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Usage

Uses

Used in Chemical Catalysis:
4,9-DibroMo-2,7-bis(2-decyltetradecyl)benzo[lMn][3,8]phenanthroline-1,3,6,8-tetraone is used as a catalyst in various chemical reactions due to its high reactivity and unique molecular structure. It can facilitate and enhance the rate of chemical reactions, making it a valuable component in the synthesis of complex organic compounds and other chemical processes.
Used in Materials Science:
In the field of materials science, 4,9-DibroMo-2,7-bis(2-decyltetradecyl)benzo[lMn][3,8]phenanthroline-1,3,6,8-tetraone is utilized for its potential to contribute to the development of new materials with specific properties. Its unique structure and reactivity can be harnessed to create materials with enhanced characteristics, such as improved thermal stability, electrical conductivity, or mechanical strength.
Used in Pharmaceutical Industry:
4,9-DibroMo-2,7-bis(2-decyltetradecyl)benzo[lMn][3,8]phenanthroline-1,3,6,8-tetraone is used as an active pharmaceutical ingredient or a key intermediate in the synthesis of various drugs. Its unique chemical properties can be leveraged to develop new therapeutic agents with novel mechanisms of action or improved pharmacokinetic profiles.
Used in Environmental Applications:
4,9-DibroMo-2,7-bis(2-decyltetradecyl)benzo[lMn][3,8]phenanthroline-1,3,6,8-tetraone can be employed in environmental remediation processes, such as the degradation of pollutants or the removal of heavy metals from contaminated sites. Its reactivity and affinity for certain substances make it a potential candidate for these applications.
Used in Nanotechnology:
In the realm of nanotechnology, 4,9-DibroMo-2,7-bis(2-decyltetradecyl)benzo[lMn][3,8]phenanthroline-1,3,6,8-tetraone is used in the design and synthesis of nanomaterials with specific properties. Its unique molecular structure can be utilized to create nanoparticles with tailored characteristics for various applications, such as drug delivery, sensing, or energy storage.

Upstream product

• 62281-07-6 2-decyl-1-tetradecylamine 
• 81-30-1 1,4,5,8-naphthalenetetracarboxylic dianhydride 
• 83204-68-6 2,6-dibromo-1,4,5,8-naphthalenetetracarboxylic acid dianhydride 

Relevant academic research and scientific papers

Conjugated polymers of rylene diimide and phenothiazine for n-channel organic field-effect transistors

A series of new n-type copolymers based on perylene diimide (PDI) or naphthalene diimide (NDI) and phenothiazine (PTZ) with different side chain length and molecular weight have been designed and synthesized by Pd-catalyzed Suzuki coupling polymerization with or without phase-transfer catalyst Aliquat 336. The effects of main chain, side chain, and molecular weight on the thermal, optical, electronic, and charge transport properties of the polymers have been investigated. Aliquat 336 improves molecular weight as well as reduces polydispersity index of the polymers. All the polymers exhibit a broad absorption extending from 300 to 900 nm. The main chain and side chain structure and molecular weight have minor effects on the HOMO (-5.8 to -5.9 eV) and LUMO (-3.7 to -3.8 eV) levels of the polymers. n-Channel field-effect transistors with bottom-gate top-contact geometry based on these copolymers exhibit electron mobilities as high as 0.05 cm2 V-1 s-1 and on/off ratios as high as 105 in nitrogen, which are among the best reported for rylene diimide-based polymers under the same test conditions.

Conjugated polymers from naphthalene bisimide

(Chemical Equation Presented) Stille coupling of regioisomerically pure dibromonaphthalene bisimides (NBI) with various stannylated thiophene-based monomers yields (very) high molecular weight donor-acceptor conjugated polymers. Electrochemical and optica

Regioirregular ambipolar naphthalenediimide-based alternating polymers: Synthesis, characterization, and application in field-effect transistors

In this work, we report the synthesis, characterization, and application of two regioirregular naphthalenediimide (NDI)-based alternating conjugated polymers, namely P1 and P2, in which nitrile-substituted moiety, 2,3-bis(thiophen-2-yl)acrylonitrile and N