Nauroozi, Djawed’s team published research in Organometallics in 2019 | CAS: 589-87-7

1-Bromo-4-iodobenzene(cas: 589-87-7) has been employed as reagent for in situ desilylation and coupling of silylated alkynes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids), as substrate in copper-free Sonogashira coupling in aqueous acetone in synthesis of β,β,dibromostyrenesRecommanded Product: 1-Bromo-4-iodobenzene

The author of 《Diethynyldiazafluoren-9-ylidene as a π Cross-Conjugated Platform for Redox Active Transition Metal Fragments》 were Nauroozi, Djawed; Bruhn, Clemens; Faust, Ruediger. And the article was published in Organometallics in 2019. Recommanded Product: 1-Bromo-4-iodobenzene The author mentioned the following in the article:

Synthetic routes were developed to attach three redox-active metal fragments to cross-conjugated 3-methylidenepentadiyne covalently expanded by diazafluorenylidene: The two alkyne termini of this new ligand were end-capped via a phenylene spacer with ethynyl ferrocene, and a [Ru(bpy)2]2+ fragment was coordinated in the diimine binding site. The photophys. and electrochem. properties of both the diferrocenyl-terminated ligand and its corresponding Ru-complex were investigated by UV-vis absorption spectroscopy and cyclic voltammetry. The absorption data reveal significant interactions of the metal centers with the cross-conjugated ligand system. In the electrochem. experiments the ferrocenyl and the ruthenium centers could be addressed individually as they are separated by almost 1 V. While the presence of the Ru-fragment manifests itself in the reduction potential of the diazafluorenylidene-ligand, communication between the ferrocenyl end-caps on one hand and between the ferrocenes and the Ru-fragment on the other appears to be reduced through the freely rotating phenylene spacers. The results came from multiple reactions, including the reaction of 1-Bromo-4-iodobenzene(cas: 589-87-7Recommanded Product: 1-Bromo-4-iodobenzene)

1-Bromo-4-iodobenzene(cas: 589-87-7) has been employed as reagent for in situ desilylation and coupling of silylated alkynes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids), as substrate in copper-free Sonogashira coupling in aqueous acetone in synthesis of β,β,dibromostyrenesRecommanded Product: 1-Bromo-4-iodobenzene

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Patel, Ashok Raj’s team published research in ChemistrySelect in 2019 | CAS: 589-87-7

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Electric Literature of C6H4BrI It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

The author of 《Synthesis of Rice Husk Derived Activated Mesoporous Carbon Immobilized Palladium Hybrid Nano-Catalyst for Ligand-Free Mizoroki-Heck/Suzuki/Sonogashira Cross-Coupling Reactions》 were Patel, Ashok Raj; Asatkar, Archana; Patel, Geetika; Banerjee, Subhash. And the article was published in ChemistrySelect in 2019. Electric Literature of C6H4BrI The author mentioned the following in the article:

Chem. activated graphitic mesoporous carbon was synthesized from rice husk biomass and subsequently immobilized with palladium nanoparticles (Pd NPs). The physiochem. characteristics like composition, morphol., structure and textural properties of the rice husk derived activated carbon supported Pd NPs (nano-Pd@RAGC) were analyzed by various anal. and spectroscopic techniques. Finally, the applications of hybrid nano-Pd@RAGC material were investigated in useful carbon-carbon bond forming reactions via Mizoroki-Heck/Suzuki/Sonogashira cross-coupling reactions under ligand-free, microwave conditions. The RAGC provided excellent stability to Pd NPs in cross coupling reactions. The catalyst was recovered simply by filtration and recycled for at least ten times.1-Bromo-4-iodobenzene(cas: 589-87-7Electric Literature of C6H4BrI) was used in this study.

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Electric Literature of C6H4BrI It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Hosseinzadeh, Rahman’s team published research in Polyhedron in 2022 | CAS: 589-87-7

1-Bromo-4-iodobenzene(cas: 589-87-7) has been employed as reagent for in situ desilylation and coupling of silylated alkynes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids), as substrate in copper-free Sonogashira coupling in aqueous acetone in synthesis of β,β,dibromostyrenesHPLC of Formula: 589-87-7

In 2022,Hosseinzadeh, Rahman; Aghili, Nora; Mavvaji, Mohammad published an article in Polyhedron. The title of the article was 《Synthesis and characterization of nano-cellulose immobilized phenanthroline-copper (I) complex as a recyclable and efficient catalyst for preparation of diaryl ethers, N-aryl amides and N-aryl heterocycles》.HPLC of Formula: 589-87-7 The author mentioned the following in the article:

Functionalized nanocellulose was prepared and employed for immobilization of phenanthroline-copper(I) complex to afford cellulose nanofibril grafted heterogeneous copper catalyst [CNF-phen-Cu(I)]. The activities of the synthesized catalyst were examined in the synthesis of diaryl ethers RC6H4OR1 (R = H, 4-Me, 4-Br, 4-NO2, etc.; R1 = Ph, 4-methylphenyl, 2-naphthyl, etc.) via C-O cross-coupling of phenols R1OH and aryl iodides RC6H4X (X = I, Br), as well as, the preparation of N-aryl amides/N-aryl heterocycles R2C6H4R3 (R2 = Ph, 1-naphthyl, 4-bromophenyl, etc.; R3 = benzoylamino, acetylamino, 1H-indol-1-yl, etc.) through C-N cross-coupling of amides/N-H heterocyclic compounds R3H with aryl halides R2C6H4X (X = I, Br). In this trend, various substrates containing electron-donating and electron-withdrawing groups were exploited to evaluate the generality of this catalytic protocol. Accordingly, the catalyst demonstrated remarkable catalytic efficiency for both C-N and C-O cross-coupling reactions, thereby resulting in good to excellent yields of the desired products. Furthermore, the recoverability experiments of the catalyst showed that it can be readily retrieved by simple filtration and successfully reused several times with negligible loss of its catalytic activity. In the experiment, the researchers used 1-Bromo-4-iodobenzene(cas: 589-87-7HPLC of Formula: 589-87-7)

1-Bromo-4-iodobenzene(cas: 589-87-7) has been employed as reagent for in situ desilylation and coupling of silylated alkynes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids), as substrate in copper-free Sonogashira coupling in aqueous acetone in synthesis of β,β,dibromostyrenesHPLC of Formula: 589-87-7

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Huang, Jiahe’s team published research in Organic Electronics in 2020 | CAS: 589-87-7

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Name: 1-Bromo-4-iodobenzene It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

Name: 1-Bromo-4-iodobenzeneIn 2020 ,《Nonvolatile bistable memory device based on polyfluorene with Ag NPs doping materials》 was published in Organic Electronics. The article was written by Huang, Jiahe; Zhang, Hongyan; Zhao, Xiaofeng; Bai, Ju; Hou, Yanjun; Wang, Shuhong; Wang, Cheng; Ma, Dongge. The article contains the following contents:

Organic elec. memory devices have broad application prospects. In the present paper, a new kind of polyfluorene-based material containing methoxytriphenylamine groups was synthesized, which exhibited good Flash-type storage characteristics. The material was further doped with Ag NPs to improve storage performance. With appropriate amount of Ag NPs, the device presented an ON/OFF current ratio up to 1.1 × 104 with excellent stability. In addition, the switching characteristics of the device were discussed through data fitting and MO calculation In the experiment, the researchers used many compounds, for example, 1-Bromo-4-iodobenzene(cas: 589-87-7Name: 1-Bromo-4-iodobenzene)

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Name: 1-Bromo-4-iodobenzene It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Pei, Xiaoyan’s team published research in Journal of Catalysis in 2021 | CAS: 589-87-7

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Application In Synthesis of 1-Bromo-4-iodobenzene It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

Pei, Xiaoyan; Xiang, Deng; Luo, Zhengxiu; Lei, Fukun; Guo, Zhanglong; Liu, Dong; Zhao, Zhigang; Ran, Maofei; Dai, Tao published an article in 2021. The article was titled 《Catalytic performance of palladium nanoparticles encapsulated within nitrogen-doped carbon during Heck reaction》, and you may find the article in Journal of Catalysis.Application In Synthesis of 1-Bromo-4-iodobenzene The information in the text is summarized as follows:

The Confinement effect is an effective strategy for enhancing the performance of catalysts during various reactions. We developed a strategy to encapsulating Palladium nanoparticles with a dopamine-derived N-doped multilayer carbon shell to catalyze the Heck reaction between iodobenzene and carbon-carbon double-bond compounds (styrene and Me acrylate). The catalytic performances of Pd nanoparticles encapsulated within a N-doped carbon layer (Pd@N-C) and those attached to the external surface of such a layer (Pd/N-C) were evaluated and compared. Pd@N-C exhibited a lower reaction activation energy (78 kJ/mol) than that of Pd/N-C (106 kJ/mol). Thus, the activity of Pd@N-C during the Heck reaction between iodobenzene and Me acrylate was approx. 20 times higher than that of Pd/N-C-200. The results of thermal filtration and recycling tests indicated that Pd@N-C showed a lower degree of leaching than that of Pd/N-C-200 owing to the spatial restriction effect of the cavity in the case of the former. Hence, the superior catalytic performance of Pd@N-C can be ascribed to the confinement of the Pd nanoparticles within the N-doped carbon layer. Finally, we useCinnamatesd these catalysts to synthesize a range of para-substituted iodobenzene derivatives, thus demonstrating the potential of Pd-encapsulating catalysts for use in the Heck reaction on the tech. scale. The experimental part of the paper was very detailed, including the reaction process of 1-Bromo-4-iodobenzene(cas: 589-87-7Application In Synthesis of 1-Bromo-4-iodobenzene)

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Application In Synthesis of 1-Bromo-4-iodobenzene It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Xu, Chen’s team published research in Science China: Chemistry in 2022 | CAS: 589-87-7

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Reference of 1-Bromo-4-iodobenzene It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

In 2022,Xu, Chen; Yin, Chenjia; Wu, Wenjun; Ma, Xiang published an article in Science China: Chemistry. The title of the article was 《Tunable room-temperature phosphorescence and circularly polarized luminescence encoding helical supramolecular polymer》.Reference of 1-Bromo-4-iodobenzene The author mentioned the following in the article:

Supramol. polymers with different functionalities have been continuously developed in the past decade because of their indispensable role in soft materials. However, pure organic supramol. polymers with stable room temperature phosphorescence (RTP) emission were very rarely reported for the difficulties of synthesis and achieving RTP in solution Herein, soluble helical supramol. polymers with circularly polarized room-temperature phosphorescence were developed via a facile host-guest strategy. Through assembly, a transition from pure fluorescence to almost pure RTP emission was achieved. Adjusting the asymmetry of guest could easily control the chiroptical property of supramol. polymers. This work provides new opportunities for the design and development of intelligent soft functional soft materials. [graphic not available: see fulltext] In addition to this study using 1-Bromo-4-iodobenzene, there are many other studies that have used 1-Bromo-4-iodobenzene(cas: 589-87-7Reference of 1-Bromo-4-iodobenzene) was used in this study.

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Reference of 1-Bromo-4-iodobenzene It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Koyanagi, Takaoki’s team published research in Organic Letters in 2019 | CAS: 589-87-7

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..SDS of cas: 589-87-7 It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

SDS of cas: 589-87-7In 2019 ,《One-Pot Electrochemical Nickel-Catalyzed Decarboxylative Sp2-Sp3 Cross-Coupling》 was published in Organic Letters. The article was written by Koyanagi, Takaoki; Herath, Ananda; Chong, Ashley; Ratnikov, Maxim; Valiere, Andrew; Chang, Jim; Molteni, Valentina; Loren, Jon. The article contains the following contents:

A one-pot electrochem. nickel-catalyzed decarboxylative sp2-sp3 cross-coupling reaction has been developed using redox-active esters prepared in situ from alkyl carboxylates and N-hydroxyphthalimide tetramethyluronium hexafluorophosphate (PITU). This undivided cell one-pot method enables C-C bond formation using inexpensive, benchtop-stable reagents with isolated yields up to 95% with good functional group tolerance, which includes nitrile, ketone, ester, alkene and selectivity over other aromatic halogens. The experimental part of the paper was very detailed, including the reaction process of 1-Bromo-4-iodobenzene(cas: 589-87-7SDS of cas: 589-87-7)

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..SDS of cas: 589-87-7 It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Kim, Youngwoong’s team published research in ACS Energy Letters in 2020 | CAS: 589-87-7

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Product Details of 589-87-7 It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

《Methoxy-Functionalized Triarylamine-Based Hole-Transporting Polymers for Highly Efficient and Stable Perovskite Solar Cells》 was written by Kim, Youngwoong; Kim, Geunjin; Jeon, Nam Joong; Lim, Chulhee; Seo, Jangwon; Kim, Bumjoon J.. Product Details of 589-87-7 And the article was included in ACS Energy Letters in 2020. The article conveys some information:

The hole-transporting layer is an essential component in a perovskite solar cell (PSC) and plays a key role in controlling both power conversion efficiency (PCE) and stability. Here, a new hole-transporting material (HTM), methoxy group-containing poly(triarylamine) (PTAA) (CH3O-PTAA) is reported for efficient PSCs with improved thermal stability. As compared to commonly used PTAA (CH3-PTAA), CH3O-PTAA exhibits enhanced doping ability and stability under thermal stress. With CH3O-PTAA, (FAPbI3)0.85(MAPbBr3)0.15-based PSCs show high PCEs > 20%, comparable to those of CH3-PTAA devices. More importantly, better long-term thermal stability with only 3% reduction from the initial PCE (6.1% reduction on average) has been achieved for encapsulated PSCs with CH3O-PTAA than that of PSCs with CH3-PTAA under dark storage conditions (ISOS-D-3) of 85° and 85% relative humidity (RH) over 1000 h. Detailed studies have been conducted to reveal the strong correlation between the doping behavior of HTMs and the performance of PSCs, which provide useful guidelines for the design of new HTMs for efficient and stable PSCs. In the experimental materials used by the author, we found 1-Bromo-4-iodobenzene(cas: 589-87-7Product Details of 589-87-7)

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Product Details of 589-87-7 It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Meng, Fan-Yi’s team published research in Nature Communications in 2022 | CAS: 589-87-7

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..SDS of cas: 589-87-7 It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

In 2022,Meng, Fan-Yi; Chen, I-Han; Shen, Jiun-Yi; Chang, Kai-Hsin; Chou, Tai-Che; Chen, Yi-An; Chen, Yi-Ting; Chen, Chi-Lin; Chou, Pi-Tai published an article in Nature Communications. The title of the article was 《A new approach exploiting thermally activated delayed fluorescence molecules to optimize solar thermal energy storage》.SDS of cas: 589-87-7 The author mentioned the following in the article:

We propose a new concept exploiting thermally activated delayed fluorescence (TADF) mols. as photosensitizers, storage units and signal transducers to harness solar thermal energy. Mol. composites based on the TADF core phenoxazine-triphenyltriazine (PXZ-TRZ) anchored with norbornadiene (NBD) were synthesized, yielding compounds PZDN and PZTN with two and four NBD units, resp. Upon visible-light excitation, energy transfer to the triplet state of NBD occurred, followed by NBD → quadricyclane (QC) conversion, which can be monitored by changes in steady-state or time-resolved spectra. The small S1-T1 energy gap was found to be advantageous in optimizing the solar excitation wavelength. Upon tuning the mol.′s triplet state energy lower than that of NBD (61 kcal/mol), as achieved by another composite PZQN, the efficiency of the NBD → QC conversion decreased drastically. Upon catalysis, the reverse QC → NBD reaction occurred at room temperature, converting the stored chem. energy back to heat with excellent reversibility. The results came from multiple reactions, including the reaction of 1-Bromo-4-iodobenzene(cas: 589-87-7SDS of cas: 589-87-7)

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..SDS of cas: 589-87-7 It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

He, Xin’s team published research in Chemistry – An Asian Journal in 2020 | CAS: 589-87-7

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Related Products of 589-87-7 It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

《Efficient Nondoped Pure Blue Organic Light-Emitting Diodes Based on an Anthracene and 9,9-Diphenyl-9,10-dihydroacridine Derivative》 was written by He, Xin; Ren, Shenghong; Liu, Hui; Zhao, Shiyuan; Liu, Futong; Du, Chunya; Min, Jiarui; Zhang, Haiquan; Lu, Ping. Related Products of 589-87-7 And the article was included in Chemistry – An Asian Journal in 2020. The article conveys some information:

Organic light-emitting diodes (OLEDs) have been greatly developed in recent years owing to their abundant advantages for full-color displays and general-purpose lightings. Blue emitters not only provide one of the primary colors of the RGB (red, green and blue) display system to reduce the power consumption of OLEDs, but are able to generate light of all colors, including blue, green, red, and white by energy transfer processes in devices. However, it remains a challenge to achieve high-performance blue electroluminescence, especially for nondoped devices. In this paper, we report a blue light emitting mol., DPAC-AnPCN, which consists of 9,9-diphenyl-9,10-dihydroacridine and p-benzonitrile substituted anthracene moieties. The asym. decoration on anthracene with different groups on its 9 and 10 positions combines the merits of the resp. constructing units and endows DPAC-AnPCN with pure blue emission, high solid-state efficiency, good thermal stability and appropriate HOMO and LUMO energy levels. Furthermore, DPAC-AnPCN can be applied in a nondoped device to effectively reduce the fabrication complexity and cost. The nondoped device exhibits pure blue electroluminescence (EL) locating at 464 nm with CIE coordinates of (0.15, 0.15). Moreover, it maintains high efficiency at relatively high luminescence. The maximum external quantum efficiency (EQE) reaches 6.04% and still remains 5.31% at the luminance of 1000 cd m-2 showing a very small efficiency roll-off. In addition to this study using 1-Bromo-4-iodobenzene, there are many other studies that have used 1-Bromo-4-iodobenzene(cas: 589-87-7Related Products of 589-87-7) was used in this study.

1-Bromo-4-iodobenzene(cas: 589-87-7) is mainly used as the OLED pharmaceutical intermediate, as reagent for in situ desilylation and coupling of silylated alkynes, as substrate in copper-free Sonogashira coupling in aqueous acetone..Related Products of 589-87-7 It is also used in synthesis of β,β,dibromostyrenes, as starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com