of the cavities can lead to a longitudinal instability of the beam. A criterion for stability of the beam against such longitudinal bunching is obtained as a restriction on the shunt impedance of the rf cavity, or the Q of the vacuum tank. This criterion contains the energy spread and intensity of the coasting beam, as well as the parameters of the accelerator. Numerical examples are given which indicate that in general the resonances with the vacuum tank will not cause instabilities, while those with an rf cavity can be prevented from causing instabilities by choosing the shunt impedance at a sufficiently low but still convenient value
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Melanocortin 1 receptor ligands and methods of use
The subject invention pertains to a modified MC1R peptide ligand comprising a peptide that is a melanocortin 1 receptor (MC1R) ligand and a functionality or linker, such as a click functionality, for conjugation to a surface or agent. The modified MC1R peptide ligand can be coupled, e.g., via a click reaction with a complementary click functionality attached, to a moiety to form an MC1R-targeted agent. Drugs, contrast agents, polymers, particles, micelles, surfaces of larger structures, or other moieties can be targeted to the MC1R. The subject invention also pertains to a MC1R peptide ligand-micelle complex comprising a peptide that is a melanocortin 1 receptor ligand connected via a click reaction product to a micelle. The micelle is stable in vivo and can target melanoma tumor cells by association of the peptide ligand with the MC1R or the tumor and selectively provide a detectable and/or therapeutic agent (such as an imageable contrast agent and/or anti-cancer agent) selectively to the tumor cell.Board of Regents, University of Texas Syste
Octatosylaminophthalocyanine: a reusable chromogenic anion chemosensor
Detailed herein is the use of 2,3,9,10,16,17,23,24-octatosylaminophthalocyanine as a chromogenic chemosensor for anions. The host:guest complexes formed during the sensing event can be regenerated by acid treatment without loss of the sensing ability. This allows the phthalocyanine chemosensor to be reused. This system also responds in a colorimetric manner when exposed to the neutral solvent molecules, dimethyl sulfoxide and methanol. A single-crystal X-ray structure of the Pc 1:2 MeOH complex was obtained. It illustrates the main interactions between the host:guest species in the solid state. Fits of the binding curves are consistent with this stoichiometry predominating in the solution state
Muon Colliders
Muon Colliders have unique technical and physics advantages and disadvantages
when compared with both hadron and electron machines. They should thus be
regarded as complementary. Parameters are given of 4 TeV and 0.5 TeV high
luminosity \mumu colliders, and of a 0.5 TeV lower luminosity demonstration
machine. We discuss the various systems in such muon colliders, starting from
the proton accelerator needed to generate the muons and proceeding through muon
cooling, acceleration and storage in a collider ring. Problems of detector
background are also discussed.Comment: 28 pages, with 12 postscript figures. To be published Proceedings of
the 9th Advanced ICFA Beam Dynamics Workshop, AIP Pres
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