Orthogonally arranged tripyrrin–BODIPY conjugates with an “edge to plane” mode
文献信息
Chun-Liang Hou, Yuhang Yao, Da Wang, Jing Zhang, Jun-Long Zhang
We designed new molecular conjugates, consisting of two strong fluorophores, tripyrrin and BODIPY moieties. Crystal structures demonstrated that the BODIPY is nearly perpendicular to the tripyrrin plane, directly linked in an orthogonal geometry, in a new “edge to plane” mode with covalently bonded chromophore peripheries. Furthermore, substitutions on BODIPY can modulate the photophysical properties, which can be explained by energy transfer via a FRET mechanism. This not only enriches the repertoire of multichromophoric system but also expands the scope of tripyrrin for constructing molecular functional materials.
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NDT & E International

Main Group Chemistry

Topics in Catalysis

Journal of Asian Natural Products Research

Journal of the Indian Institute of Science

Herald of the Russian Academy of Sciences

Chinese Journal of Chemistry

Critical Reviews in Solid State and Materials Sciences

Bioorganic & Medicinal Chemistry Letters

Polycyclic Aromatic Compounds
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Organic Chemistry Frontiers

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry



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