Dihydroazulene‐Boron Subphthalocyanine Conjugates with Oligo(phenyleneethynylene) Bridging Unit: Photoswitchable Fluorophores

Autor: Esmeralda Bukuroshi, Anne Ugleholdt Petersen, Cecilie Jensen, Mathias Kirkholt Lund, Martin Kühnel, Kasper Nørgaard, Timothy P. Bender, Mogens Brøndsted Nielsen

Publikováno v: Bukuroshi, E, Ugleholdt Petersen, A, Jensen, C, Kirkholt Lund, M, Kühnel, M, Nørgaard, K, Bender, T P & Brøndsted Nielsen, M 2023, ' Dihydroazulene-Boron Subphthalocyanine Conjugates with Oligo(phenyleneethynylene) Bridging Unit : Photoswitchable Fluorophores ', European Journal of Organic Chemistry, vol. 26, no. 24, e202300284 . https://doi.org/10.1002/ejoc.202300284

In this work, we have linked the dihydroazulene (DHA)/vinylheptafulvene (VHF) photo-/thermoswitch and the boron subphthalocyanine (BsubPc) fluorophore via an axial oligo(phenyleneethynylene) bridging unit into new DHA-BsubPc conjugates. The objective

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::587da4fbc912b7a2c0c9292fcffc1ed8
https://doi.org/10.1002/ejoc.202300284

Molecular engineering of α and β peripherally tri-halogenated substituted boron subphthalocyanines as mixed alloys to control physical and electrochemical properties for organic photovoltaic applications

Autor: Esmeralda Bukuroshi, Timothy P. Bender, Zheng-Hong Lu, Devon Holst, Thanmayee Mudigonda, Kyle Nova, Antoine Dumont, Siena Wong

Publikováno v: Molecular Systems Design & Engineering. 6:308-326

The chirality feature of C1 and C3 boron subphthalocyanines (BsubPcs) is an attractive property in material science and supramolecular chemistry. Normally in the field, enantiomeric mixtures are separated through a standard process. The goal of this

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6c91a3be681a14120de9f9a91a5e3a20
https://doi.org/10.1039/d0me00175a

Axial/Peripheral Chloride/Fluoride-Substituted Boron Subphthalocyanines as Electron Acceptors

Autor: Amir Mizrahi, Zeev Gross, Jenya Vestfrid, Timothy P. Bender, Esmeralda Bukuroshi

Publikováno v: Inorganic Chemistry. 59:2641-2645

Chloroboron subphthalocyanines (Cl-BsubPc) are robust compounds that can be readily modified at the axial and peripheral positions. Peripherally chlorinated derivatives were recently found to be advantageous regarding integration into organic electro

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https://doi.org/10.1021/acs.inorgchem.9b03529

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

Autor: Esmeralda Bukuroshi, Timothy P. Bender, Zeev Gross, Jenya Vestfrid

Publikováno v: New Journal of Chemistry. 43:16730-16737

A sub-group of the phthalocyanine family, the boron subphthalocyanines (BsubPcs), have robust chemistry and can be readily modified at the axial and peripheral positions to tune their physical properties. Our laboratory recently discovered that perip

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https://doi.org/10.1039/c9nj04093e

Correction to 'A Comprehensive Scope of Peripheral and Axial Substituent Effect on the Spectroelectrochemistry of Boron Subphthalocyanines'

Autor: Hasan Raboui, Kathleen L. Sampson, Karl M. Kadish, Xiaoqin Jiang, Timothy P. Bender, Aleksa Dovijarski, Esmeralda Bukuroshi

Publikováno v: The journal of physical chemistry. A. 122(38)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ff9b13bec4f13432717b5bfea549aad
https://pubmed.ncbi.nlm.nih.gov/29672045