CAS:312924-93-9 | 3,7-Dibromo-10-hexylphenothiazine

Introduction of CAS:312924-93-9 | 3,7-Dibromo-10-hexylphenothiazine

3, 7-dibromo-10-hexyl phenothiazine is an organic compound with the formula C14H18Br2S. Its structure contains a phenothiazine ring and is replaced by bromine atoms at position 3 and 7 of the phenothiazine ring, while a hexyl (C6H13-) group is attached at position 10.
This compound may have some potential applications in the field of organic synthesis and materials science:

Materials science: Due to its inclusion of phenothiazine rings and hexyl groups, this compound may be used in the field of materials science, for example as a fluorescent marker, a precursor to organic semiconductor materials, or a component of liquid crystal materials.

Specification of CAS:312924-93-9 | 3,7-Dibromo-10-hexylphenothiazine

Research Application of CAS:312924-93-9 | 3,7-Dibromo-10-hexylphenothiazine

Synthesis and Electronic Properties

3,7-Diaminophenothiazine derivatives, including 3,7-dibromo-10-hexylphenothiazine, are synthesized via Buchwald-Hartwig coupling and display remarkable semiquinone formation constants and two reversible oxidations at low potentials. Their electronic structure is explored through DFT computations, demonstrating their potential in electronic applications (Pereteanu & Müller, 2013).

Photophysical and Electrochemical Properties

Phenothiazine derivatives, including 3,7-dibromo-10-hexylphenothiazine, are used to create novel conjugated donor-acceptor molecules with enhanced charge transfer characteristics. These molecules are valuable in organic light-emitting diode (OLED) applications due to their ability to fine-tune LUMO energy levels without significantly affecting HOMO energy levels (Zhang et al., 2007).

Photovoltaic Properties

Conjugated copolymers derived from phenothiazines, including 3,7-dibromo-10-hexylphenothiazine, exhibit promising photovoltaic properties. These polymers show good thermal stability and efficient blue-green light emission, suitable for polymer solar cell applications (Tang et al., 2007).

Bromination Mechanism Studies

Studies on the bromination of 10-substituted phenothiazines, such as 3,7-dibromo-10-hexylphenothiazine, provide insights into electrophilic aromatic substitution mechanisms. These studies are crucial for understanding the chemical behavior and potential applications of these compounds in various fields (Chiou et al., 1976).

Conjugated Polymers and Semiconductors

Phenothiazine-based conjugated polymers show potential as hole transport materials in electronic devices due to their favorable ionization potentials and greenish-blue photoluminescence. This makes them good candidates for applications in electroluminescent and other semiconductor devices (Kong et al., 2003).

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