CAS:76275-14-4 | 9,10-Dibutoxyanthracene

Introduction of CAS:76275-14-4 | 9,10-Dibutoxyanthracene

9,10-Dibutoxyanthracene is a photosensitizer for UV cationic polymerization . It has a unique absorption zone of long UV wavelengths over 400 nm . It is commonly used as an electron transfer sensitizer for photopolymerization due to its favorable optical properties .

Anthracene, the base molecule of 9,10-Dibutoxyanthracene, consists of a conjugated skeleton that absorbs UV light at wavelengths of ≥300 nm . The properties of 9,10-disubstituted anthracenes differ greatly depending on the substituents present.

9,10-Dibutoxyanthracene has a unique absorption zone of long UV wavelengths over 400 nm . It is used to increase the reactivity of epoxides, which are important additives in coatings and adhesives.

Specification of CAS:76275-14-4 | 9,10-Dibutoxyanthracene

Research Application of CAS:76275-14-4 | 9,10-Dibutoxyanthracene

Photodegradation and Oxygen Scavenging

9,10-Dibutoxyanthracene demonstrates significant potential in the field of photopolymerization, acting as an electron transfer sensitizer due to its favorable optical properties. Research has revealed its ability to produce endoperoxide species in the presence of oxygen, which subsequently decomposes to form secondary products. This indicates its utility as a photo-induced oxygen scavenger, highlighting its role in singlet oxygen scavenging applications and suggesting its potential in developing photoresponsive materials (Seto et al., 2022).

Fluorescent pH Sensors and Biological Probes

Anthracene derivatives, including those related to 9,10-Dibutoxyanthracene, have been synthesized to exhibit aggregation-induced emission (AIE) characteristics. These compounds are nonluminescent in dilute solutions but display efficient fluorescence upon molecular aggregation. Such properties make them suitable for applications as pH sensors and biological probes, capable of interacting with proteins or DNA to amplify emission, which could be particularly useful in medical diagnostics and research (Lu et al., 2010).

Supramolecular Assembly and Fluorescence Emission

The integration of 9,10-Distyrylanthracene derivatives into supramolecular structures, such as bridging bis(pillar[5]arene)s, has been explored. This assembly induces yellow fluorescence emission in both solution and solid states, pointing towards its potential in developing new fluorescent materials for sensing and imaging applications (Song et al., 2015).

Organic Light-Emitting Diodes (OLEDs)

Research into electroluminescent 9,10-diaryl anthracenes has underscored their promise as host and hole-transporting materials for OLED applications, particularly blue OLEDs. Their high thermal stability, electrochemical reversibility, and wide band gap are beneficial for the development of efficient OLEDs. This includes studies on the rearrangement of cyclotriveratrylene (CTV) diketone to 9,10-diaryl anthracenes, enhancing their functionality for electronic applications (Sarsah et al., 2013).

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