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Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and AlkynesWe thank the National Institute of General Medical Sciences, the National Institutes of Health (GM 28284), the National Science Foundation (CHE-9985553), the W. M. Keck Foundation, the Skaggs Institute for Chemical Biology, the MRSEC Program of the National Science Foundation (award no. DMR-0213618 for the Center for Polymeric Interfaces and Macromolecular Assemblies), the NIRT Program of the National Science Foundation (grant no. 0210247), IBM Corporation, DOE-BES, and NSF International/DAAD for financial support. We are also grateful to Prof. M. G. Finn for helpful discussions.
- Published in:
- Angewandte Chemie, 2004, v. 116, n. 30, p. 4018, doi. 10.1002/ange.200454078
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Titelbild: Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and Alkynes (Angew. Chem. 30/2004).
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- Angewandte Chemie, 2004, v. 116, n. 30, p. 3951, doi. 10.1002/ange.200490100
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Round-Robin Studies as a Method for Testing and Validating High-Efficiency ITO-Free Polymer Solar Cells Based on Roll-to-Roll-Coated Highly Conductive and Transparent Flexible Substrates.
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- Advanced Energy Materials, 2012, v. 2, n. 9, p. 1091, doi. 10.1002/aenm.201200079
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Novel Hyperbranched Poly([1,2,3]-triazole)s Derived from AB2 Monomers by a 1,3‐Dipolar Cycloaddition.
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- Macromolecular Rapid Communications, 2004, v. 25, n. 12, p. 1175, doi. 10.1002/marc.200400097
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Round-Robin Studies on Roll-Processed ITO-free Organic Tandem Solar Cells Combined with Inter-Laboratory Stability Studies.
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- Energy Technology, 2015, v. 3, n. 4, p. 423, doi. 10.1002/ente.201402095
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Improved Light Utilization Efficiency for an ITO‐Free Semitransparent Organic Solar Cell Using a Multilayer Silver Back Electrode as Infrared Mirror.
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- Solar RRL, 2023, v. 7, n. 21, p. 1, doi. 10.1002/solr.202300561
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Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and AlkynesWe thank the National Institute of General Medical Sciences, the National Institutes of Health (GM 28284), the National Science Foundation (CHE-9985553), the W. M. Keck Foundation, the Skaggs Institute for Chemical Biology, the MRSEC Program of the National Science Foundation (award no. DMR-0213618 for the Center for Polymeric Interfaces and Macromolecular Assemblies), the NIRT Program of the National Science Foundation (grant no. 0210247), IBM Corporation, DOE-BES, and NSF International/DAAD for financial support. We are also grateful to Prof. M. G. Finn for helpful discussions.
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- Angewandte Chemie International Edition, 2004, v. 43, n. 30, p. 3928, doi. 10.1002/anie.200454078
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- Publication type:
- Article
Cover Picture: Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and Alkynes (Angew. Chem. Int. Ed. 30/2004).
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- Angewandte Chemie International Edition, 2004, v. 43, n. 30, p. 3863, doi. 10.1002/anie.200490100
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- Article
Cycloaddition Reactions and Dendritic Polymer Architectures - A Perfect Match.
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- Macromolecular Symposia, 2007, v. 254, n. 1, p. 16, doi. 10.1002/masy.200750803
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Hyperbranched thermolabile polycarbonates derived from a A<sub>2</sub>+B<sub>3</sub> monomer system.
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- Macromolecular Symposia, 2004, v. 210, n. 1, p. 101, doi. 10.1002/masy.200450612
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