Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Anna-Bea Bornhof"'
Autor:
Eric Vauthey, Anna Bea Bornhof, Tomáš Šolomek, Stefan Matile, Christopher A. Rumble, Hsin-Hua Huang, Alexander Aster, Naomi Sakai
Publikováno v:
Chemical Science
Chemical Science, Vol. 12, No 13 (2021) pp. 4908-4915
Chemical Science, Vol. 12, No 13 (2021) pp. 4908-4915
1,4,5,8-Naphthalenediimides (NDIs) are widely used motifs to design multichromophoric architectures due to their ease of functionalisation, their high oxidative power and the stability of their radical anion. The NDI building block can be incorporate
Autor:
Anna‐Bea Bornhof, Mikiko Vázquez‐Nakagawa, Laura Rodríguez‐Pérez, María Ángeles Herranz, Naomi Sakai, Nazario Martín, Stefan Matile, Javier López‐Andarias
Publikováno v:
Angewandte Chemie. 131:16243-16246
Publikováno v:
Journal of Physical Chemistry Letters, Vol. 12 (2021) pp. 1052-1057
The absorption band shape of chromophores in liquid solution at room temperature is usually dominated by pure electronic dephasing dynamics, which occurs on the sub-100 fs time scale. Herein, we report on a series of dyads consisting of a naphthalene
Autor:
Antonio Bauzá, Marion Pupier, Naomi Sakai, Alexander Aster, Antonio Frontera, Stefan Matile, Anna-Bea Bornhof, Eric Vauthey
Publikováno v:
Journal of the American Chemical Society, Vol. 140, No 14 (2018) pp. 4884-4892
In this report, we demonstrate that synergistic effects between π–π stacking and anion−π interactions in π-stacked foldamers provide access to unprecedented catalytic activity. To elaborate on anion–(π)n–π catalysis, we have designed, s
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
The de novo syntheses of chemically stable chlorins with five‐membered heterocyclic (furane, thiophene, formylfurane and formylthiophene) substituents in selected meso‐ and β‐positions are reported. Heterocycle incorporation in the 3‐ and 13
Autor:
Javier López-Andarias, Nazario Martín, María Herranz, Naomi Sakai, Anna-Bea Bornhof, Laura Rodríguez-Pérez, Mikiko Vázquez-Nakagawa, Stefan Matile
Publikováno v:
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
instname
E-Prints Complutense. Archivo Institucional de la UCM
E-Prints Complutense: Archivo Institucional de la UCM
Universidad Complutense de Madrid
Angewandte Chemie: International Edition, Vol. 58, No 45 (2019) pp. 16097-16100
instname
E-Prints Complutense. Archivo Institucional de la UCM
E-Prints Complutense: Archivo Institucional de la UCM
Universidad Complutense de Madrid
Angewandte Chemie: International Edition, Vol. 58, No 45 (2019) pp. 16097-16100
Induced π acidity from polarizability is currently emerging as most effective to stabilize anionic transition states on aromatic π surfaces, that is anion-π catalysis. To access extreme polarizability, we here propose a shift of attention from hom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::487e8d69c511791daa685260a3a581c3
http://hdl.handle.net/20.500.12614/1718
http://hdl.handle.net/20.500.12614/1718
Autor:
Yingjie Zhao, Anna Bea Bornhof, Le Liu, Javier López-Andarias, Naomi Sakai, Stefan Matile, Yoann Cotelle, Masaaki Akamatsu
Publikováno v:
Accounts of Chemical Research
Accounts of Chemical Research, American Chemical Society, 2018, 51 (9), pp.2255-2263. ⟨10.1021/acs.accounts.8b00223⟩
Accounts of Chemical Research, Vol. 51, No 9 (2018) pp. 2255-2263
Accounts of Chemical Research, 2018, 51 (9), pp.2255-2263. ⟨10.1021/acs.accounts.8b00223⟩
Accounts of Chemical Research, American Chemical Society, 2018, 51 (9), pp.2255-2263. ⟨10.1021/acs.accounts.8b00223⟩
Accounts of Chemical Research, Vol. 51, No 9 (2018) pp. 2255-2263
Accounts of Chemical Research, 2018, 51 (9), pp.2255-2263. ⟨10.1021/acs.accounts.8b00223⟩
The objective of this Account is to summarize the first five years of anion-π catalysis. The general idea of anion-π catalysis is to stabilize anionic transition states on aromatic surfaces. This is complementary to the stabilization of cationic tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5de6658d827bcd4cee633cf2e3fe0029
https://hal.archives-ouvertes.fr/hal-03274541
https://hal.archives-ouvertes.fr/hal-03274541
Autor:
Anna-Bea, Bornhof, Antonio, Bauzá, Alexander, Aster, Marion, Pupier, Antonio, Frontera, Eric, Vauthey, Naomi, Sakai, Stefan, Matile
Publikováno v:
Journal of the American Chemical Society. 140(14)
In this report, we demonstrate that synergistic effects between π-π stacking and anion-π interactions in π-stacked foldamers provide access to unprecedented catalytic activity. To elaborate on anion-(π)
Publikováno v:
The Journal of organic chemistry. 82(23)
Bromoporphyrins were prepared by the metal-mediated self-condensation of brominated 1-formyldipyrromethanes. Depending on the conditions, Mg(II)-2,12-dibromoporphyrin and Mg(II)-2-bromoporphyrin could be obtained in up to 11% and 17% isolated yield,
Publikováno v:
Chemistry - A European Journal. 23:4229-4229