Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Bruno Dacunha-Marinho"'
Autor:
Carlos Lázaro, Juan Antelo, Ivan Carabante, Alba Otero-Fariña, Pedro V. Verdes, Bruno Dacunha-Marinho, Sarah Fiol
Publikováno v:
Minerals, Vol 12, Iss 6, p 726 (2022)
Schwertmannite is a metastable mineral playing a crucial role in the immobilization of metal(oid)s in acid mine drainage (AMD) systems. High temperatures associated with wildfires could lead to a sudden schwertmannite transformation, changing the mob
Externí odkaz:
https://doaj.org/article/6ee19e96b6cf4c2aa1fac2cf61647b30
Autor:
Augusto Rivera, Mauricio Maldonado, Jaime Ríos-Motta, Diego González-Salas, Bruno Dacunha-Marinho
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 10, Pp o2553-o2553 (2009)
In the title structure, C18H20N4, the aromatic rings are almost orthogonal [81.6 (2)°]. The molecule has symmetry 2 since it is situated on a crystallographic twofold axis. There are only weak intermolecular interactions present in the structure, no
Externí odkaz:
https://doaj.org/article/c4db1fac957c441b9f6602f215980a25
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 2, Pp o283-o284 (2009)
The title compound, 2C21H34N4O3S2+·4I−·5H2O, was prepared exclusively as the E isomer by methylation of the corresponding N-phenylpyridin-4-amine. There are two symmetry-independent molecules in the asymmetric unit with no significant differences
Externí odkaz:
https://doaj.org/article/bec84e7b3bc94485acac977b87ad5f41
Autor:
Bruno Dacunha-Marinho, Juan J. Torres-Labandeira, Pedro José Rolim Neto, Marcílio S. S. Cunha-Filho, José Lamartine Soares-Sobrinho
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 3, Pp o634-o634 (2008)
The conformation of the title compound [systematic name: N-benzyl-2-(2-nitroimidazol-1-yl)acetamide], C12H12N4O3, can be described in terms of the relative orientation of three planar fragments, the imidazol group (A), benzyl group (B), and the aceta
Externí odkaz:
https://doaj.org/article/a70af60acdb649b7ac799712360bc471
Autor:
Xiang Zhang, Bruno Dacunha-Marinho, Antonios G. Mikos, Luis Diaz-Gomez, Panayiotis D. Kontoyiannis, Pulickel M. Ajayan, John A. Jansen, Maryam E. Elizondo, Gerry L. Koons, Anthony J. Melchiorri
Publikováno v:
Tissue Engineering. Part C: Methods, 26, 6, pp. 292-305
Tissue Engineering. Part C: Methods, 26, 292-305
Tissue Eng Part C Methods
Tissue Engineering. Part C: Methods, 26, 292-305
Tissue Eng Part C Methods
In this study, we describe the additive manufacturing of porous three-dimensionally (3D) printed ceramic scaffolds prepared with hydroxyapatite (HA), β-tricalcium phosphate (β-TCP), or the combination of both with an extrusion-based process. The sc
Autor:
Sander G. A. van Assema, J. Chris Slootweg, José M. Otero, Antonio L. Llamas-Saiz, Mark J. van Raaij, Mark Overhand, Bas Lastdrager, Koop Lammertsma, Sebastian Burck, Andreas W. Ehlers, Bruno Dacunha-Marinho
Publikováno v:
Chemistry: A European Journal, 15(33), 8134-45. Wiley-VCH Verlag
Burck, S, van Assema, S G A, Lastdrager, B, Slootweg, J C, Ehlers, A W, Otero, J M, Dacunha-Marinho, B, Llamas-Saiz, A L, Overhand, M, van Raaij, M J & Lammertsma, K 2009, ' Bisphosphine-functionalized cyclic decapeptides based on the natural product Gramicidin S: a potential scaffold for transition-metal coordination ', Chemistry: A European Journal, vol. 15, no. 33, pp. 8134-45 . https://doi.org/10.1002/chem.200901127
Burck, S, van Assema, S G A, Lastdrager, B, Slootweg, J C, Ehlers, A W, Otero, J M, Dacunha-Marinho, B, Llamas-Saiz, A L, Overhand, M, van Raaij, M J & Lammertsma, K 2009, ' Bisphosphine-functionalized cyclic decapeptides based on the natural product Gramicidin S: a potential scaffold for transition-metal coordination ', Chemistry: A European Journal, vol. 15, no. 33, pp. 8134-45 . https://doi.org/10.1002/chem.200901127
The natural product Gramicidin S is a promising scaffold for novel oligopeptide-based bisphosphine ligands, combining the advantageous rigid chiral backbone with the close proximity of phosphine substituents. The required unnatural, phosphine-contain
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 64:o353-o356
The title flavonoid [systematic name: (2S)-7-hydroxy-5-methoxy-6,8-dimethyl-2-phenyl-3,4-dihydrochromen-4(2H)-one], C18H18O4, displays statistical conformational disorder, with three conformations of the molecule involving three orientations of the p
Autor:
Juan J. Torres-Labandeira, Marcilio Cunha-Filho, Ramón Martínez-Pacheco, Bruno Dacunha-Marinho, Mariana Landin
Publikováno v:
AAPS PharmSciTech. 8:E68-E77
The aim of the present investigation was to develop a novel dosage form of rifampicin and isoniazid to minimize degradation of rifampicin in acidic medium and to modulate the release of rifampicin in the stomach and isoniazid in the intestine. Gastro
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 62:o473-o475
Autor:
Jaime Ríos-Motta, Augusto Rivera, Bruno Dacunha-Marinho, Diego González-Salas, Mauricio Maldonado
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 10, Pp o2553-o2553 (2009)
Acta Crystallographica Section E: Structure Reports
Acta Crystallographica Section E: Structure Reports
In the title structure, C18H20N4, the aromatic rings are almost orthogonal [81.6 (2)°]. The molecule has symmetry 2 since it is situated on a crystallographic twofold axis. There are only weak intermolecular interactions present in the structure, no