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For: Polgar AM, Hudson ZM. Thermally activated delayed fluorescence materials as organic photosensitizers. Chem Commun (Camb) 2021;57:10675-88. [PMID: 34569578 DOI: 10.1039/d1cc04593h] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Cao X, Pan K, Miao J, Lv X, Huang Z, Ni F, Yin X, Wei Y, Yang C. Manipulating Exciton Dynamics toward Simultaneous High-Efficiency Narrowband Electroluminescence and Photon Upconversion by a Selenium-Incorporated Multiresonance Delayed Fluorescence Emitter. J Am Chem Soc 2022. [DOI: 10.1021/jacs.2c09543] [Reference Citation Analysis]
2 Cappello D, Buguis FL, Gilroy JB. Tuning the Properties of Donor–Acceptor and Acceptor–Donor–Acceptor Boron Difluoride Hydrazones via Extended π-Conjugation. ACS Omega. [DOI: 10.1021/acsomega.2c04401] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Zhao X, Zhao J. Long-lived charge separated state and thermally activated delayed fluorescence in anthraquinone-phenoxazine electron donor-acceptor dyads. Chem Commun (Camb) 2022. [PMID: 35726708 DOI: 10.1039/d2cc01958b] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Liang H, Liu X, Tang L, Mahmood Z, Chen Z, Chen G, Ji S, Huo Y. Heavy atom-free triplet photosensitizer based on thermally activated delayed fluorescence material for NIR-to-blue triplet-triplet annihilation upconversion. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.05.029] [Reference Citation Analysis]
5 Olesund A, Johnsson J, Edhborg F, Ghasemi S, Moth-Poulsen K, Albinsson B. Approaching the Spin-Statistical Limit in Visible-to-Ultraviolet Photon Upconversion. J Am Chem Soc 2022. [PMID: 35175751 DOI: 10.1021/jacs.1c13222] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
6 Wang X, Marom N. An energetics assessment of benzo[ a ]tetracene and benzo[ a ]pyrene as triplet–triplet annihilation emitters. Mol Syst Des Eng . [DOI: 10.1039/d2me00004k] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Polgar AM, Huang SH, Hudson ZM. Donor modification of thermally activated delayed fluorescence photosensitizers for organocatalyzed atom transfer radical polymerization. Polym Chem . [DOI: 10.1039/d2py00470d] [Reference Citation Analysis]
8 Hojo R, Mayder DM, Hudson ZM. Deep-blue emission and thermally activated delayed fluorescence via Dimroth rearrangement of tris(triazolo)triazines. J Mater Chem C. [DOI: 10.1039/d2tc01153k] [Reference Citation Analysis]
9 Cardeynaels T, Etherington MK, Paredis S, Batsanov AS, Deckers J, Stavrou K, Vanderzande D, Monkman AP, Champagne B, Maes W. Dominant dimer emission provides colour stability for red thermally activated delayed fluorescence emitter. J Mater Chem C 2022;10:5840-8. [DOI: 10.1039/d1tc04913e] [Reference Citation Analysis]