Colorantes orgánicos para materiales fotónicos
COLORGANIC
Universidad Autónoma de Madrid
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Universidad Autónoma de Madrid (29)
2022
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Halogen-free photosensitizers based on meso-enamine-BODIPYs for bioimaging and photodynamic therapy
Journal of Materials Chemistry B, Vol. 11, Núm. 1, pp. 169-179
2021
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Mitochondria selective trackers for long-term imaging based on readily accessible neutral BODIPYs
Chemical Communications, Vol. 57, Núm. 43, pp. 5318-5321
2020
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BODIPYs revealing lipid droplets as valuable targets for photodynamic theragnosis
Chemical Communications, Vol. 56, Núm. 6, pp. 940-943
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Exploring BODIPY Derivatives as Singlet Oxygen Photosensitizers for PDT
Photochemistry and Photobiology, Vol. 96, Núm. 3, pp. 458-477
2019
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Tailoring the Molecular Skeleton of Aza-BODIPYs to Design Photostable Red-Light-Emitting Laser Dyes
ChemPhotoChem, Vol. 3, Núm. 2, pp. 75-85
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Tailoring the Molecular Skeleton of Aza-BODIPYs to Design Photostable Red-Light-Emitting Laser Dyes
ChemPhotoChem
2017
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A versatile fluorescent molecular probe endowed with singlet oxygen generation under white-light photosensitization
Dyes and Pigments, Vol. 142, pp. 77-87
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AcetylacetonateBODIPY-Biscyclometalated Iridium(III) Complexes: Effective Strategy towards Smarter Fluorescent Photosensitizer Agents
Chemistry - A European Journal, Vol. 23, Núm. 42, pp. 10139-10147
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Rational Design of Advanced Photosensitizers Based on Orthogonal BODIPY Dimers to Finely Modulate Singlet Oxygen Generation
Chemistry - A European Journal, Vol. 23, Núm. 20, pp. 4837-4848
2014
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Circularly polarized luminescence by visible-light absorption in a chiral o-bodipy dye: Unprecedented design of cpl organic molecules from achiral chromophores
Journal of the American Chemical Society, Vol. 136, Núm. 9, pp. 3346-3349
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Increased laser action in commercial dyes from fluorination regardless of their skeleton
Laser Physics Letters, Vol. 11, Núm. 11
2010
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The role of the C(2) configuration and methyl substitution on the catalytic activity of novel 2,3,3- and 2,7,7-trimethyl-substituted γ- aminonorbornan-2-ols
Chirality, Vol. 22, Núm. 8, pp. 778-787
2007
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First efficient synthesis of enantiopure homoketopinic acid
Letters in Organic Chemistry, Vol. 4, Núm. 2, pp. 123-125
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Surprising obtention of an enantiopure eight-membered cyclic ether from camphor
Tetrahedron Letters, Vol. 48, Núm. 30, pp. 5185-5188
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The role of conformational flexibility on the catalytic activity of norbornane-derived β-, γ- and δ-amino alcohols
Tetrahedron Asymmetry, Vol. 18, Núm. 6, pp. 742-749
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Unexpected reactivity of 1-amine-2-methylenenorbornane hydrochlorides with m-CPBA
Tetrahedron Letters, Vol. 48, Núm. 34, pp. 5981-5983
2006
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A novel modification of the Ritter reaction: stereoselective synthesis of bridgehead-fused Δ2-norbornanethiazolines from thiocamphor and thiofenchone
Tetrahedron Asymmetry, Vol. 17, Núm. 21, pp. 2970-2975
2005
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A new type of anomalous ozonolysis in strained allylic bicycloalkan-1-ols
Tetrahedron Letters, Vol. 46, Núm. 31, pp. 5157-5159
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Palladium(II)-catalyzed ring expansion of a 1-alkenyl cyclopentanol
Tetrahedron Letters, Vol. 46, Núm. 20, pp. 3509-3511
2004
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A short and convenient procedure for the stereoselective synthesis of 2-hydroxy-1-norbornanesulfonamides
Tetrahedron Asymmetry, Vol. 15, Núm. 2, pp. 293-298