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Donor–Donor′–Acceptor Triads Based on [3.3]Paracyclophane with a 1,4‐Dithiafulvene Donor and a Cyanomethylene Acceptor: Synthesis, Structure, and Electrochemical and Photophysical Properties.
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- Chemistry - A European Journal, 2018, v. 24, n. 44, p. 11407, doi. 10.1002/chem.201801774
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- Article
Macrocyclic Oligothiophene with Stereogenic [2.2]Paracyclophane Scaffolds: Chiroptical Properties from π-Transannular Interactions.
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- Chemistry - A European Journal, 2017, v. 23, n. 14, p. 3267, doi. 10.1002/chem.201605842
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- Article
Dimeric Tetrathiafulvalene Linked to pseudo-ortho-[2.2]Paracyclophane: Chiral Electrochromic Properties and Use as a Chiral Dopant.
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- Chemistry - An Asian Journal, 2014, v. 9, n. 10, p. 2751, doi. 10.1002/asia.201402667
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- Article
Photoinduced Color Change and Photomechanical Effect of Naphthalene Diimides Bearing Alkylamine Moieties in the Solid State.
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- Chemistry - A European Journal, 2014, v. 20, n. 24, p. 7309, doi. 10.1002/chem.201304849
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Cyclophanes within Cyclophanes: The Synthesis of a Pyromellitic Diimide-Based Macrocycle as a Structural Unit in a Molecular Tube and Its Inclusion PhenomenaMolecular Tubes and Capsules, Part 1. We gratefully acknowledge the financial support by a Theme Project of Molecular Architecture of Organic Compounds for Functional Design (Prof. Tahsin J. Chow) from the Institute of Chemistry, Academia Sinica, Taiwan R.O.C. We are also grateful for partial financial support by the Joint Project of Chemical Synthesis Core Research Institutions, Research and Education for Inter-University Research Project, MEXT, Japan.
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- Angewandte Chemie, 2006, v. 118, n. 22, p. 3725, doi. 10.1002/ange.200504499
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Cyclophanes within Cyclophanes: The Synthesis of a Pyromellitic Diimide-Based Macrocycle as a Structural Unit in a Molecular Tube and Its Inclusion PhenomenaMolecular Tubes and Capsules, Part 1. We gratefully acknowledge the financial support by a Theme Project of Molecular Architecture of Organic Compounds for Functional Design (Prof. Tahsin J. Chow) from the Institute of Chemistry, Academia Sinica, Taiwan R.O.C. We are also grateful for partial financial support by the Joint Project of Chemical Synthesis Core Research Institutions, Research and Education for Inter-University Research Project, MEXT, Japan.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 22, p. 3643, doi. 10.1002/anie.200504499
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- Article