1159905-88-0

Usage

Uses

Used in Organic Chemistry:
4,7-dibroMo-2-dodecylisoindoline-1,3-dione is utilized as a precursor for the synthesis of various organic compounds, playing a crucial role in the creation of new chemical entities with specific properties.
Used in Pharmaceutical Production:
4,7-dibroMo-2-dodecylisoindoline-1,3-dione is employed in the production of pharmaceuticals due to its potential to contribute to the development of new drugs, leveraging its unique structure and chemical reactivity.
Used in Agrochemical Production:
4,7-dibroMo-2-dodecylisoindoline-1,3-dione is also used in the manufacturing of agrochemicals, where its chemical properties can be harnessed to create effective products for agricultural applications.
Used in Medicinal Chemistry Research:
As a potential candidate for research in medicinal chemistry, 4,7-dibroMo-2-dodecylisoindoline-1,3-dione is explored for its possible biological activities, which may lead to the discovery of new therapeutic agents.
Used in Drug Discovery:
4,7-dibroMo-2-dodecylisoindoline-1,3-dione is valuable in drug discovery processes, where its unique structural features are investigated for potential interactions with biological targets, contributing to the advancement of novel pharmaceuticals.
It is important to handle 4,7-dibroMo-2-dodecylisoindoline-1,3-dione with care and follow safety regulations, given its potential health hazards.

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Relevant academic research and scientific papers

Multifunctional materials for OFETs, LEFETs and NIR PLEDs

A family of phthalimide-thiophene copolymers with linear and branched alkyl chains attached to the imide nitrogen have been synthesized. Their optical and electronic properties were investigated along with their applications in OFETs and LEFETs. The phthalimide-thiophene copolymer having a C16 straight alkyl chain on the phthalimide yielded the highest mobilities and PLQE with mobilities of 1 × 10-3 cm2 V-1 s -1 for holes and 1 × 10-2 cm2 V -1 s-1 for electrons with a PLQE of ～28% in the solid state. Since these polymers are ambipolar and emissive, they have proven to be useful for applications as a host material for NIR PLEDs. In this study a 1% loading of NIR emitting DAD segments based on bisthienyl(thiadiazoloquinoxaline) or bisthienyl(benzotriazolothiadiazole) were incorporated into the phthalimide-thiophene polymerization. Using the branched CH(C8H 17)2 alkyl chain on the host phthalimide-thiophene copolymer combined with the bisthienyl(benzotriazolothiadiazole) emitter resulted in the most efficient (emission maximum ≥ 850 nm) single layer NIR-emitting PLED to date with an EQE of 0.27% emitting at 885 nm.

Optimal ambipolar charge transport of thienylenevinylene-based polymer semiconductors by changes in conformation for high-performance organic thin film transistors and inverters

We report the synthesis and characterization of thienylenevinylene-based donor-acceptor alternating copolymers (PTVPhI-Eh and PTVPhI-C12) as highly efficient ambipolar semiconductors in a thin film transistor. These polymers exhibit significantly improved hole and electron mobilities after thermal annealing. To determine the relationship between ambipolar charge transport and thermal annealing, we investigated these polymers using various analyses such as optical spectroscopy, Raman spectroscopy, computational quantum chemical calculation, X-ray diffraction, atomic force microscopy, and ambipolar charge mobility measurements. In pristine films, the polymer chains exhibited weak intra- and interchain ordering. However, when samples were annealed at sufficiently high temperatures, they exhibited a more ordered intra- and interchain conformation. As a result, we found a strong relationship between intra- and interchain conformational changes of the polymers and corresponding ambipolar charge transport properties during thermal annealing processes. Finally, we demonstrate complementary-like ambipolar inverters using a PTVPhI-Eh polymer. The largely shifted inverting voltage was improved for the thermally annealed inverters, which exhibited large voltage gains (～40).