Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Miguel García-Iglesias"'
Autor:
Nicolás M. Casellas, Gaole Dai, Evelyn Y. Xue, Alba Fonseca, Dennis K. P. Ng, Miguel García-Iglesias, Tomás Torres
Publikováno v:
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
instname
instname
A subphthalocyanine substituted with nine tetra(ethylene glycol) chains on the periphery has been synthesised. This novel amphiphilic and cone-shaped compound can self-assemble in water into spherical nanoparticles with a hydrodynamic diameter of 154
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::471468510fc8bd1f1334224030447add
https://pubmed.ncbi.nlm.nih.gov/34919102
https://pubmed.ncbi.nlm.nih.gov/34919102
Publikováno v:
Chemistry-A European Journal, 2021, 27(43), 11056-11060
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry-A European Journal, 27(43), 11056-11060. Wiley-VCH Verlag
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
instname
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Biblos-e Archivo. Repositorio Institucional de la UAM
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry-A European Journal, 27(43), 11056-11060. Wiley-VCH Verlag
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
instname
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Biblos-e Archivo. Repositorio Institucional de la UAM
An amine functionalized C3‐symmetric benzotrithiophene (BTT) monomer has been designed and synthetized in order to form pH responsive one‐dimensional supramolecular polymers in aqueous media. While most of the reported studies looked at the effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c1d29e1fb716eee89e0a91b55c626ff
http://hdl.handle.net/10902/22781
http://hdl.handle.net/10902/22781
Autor:
David González-Rodríguez, Fátima Aparicio, Miguel García-Iglesias, Violeta Vázquez-González, David Serrano-Molina, María José Mayoral
Publikováno v:
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
ChemPlusChem
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Universidad Autónoma de Madrid
ChemPlusChem
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
This is the peer reviewed version of the following article: ChemPlusChem 84.5 (2019): 488-492, which has been published in final form at https://doi.org/10.1002/cplu.201900207. This article may be used for non-commercial purposes in accordance with W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17aef2e3597d05bc6a1c3a1fbc0c8910
https://hdl.handle.net/10486/687525
https://hdl.handle.net/10486/687525
Autor:
José Augusto Berrocal, Miguel García-Iglesias, Martijn Kemerink, Tim D. Cornelissen, Indre Urbanaviciute, Nicolás M. Casellas, Tomás Torres
Publikováno v:
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
instname
Chemical Communications, ChemComm, 55(60), 8828-8831. Royal Society of Chemistry
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Chemical Communications, ChemComm, 55(60), 8828-8831. Royal Society of Chemistry
The combination of switchable dipolar side groups and the semiconducting core of the newly synthetized C-3-symmetric benzotrithiophene molecule (BTTTA) leads to an ordered columnar material showing continuous tunability from injection- to bulk-limite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f730512e085e9f0e93fadc650feff3a
http://hdl.handle.net/20.500.12614/1860
http://hdl.handle.net/20.500.12614/1860
Autor:
Martijn Kemerink, E. W. Meijer, Anja R. A. Palmans, Miguel García-Iglesias, Bas F. M. de Waal, Andrey V. Gorbunov
Publikováno v:
Journal of the American Chemical Society, 138(19), 6217-6223. American Chemical Society
ResearcherID
ResearcherID
A synthetic method for the end-functionalization of vinylidene fluoride oligomers (OVDF) via a radical reaction between terminal olefins and I-OVDF is described. The method shows a wide substrate scope and excellent conversions, and permits the prepa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c563c91ddf6095bf9f2948ef18b8b63c
https://doi.org/10.1021/jacs.6b01908
https://doi.org/10.1021/jacs.6b01908
Autor:
Tomás Torres, Alba Fonseca, Ana Belen Dominguez, Andrés de la Escosura, Miguel Angel Revuelta, Gonzalo Duran, Veronica Almeida, Asma Rahali, Miguel García-Iglesias, Gema de la Torre, M. Salomé Rodríguez-Morgade
Publikováno v:
ECS Meeting Abstracts. :946-946
Photodynamic therapy combines light, molecular oxygen and a PS for the production of reactive oxygen species (ROS), such as singlet oxygen (1O2) and free radicals, leading to oxidative stress and eventual cell death. Phthalocyanines (Pcs) fulfil many
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb5ebe5173da514bc9543e14a0248a8a
https://doi.org/10.1149/ma2020-0112946mtgabs
https://doi.org/10.1149/ma2020-0112946mtgabs
Publikováno v:
Chemistry : A European Journal, 21(1), 377-385. Wiley-VCH Verlag
The synthesis of C3 - and C2 -symmetric benzene-1,3,5-tricarboxamides (BTAs) containing well-defined oligodimethylsiloxane (oDMS) and/or alkyl side chains has been carried out. The influence of the bulkiness of the oDMS chains in the aggregation beha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d8b65ad1923c34761d5e2f1b21134d0
https://research.tue.nl/en/publications/f4830bfc-b923-4119-83de-b688f0e3a1bd
https://research.tue.nl/en/publications/f4830bfc-b923-4119-83de-b688f0e3a1bd
Autor:
Anja R. A. Palmans, Ghislaine Vantomme, Huub M. M. ten Eikelder, E. W. Meijer, Albert J. Markvoort, Miguel García-Iglesias, Anindita Das
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, 2017, 139(20), 7036-7044
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Journal of the American Chemical Society, 139(20), 7036-7044. American Chemical Society
Journal of the American Chemical Society, 2017, 139(20), 7036-7044
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Journal of the American Chemical Society, 139(20), 7036-7044. American Chemical Society
Supramolecular copolymers, non-covalent analogues of synthetic copolymers, constitute a new and promising class of polymers. In contrast to their covalent counterparts, the details of their mechanism of formation, as well as the factors determining t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81dca9b24b1b95b32f3a40aff7c0f8f3
https://pubmed.ncbi.nlm.nih.gov/28485145
https://pubmed.ncbi.nlm.nih.gov/28485145
Autor:
Elisa Huerta, Miguel García-Iglesias
Publikováno v:
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Journal of Porphyrins and Phthalocyanines, 21(11), 745-750. Wiley
Universidad Autónoma de Madrid
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Journal of Porphyrins and Phthalocyanines, 21(11), 745-750. Wiley
The self-assembly of α-D-glucose octafunctionalized Zn(II) phtalocyanine (ZnPc) in aqueous media has been investigated using different techniques such as UV, CD and diffusion-ordered 1H-NMR spectroscopy (DOSY). The formation of supramolecular column
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e4132556c0343495cd8985a3976074e
http://hdl.handle.net/10486/681794
http://hdl.handle.net/10486/681794
Publikováno v:
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
instname
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Biblos-e Archivo. Repositorio Institucional de la UAM
Octameric near-IR dye nanoclusters are produced by complexation of potassium cations with a phthalocyanine-guanosine conjugate. The combination of hydrogen-bonding, K+ coordination, π-π stacking and steric interactions between the chiral side group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40e4403d01de0bee988206754891883b
https://doi.org/10.1039/c6cc04152c
https://doi.org/10.1039/c6cc04152c