Search results for "Experimental"
showing 10 items of 18236 documents
Regulación emocional como proceso de transdiagnóstico a través de los trastornos depresivos y ansiedad.
2020
Frente al enfoque tradicional centrado en trastornos específicos, los modelos transdiagnósticos hipotetizan procesos y mecanismos compartidos por diversos trastornos psicológicos. En relación con los trastornos de ansiedad y los trastornos depresivos, entre los procesos comunes que más interés despiertan, se encuentra la regulación emocional (RE). Las estrategias de RE inicialmente se clasificaron como adaptativas o desaptativas en función de sus consecuencias. Sin embargo, una segunda generación de estudios enfatiza la importancia del contexto y la flexibilidad. En el ámbito psicopatológico se han aplicado los modelos surgidos de la investigación básica y, por otra parte, se han generado t…
Search for photonic signatures of gauge-mediated supersymmetry in 8TeV pp collisions with the ATLAS detector
2015
A search is presented for photonic signatures motivated by generalized models of gauge-mediated supersymmetry breaking. This search makes use of 20.3 fb[superscript −1] of proton-proton collision data at √s = 8 TeV recorded by the ATLAS detector at the LHC, and explores models dominated by both strong and electroweak production of supersymmetric partner states. Four experimental signatures incorporating an isolated photon and significant missing transverse momentum are explored. These signatures include events with an additional photon, lepton, b-quark jet, or jet activity not associated with any specific underlying quark flavor. No significant excess of events is observed above the Stand…
Recommendations of the LHC Dark Matter Working Group: Comparing LHC searches for dark matter mediators in visible and invisible decay channels and ca…
2019
Physics of the Dark Universe 26, 100377 (2019). doi:10.1016/j.dark.2019.100377
CCDC 1900330: Experimental Crystal Structure Determination
2019
Related Article: Lucas H. G. KalinkeDanielle CangussuFrancesc LloretRosaria BrunoDonatella ArmentanoEmilio PardoJesus Ferrando-Soria, Jesus Ferrando-Soria|2019|Cryst.Growth Des.|19|3905|doi:10.1021/acs.cgd.9b00324
CCDC 1438663: Experimental Crystal Structure Determination
2016
Related Article: David Van Craen, Markus Albrecht, Gerhard Raabe, Fangfang Pan, Kari Rissanen|2016|Chem.-Eur.J.|22|3255|doi:10.1002/chem.201600158
CCDC 2069786: Experimental Crystal Structure Determination
2021
Related Article: Christian Mevissen, David Sommer, Sabarina Vasanthakumar, Khai-Nghi Truong, Kari Rissanen, Markus Albrecht|2021|Dalton Trans.|50|9372|doi:10.1039/D1DT01707A
CCDC 1512900: Experimental Crystal Structure Determination
2017
Related Article: Shobhraj Haldar, Gonela Vijaykumar, Luca Carrella, Steven Batha, Ghezai T. Musie, Manindranath Bera|2017|ACS Omega|2|1535|doi:10.1021/acsomega.7b00189
CCDC 706867: Experimental Crystal Structure Determination
2012
Related Article: L.Lopez-Banet, M.D.Santana, G.Garcia, J.Perez, L.Garcia, L.Lezama, M.Liu|2012|Polyhedron|31|575|doi:10.1016/j.poly.2011.10.014
The Impact of a 1,2,3-Triazole Motif on the Photophysical Behavior of Non-K Tetrasubstituted Pyrene with a Substitution Pattern Providing the Long Ax…
2022
1,3,6,8-Tetrasubstituted pyrene derivatives with two types of substituents (4-(2,2-dimethylpropyloxy)pyridine, 1-decyl-1,2,3-triazole, 1-benzyl-1,2,3-triazole, and pyrazole), substituted in such a way that provides the long axial symmetry, are prepared and characterized in the present study. To the best of our knowledge, the pyrene derivative containing the same heteroaryl motif (triazole) but substituted by two various alkyls, straight decyl and benzyl-based side chains (C), is reported for the first time. For comparison, compounds with one kind of triazole motif and substituted pyridine or pyrazole groups were prepared (A and B). The photophysical properties of all molecules were evaluate…
CCDC 1443465: Experimental Crystal Structure Determination
2017
Related Article: Rajendhraprasad Tatikonda, Elina Kalenius, Matti Haukka|2016|Inorg.Chim.Acta|453|298|doi:10.1016/j.ica.2016.08.015