Crystal structure of 4,4′-dibromo-2′,5′-dimethoxy-[1,1′-biphenyl]-2,5-dione (BrHBQBr)

Autor: Joseph E. Meany, Steven P. Kelley, Robert M. Metzger, Robin D. Rogers, Stephen A. Woski

Publikováno v: Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 12, Pp 1454-1456 (2015)

In the title compound, C14H10Br2O4, the dihedral angle between the aromatic rings is 67.29 (19)°. Both methoxy-group C atoms lie close to the plane of their attached ring [deviations = −0.130 (4) and 0.005 (5) Å]. In the crystal, molecules pack i

Externí odkaz: https://doaj.org/article/544abc05b7f04e78aec006ddc471be70

Correction to: The Intensive Care Global Study on Severe Acute Respiratory Infection (IC-GLOSSARI): a multicenter, multinational, 14-day inception cohort study

Autor: R. Di Pasquale, F. Zand, C. Chavez, P. Hopkins, G. Almekhlafi, H. Haake, A. Martinho, A. Jung, R. Montoiro Allue, T. Pellis, R. Ferrer Roca, S. Busani, A. Gordon, N. Salahuddin, F. Belda, J. Rubio Mateo-Sidron, A. Goldmann, P. Deschamps, K. Mach, J. Nentwich, F. Rubulotta, G. Lunch, A. Jonas, R. Matos, A. Carvalho, T. Vymazal, M. Guillot, D. Morocho, D. Barrios, K. Koopmans, J. Machon, D. Tomescu, X. Wu, N. Cimic, C. de Cabo, M. Kol, M. Papanikolaou, C. Aragon, S. Afonso, S. Mukkera, T. Szakmany, Z. Mitrev, A. Alsheikhly, P. Garcia Olivares, M. de la Torre-Prados, A. Donnelly, M. Girardis, V. Schiavone, N. Unni, A. Vujiaklija Brajkovic, J. van den Bosch, F. Udwadia, R. Losser, L. Bormans, J. Tomás Marsilla, F. Bloos, A. Puerto-Morlan, F. Guarracino, M. Faraz, E. Meany, K. Ravi, J. Vincent, K. Zacharowski, R. Shetty, B. Misset, V. Pota, L. Sanchez-Hurtado, B. Villamagua, C. Pierrakos, C. Nutt, S. Humphreys, P. Dennesen, M. de Groot, J. Robles, J. Meyer, W. Samaniego, Q. Zhai, L. Yu, V. Koulouras, P. Gottardo, E. Caser, M. Cecconi, S. John, I. von Osten, G. Kekstas, C. Leite Mendes, H. Jamaati, A. Raj, P. Csabi, N. Catorze, R. Gueret, F. Sifrer, G. Plantefeve, A. Macri, S. Den Boer, C. Ortiz-Leyba, M. Gurjar, J. Palo, S. Hoersch, G. Kyriazopoulos, M. Balla, Z. Kheladze, M. Hobrok, T. Nguyen, L. Srinivasa, S. Henderson, G. Dominguez, A. Maghrabi, S. Mathew, M. Blahut-Zugaj, S. Spadaro, A. Lange, K. Fiedler, L. Chao, G. Pellerano, A. Rojas, L. Brochard, S. Brett, I. Soultati, A. Albis, J. Timsit, R. Quispe Sierra, A. Pais-de-Lacerda, N. Di Tomasso, E. Scarlatescu, Y. Sakr, M. Hegazi, A. Gottschalk, N. Anguel, C. Volta, M. Alvarez, K. Psaroulis, P. Monedero, L. Fernandes, M. Niesen, G. Francois, D. Debels, M. Stotz, R. Riessen, J. Auer, E. Massa, Y. Ikeda-Maquiling, J. Izura, M. Chruscikowski, F. Franco, G. Aguilar, R. Bigornia, J. Teboul, K. Bhowmick, R. Srinivasan, J. Mallat, G. Bellani, C. Van Haren, F. Philippart, F. Honig, I. Gornik, D. Filipescu, M. Fulop, M. Albarrak, S. Behrens, E. Bermudez-Aceves, K. Schwarzkopf, N. Ramakrishnan, P. Mazzini, K. Mccalman, V. Tomic, R. Catalan, M. Giannakou, D. Molano, M. Savioli, M. Watters, X. Zhang, X. Jing, P. Araujo Aguilar, C. Joya, R. Beale, M. Garfield, A. Nichol, G. Barraza, H. Siegel, D. Gkika, L. Bouadma, T. Helmes, A. Bendtsen, R. Moreno, U. Kaisers, B. Thompson, A. Araujo, C. Teixeira, T. Hurst, M. Ostermann, T. Anguseva, I. Serra, M. Deja, J. Blanquer, A. Faltlhauser, J. Strachan, V. Corcoles Gonzalez, U. Goebel, V. Karosas, J. Wauters, F. Taccone, A. Wieczorek, C. Fernandez Gonzalez, R. Smith, A. Kübler, N. Petrucci, G. Kluge, T. Pham, U. Jaschinski, M. Vander Laenen, A. Molin, G. Barberet, M. Kuiper, C. Santos, R. Medici, J. Nielsen, S. Whittle, P. Meybohm, E. Schreurs, C. Dao, J. Bedford, R. Cardiga, G. Schatzl, M. Baumgaertel, O. Balogun, J. Gutierrez Rubio, I. Martins, G. Vlachogianni, K. Guerra, E. Novy, A. Gatta, M. Mikaszewska-Sokolewicz, B. Adamik, J. Baltazar-Torres, S. Hraech, D. Higgs, A. Ferguson, F. Cecchini, E. Zogheib, S. Dixit, M. Darmon, Z. Costa, S. O’Kane, B. Siepe, S. Ñamendys-Silva, R. Ferrer, M. Popescu, B. Floccard, O. Beck, M. Christ, F. Daviaux, N. Smalley, P. Alexander, J. Lopez-Delgado, K. Reinhart, R. Jha, J. Chiche, C. Lovesio, J. Fried, D. Rodriguez, P. Vera Aratcoz, A. Cortegiani, T. Aisa, N. Remache-Vargas, E. Salgado-Yepez, A. Olmo, E. Rupnik, M. Haap, C. Motherway, M. Sungur, R. Stoica, R. Nikandish, P. Reddy, M. Miclo, N. Chinellato, E. Mouloudi, O. O’Neill, J. Lehmke, G. Nikos, P. Bauer, M. Barger, H. Atalan, J. Ferrer Agüero, A. Bellini, G. Janssen, S. Allgaeuer, G. Strandvik, P. Simon, D. Castanares, H. Ceunen, A. Rhodes, S. Simran, S. Hashemian, A. Pravin, I. Sagoschen, E. Rezende, H. Wong, J. Sole Violan, V. Castelain, S. Raineri, K. Indraratna, E. Nives Carbonell, T. Suonsyrjä, D. Wu, G. Brescia, H. Gruber, M. Sim, T. Lazowski, C. Gonzalez, C. Dellera, J. Rajasinhe

Publikováno v: Intensive Care Medicine
Intensive care medicine, Vol. 44, no.1, p. 144-152 (2018)

Purpose In this prospective, multicenter, 14-day inception cohort study, we investigated the epidemiology, patterns of infections, and outcome in patients admitted to the intensive care unit (ICU) as a result of severe acute respiratory infections (S

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a45d2fbb2753989844e4a1b44b624fa
http://europepmc.org/articles/PMC7608195

Crystal structure of 4,4′-dibromo-2′,5′-dimethoxy-[1,1′-biphenyl]-2,5-dione (BrHBQBr)

Autor: Robert M. Metzger, Robin D. Rogers, Joseph E. Meany, Steven P. Kelley, Stephen A. Woski

Publikováno v: Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 12, Pp 1454-1456 (2015)
Acta Crystallographica Section E: Crystallographic Communications

In the crystal, mol­ecules pack in a centrosymmetric fashion and inter­act via a mixture of weak π–π stacking inter­actions, weak C—H⋯O hydrogen bonding, and Br⋯Br halogen bonding. This induces a geometry quite different than that predic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f67ebac4bbeba4753e3364009400a48c
http://scripts.iucr.org/cgi-bin/paper?S2056989015020472

Mass-Producing Graphene

Autor: Les Johnson, Joseph E. Meany

Publikováno v: American Scientist. 106:176

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::365408a18a63249928519670bea24c38
https://doi.org/10.1511/2018.106.3.176

A comparative study of the enolization of pyruvate and the reversible dehydration of pyruvate hydrate

Autor: G. Smith, Y. Pocker, J. Damitio, J. E. Meany

Publikováno v: Journal of the American Chemical Society. 114:3081-3087

The enolization of pyruvate and the reversible dehydration of pyruvate hydrate were studied at 25.0 o C using spectrophotometric methods. The enolization of pyruvate was followed at 353 nm by monitoring the rate of uptake of triiodide ion. The dehydr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e84c388334c2d2a5be6a405e413ee173
https://doi.org/10.1021/ja00034a049