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Strong Chiroptical Effects in the Absorption and Emission of Macrocycles Based on the 2,5‐Diaminoterephthalate Minimal Fluorophore.
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- Chemistry - A European Journal, 2023, v. 29, n. 45, p. 1, doi. 10.1002/chem.202300932
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Cover Feature: Strong Chiroptical Effects in the Absorption and Emission of Macrocycles Based on the 2,5‐Diaminoterephthalate Minimal Fluorophore (Chem. Eur. J. 45/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 45, p. 1, doi. 10.1002/chem.202302066
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- Article
Effects of Amino Group Substitution on the Photophysical Properties and Stability of Near‐Infrared Fluorescent P‐Rhodamines.
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- Chemistry - A European Journal, 2020, v. 26, n. 35, p. 7912, doi. 10.1002/chem.202000957
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Syntheseanwendungen der oxidativen aromatischen Kupplung – von Biphenolen zu Nanographenen.
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- Angewandte Chemie, 2020, v. 132, n. 8, p. 3020, doi. 10.1002/ange.201904934
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Synthetic Applications of Oxidative Aromatic Coupling—From Biphenols to Nanographenes.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 8, p. 2998, doi. 10.1002/anie.201904934
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- Article
A Highly Photostable Near‐Infrared Labeling Agent Based on a Phospha‐rhodamine for Long‐Term and Deep Imaging.
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- Angewandte Chemie, 2018, v. 130, n. 32, p. 10294, doi. 10.1002/ange.201804731
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A Highly Photostable Near‐Infrared Labeling Agent Based on a Phospha‐rhodamine for Long‐Term and Deep Imaging.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 32, p. 10137, doi. 10.1002/anie.201804731
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- Article
Selective Conversion of P=O-Bridged Rhodamines into P=O-Rhodols: Solvatochromic Near-Infrared Fluorophores.
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- Chemistry - A European Journal, 2017, v. 23, n. 53, p. 13028, doi. 10.1002/chem.201703456
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Synthesis and optical properties of water-soluble diketopyrrolopyrroles.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 1, p. 72, doi. 10.1007/s10593-017-2023-y
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Z-Shaped Pyrrolo[3,2- b]pyrroles and Their Transformation into π-Expanded Indolo[3,2- b]indoles.
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- Chemistry - A European Journal, 2016, v. 22, n. 15, p. 5198, doi. 10.1002/chem.201505052
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Back Cover: Z-Shaped Pyrrolo[3,2- b]pyrroles and Their Transformation into π-Expanded Indolo[3,2- b]indoles (Chem. Eur. J. 15/2016).
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- Chemistry - A European Journal, 2016, v. 22, n. 15, p. 5432, doi. 10.1002/chem.201600768
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- Article
Polar Diketopyrrolopyrrole-Imidazolium Salts as Selective Probes for Staining Mitochondria in Two-Photon Fluorescence Microscopy.
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- Chemistry - A European Journal, 2015, v. 21, n. 25, p. 9101, doi. 10.1002/chem.201500738
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- Article
Back Cover: Polar Diketopyrrolopyrrole-Imidazolium Salts as Selective Probes for Staining Mitochondria in Two-Photon Fluorescence Microscopy (Chem. Eur. J. 25/2015).
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- Chemistry - A European Journal, 2015, v. 21, n. 25, p. 9264, doi. 10.1002/chem.201590111
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Diketopyrrolopyrroles: Synthesis, Reactivity, and Optical Properties.
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- Advanced Optical Materials, 2015, v. 3, n. 3, p. 280, doi. 10.1002/adom.201400559
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Two-Photon-Induced Fluorescence in New π-Expanded Diketopyrrolopyrroles.
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- Chemistry - A European Journal, 2014, v. 20, n. 39, p. 12493, doi. 10.1002/chem.201402569
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Oxidative aromatische Kupplung und Scholl-Reaktion im Vergleich.
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- Angewandte Chemie, 2013, v. 125, n. 38, p. 10084, doi. 10.1002/ange.201210238
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Comparison of Oxidative Aromatic Coupling and the Scholl Reaction.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 38, p. 9900, doi. 10.1002/anie.201210238
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- Article