Category: 523-27-3

Yang, Chun; Su, Meihui; Luo, Pei; Liu, Yanan; Yang, Feng; Li, Changhua published an article in 2021. The article was titled 《A Photosensitive Polymeric Carrier with a Renewable Singlet Oxygen Reservoir Regulated by Two NIR Beams for Enhanced Antitumor Phototherapy》, and you may find the article in Small.Application In Synthesis of 9,10-Dibromoanthracene The information in the text is summarized as follows:

Photodynamic therapy (PDT), which utilizes photosensitizer to convert mol. oxygen into singlet oxygen (1O2) upon laser irradiation to ablate tumors, will exacerbate the already oxygen shortage of most solid tumors and is thus self-limiting. Herein, a sophisticated photosensitive polymeric material (An-NP) that allows sustained 1O2 generation and sufficient oxygen supply during the entire phototherapy is engineered by alternatively applying PDT and photothermal therapy (PTT) controlled by two NIR laser beams. In addition to a photosensitizer that generates 1O2, An-NP consists of two other key components: a molecularly designed anthracene derivative capable of trapping/releasing 1O2 with superior reversibility and a dye J-aggregate with superb photothermal performance. Thus, in 655 nm laser-triggered PDT process, An-NP generates abundant 1O2 with extra 1O2 being trapped via the conversion into EPO-NP; while in the subsequent 785 nm laser-driven PTT process, the converted EPO-NP undergoes thermolysis to liberate the captured 1O2 and regenerates An-NP. The intratumoral oxygen level can be replenished during the PTT cycle for the next round of PDT to generate 1O2. The working principle and phototherapy efficacy are preliminarily demonstrated in living cells and tumor-bearing mice, resp. In the experiment, the researchers used many compounds, for example, 9,10-Dibromoanthracene(cas: 523-27-3Application In Synthesis of 9,10-Dibromoanthracene)

9,10-Dibromoanthracene(cas: 523-27-3) is a dibrominated polycyclic aromatic hydrocarbon (PAH). 9,10-Dibromoanthracene is often used as an energy acceptor and activator in reactions that produce chemiluminescence.Application In Synthesis of 9,10-Dibromoanthracene

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Quality Control of 9,10-DibromoanthraceneIn 2022 ,《POSS-based fluorescence sensor for rapid analysis of β-carotene in health products》 appeared in Luminescence. The author of the article were Li, Dan; Zhou, Peipei; Hu, Yufei; Li, Gongke; Xia, Ling. The article conveys some information:

In recent years, fluorescent organic-inorganic hybrid nanomaterials have received much interest as potential fluorescent sensor materials. In this study, fluorescent organic-inorganic hybrid nanomaterials (POSS@ANT) were created using polyhedral oligomeric silsesquioxane as the precursor and 9,10-bromoanthracene as the monomer. The morphol. and composition of POSS@ANT, as well as its pore characteristics and fluorescence properties were studied. POSS@ANT displayed steady fluorescence emission at an excitation wavelength of 374 nm. Next, a β-carotene fluorescence sensor was developed using the capacity of β-carotene to quench the fluorescence of POSS@ANT. The quenching process is linked to acceptor electron transfer and energy transfer, and the sensor has a high selectivity for β-carotene. This β-carotene fluorescence anal. method that we established has a linear range of 0.2-4.3 mg/L and a detection limit of 0.081 mg/L. Finally, it was used to quantify β-carotene in health products, the recovery rate was 91.1-109.9%, the relative standard deviation (RSD) was 2.2-4.3%, and the results were comparable with the results of high-performance liquid chromatog. The approach is reliable and can be used to determine β-carotene in health products. The results came from multiple reactions, including the reaction of 9,10-Dibromoanthracene(cas: 523-27-3Quality Control of 9,10-Dibromoanthracene)

9,10-Dibromoanthracene(cas: 523-27-3) is a dibrominated polycyclic aromatic hydrocarbon (PAH). 9,10-Dibromoanthracene is often used as an energy acceptor and activator in reactions that produce chemiluminescence.Quality Control of 9,10-Dibromoanthracene

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

《Conjugated polymer self-assembled with graphene: Synthesis and electrochemical 1-hydroxypyrene sensor》 was published in Polymer in 2020. These research results belong to Pang, Yuehong; Yang, Nianci; Shen, Xiaofang; Zhang, Yi; Feng, Liheng. COA of Formula: C14H8Br2 The article mentions the following:

Urinary 1-hydroxypyrene (1-OHP), one of the metabolite of polycyclic aromatic hydrocarbons (PAHs), has been extensively applied as a biomarker of animals and human exposure to PAHs. Herein, we synthesized a novel conjugated polymer poly-8-methoxy-7-methyl-5-(10-anthracen-9-yl)quinolone (PMMAYQ) using Suzuki coupling reaction, and then fabricated a homogeneous PMMAYQ/grahene multilayer film via layer-by-layer self-assembly technique and applied for electrochem. sensing of 1-OHP. Under the optimal conditions, {PMMAYQ-Graphene}16 modified glass carbon electrode exhibited excellent response for detection of 1-OHP. A linear range from 0.5 to 120 nM was obtained with a low detection limit of 0.07 nM (S/N = 3) and a sensitivity of 0.5539μA/μM. The electrochem. sensor exhibited excellent stability, accepted repeatability, and good selectivity. The developed method was employed for determination of 1-OHP in human urine samples and recoveries in the range of 95.6%-107.1% were achieved. The experimental process involved the reaction of 9,10-Dibromoanthracene(cas: 523-27-3COA of Formula: C14H8Br2)

9,10-Dibromoanthracene(cas: 523-27-3) can be sublimated and oxidized to generate anthraquinone. Soluble in hot benzene and hot toluene, slightly soluble in alcohol, ether and cold benzene, insoluble in water.COA of Formula: C14H8Br2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Sei, Kento; Wang, Qi; Tokumura, Masahiro; Miyake, Yuichi; Amagai, Takashi published an article in 2021. The article was titled 《Accurate and ultrasensitive determination of 72 parent and halogenated polycyclic aromatic hydrocarbons in a variety of environmental samples via gas chromatography-triple quadrupole mass spectrometry》, and you may find the article in Chemosphere.Quality Control of 9,10-Dibromoanthracene The information in the text is summarized as follows:

Polycyclic aromatic hydrocarbons (PAHs) and their halogenated derivatives (XPAHs) are ubiquitous in various environmental media. Anal. problems, however, make it difficult to accurately determine their concentrations To develop a satisfactory anal. method suitable for a diversity of PAHs and XPAHs in multiple environmental samples, we evaluated three com. anal. columns (DB-5MS, Select PAH, and Rxi-PAH) for better chromatog. separation and optimized the anal. conditions for gas chromatog.-triple quadrupole mass spectrometry (GC-MS/MS). Comparison of the abilities of the columns to sep. peaks revealed that the Rxi-PAH was the best column for both PAH and XPAH analyses. Optimization of anal. conditions for GC-MS/MS resulted in sensitivities for PAHs and XPAHs that were 4.2-fold-2600-fold higher than the sensitivities of GC-high-resolution MS (GC-HRMS) (an example of a traditional anal. method). Although there were no statistically significant differences between the instrumental detection limits (IDLs) of PAHs and XPAHs measured by GC-HRMS, the IDLs of XPAHs were significantly lower than those of PAHs when measured by GC-MS/MS. This difference could be attributed to the unique ionization patterns of XPAHs in the GC-MS/MS anal., which suppressed background noise and increased the anal. sensitivity. Analyses of PAHs and XPAHs in grilled chicken, vehicle exhaust, sea sediment, ambient air, and indoor dust via the anal. method optimized in this study revealed that the proposed method was sufficiently sensitive, comprehensive, and versatile for risk assessment purposes, and could eliminate interferences associated with the co-elution of target PAHs and XPAHs. In the experimental materials used by the author, we found 9,10-Dibromoanthracene(cas: 523-27-3Quality Control of 9,10-Dibromoanthracene)

9,10-Dibromoanthracene(cas: 523-27-3) is a dibrominated polycyclic aromatic hydrocarbon (PAH). 9,10-Dibromoanthracene is often used as an energy acceptor and activator in reactions that produce chemiluminescence.Quality Control of 9,10-Dibromoanthracene

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

In 2022,Cheng, Guoqing; Hayashi, Takuya; Miyake, Yuya; Sato, Takashi; Tabata, Hiroshi; Katayama, Mitsuhiro; Komatsu, Naoki published an article in ACS Nano. The title of the article was 《Interlocking of Single-Walled Carbon Nanotubes with Metal-Tethered Tetragonal Nanobrackets to Enrich a Few Hundredths of a Nanometer Range in Their Diameters》.Formula: C14H8Br2 The author mentioned the following in the article:

The authors have separated C nanotubes through host-guest complexation using host mols. named nanotweezers and nanocalipers. A host mol. named tetragonal M-nanobrackets, consisting of a pair of dipyrrin nanocalipers corresponding to two brackets and tethered by two metals (M), is designed, synthesized, and employed to sep. single-walled C nanotubes (SWNTs). A facile three-step process including 1-pot Suzuki coupling is developed to prepare M-nanobrackets in a 37% total yield (M = Cu). Upon extraction of SWNTs with a square nanobracket and Cu(II), in situ formed tetragonal M-nanobrackets interlock SWNTs to disperse them in iso-PrOH. Interlocking is confirmed by absorption and Raman spectroscopy as well as transmission electron and at. force microscopy. Especially, Raman spectroscopy was used to prove the interlocking of SWNTs; Cu-nanobrackets inherent resonance Raman signals and affect the SWNT signals, or a radial breathing vibration, due to the rigid rectangular structure of Cu-nanobrackets. The interlocking is facilely and thoroughly released through demetalation to recover pristine SWNTs and the square nanobracket. Such chem. controlled locking and unlocking for SWNTs are one of the characteristics of the authors’ separation process. This enables a precise evaluation by Raman, photoluminescence, and absorption spectroscopy of the diameter selectivity to SWNTs, revealing the diameter enrichment of only three kinds of SWNTs, (7,6), (9,4), and (8,5), in the 0.02 nm diameter range from 0.90 to 0.92 nm among ~20 kinds of SWNTs from 0.76 to 1.17 nm in their diameter range.9,10-Dibromoanthracene(cas: 523-27-3Formula: C14H8Br2) was used in this study.

9,10-Dibromoanthracene(cas: 523-27-3) can be sublimated and oxidized to generate anthraquinone. Soluble in hot benzene and hot toluene, slightly soluble in alcohol, ether and cold benzene, insoluble in water.Formula: C14H8Br2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

In 2022,Wang, Dinghui; Wang, Jun; Wang, Yan; Yang, Yingwei published an article in Molecules. The title of the article was 《A Fluorescent Linear Conjugated Polymer Constructed from Pillararene and Anthracene》.Safety of 9,10-Dibromoanthracene The author mentioned the following in the article:

Over the past few years, conjugated polymers (CPs) have aroused much attention owing to their rigid conjugated structures, which can perform well in light harvesting and energy transfer and offer great potential in materials chem. In this article, we fabricate a new luminescent linear CP p(P[5](OTf)2-co-9,10-dea) via the Sonogashira coupling of 9,10-diethynylanthracene and trifluoromethanesulfonic anhydride (OTf) modified pillar[5]arene, generating enhanced yellow-green fluorescence emission at around 552 nm. The reaction condition was screened to get a deeper understanding of this polymerization approach, resulting in an excellent yield as high as 92% ultimately. Besides the optical properties, self-assembly behaviors of the CP in low/high concentrations were studied, where interesting adjustable morphologies from tube to sheet were observed In addition, the fluorescence performance and structural architecture can be disturbed by the host-guest reorganization between the host CP and the guest adiponitrile, suggesting great potential of this CP material in the field of sensing and detection. In addition to this study using 9,10-Dibromoanthracene, there are many other studies that have used 9,10-Dibromoanthracene(cas: 523-27-3Safety of 9,10-Dibromoanthracene) was used in this study.

9,10-Dibromoanthracene(cas: 523-27-3) is a dibrominated polycyclic aromatic hydrocarbon (PAH). 9,10-Dibromoanthracene is often used as an energy acceptor and activator in reactions that produce chemiluminescence.Safety of 9,10-Dibromoanthracene

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Recommanded Product: 9,10-DibromoanthraceneIn 2020 ,《””Metal-Free”” Fluorescent Supramolecular Assemblies for Distinct Detection of Organophosphate/Organochlorine Pesticides》 was published in ACS Omega. The article was written by Sharma, Pooja; Kumar, Manoj; Bhalla, Vandana. The article contains the following contents:

The “”metal-free””, easy-to-prepare fluorescent supramol. assemblies based on anthracene/perylene bisamide (PBI) derivatives have been developed for the distinct detection of organophosphate (CPF) and organochlorine (DCN) pesticides in aqueous media. The supramol. assemblies of anthracene derivative show rapid and highly selective “”on-on”” response toward organophosphate (CPF), which is attributed to the formation of CPF-induced formation of “”closely packed”” assemblies. A detection limit in the nanomolar range is observed for CPF. On the other hand, the inner filter effect is proposed as the mechanism for the “”on-off”” detection of DCN using supramol. assemblies of the anthracene derivative This is the first report on the development of fluorescent materials having the potential to differentiate between organophosphate and organochlorine pesticides. The assemblies of anthracene derivative (I) also act as “”enzyme mimic”” as organophosphate pesticide show a preferential affinity for assemblies of derivative I over acetylcholinesterase enzyme. Further, the real-time applications of supramol. assemblies have also been explored for the detection of CPF and DCN in spiked water and in agricultural products such as grapes and apples. The experimental part of the paper was very detailed, including the reaction process of 9,10-Dibromoanthracene(cas: 523-27-3Recommanded Product: 9,10-Dibromoanthracene)

9,10-Dibromoanthracene(cas: 523-27-3) is a dibrominated polycyclic aromatic hydrocarbon (PAH). 9,10-Dibromoanthracene is often used as an energy acceptor and activator in reactions that produce chemiluminescence.Recommanded Product: 9,10-Dibromoanthracene

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

《9,10-Di(hydroxymethylphenyl)anthracenes: Highly efficient triplet annihilators with small singlet-triplet energy gap (ΔEST) and planar configuration》 was published in Dyes and Pigments in 2020. These research results belong to Yu, Xue; Fan, Congbin; Dai, Guoliang; Wang, Xiaomei; Ye, Changqing; Tao, Xutang. Recommanded Product: 523-27-3 The article mentions the following:

A series of 9,10-di(hydroxymethylphenyl)anthracene chromophores (named as E-o-DHMPA, Z-o-DHMPA, m-DHMPA and p-DHMPA) are designed to tailor triplet-triplet annihilation upconversion through isomer engineering. It was found that improving mol. planarity makes for mol. π-π interaction, meanwhile, mol. excited singlet energy level (ES1) shows decreasing; however, the triple energy level (ET1) exhibits almost equal. Thus, small singlet-triplet energy gap (ΔEST) of chromophores could be designed. Selective excitation of sensitizer (palladiumIItetrabromophenylporphyrin, PdBrTPP) in solution containing annihilator results in the upconversion (UC) efficiency (ΦUC) increasing from E-o-DHMPA (15.9%), Z-o-DHMPA (18.7%), m-DHMPA (26.0%) to p-DHMPA (26.8%), accompanied by the excitation threshold intensity (Ith, mW·cm-2) decreasing from E-o-DHMPA (292.74), Z-o-DHMPA (174.41), m-DHMPA (36.58) to p-DHMPA (29.78), which are in agreement with the ΔEST decreasing and planarity improving of these isomers. Annihilator with small energy gap (ΔEST) and planar configuration has contribution to triplet-triplet annihilation (TTA), supported by the fact of the Ith value reducing, and thereby increasing UC efficiency (ΦUC), which provides a new strategy for mol. design to develop new triplet annihilator. Finally, the TTA-UC powered photolysis of bilirubin was conducted for the first time, suggesting that TTA-UC can act as an effective light source used in the light therapy for neonatal hyperbilirubinemia. In the part of experimental materials, we found many familiar compounds, such as 9,10-Dibromoanthracene(cas: 523-27-3Recommanded Product: 523-27-3)

9,10-Dibromoanthracene(cas: 523-27-3) is synthesized by the bromination of anthracene. The bromination reaction is carried out at room temperature using carbon tetrachloride as a solvent. Using 80-85% anthracene as raw material, adding bromine to react for half an hour, the yield is 83-88%.Recommanded Product: 523-27-3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Chen, Jinqing; Zhong, Hong; Lv, Haowei; Liu, Ruixia; Wang, Ruihu published an article in 2021. The article was titled 《Regulating Utilization Efficiency of the Photogenerated Charge Carriers by Constructing Donor-π-Acceptor Polymers for Upgrading Photocatalytic CO2 Reduction》, and you may find the article in ChemSusChem.Computed Properties of C14H8Br2 The information in the text is summarized as follows:

Photocatalytic CO2 reduction offers a promising approach for managing global carbon balance. The smooth delivery of the photoexcited electrons to the active sites without the extra photosensitizers is still challenging. Herein, a series of donor-π-acceptor conjugated organic polymers (COPs) were produced using anthracene, cobalt-coordinated bipyridyl, and benzene as donor, acceptor, and π linker units, resp. The introduction of Ph linker significantly improved the activities of photocatalytic CO2 reduction upon visible light illumination. Structure-performance relationship examinations uncovered that donor-π-acceptor structure promotes mobility of charge carriers and utilization efficiency on the catalytically active sites, resulting in high photocatalytic activity and durability for CO2 photoreduction The in-depth insights into the electron transport processes open new perspectives for further optimization and rational design of photoactive polymers with high efficiency for solar-energy conversion.9,10-Dibromoanthracene(cas: 523-27-3Computed Properties of C14H8Br2) was used in this study.

9,10-Dibromoanthracene(cas: 523-27-3) is a dibrominated polycyclic aromatic hydrocarbon (PAH). 9,10-Dibromoanthracene is often used as an energy acceptor and activator in reactions that produce chemiluminescence.Computed Properties of C14H8Br2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Urgel, Jose I.; Bock, Julian; Di Giovannantonio, Marco; Ruffieux, Pascal; Pignedoli, Carlo A.; Kivala, Milan; Fasel, Roman published their research in RSC Advances in 2021. The article was titled 《On-surface synthesis of π-conjugated ladder-type polymers comprising nonbenzenoid moieties》.Synthetic Route of C14H8Br2 The article contains the following contents:

On-surface synthesis provides a powerful approach toward the atomically precise fabrication of π-conjugated ladder polymers (CLPs). We report herein the surface-assisted synthesis of nonbenzenoid CLPs from cyclopenta-annulated anthracene monomers on Au(111) under ultrahigh vacuum conditions. Successive thermal annealing steps reveal the dehalogenative homocoupling to yield an intermediate 1D polymer and the subsequent cyclodehydrogenation to form the fully conjugated ladder polymer. Notably, neighboring monomers may fuse in two different ways, resulting in six- and five-membered rings, resp. The structure and electronic properties of the reaction products have been investigated via low-temperature scanning tunneling microscopy and spectroscopy, complemented by d.-functional theory calculations Our results provide perspectives for the on-surface synthesis of nonbenzenoid CLPs with the potential to be used for organic electronic devices. In the experimental materials used by the author, we found 9,10-Dibromoanthracene(cas: 523-27-3Synthetic Route of C14H8Br2)

9,10-Dibromoanthracene(cas: 523-27-3) can be sublimated and oxidized to generate anthraquinone. Soluble in hot benzene and hot toluene, slightly soluble in alcohol, ether and cold benzene, insoluble in water.Synthetic Route of C14H8Br2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary