Search results for "RIG"

showing 10 items of 9548 documents

"Table 16" of "Search for pairs of highly collimated photon-jets in $pp$ collisions at $\sqrt{s}$ = 13 TeV with the ATLAS detector"

2018

Selection efficiency for reconstructed photons originating from the decay $a\rightarrow 3\pi^0\rightarrow 6\gamma$ with $m_a$ = 0.7 GeV.

$pp\rightarrow X \rightarrow aa \rightarrow 6\pi^0$Astrophysics::High Energy Astrophysical PhenomenaHigh Energy Physics::PhenomenologySelection efficiencyHigh Energy Physics::Experiment13000Photon-jet
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"Table 15" of "Search for pairs of highly collimated photon-jets in $pp$ collisions at $\sqrt{s}$ = 13 TeV with the ATLAS detector"

2018

Selection efficiency for reconstructed photons originating from the decay $a\rightarrow 3\pi^0\rightarrow 6\gamma$ with $m_a$ = 0.5 GeV.

$pp\rightarrow X \rightarrow aa \rightarrow 6\pi^0$Astrophysics::High Energy Astrophysical PhenomenaHigh Energy Physics::PhenomenologySelection efficiencyHigh Energy Physics::Experiment13000Photon-jet
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"Table 20" of "Search for pairs of highly collimated photon-jets in $pp$ collisions at $\sqrt{s}$ = 13 TeV with the ATLAS detector"

2018

Selection efficiency for reconstructed photons originating from the decay $a\rightarrow 3\pi^0\rightarrow 6\gamma$ with $m_a$ = 10 GeV.

$pp\rightarrow X \rightarrow aa \rightarrow 6\pi^0$Astrophysics::High Energy Astrophysical PhenomenaHigh Energy Physics::PhenomenologySelection efficiencyHigh Energy Physics::Experiment13000Photon-jet
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"Table 19" of "Search for pairs of highly collimated photon-jets in $pp$ collisions at $\sqrt{s}$ = 13 TeV with the ATLAS detector"

2018

Selection efficiency for reconstructed photons originating from the decay $a\rightarrow 3\pi^0\rightarrow 6\gamma$ with $m_a$ = 5 GeV.

$pp\rightarrow X \rightarrow aa \rightarrow 6\pi^0$Astrophysics::High Energy Astrophysical PhenomenaHigh Energy Physics::PhenomenologySelection efficiencyHigh Energy Physics::Experiment13000Photon-jet
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Aggregation of [Ln(12)(III)] clusters by the dianion of 3-formylsalicylic acid. Synthesis, crystal structures, magnetic and luminescence properties

2019

Three isostrucutral dodecanuclear clusters with the general formula [Ln(12)(fsa)(12)(mu f(3)-OH)(12)(DMF)(12)]center dot nDMF (fsa(2-) is the dianion of 3-formylsalicylic acid; Ln = Eu 1, Gd 2, Dy 3) have been obtained from the reaction of fromylsalicyclic acid (H(2)fsa), tetrabutylammonium hydroxide and Ln(NO3)(3)center dot 6H(2)O in methanol/DMF. Their structure consists of four vertex-sharing heterocubanes. Each heterocubane unit is assembled from four Ln(III) ions, three mu(3)-OH groups and one mu(3)-oxygen atom arising from the fsa(2-) carboxylato group. The photophysical properties of the europium derivative investigated at both 300 and 80 K sustain a relative intense emission obtaine…

---Materials science010405 organic chemistryTetrabutylammonium hydroxidechemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciences0104 chemical sciencesIonInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryAtomDysprosiumMagnetic refrigerationEuropiumLuminescence
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The research reactor TRIGA Mainz – a strong and versatile neutron source for science and education

2019

Abstract The TRIGA Mark II-reactor at the Johannes Gutenberg University Mainz (JGU) is one of three research reactors in Germany. The TRIGA Mainz became first critical on August 3rd, 1965. It can be operated in the steady state mode with a maximum power of 100 kWth and in the pulse mode with a peak power of 250 MWth and a pulse length of 30 ms. The TRIGA Mainz is equipped with a central thimble, a rotary specimen rack, three pneumatic transfer systems, four beam tubes, and a graphite thermal column. The TRIGA Mainz is intensively used both for basic and applied research in nuclear chemistry and nuclear physics. Two sources for ultra-cold neutrons (UCN) are operational at two beam ports. At …

010308 nuclear & particles physicsChemistryNuclear engineering0103 physical sciencesNeutron sourceResearch reactorPhysical and Theoretical Chemistry010306 general physics01 natural sciencesTRIGARadiochimica Acta
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Sulfur, tin and gold derivatives of 1-(2'-pyridyl)-ortho-carborane, 1-R-2-X-1,2-C2B10H10 (R = 2'-pyridyl, X = SH, SnMe3 or AuPPh3).

2004

Reaction of the lithium salt of 1-(2'-pyridyl)-ortho-carborane, Li[1-R-1,2-C(2)B(10)H(10)](R = 2'-NC(5)H(4)), with sulfur, followed by hydrolysis, gave the mercapto-o-carborane, 1-R-2-SH-1,2-C(2)B(10)H(10) which forms chiral crystals containing helical chains of molecules linked by intermolecular S-H...N hydrogen bonds. The cage C(1)-C(2) and exo C(2)-S bond lengths (1.730(3) and 1.775(2)[Angstrom], respectively) are indicative of exo S=C pi bonding. The tin derivative 1-R-2-SnMe(3)-1,2-C(2)B(10)H(10), prepared from Li[1-R-1,2-C(2)B(10)H(10)] and Me(3)SnCl, crystallises with no significant intermolecular interactions. The pyridyl group lies in the C(1)-C(2)-Sn plane, oriented to minimise th…

010405 organic chemistryChemistryHydrogen bondStereochemistryIntermolecular forcechemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic ChemistryBond lengthCrystallographyTrigonal bipyramidal molecular geometryCarboraneMoleculeTinDalton transactions (Cambridge, England : 2003)
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A trigonal prismatic anionic iron(iii) complex of a radical o-iminobenzosemiquinonate derivative: structural and spectral analyses

2017

A new iron(III) complex, [Et3NH][FeIII(L2−˙)2] (1) with a substituted o-aminophenol based ligand is reported. Complex 1 is an anionic complex with a triethylammonium cation in the lattice. It contains two O,O,N-coordinated o-iminobenzosemiquinonate(2−) radical anions with an Fe(III) centre in a high-spin configuration. The crystal structure of 1 was determined by X-ray diffraction, which revealed a trigonal prismatic coordination environment whose electronic structure was established by various physical methods including EPR, Mossbauer spectroscopy and variable-temperature (2–300 K) magnetic susceptibility measurements. Electrochemical analysis indicated primarily ligand-centred redox proce…

010405 organic chemistryChemistryLigandGeneral ChemistryCrystal structureElectronic structure010402 general chemistryTrigonal prismatic molecular geometry01 natural sciencesMagnetic susceptibilityCatalysis0104 chemical scienceslaw.inventionCrystallographylawMössbauer spectroscopyMaterials ChemistryGround stateElectron paramagnetic resonanceNew Journal of Chemistry
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Combining Cyanometalates and Coordination Clusters: An Alternative Synthetic Route toward Original Molecular Materials

2013

International audience; With the discovery of molecules or molecule-based compounds that can display blocked magnetization, magnetic ordering or switchable magnetic bistability, the research efforts devoted to molecular magnetic materials have considerably increased over the past two decades, fully exploiting the advantages of the bottom-up approach. 1-4 This research field focuses on promising properties for potential technological applications such as information storage, quantum computing and spintronics at the molecular scale, but it also provides fundamental insights into original quantum phenomena. 5,6 Coordination chemists have developed efficient synthetic tools for the preparation …

010405 organic chemistryChemistryStereochemistrychemistry.chemical_elementGeneral ChemistryTrigonal crystal system010402 general chemistryCondensed Matter Physics01 natural sciencesCopper0104 chemical sciencesCoordination networkCluster (physics)[CHIM]Chemical SciencesGeneral Materials Science[CHIM.COOR]Chemical Sciences/Coordination chemistryMolecular materials
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Oxotris(oxalate)niobate(V): An oxalate delivery agent in the design of building blocks

2018

This work concerns the oxalate delivery process that occurs when using (NH4)3[NbO(C2O4)3]·6H2O as a suitable oxalate source in the synthesis of two compounds, [Cu(dmphen)(C2O4)(H2O)] (1) and [{Cu(dmphen)(CH3OH)}2(μ-C2O4)](ClO4)2 (2) (dmphen = 2,9-dimethyl-1,10-phenanthroline). {[Fe{HB(pz)3}(CN)2(μ-CN)]2[{Cu(dmphen)}2(μ-C2O4)]}∙xCH3OH (3) (2.0 ≤ x ≤ 2.4) was obtained by reacting 2 and PPh4[Fe{HB(pz)3}(CN)3]∙H2O [ = tetraphenylphosphonium and = tris(pyrazolyl)borate]. Crystal structures of 1–3 have been determined by single-crystal X-ray diffraction experiments: 1 is a mononuclear trigonal bipyramidal copper(II) species, 2 is a centrosymmetric oxalato-bridged dicopper(II) complex, and 3 consi…

010405 organic chemistryChemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesCopperOxalate0104 chemical scienceschemistry.chemical_compoundCrystallographyTrigonal bipyramidal molecular geometryIntramolecular forceMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryBoronNatural bond orbital
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