Mezzetta, Andrea’s team published research in Molecules in 2021 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Recommanded Product: 629-03-8

Mezzetta, Andrea; Guglielmero, Luca; Mero, Angelica; Tofani, Giorgio; D’Andrea, Felicia; Pomelli, Christian Silvio; Guazzelli, Lorenzo published their research in Molecules in 2021. The article was titled 《Expanding the Chemical Space of Benzimidazole Dicationic Ionic Liquids》.Recommanded Product: 629-03-8 The article contains the following contents:

Benzimidazole dicationic ionic liquids (BDILs) have not yet been widely explored in spite of their potential. Therefore, two structurally related families of BDILs, paired with either bromide or bistriflimide anions and bearing alkyl spacers ranging from C3 to C6, have been prepared Their thermal properties have been studied by thermogravimetric anal. (TGA) and differential scanning calorimetry (DSC), while their elec. properties have been assessed by cyclic voltammetry (CV). TG anal. confirmed the higher stability of the bistriflimide BDILs over the bromide BDILs, with minor variation within the two families. Conversely, DSC and CV allowed for ascertaining the role played by the spacer length. In particular, the thermal behavior changed dramatically among the members of the bistriflimide family, and all three possible thermal behavior types of ILs were observed Furthermore, cyclic voltammetry showed different electrochem. window (C3(C1BenzIm)2/2Tf2N < C4(C1BenzIm)2/2Tf2N, C5(C1BenzIm)2/2Tf2N < C6(C1BenzIm)2/2Tf2N) as well as a reduction peak potential, shape, and intensity as a function of the spacer length. The results obtained highlight the benefit of accessing a more structurally diverse pool of compounds offered by dicationic ILs when compared to the parent monocationic ILs. In particular, gains are to be found in the ease of fine-tuning their properties, which translates in facilitating further investigations toward BDILs as designer solvents and catalysts. The experimental process involved the reaction of 1,6-Dibromohexane(cas: 629-03-8Recommanded Product: 629-03-8)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Recommanded Product: 629-03-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Wang, Weiwei’s team published research in Green Chemistry in 2021 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Related Products of 629-03-8

Wang, Weiwei; Zhang, Yaqin; Yang, Zifeng; Zhang, Zhencai; Fang, Wenjuan; Niu, Donghui; He, Hongyan; Xu, Fei published an article in 2021. The article was titled 《Efficient synthesis of isosorbide-based polycarbonate with scalable dicationic ionic liquid catalysts by balancing the reactivity of the endo-OH and exo-OH》, and you may find the article in Green Chemistry.Related Products of 629-03-8 The information in the text is summarized as follows:

In this study, a series of high-activity imidazole-based dicationic ionic liquids (DILs) were designed and prepared as efficient catalysts for balancing the reactivity between the endo-hydroxyl group (endo-OH) and the exo-hydroxyl group (exo-OH) of isosorbide (ISO) to synthesize high mol. weight poly(isosorbide carbonate) (PIC). Meanwhile, the thermal performance of PIC was precisely optimized by regulating the chain configuration. When the trace amounts (4.5 x 10-5 based on the ISO molar amount) of bis-(3-methyl-1-imidazole)-ethylene dibromide ([C2(Min)2][Br]2) were used, the weight average mol. weight (Mw) of PIC reached 98 700 g mol-1. It could be concluded from the results of the experiment and the stimulation that the high catalytic activity of DILs was attributed to the strong electrostatic interaction between the cation and the substrate and the effective balance of the reactivity of the endo-OH and the exo-OH. Furthermore, we found that the reduction of hydroxyl groups in the terminal groups and the increase of endo-endo (a1) structure in the repeating unit improved the thermal properties of PIC. Finally, 1H NMR, Fourier IR spectroscopy, and d. functional theory (DFT) calculations were used to verify the reaction process through anion and cation multi-site synergistic effect and a possible electrophilic-nucleophilic reaction mechanism was successfully obtained.1,6-Dibromohexane(cas: 629-03-8Related Products of 629-03-8) was used in this study.

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Related Products of 629-03-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Jin, Meng’s team published research in Bioorganic Chemistry in 2020 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Synthetic Route of C6H12Br2

《Synthesis of a novel fluorescent berberine derivative convenient for its subcellular localization study》 was published in Bioorganic Chemistry in 2020. These research results belong to Jin, Meng; Ji, Xiuna; Stoika, Rostyslav; Liu, Kechun; Wang, Lizhen; Song, Yang. Synthetic Route of C6H12Br2 The article mentions the following:

Berberine is a naturally occurred isoquinoline alkaloid that shows great potential for developing anticancer drugs. However, the problem stays of poor understanding of the mechanisms of anticancer action of berberine. It depends on evaluation of berberine’s pharmacokinetics, namely monitoring of its uptake and distribution in cells, tissues and organs. In order to address these problems, we have designed and synthesized a novel berberine derivative BBR-BODIPY bearing a fluorescent tag that allows screening its interaction with the targeted cells. It was shown that the synthesized fluorescent derivative could penetrate into human breast carcinoma MCF7 cells, and then induced apoptosis detected by the Western Blot anal. as changed expression of apoptosis-related proteins, including Bax, Bcl2, and Cyto C released from mitochondria, Cleaved Caspase 9, Cleaved PARP, Pro-Caspase 3, and Cleaved Caspase 3. The results of MitoTracker anal. followed by the confocal microscopy of sub-cellular localization of BBR-BODIPY in the MCF7 cells demonstrated excellent cell-penetrating ability of this compound even at low concentrations, and mitochondria was the main site of its accumulation. Together with the results of Western Blot anal., these data indicated that the mitochondria pathway might be involved in berberine-induced apoptosis. In the experiment, the researchers used many compounds, for example, 1,6-Dibromohexane(cas: 629-03-8Synthetic Route of C6H12Br2)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Synthetic Route of C6H12Br2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Azum, Naved’s team published research in Scientific Reports in 2020 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.SDS of cas: 629-03-8

《Kinetic study of the metal-dipeptide complex with ninhydrin facilitated by gemini (m-s-m) surfactant micelles》 was written by Azum, Naved; Kumar, Dileep. SDS of cas: 629-03-8 And the article was included in Scientific Reports in 2020. The article conveys some information:

The three Gemini (m-s-m; m (head group) = 16 and s (spacer) = 4, 5, 6) surfactants have been synthesized and their impact on reaction of zinc(II)-glycylleucine complex ([Zn(II)-Gly-Leu]+) and ninhydrin were studied at temperature (343 K) and pH (5.0) using spectroscopic method. Influence of several factors, viz., [Zn(II)-Gly-Leu]+, [ninhydrin], temperature and pH were also carried out on title reaction in geminis. Rates of reaction are the first-order path in concentration of [Zn(II)-Gly-Leu]+ complex and fractional order path in concentration of ninhydrin. The catalysis of gemini 16-s-16 surfactant micelles was investigated below and above their critical micelle concentration (cmc) value and detailed elaboration were provided in the text. In the present case, rate constants, kψ, increased on increasing geminis ([gemini] are below their cmc, region I) and stayed nearly constant (region II). The shape of (region I and II) surfactants ([gemini] = 0 to 400 × 10-5 mol dm-3) are similar to a cetyltrimethylammonium bromide, CTAB (single hydrophilic head group and hydrophobic part). Later, a sharp increment in rate was observed with higher [gemini] (region III, (Fig. 5)). The study was catalyzed and accelerated quite enough by geminis (at concentrations below their cmc) compared to aqueous An appropriate mechanism has been proposed for accounting for the distribution of reactants between aqueous and micellar pseudo phases. Resulting kinetic data were used to determine the binding constants of micelle-substrate (KB) and micelle-ninhydrin (KNin). The results came from multiple reactions, including the reaction of 1,6-Dibromohexane(cas: 629-03-8SDS of cas: 629-03-8)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.SDS of cas: 629-03-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Odewunmi, Nurudeen A.’s team published research in ACS Omega in 2020 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Application of 629-03-8

《Comparative Studies of the Corrosion Inhibition Efficacy of a Dicationic Monomer and Its Polymer against API X60 Steel Corrosion in Simulated Acidizing Fluid under Static and Hydrodynamic Conditions》 was published in ACS Omega in 2020. These research results belong to Odewunmi, Nurudeen A.; Solomon, Moses M.; Umoren, Saviour A.; Ali, Shaikh A.. Application of 629-03-8 The article mentions the following:

N1,N1-diallyl-N6,N6,N6-tripropylhexane-1,6-diaminium chloride (NDTHDC) and its polymer poly(N1,N1-diallyl-N6,N6,N6-tripropylhexane-1,6-diaminium chloride) (poly-NDTHDC) were synthesized and tested against API X60 carbon steel corrosion in 15 wt % HCl solution Weight loss, electrochem., and surface anal. techniques were used. Results show that poly-NDTHDC is better than NDTHDC. Moreover, 1000 mg/L NDTHDC protected the studied surface by 79.1% at 25 °C, while 100 mg/L poly-NDTHDC afforded 86.1% protection. Inhibition efficiency increases with temperature (up to 60 °C) but depreciates thereafter. NDTHDC and poly-NDTHDC perform better under the hydrodynamic condition than the static condition. TGA and FTIR results reveal that poly-NDTHDC is chem. and thermally stable. In the experiment, the researchers used 1,6-Dibromohexane(cas: 629-03-8Application of 629-03-8)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Application of 629-03-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Su, Hongmei’s team published research in Dalton Transactions in 2020 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Application In Synthesis of 1,6-Dibromohexane

《Behavior, mechanism and equilibrium studies of Au(III) extraction with an ionic liquid [C4-6-C4BIm]Br2》 was written by Su, Hongmei; Wang, Qi; Wang, Ning; Yang, Yanzhao. Application In Synthesis of 1,6-Dibromohexane And the article was included in Dalton Transactions in 2020. The article conveys some information:

The first gemini-type benzimidazole ionic liquid ([C4-6-C4BIm]Br2) with two sites of action was synthesized and applied for gold extraction The effects of [C4-6-C4BIm]Br2 concentration, initial gold(III) concentration, acidity, and the loading capacity of [C4-6-C4BIm]Br2 were examined in detail. It was found that [C4-6-C4BIm]Br2 has excellent extraction ability for obtaining high purity gold. The anion exchange mechanism between [C4-6-C4BIm]Br2 and Au(III) was proved by Job’s method and 1H NMR and FTIR spectroscopy. Quantum chem. calculations were carried out to prove the mechanism theor. The extraction equilibrium process was modeled using Langmuir and Freundlich isotherms. Thermodn. parameters ΔH, ΔG and ΔS indicated that the extraction process was exothermic and spontaneous. The pseudo-second-order kinetic model well fitted the exptl. data (R = 0.99). In addition, [C4-6-C4BIm]Br2 has high selectivity for Au(III) compared to other base metals. In summary, [C4-6-C4BIm]Br2 has great application prospects in industry due to its excellent characteristics such as low cost, easy availability, and high extraction capacity. After reading the article, we found that the author used 1,6-Dibromohexane(cas: 629-03-8Application In Synthesis of 1,6-Dibromohexane)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Application In Synthesis of 1,6-Dibromohexane

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yuan, Yongjie’s team published research in Polymer Chemistry in 2019 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.HPLC of Formula: 629-03-8

The author of 《Synthesis, properties and photo-responsive behavior of luminescent side chain polymers containing D-π-A α-cyanostilbene units》 were Yuan, Yongjie; He, Lifang; Li, Jindi; Zhang, Hailiang. And the article was published in Polymer Chemistry in 2019. HPLC of Formula: 629-03-8 The author mentioned the following in the article:

A series of luminescent side chain polymers containing a D-π-A structure and different flexible spacer lengths, namely, poly[(Z)-ω-(4-(1-cyano-2-(4-cyanophenyl)vinyl)phenoxy)alkyl methacrylate]s (PMmPVPCN, m = 2, 4, 6, 8), were successfully prepared With the combination of aggregation-induced emission enhancement (AIEE) luminogens and mesogens, the resultant polymers are expected to possess both liquid crystal characteristics and AIEE characteristics. The phase structure of PMmPVPCN was explored by differential scanning calorimetry (DSC), polarized optical microscopy (POM), and one-dimensional wide-angle X-ray diffraction (1D WAXD). Photophys. properties of PMmPVPCN were studied by UV spectra and fluorescence spectra. Test results suggested that the phase structure of PMmPVPCN transformed from the amorphous phase (PMmPVPCN, m = 2, 4) to the nematic phase (PMmPVPCN, m = 6, 8) with the increase of polymer spacer length. All the synthetic monomers and polymers exhibited AIEE properties and the luminescence behavior of PMmPVPCN was associated with their chem. structure. The solid fluorescence quantum yields of PMmPVPCN increased from 22.4% to 42.7% with increasing spacer length. The polymer films also showed reversible fluorescence photo-responsive properties. The emission color and the emission intensity of polymer films changed when exposed to a 365 nm UV lamp. The change process was reversible and they could turn back to their original state when irradiated with a 254 nm UV lamp or heated at higher temperature In the experiment, the researchers used 1,6-Dibromohexane(cas: 629-03-8HPLC of Formula: 629-03-8)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.HPLC of Formula: 629-03-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yu, Zhen-Qiang’s team published research in Chemical Science in 2021 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Category: bromides-buliding-blocks

Yu, Zhen-Qiang; Li, Xiaodong; Wan, Wei; Li, Xin-Shun; Fu, Kuo; Wu, Yue; Li, Alexander D. Q. published their research in Chemical Science in 2021. The article was titled 《Cooperatively assembled liquid crystals enable temperature-controlled Forster resonance energy transfer》.Category: bromides-buliding-blocks The article contains the following contents:

Balancing the rigidity of a π-conjugated structure for strong emission and the flexibility of liquid crystals for self-assembly is the key to realizing highly emissive liquid crystals (HELCs). Here we show that (1) integrating organization-induced emission into dual mol. cooperatively-assembled liquid crystals, (2) amplifying mesogens, and (3) elongating the spacer linking the emitter and the mesogen create advanced materials with desired thermal-optical properties. Impressively, assembling the fluorescent acceptor Nile red into its host donor designed according to the aforementioned strategies results in a temperature-controlled Forster resonance energy transfer (FRET) system. Indeed, FRET exhibits strong S-curve dependence as temperature sweeps through the liquid crystal phase transformation. Such thermochromic materials, suitable for dynamic thermo-optical sensing and modulation, are anticipated to unlock new and smart approaches for controlling and directing light in stimuli-responsive devices. The results came from multiple reactions, including the reaction of 1,6-Dibromohexane(cas: 629-03-8Category: bromides-buliding-blocks)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules; synthesis of water-soluble thermoresponsive polylactides.Category: bromides-buliding-blocks

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Ma, Xiao-Qiang’s team published research in Dyes and Pigments in 2019 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Computed Properties of C6H12Br2

In 2019,Dyes and Pigments included an article by Ma, Xiao-Qiang; Wang, Yun; Wei, Tai-Bao; Qi, Li-Hua; Jiang, Xiao-Mei; Ding, Jin-Dong; Zhu, Wen-Bo; Yao, Hong; Zhang, You-Ming; Lin, Qi. Computed Properties of C6H12Br2. The article was titled 《A novel AIE chemosensor based on quinoline functionalized Pillar[5]arene for highly selective and sensitive sequential detection of toxic Hg2+ and CN-》. The information in the text is summarized as follows:

Aggregation-induced emission (AIE) is widely used for fluorescence on-off-on detection ions and mol. Herein, the authors report a novel AIE chemosensor through self-assembly of quinoline functionalized pillar[5]arene (SPQ5). The SPQ5 can bind with Hg2+ tightly through coordinating reaction. By introducing Hg2+ into AIE-based chemosensor, metal-coordinated chemosensor (SPQ5-Hg2+) was obtained, the SPQ5-Hg2+ could high selectively and sensitively detection of CN- by competitive coordinating interactions. The LODs of SPQ5 for Hg2+ and CN- are 2.53 × 10-8 M and 7.71 × 10-8 M, resp. Hg2+ test kit was prepared by loading the SPQ5 chemosensor on a silica gel plate, which could more convenient and efficiency detection Hg2+ and CN-. The chemosensor SPQ5 could instant sense the Hg2+ and CN- by the changing of fluorescence color and fluorescence intensity. Notably, the fluorescence intensity changes of SPQ5 upon the addition of Hg2+ and CN- were used as an IMP logic gate at the mol. level, using Hg2+ and CN- as chem. inputs and the fluorescence intensity signal as the output. However, the test kit by loading SPQ5 on a silica gel plate was prepared for convenient detection of Hg2+. This study provides a practical application for the sensing of toxic ions in aqueous solution by the construction of supramol. system. In the part of experimental materials, we found many familiar compounds, such as 1,6-Dibromohexane(cas: 629-03-8Computed Properties of C6H12Br2)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Computed Properties of C6H12Br2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Wu, Hong Yue’s team published research in Electrochimica Acta in 2019 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Quality Control of 1,6-Dibromohexane

In 2019,Electrochimica Acta included an article by Wu, Hong Yue; Yang, Qian; Gao, Xue Lang; Zhu, Zhao Yu; Sun, Qi Hui; Zhang, Qiu Gen; Zhu, Ai Mei; Liu, Qing Lin. Quality Control of 1,6-Dibromohexane. The article was titled 《Novel crosslinked aliphatic anion exchange membranes with pendant pentafluorophenyl groups》. The information in the text is summarized as follows:

To enhance the performance of anion exchange membranes (AEMs) by constructing effective ion channels, the authors synthesized novel aliphatic polymers with pentafluorophenyl pendent groups via superacid catalyzed polyhydroxyalkylation and quaternization by grafting multi-cation crosslinker through the Menshutkin reaction. The procedure adopted in this study for preparing the AEMs circumvented the use of precious metal catalysts and made it easy to control the reaction conditions. Compared with the traditional aliphatic AEMs, the AEMs prepared by the new strategy exhibited well-developed microphase-separated structures by increasing the hydrophilic/hydrophobic difference between the polymer backbones and the side chains. Also, the multi-cation crosslinker not only provides ion exchange groups but also constrains the swelling of the AEMs. As the authors expected, the well-defined ion channels were validated by TEM and small angle x-ray scattering (SAXS). The CPFBP-TQA-100 membrane shows a highest ion conductivity of 76.85 mS cm-1 and a swelling ratio of only 24.8% at 80°. A maximum power d. of 116.7 mW cm-2 is achieved by a single cell using the CPFBP-TQA-100 membrane at a c.d. of 300 mA cm-2 at 80°. Besides, all the AEMs display excellent thermal stability and reasonable alk. stability. The results came from multiple reactions, including the reaction of 1,6-Dibromohexane(cas: 629-03-8Quality Control of 1,6-Dibromohexane)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Quality Control of 1,6-Dibromohexane

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary