Category: 913836-27-8

Xiong, Wenjing published the artcileSynthesis and optoelectronic properties of a dinuclear iridium (III) complex containing a picolinic acid derivative by nonconjugated linkage with a D-A-D core, Related Products of bromides-buliding-blocks, the main research area is diiridium complex picolinic acid derivative preparation mol structure optimized; dinuclear iridium complex picolinic acid derivative organic electroluminescent device; electrochem electroluminescence photoluminescence OLED iridium picolinic acid complex preparation.

A novel dinuclear iridium (III) complex containing a non-conjugated bridging picolinic acid ligand of (C8TPAPhOC2FIrpic)2BT with a D-A-D core was synthesized and characterized, in which the D-A-D core consists of benzo[c][1,2,5]thiadiazole (BT) and triphenylamino (TPA) units. Its optophys., electrochem. and electroluminescent characteristics were primarily studied. It is found this dinuclear iridium (III) complex exhibited similar photoluminescent and electroluminescent profiles, but higher brightness and efficiency in compared with the picolinic acid ligand in the single-emissive-layer organic light-emitting devices. The maximum luminance of 7404 cd/m2 and current efficiency of 0.81 cd/A was obtained in the (C8TPAPhOC2FIrpic)2BT-based devices. The efficient energy transfer is observed from the terminal iridium complex unit to the picolinic acid ligand. This work demonstrates that the picolinic acid ligand with a D-A-D core can facilitate dinuclear iridium (III) complex to exhibit the ancillary ligand-based red emission.

Journal of Organometallic Chemistry published new progress about Band gap. 913836-27-8 belongs to class bromides-buliding-blocks, name is 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, and the molecular formula is C14H20BBrO3, Related Products of bromides-buliding-blocks.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Nishihara, Ryo published the artcileAzide- and Dye-Conjugated Coelenterazine Analogues for a Multiplex Molecular Imaging Platform, Recommanded Product: 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, the main research area is azide dye conjugation coelenterazine analog luminescence mol imaging luciferase.

Native coelenterazine (nCTZ) is a common substrate to most marine luciferases and photoproteins. In this study, nine novel dye- and azide-conjugated CTZ analogs were synthesized by conjugating a series of fluorescent dyes or an azide group to the C-2 or C-6 position of the nCTZ backbone to obtain bulkiness-driven substrate specificity and potential chemiluminescence/bioluminescence resonance energy transfer (C/BRET). The investigation on the optical properties revealed that azide-conjugated CTZs emit greatly biased bioluminescence to ALucs and ca. 130 nm blue-shifted bioluminescence with RLuc8.6 in living animal cells or lysates. The corresponding kinetic study explains that azide-conjugated CTZ exerts higher catalytic efficiency than nCTZ. Nile red-conjugated CTZ completely showed red-shifted CRET spectra and characteristic BRET spectra with artificial luciferase 16 (ALuc16). No or less spectral overlap occurs among [Furimazine-NanoLuc], [6-N3-CTZ-ALuc26], [6-pi-OH-CTZ-RLuc8.6], and [6-N3-CTZ-RLuc8.6] pairs, because of the substrate-driven luciferase specificity and color shifts, providing a crosstalk-free multiplex bioassay platform. The unique bioluminescence system appends a new toolbox to bioassays and multiplex mol. imaging platforms. This study is the first example that systematically synthesized fluorescent dye-conjugated CTZs and applied them for a bioluminescence assay system.

Bioconjugate Chemistry published new progress about Biological imaging. 913836-27-8 belongs to class bromides-buliding-blocks, name is 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, and the molecular formula is C14H20BBrO3, Recommanded Product: 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Chen, Ya-Jing published the artcileEnantioselective Rhodium-Catalyzed Arylation of Cyclic N-Sulfamidate Alkylketimines: A New Access to Chiral β-Alkyl-β-aryl Amino Alcohols, Safety of 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, the main research area is sulfamidate preparation enantioselective addition arylboronate cyclic sulfamidate alkylketimine; rhodium catalyzed arylation sulfamidate preparation alkylarylamino alc conversion.

The enantioselective rhodium-catalyzed 1,2-addition of arylboronates to cyclic N-sulfamidate alkylketimines was developed. With a rhodium/diene complex as catalyst, high enantioselectivity and broad functional group tolerance were observed The resulting sulfamidates can easily be converted into chiral β-alkyl-β-aryl amino alcs.

Organic Letters published new progress about 1,2-Addition reaction. 913836-27-8 belongs to class bromides-buliding-blocks, name is 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, and the molecular formula is C14H20BBrO3, Safety of 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Li, Zhiqiang published the artcilePhotoresponsive supramolecular coordination polyelectrolyte as smart anticounterfeiting inks, Synthetic Route of 913836-27-8, the main research area is photoresponsive supramol coordination polyelectrolyte anticounterfeiting ink.

While photoluminescence printing is a widely applied anticounterfeiting technique, there are still challenges in developing new generation anticounterfeiting materials with high security. Here we report the construction of a photoresponsive supramol. coordination polyelectrolyte (SCP) through hierarchical self-assembly of lanthanide ion, bis-ligand and diarylethene unit, driven by metal-ligand coordination and ionic interaction. Owing to the conformation-dependent photochromic fluorescence resonance energy transfer between the lanthanide donor and diarylethene acceptor, the ring-closure/ring-opening isomerization of the diarylethene unit leads to a photoreversible luminescence on/off switch in the SCP. The SCP is then utilized as security ink to print various patterns, through which photoreversible multiple information patterns with visible/invisible transformations are realized by simply alternating the irradiation with UV and visible light. This work demonstrates the possibility of developing a new class of smart anticounterfeiting materials, which could be operated in a noninvasive manner with a higher level of security.

Nature Communications published new progress about Inks (anticounterfeiting). 913836-27-8 belongs to class bromides-buliding-blocks, name is 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, and the molecular formula is C14H20BBrO3, Synthetic Route of 913836-27-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Cruz, Cole L. published the artcileNickel-catalyzed reductive coupling of unactivated alkyl bromides and aliphatic aldehydes, Formula: C14H20BBrO3, the main research area is aliphatic aldehyde alkyl bromide reductive coupling nickel catalyst; silyl secondary alc preparation.

A mild, convenient coupling of aliphatic aldehydes e.g., BnCH2CHO and unactivated alkyl bromides e.g., Br(CH2)3C(O)OEt has been developed. The catalytic system features the use of a common Ni(II) precatalyst and a readily available bioxazoline ligand and affords silyl-protected secondary alcs. e.g., BnCH2CH(OTES)(CH2)3C(O)OEt. The reaction is operationally simple, utilizes Mn as a stoichiometric reductant, and tolerates a wide range of functional groups. The use of 1,5-hexadiene as an additive is an important reaction parameter that provides significant benefits in yield optimizations. Initial mechanistic experiments support a mechanism featuring an alpha-silyloxy Ni species that undergoes formal oxidative addition to the alkyl bromide via a reductive cross-coupling pathway.

Chemical Science published new progress about Aliphatic aldehydes Role: RCT (Reactant), RACT (Reactant or Reagent). 913836-27-8 belongs to class bromides-buliding-blocks, name is 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, and the molecular formula is C14H20BBrO3, Formula: C14H20BBrO3.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Liu, Xiao published the artcileMultistimuli-responsive hydrogels with both anisotropic mechanical performance and anisotropic luminescent behavior, Name: 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, the main research area is multiresponsive hydrogel luminescent anisotropy mech property.

Anisotropic luminescence emission is the basis to achieve some key parameters in optoelectronic fields. As compared with mech. anisotropy, however, achieving anisotropic emitting behavior is still challenging. Thus, integrating multiple stimuli into one luminescent hydrogel orthogonally while retaining its anisotropic structure remains an open challenge. Herein, we report the construction of a multistimuli-responsive mech./luminescent dual anisotropic hydrogel through the copolymerization of superparamagnetic nanoparticle-coated alumina (Fe/Al2O3) platelets, lanthanide complex, photochromic diarylethene mol., and N-isopropylacrylamide (NIPA) in an oriented magnetic field. The aligned Fe/Al2O3 platelets impart the hydrogel an anisotropic mech. property, and the orientation-dependent “”shading effect”” of the aligned Fe/Al2O3 platelets on the lanthanide complex also endow the hydrogel with anisotropic emission behavior. Significantly, photoreversible luminescence on/off switch and thermoreversible anisotropic deformation are realized in the hydrogel based on the conformation-dependent fluorescence resonance energy transfer between the lanthanide donor and photochromic diarylethene acceptor, and phase transition of polymerized NIPA, resp. As a proof-of-concept, multidimensional intelligent anticounterfeiting is demonstrated by using this hydrogel. Thus, this work demonstrates a general preparation strategy of multistimuli-responsive dual anisotropic hydrogels for purposely designed applications, offering insights in the field fundamentally and practically.

Chemical Engineering Journal (Amsterdam, Netherlands) published new progress about Anisotropic materials. 913836-27-8 belongs to class bromides-buliding-blocks, name is 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, and the molecular formula is C14H20BBrO3, Name: 2-(4-(2-Bromoethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary