Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Marcos Juanes"'
Autor:
Alfredo Echarri Sucunza, Patricia Fernández del Valle, Jose Antonio Iglesias Vázquez, Youcef Azeli, Jose María Navalpotro Pascual, Juan Valenciano Rodriguez, Cristian Fernández Barreras, Sonia Royo Embid, Carmen Gutiérrez-García, María Isabel Ceniceros Rozalén, Cesar Manuel Guerra García, Carmen del Pozo Pérez, María José Luque-Hernández, Silvia Sola Muñoz, Ana Belén Forner Canos, María Isabel Herrera Maíllo, Marcos Juanes García, Natividad Ramos García, Belén Muñoz Isabel, Junior Jose García Mendoza, José Antonio Cortés Ramas, Faustino Redondo Revilla, Inmaculada Mateo-Rodríguez, Félix Rivera Sanz, Emily Knox, Antonio Daponte Codina, José Ignacio Ruiz Azpiazu, Fernando Rosell Ortiz
Publikováno v:
Resuscitation Plus, Vol 18, Iss , Pp 100635- (2024)
Introduction: Recent data are not available on ongoing CPR for emergency services with an onboard physician. The aim of the present study was to identify factors associated with the decision to transport patients to hospital with ongoing CPR and exam
Externí odkaz:
https://doaj.org/article/4d47c45c3ec44c1387a270ca03d8fea8
Autor:
Marcos Juanes, Rizalina Tama Saragi, Cristóbal Pérez, Luca Evangelisti, Lourdes Enríquez, Martín Jaraíz, Alberto Lesarri
Publikováno v:
Molecules, Vol 27, Iss 8, p 2584 (2022)
Weakly-bound intermolecular clusters constitute reductionist physical models for non-covalent interactions. Here we report the observation of the monomer, the dimer and the monohydrate of 2-adamantanol, a secondary alcohol with a bulky ten-carbon ali
Externí odkaz:
https://doaj.org/article/05dcf3fde87448c390cbdd929b509d82
Molecular Recognition, Transient Chirality and Sulfur Hydrogen Bonding in the Benzyl Mercaptan Dimer
Autor:
Rizalina Tama Saragi, Marcos Juanes, Ruth Pinacho, José Emiliano Rubio, José A. Fernández, Alberto Lesarri
Publikováno v:
Symmetry, Vol 13, Iss 11, p 2022 (2021)
The homodimers of transiently chiral molecules offer physical insight into the process of molecular recognition, the preference for homo or heterochiral aggregation and the nature of the non-covalent interactions stabilizing the adducts. We report th
Externí odkaz:
https://doaj.org/article/516cd5165c6e4f1da71ca18f7c719865
Autor:
Sucunza, Alfredo Echarri, Fernández del Valle, Patricia, Vázquez, Jose Antonio Iglesias, Azeli, Youcef, Navalpotro Pascual, Jose María, Rodriguez, Juan Valenciano, Barreras, Cristian Fernández, Embid, Sonia Royo, Gutiérrez-García, Carmen, Rozalén, María Isabel Ceniceros, García, Cesar Manuel Guerra, del Pozo Pérez, Carmen, Luque-Hernández, María José, Muñoz, Silvia Sola, Canos, Ana Belén Forner, Maíllo, María Isabel Herrera, García, Marcos Juanes, García, Natividad Ramos, Isabel, Belén Muñoz, Mendoza, Junior Jose García, Ramas, José Antonio Cortés, Revilla, Faustino Redondo, Mateo-Rodríguez, Inmaculada, Sanz, Félix Rivera, Knox, Emily, Codina, Antonio Daponte, Azpiazu, José Ignacio Ruiz, Ortiz, Fernando Rosell
Publikováno v:
In Resuscitation Plus June 2024 18
Akademický článek
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Autor:
Rizalina Tama Saragi, Camilla Calabrese, Marcos Juanes, Ruth Pinacho, José Emiliano Rubio, Cristóbal Pérez, Alberto Lesarri
Publikováno v:
The Journal of Physical Chemistry Letters. 14:207-213
Producción Científica
π-Stacking is a common descriptor for face-to-face attractive forces between aromatic hydrocarbons. However, the physical origin of this interaction remains debatable. Here we examined π-stacking in a model homodimer fo
π-Stacking is a common descriptor for face-to-face attractive forces between aromatic hydrocarbons. However, the physical origin of this interaction remains debatable. Here we examined π-stacking in a model homodimer fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be4296ae65563a7ea68e18b085628e33
https://doi.org/10.1021/acs.jpclett.2c03299
https://doi.org/10.1021/acs.jpclett.2c03299
Autor:
Yan Jin, Wenqin Li, Rizalina Tama Saragi, Marcos Juanes, Cristóbal Pérez, Alberto Lesarri, Gang Feng
Producción Científica
Non-covalent interactions between sulfur centers and aromatic rings play important roles in biological chemistry. We examined here the sulfur–arene interactions between the fused aromatic heterocycle benzofuran and two
Non-covalent interactions between sulfur centers and aromatic rings play important roles in biological chemistry. We examined here the sulfur–arene interactions between the fused aromatic heterocycle benzofuran and two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f061595ed1b373f7763ea0e41b9b735
https://doi.org/10.1039/d3cp01146a
https://doi.org/10.1039/d3cp01146a
Autor:
Ander Camiruaga, Rizalina Tama Saragi, Fernando Torres-Hernández, Marcos Juanes, Imanol Usabiaga, Alberto Lesarri, José A. Fernández
Publikováno v:
Physical chemistry chemical physics : PCCP. 24(40)
Gas-phase spectroscopic studies of alcohol clusters offer accurate information on the influence of non-covalent interactions on molecular recognition, and are of paramount importance to model supramolecular and biological chemical processes. Here, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b64d99c3c5de4fc00e8697a7c64cb5c5
https://pubmed.ncbi.nlm.nih.gov/36214363
https://pubmed.ncbi.nlm.nih.gov/36214363
Autor:
Prakash Panwaria, Marcos Juanes, Kamal K. Mishra, Rizalina Saragi, Kshetrimayum Borish, Imanol Usabiaga, Ander Camiruaga, José A. Fernández, Alberto Lesarri, Aloke Das
Publikováno v:
Chemphyschem : a European journal of chemical physics and physical chemistry. 23(24)
Herein, we have investigated the structure of phenyl formate⋅⋅⋅water (PhOF⋅⋅⋅H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a2a3e24818d309eaa3769a56416c482
https://pubmed.ncbi.nlm.nih.gov/35984348
https://pubmed.ncbi.nlm.nih.gov/35984348
Publikováno v:
UVaDOC. Repositorio Documental de la Universidad de Valladolid
Universidad Politécnica de Madrid
Universidad Politécnica de Madrid
Producción Científica
We characterized the bis-quinolizidine tetracyclic alkaloid (5S, 6S, 7R, 11R)-matrine in a supersonic jet expansion, using chirped-pulsed broadband microwave spectroscopy. Previous crystal diffraction analyses suggested 1
We characterized the bis-quinolizidine tetracyclic alkaloid (5S, 6S, 7R, 11R)-matrine in a supersonic jet expansion, using chirped-pulsed broadband microwave spectroscopy. Previous crystal diffraction analyses suggested 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbd4ada62e753197b68ecbe431182755
https://doi.org/10.1021/acs.joc.0c02689
https://doi.org/10.1021/acs.joc.0c02689