Zobrazeno 1 - 10
of 104
pro vyhledávání: '"M. Victoria Martínez‐Díaz"'
Autor:
Jorge Labella, Gonzalo Durán‐Sampedro, Swathi Krishna, M. Victoria Martínez‐Díaz, Dirk M. Guldi, Tomás Torres
Publikováno v:
Angewandte Chemie International Edition. 62
Large π-conjugated systems are key in the area of molecular materials. Herein, we prepare via AuI - catalyzed cyclization a series of fully π-conjugated anthracene-fused oligo-BODIPYs. Their structural and optoelectronic properties were studied by
Autor:
Giulia Lavarda, Jorge Labella, M. Victoria Martínez-Díaz, M. Salomé Rodríguez-Morgade, Atsuhiro Osuka, Tomás Torres
Publikováno v:
Chemical Society reviews. 51(23)
Half a century after the synthesis of the first subporphyrinoid, the study of tripyrrole and trisoindole porphyrin analogues constitutes a fervent and rapidly expanding research area. The outstanding structural, electronic and optical features of the
Autor:
Cristina Momblona, Jorge Labella, Marta Gómez-Gómez, David Guzmán, Pavel Čulík, Hiroyuki Kanda, M. Victoria Martínez-Díaz, Dirk M. Guldi, Mohammad Khaja Nazeeruddin, Tomás Torres
Publikováno v:
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
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Due to their strong acceptor properties and enhanced charge transport capabilities, non-fullerene electron acceptors based on [Formula: see text]-extended derivatives – subnaphthalocyanines (SubNc) or subphtalocyanine dimers (SubPc[Formula: see tex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::052ce51ea67aa05ec7f5d3ac23ea8675
http://hdl.handle.net/20.500.12614/3230
http://hdl.handle.net/20.500.12614/3230
Autor:
Radim Kučera, Tomás Torres, Veronika Novakova, Miloslav Machacek, Magdalena Kozlikova, Jiri Demuth, M. Victoria Martínez-Díaz, Lucia Gallego
Publikováno v:
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
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Because cancer is the second leading cause of death globally, investigation of new photosensitizers for photodynamic therapy is highly desirable. In this work, different peripherally substituted subphthalocyanines (SubPcs) with either a benzocrown mo
Autor:
Lara Martínez-Fernández, Inés Corral, Jorge Labella, Lara Tejerina, M. Victoria Martínez-Díaz, Tomás Torres
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
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Chemistry (Weinheim an Der Bergstrasse, Germany)
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
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Chemistry (Weinheim an Der Bergstrasse, Germany)
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
Subphthalocyanine (SubPc) chemistry has been limited so far by their high sensitivity toward strong nucleophiles. In particular, the substitution of the axial chlorine atom by a nucleophilic group in the case of less‐reactive SubPcs, such as those
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93e762c8fd16da8b8d3056c2ad22dac9
https://hdl.handle.net/10486/700270
https://hdl.handle.net/10486/700270
Autor:
Mutsumi Kimura, Tomás Torres, Satoshi Yamamoto, M. Victoria Martínez-Díaz, Ismael López-Duarte, Lara Tejerina
Publikováno v:
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
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instname
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba427a3f32fe26c2199078f076c95da2
http://hdl.handle.net/20.500.12614/768
http://hdl.handle.net/20.500.12614/768
Publikováno v:
Chemical Science
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
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Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
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Here we report gold(i)-catalyzed cycloisomerization as a new powerful synthetic tool for the preparation of π-extended BODIPY derivatives. The catalytic system PPhF3AuCl/AgSbF6 enables the synthesis of [b]-[2,1]naphtho-fused-BODIPYs (2a–2c) under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbb60e7f215757e14348c19f39e381e0
http://hdl.handle.net/20.500.12614/730
http://hdl.handle.net/20.500.12614/730
Autor:
Tomás Torres, Timothy Clark, Víctor Mariñas, German Zango, Marcel Krug, Dirk M. Guldi, Swathi Krishna, M. Victoria Martínez-Díaz
Publikováno v:
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Chemical Science
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
Universidad Autónoma de Madrid
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Chemical Science
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
The development of new chromophoric receptors capable of binding curved carbon nanostructures is central to the quest for improved fullerene-based organic photovoltaics. We herein report the synthesis and characterization of a subphthalocyanine-based
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e486766b667b05763b46ff6ddc535398
http://hdl.handle.net/10486/696967
http://hdl.handle.net/10486/696967
Autor:
Tomás Torres, Nikolai V. Tkachenko, Lara Tejerina, V. Golovanov, Mine Ince, Maxence Urbani, Hanna Hakola, M. Victoria Martínez-Díaz, Kirsi Virkki, Viktoria Golovanova
Publikováno v:
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
instname
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Phthalocyanines (Pc) are well-known light-harvesting compounds. However, despite the tremendous efforts on phthalocyanine synthesis, the achieved energy conversion efficiencies for Pc-based dye-sensitized solar cells are moderate. To cast light on th
Autor:
M. Victoria Martínez-Díaz, Jorge Labella, Miguel Martínez-García, Giovanni Bottari, Tomás Torres, Luis M. Mateo, Mine Ince, Elisa López-Serrano
Publikováno v:
ECS Meeting Abstracts. :633-633
The development of new chromophoric receptors able to bind curved carbon nanostructures is at the epicenter of the quest for fullerene-based organic photovoltaics with improved performances. Herein, a subphthalocyanine-based multicomponent ensemble c