2018
DOI: 10.1002/slct.201801500
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Dibenzo[a, c]phenazine‐Based Donor‐Acceptor (D–A) Tetra Branched Molecules: Fine Tuning of Optical Properties

Abstract: Four dibenzo[a, c]phenazine based donor–acceptor tetra branched molecules were synthesized. The optical (including absorption, steady state and time resolved fluorescence) and electrochemical properties of these compounds were investigated. The emitting behavior of these molecules depends on the donor strength of the side‐arms. Tuning of optical properties has been performed by varying side‐arms. Electron deficient 4‐(2‐benzothiazolyl)phenyl side‐arm compound emit light in the blue region. Weak donor (4‐methox… Show more

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Cited by 7 publications
(4 citation statements)
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“…These observations can be attributed to the unique structure of DPPI with imidazole and triphenylamine groups, which are sensitive to the micro-environments changed by the addition of TEA [ 44 , 45 , 46 ]. On one hand, TEA provides active hydrogen protons that result in acid-base interactions; on the other hand, it causes the electronic distribution and energy state changes in the ILCT-structured DPPI ligand due to molecular interactions [ 47 ], and leads to the color emission variations and the TEA detecting capabilities of the Eu 3+ -complex [ 48 , 49 ].…”
Section: Resultsmentioning
confidence: 99%
“…These observations can be attributed to the unique structure of DPPI with imidazole and triphenylamine groups, which are sensitive to the micro-environments changed by the addition of TEA [ 44 , 45 , 46 ]. On one hand, TEA provides active hydrogen protons that result in acid-base interactions; on the other hand, it causes the electronic distribution and energy state changes in the ILCT-structured DPPI ligand due to molecular interactions [ 47 ], and leads to the color emission variations and the TEA detecting capabilities of the Eu 3+ -complex [ 48 , 49 ].…”
Section: Resultsmentioning
confidence: 99%
“…In recent years, phenazine-based derivatives have exhibited high light absorption capacity, superior photoelectric conversion efficiency, and excellent light stability. 30,31 Moreover, the nitrogen atom on the phenazine ring carries a lone pair of electrons, which can attract surrounding electrons through the π electron cloud on the heterocycle, giving the phenazine-based derivatives strong electron-accepting ability. They are commonly used in organic light-emitting diodes (OLEDs), 32,33 dye-sensitized solar cells (DSSCs), 34,35 electrochromic devices (ECDs), 36,37 and other fields.…”
Section: Introductionmentioning
confidence: 99%
“…Phenazine scaffold are significant group of azo-polycyclic compounds that are widely found in various natural products and synthetic dyes [20] Further, the synthesized phenazine frameworks are identified as various pharmaceutical activities such as antitumor, antiinflammatory, antimicrobial, antifungal, antimalarial, antileishmanial, antihepatitis C viral replication and also act as insecticidal activities [21] Apart from their biological activities, the several natural and synthesized phenazine derivatives are used in various material chemistry applications such as organic semiconductors, [22] dye-sensitized solar cells (DSSCs), [23] promoter for proliferation, [24] electroluminescence devices, [25] photo-sensitizers in photodynamic therapy, [26] etc.…”
Section: Introductionmentioning
confidence: 99%