Four new blue light-emitting materials based on benzo[1,2-d:4,5-d′]bisoxazole (BBO) have been synthesized, characterized, and fabricated into organic light-emitting diode (OLED) devices. Using a combination of theoretical and experimental methods, we investigated the effect of conjugation by comparing bulky alkyl groups and planar aromatic groups along the 2,6-axis. Two of these molecules, PB2Cz and PB3Cz, are cross-conjugated cruciform-type BBOs with phenyl and carbazole groups along the 2,6 and 4,8 axes, respectively. The other two molecules, AB2Cz and AB3Cz, have extended conjugation via the carbazole groups along the 4,8-axis and bulky adamantyl groups along the 2,6-axis. Concurrently, we explored the effect of regioisomerism on optoelectronic and device properties arising from attaching carbazole at the 2- (2Cz) or 3- (3Cz) position along the 4,8-axis. The materials’ geometric and electronic properties were predicted using time-dependent density functional theory (TD-DFT) calculations at the mPW3PBE/SV level. The molecules’ photoluminescent properties were measured in solution and film states. The BBO molecules were used as dopants in mixed host/guest OLED devices, producing teal to deep blue emission. Specifically, the AB2Cz and AB3Cz, with adamantyl on the 2,6-axis, exhibit blue to deep-blue emissions of 414–422 nm (CIEx < 0.20, CIEy < 0.10). In comparison, PB2Cz and PB3Cz have slightly longer emission wavelengths of 472–476 nm (CIEx < 0.16, CIEy < 0.28) and high brightness of 2700–3500 cdm–2. The BBOs with 2Cz resulted in more efficient devices with EQEs of ∼2.8–3.2%, while the 3Cz BBOs had EQEs of ∼1.1–1.5%. This work provides insight into designing efficient, purely organic blue-fluorescent OLED materials based on the BBO moiety. 
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                            A computational and experimental investigation of deep-blue light-emitting tetraaryl-benzobis[1,2- d :4,5- d ′]oxazoles
                        
                    
    
            In an effort to design deep-blue light emitting materials for use in OLEDs, the optical and electronic properties of a series of tetraarylbenzobis[1,2- d :4,5- d ′]oxazole (BBO) cruciforms were evaluated using density functional theory (DFT) and time-dependent DFT (TD-DFT). Of the nine possible combinations of phenyl-, furan-2-yl-, and thiophen-2-yl-substituted BBO cruciforms, five were predicted to have ideal optical and electronic properties for use in blue-light emitting diodes. These five cruciforms were synthesized and then characterized electrochemically and spectroscopically. Additionally, they were solution-processed into functional organic light-emitting diodes (OLED). Several of the OLEDs exhibited deep-blue EL ( λ EL < 452 nm; CIE y ≤ 0.12) with maximum luminance efficacies reaching 0.39 lm W −1 and maximum current efficiencies of 0.59 cd A −1 . A comparison of identical device architectures showed that heterocycles such as furan and thiophene helped improve device efficiencies with only a minor red-shift of the electroluminescence (EL). Although these BBO cruciforms produced the desired deep-blue emission their modest performance in host–guest OLEDs demonstrates the incorporation of heterocycles onto the BBO cruciform motif is detrimental to the fluroescence quantum yield. These results add to the knowledge base on structure–property relationships that will inform the design of better blue emitting materials. 
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                            - PAR ID:
- 10358294
- Date Published:
- Journal Name:
- Materials Advances
- Volume:
- 3
- Issue:
- 9
- ISSN:
- 2633-5409
- Page Range / eLocation ID:
- 3842 to 3852
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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