Synthesis, photophysical and electrochemical properties of bay-axial perylene diimide–subphthalocyanine dyads
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Structural Modulation of the Dipolar−Octupolar Contributions to the NLO Response in Subphthalocyanines
2. Chiral Self-Discrimination in a M3L2 Subphthalocyanine Cage
3. Inclusion of C60fullerene in a M3L2subphthalocyanine cage
4. Synthesis and Nonlinear Optical, Photophysical, and Electrochemical Properties of Subphthalocyanines
5. Corrole−Fullerene Dyads: Formation of Long-Lived Charge-Separated States in Nonpolar Solvents
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1. Synthesis and Physical Properties of a Perylene Diimide-Embedded Chiral Conjugated Macrocycle;Organic Letters;2023-02-14
2. Recent advances in subphthalocyanines and related subporphyrinoids;Chemical Society Reviews;2022
3. Controlling the optical properties of boron subphthalocyanines and their analogues;Molecular Systems Design & Engineering;2021
4. Propeller-Like All-Fused Perylene Diimide Based Electron Acceptors With Chalcogen Linkage for Efficient Polymer Solar Cells;Frontiers in Chemistry;2020-04-29
5. Fluorinated boron subphthalocyanines: Lewis acid based templating chemistry facilitates random halide exchange, and fluoride versus chloride affects the basic photophysical properties and the solid-state arrangement;New Journal of Chemistry;2019
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