Category: 626-05-1

Lin, Na; Huang, Lei; Ding, Huan-huan; Zhang, Yue; Dong, Wen-jing; Xia, Bin-yuan; Ren, Wen-sheng; Zhao, Dong published their research in Organic Chemistry Frontiers in 2021. The article was titled 《Synthesis of para-linked azacalix[n]pyridine[n]pyrazines and their uranyl ion binding properties》.Application of 626-05-1 The article contains the following contents:

Based on the fragment coupling strategy, the novel macrocycles, para-linked azacalix[n]pyridine[n]pyrazines (n = 2 and 4) with coexisting different heteroaromatics, were synthesized readily starting from 2,5-dibromopyrazine and 2,6-dibromopyridine. According to the X-ray diffraction anal., the macrocycle azacalix[4]pyridine[4]pyrazine adopted a unique boat-type conformation with a large rectangular cavity in the solid state. The complexation between the azacalix[n]pyridine[n]pyrazines and uranyl ions was investigated by DFT calculations and 1H NMR and UV-vis titration experiments It was found that they were strong host mols. to form 1 : 1 complexes with uranyl ions with an association constant of up to (1.38 +/= 0.04) x 105 M-1. After reading the article, we found that the author used 2,6-Dibromopyridine(cas: 626-05-1Application of 626-05-1)

2,6-Dibromopyridine(cas: 626-05-1) belongs to pyridine. Pyridine’s structure is isoelectronic with that of benzene, but its properties are quite different. Pyridine is completely miscible with water, whereas benzene is only slightly soluble. Like all hydrocarbons, benzene is neutral (in the acid–base sense), but because of its nitrogen atom, pyridine is a weak base.Application of 626-05-1

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

The author of 《Construction of Nitrogen-containing Polycyclic Aromatic Compounds by Intramolecular Oxidative C-H/C-H Coupling of Bis(9H-carbazol-9-yl)benzenes and Their Properties》 were Taniguchi, Taisei; Itai, Yuhei; Nishii, Yuji; Tohnai, Norimitsu; Miura, Masahiro. And the article was published in Chemistry Letters in 2019. Category: pyridine-derivatives The author mentioned the following in the article:

Treatment of 1,3- and 1,4-bis(3,6-di-tert-butyl-9H-carbazol-9-yl)benzenes with an oxidizing system of Pd(II)/Ag(I) has been found to induce double intramol. C-H/C-H coupling to give the corresponding highly π-extended polycyclic compds I (X = CH, N), II and III. In contrast, a singly cyclized product IV in a different manner has been isolated from the reaction of 1,2-bis(3,6-di-tert-butyl-9H-carbazol-9-yl)benzene. Cardinal optoelectronic properties of the products have also been estimated2,6-Dibromopyridine(cas: 626-05-1Category: pyridine-derivatives) was used in this study.

2,6-Dibromopyridine(cas: 626-05-1) belongs to pyridine. Pyridine derivatives lend themselves to many roles in the spirited field of supramolecular chemistry – whether as the ligand backbone of metal-organic polymers or presiding over the key electronic stations of nanodevices. In biochemistry, pyridine-containing cofactors are necessary nutrients on which our lives depend. Category: pyridine-derivatives

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Synthetic Route of C5H3Br2NIn 2021 ,《Electronic and geometric structure effects on one-electron oxidation of first-row transition metals in the same ligand framework》 appeared in Dalton Transactions. The author of the article were Boniolo, Manuel; Chernev, Petko; Cheah, Mun Hon; Heizmann, Philipp A.; Huang, Ping; Shylin, Sergii I.; Salhi, Nessima; Hossain, Kamal Md; Gupta, Arvind K.; Messinger, Johannes; Thapper, Anders; Lundberg, Marcus. The article conveys some information:

Developing new transition metal catalysts requires understanding of how both metal and ligand properties determine reactivity. Since metal complexes bearing ligands of the Py5 family (2,6-bis-[(2-pyridyl)methyl]pyridine) were employed in many fields in the past 20 years, authors set out here to understand their redox properties by studying a series of base metal ions (M = Mn, Fe, Co, and Ni) within the Py5OH (pyridine-2,6-diylbis[di-(pyridin-2-yl)methanol]) variant. Both reduced (MII) and the one-electron oxidized (MIII) species were carefully characterized using a combination of x-ray crystallog., x-ray absorption spectroscopy, cyclic voltammetry, and d.-functional theory calculations The observed metal-ligand interactions and electrochem. properties do not always follow consistent trends along the periodic table. this observation cannot be explained by only considering orbital and geometric relaxation, and spin multiplicity changes needed to be included into the DFT calculations to reproduce and understand these trends. In addition, exchange reactions of the sixth ligand coordinated to the metal, were analyzed. Finally, by including published data of the extensively characterized Py5OMe (pyridine-2,6-diylbis[di-(pyridin-2-yl)methoxymethane])complexes, the special characteristics of the less common Py5OH ligand were extracted This comparison highlights the non-innocent effect of the distal OH functionalization on the geometry, and consequently on the electronic structure of the metal complexes. Together, this gives a complete anal. of metal and ligand degrees of freedom for these base metal complexes, while also providing general insights into how to control electrochem. processes of transition metal complexes. The experimental part of the paper was very detailed, including the reaction process of 2,6-Dibromopyridine(cas: 626-05-1Synthetic Route of C5H3Br2N)

2,6-Dibromopyridine(cas: 626-05-1) belongs to pyridine. The basicity and metallophilic high donor number of these π-deficient systems has long favored them as ligands in metal catalysis. The last decade saw pyridine assume a stronger role as functional group for directed C–H oxidation/activation.Synthetic Route of C5H3Br2N

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Electric Literature of C5H3Br2NIn 2020 ,《Controlling Singlet Fission with Coordination Chemistry-Induced Assembly of Dipyridyl Pyrrole Bipentacenes》 was published in ACS Central Science. The article was written by Ribson, Ryan D.; Choi, Gyeongshin; Hadt, Ryan G.; Agapie, Theodor. The article contains the following contents:

Singlet fission has the potential to surpass current efficiency limits in next-generation photovoltaics and to find use in quantum information science. Despite the demonstration of singlet fission in various materials, there is still a great need for fundamental design principles that allow for tuning of photophys. parameters, including the rate of fission and triplet lifetimes. Here, we describe the synthesis and photophys. characterization of a novel bipentacene dipyridyl pyrrole (HDPP-Pent) and its Li- and K-coordinated derivatives HDPP-Pent undergoes singlet fission at roughly 50% efficiency (τSF = 730 ps), whereas coordination in the Li complex induces significant structural changes to generate a dimer, resulting in a 7-fold rate increase (τSF = 100 ps) and more efficient singlet fission with virtually no sacrifice in triplet lifetime. We thus illustrate novel design principles to produce favorable singlet fission properties, wherein through-space control can be achieved via coordination chem.-induced multipentacene assembly. Series of ligand-bridged bipentacenes display differential rates/yields of singlet fission as a result of distinct solution-state structures arising from the identity of the coordinated alkali metal. In the experimental materials used by the author, we found 2,6-Dibromopyridine(cas: 626-05-1Electric Literature of C5H3Br2N)

2,6-Dibromopyridine(cas: 626-05-1) belongs to pyridine. Pyridines, quinolines, and isoquinolines have found a function in almost all aspects of organic chemistry. Pyridine has found use as a solvent, base, ligand, functional group, and molecular scaffold. As structural elements, these moieties are potent electron-deficient groups, metal-directing functionalities, fluorophores, and medicinally important pharmacophores. Electric Literature of C5H3Br2N

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Product Details of 626-05-1In 2021 ,《Rare Fluorescence Red-Shifted Metal-Organic Framework Sensor for Methylamine Derived from an N-Donor Ligand》 was published in Crystal Growth & Design. The article was written by Yao, Shu-Li; Xu, Hui; Zheng, Teng-Fei; Liu, Sui-Jun; Chen, Jing-Lin; Wen, He-Rui. The article contains the following contents:

A three-dimensional (3D) metal-organic framework (MOF) [Cd(bbip)(NDC)]n(JXUST-8, bbip = 2,6-bis(benzimidazol-1-yl)pyridine, and H2NDC = 2,6-naphthalenedicarboxylic acid) with 8-connected bcg topol. was solvothermally synthesized and fully characterized. The fluorescence experiments demonstrate that JXUST-8 could selectively distinguish methylamine (MA) by fluorescence red shift, and the detection limit is 0.341 ppm. It is noteworthy that red shift emission could enlarge the fluorescence signal, which is beneficial to realize sensing. In addition, JXUST-8 performs relatively good thermal stability, chem. stability, and reusability. Importantly, JXUST-8 could be considered as the first example of a bbip-based MOF as well as the second case of a fluorescence red shifted MOF sensor toward MA. In the experiment, the researchers used many compounds, for example, 2,6-Dibromopyridine(cas: 626-05-1Product Details of 626-05-1)

2,6-Dibromopyridine(cas: 626-05-1) belongs to pyridine. Pyridines, quinolines, and isoquinolines have found a function in almost all aspects of organic chemistry. Pyridine has found use as a solvent, base, ligand, functional group, and molecular scaffold. As structural elements, these moieties are potent electron-deficient groups, metal-directing functionalities, fluorophores, and medicinally important pharmacophores. Product Details of 626-05-1

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Nair, Shruthi S.; Bysewski, Oliver A.; Kupfer, Stephan; Waechtler, Maria; Winter, Andreas; Schubert, Ulrich S.; Dietzek, Benjamin published an article in 2021. The article was titled 《Excitation Energy-Dependent Branching Dynamics Determines Photostability of Iron(II)-Mesoionic Carbene Complexes》, and you may find the article in Inorganic Chemistry.COA of Formula: C5H3Br2N The information in the text is summarized as follows:

Photoactive metal complexes containing earth-abundant transition metals recently gained interest as photosensitizers in light-driven chem. In contrast to the traditionally employed ruthenium or iridium complexes, iron complexes developed to be promising candidates despite the fact that using iron complexes as photosensitizers poses an inherent challenge associated with the low-lying metal-centered states, which are responsible for ultrafast deactivation of the charge-transfer states. Nonetheless, recent developments of strongly σ-donating carbene ligands yielded highly promising systems, in which destabilized metal-centered states resulted in prolonged lifetimes of charge-transfer excited states. In this context, we introduce a series of novel homoleptic Fe-triazolylidene mesoionic carbene complexes. The excited-state properties of the complexes were investigated by time-resolved femtosecond transient absorption spectroscopy and quantum chem. calculations Pump wavelength-dependent transient absorption reveals the presence of distinct excited-state relaxation pathways. We relate the excitation-wavelength-dependent branching of the excited-state dynamics into various reaction channels to solvent-dependent photodissociation following the population of dissociative metal centered states upon excitation at 400 nm. In addition to this study using 2,6-Dibromopyridine, there are many other studies that have used 2,6-Dibromopyridine(cas: 626-05-1COA of Formula: C5H3Br2N) was used in this study.

2,6-Dibromopyridine(cas: 626-05-1) belongs to pyridine. Pyridine derivatives lend themselves to many roles in the spirited field of supramolecular chemistry – whether as the ligand backbone of metal-organic polymers or presiding over the key electronic stations of nanodevices. In biochemistry, pyridine-containing cofactors are necessary nutrients on which our lives depend. COA of Formula: C5H3Br2N

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

《Four congenetic zinc(II) MOFs from delicate solvent-regulated strategy: Structural diversities and fluorescent properties》 was written by Wen, Gui-Lin; Liu, Bo; Liu, Dao-Fu; Wang, Feng-Wu; Li, Li; Zhu, Liang; Song, Dong-Mei; Huang, Chao-Xiu; Wang, Yao-Yu. COA of Formula: C5H3Br2NThis research focused onzinc carboxylphenyl pyridine MOF preparation crystal structure thermal stability; fluorescence zinc carboxylphenyl pyridine MOF. The article conveys some information:

Four new congenetic zinc(II) MOFs, namely [Zn5(bdcpp)3(DMF)(H2O)4]n·x(solvent) (1), [Zn2(bdcpp)(Hbdcpp)]n·y(solvent) (2), [Zn2(bdcpp)(DMF)(H2O)2]n (3), and [Zn2(bdcpp)(NMP)(H2O)2]n (4) (H4bdcpp = 2,6-bis(2′,4′-dicarboxylphenyl)pyridine, DMF = N,N’-dimethylformamide, NMP = N-methyl-2-pyrrolidone), were synthesized solvothermally with different solvent systems. Stabilized by Zn2(COO)4 paddle-wheel building blocks, the resulting MOFs 1-4 represent diverse structural features. Structurally, 1 is a rarely 3,4-c binodal 2D bilayered framework, 2 possesses a 4-c 2D (4,4) sql planar network accommodating two kinds of hetero chiral helix chains, 3 and 4 are isostructural 1D loop ladder chains except different solvent mols. occupying the axial terminals of Zn2(COO)4 paddle-wheels. This approach based on solvent-regulated strategy aiming to allow the structural fine-tuning provides a good role model in reticular chem. Complexes 1-3 display excellent solid-state photoluminescence stemming from the metal-to-ligand charge transfer or intraligand charge transmission. The results came from multiple reactions, including the reaction of 2,6-Dibromopyridine(cas: 626-05-1COA of Formula: C5H3Br2N)

2,6-Dibromopyridine(cas: 626-05-1) belongs to pyridine. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Additionally, pyridine-based natural products continue to be discovered and studied for their properties and to understand their biosynthesis.COA of Formula: C5H3Br2N

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

In 2022,Wolinska, Ewa; Rozbicki, Przemyslaw; Branowska, Danuta published an article in Monatshefte fuer Chemie. The title of the article was 《Chiral pyridine oxazoline and 1,2,4-triazine oxazoline ligands incorporating electron-withdrawing substituents and their application in the Cu-catalyzed enantioselective nitroaldol reaction》.Formula: C5H3Br2N The author mentioned the following in the article:

Eight pyridine-containing and four 1,2,4-triazine-containing chiral oxazoline ligands incorporating electron-withdrawing substituents have been oxazolines I (R1 = Ph, t-Bu; R2 = H, F; R3 = H, Cl; R4 = H, F, Cl, nitro; R5 = H, Br), II and III synthesized by two-step route including Buchwald-Hartwig amination. Enantio-inducing activity of the ligands has been assessed in the copper-catalyzed asym. nitroaldol reactions and the influence of the electron-withdrawing substituents on the ligands’ activity has been investigated. In the experiment, the researchers used 2,6-Dibromopyridine(cas: 626-05-1Formula: C5H3Br2N)

2,6-Dibromopyridine(cas: 626-05-1) belongs to pyridine. When pyridine is adsorbed on oxide surfaces or in porous materials, the following species are commonly observed: (i) pyridine coordinated to Lewis acid sites, (ii) pyridine H-bonded to weakly acidic hydroxyls, and (iii) protonated pyridine. At high coverage, physisorbed pyridine and protonated dimers can also be observed.Formula: C5H3Br2N

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

《Encapsulation of Phosphorescent Pt(II) Complexes in Zn-Based Metal-Organic Frameworks toward Oxygen-Sensing Porous Materials》 was written by Knedel, Tim-Oliver; Buss, Stefan; Maisuls, Ivan; Daniliuc, Constantin G.; Schluesener, Carsten; Brandt, Philipp; Weingart, Oliver; Vollrath, Annette; Janiak, Christoph; Strassert, Cristian A.. Name: 2,6-Dibromopyridine And the article was included in Inorganic Chemistry in 2020. The article conveys some information:

In this work, two tailored phosphorescent Pt(II) complexes are synthesized bearing a cyclometalating tridentate thiazole-based C^N*N pincer luminophore (L) and exchangeable chlorido ([PtCl(L)]) or cyanido ([PtCN(L)]) coligands. While both complexes showed photoluminescence from metal-perturbed ligand-centered triplet states (3MP-LC), [PtCN(L)] reached the highest phosphorescence quantum yields and displayed a significant sensitivity toward quenching by 3O2. They were encapsulated into two Zn-based metal-organic frameworks, namely, MOF-5 and ZIF-8. The incorporation of the organometallic compounds in the resulting composites [PtCl(L)]@ZIF-8, [PtCN(L)]@ZIF-8, [PtCl(L)]@MOF-5 and [PtCN(L)]@MOF-5 was verified by powder X-ray diffractometry, SEM, time-resolved photoluminescence spectroscopy and microscopy, as well as N2- and Ar-gas sorption studies. The amount of encapsulated complex was determined by graphite furnace at. absorption spectroscopy, showing a maximum loading of 3.7 wt %. If compared with their solid state forms, the solid-solution composites showed prolonged 3O2-sensitive excited state lifetimes for the complexes at room temperature, reaching up to 18.4μs under an Ar atm., which is comparable with the behavior of the complex in liquid solutions or even frozen glassy matrixes at 77 K. Two tailored phosphorescent Pt(II) complexes were synthesized bearing a cyclometalating tridentate thiazole-based C^N*N pincer luminophore and exchangeable coligands. They were encapsulated into two Zn-based metal-organic frameworks, namely, MOF-5 and ZIF-8. If compared with their liquid solutions, the solid-solution composites showed prolonged 3O2-sensitive excited state lifetimes for the complexes at room temperature, reaching up to 18.4μs under an Ar atm., which is comparable with the behavior of the complex in frozen glassy matrixes at 77 K.2,6-Dibromopyridine(cas: 626-05-1Name: 2,6-Dibromopyridine) was used in this study.

2,6-Dibromopyridine(cas: 626-05-1) belongs to pyridine. Pyridine derivatives lend themselves to many roles in the spirited field of supramolecular chemistry – whether as the ligand backbone of metal-organic polymers or presiding over the key electronic stations of nanodevices. In biochemistry, pyridine-containing cofactors are necessary nutrients on which our lives depend. Name: 2,6-Dibromopyridine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Weilhard, Andreas; Argent, Stephen P.; Sans, Victor published an article in 2021. The article was titled 《Efficient carbon dioxide hydrogenation to formic acid with buffering ionic liquids》, and you may find the article in Nature Communications.Quality Control of 2,6-Dibromopyridine The information in the text is summarized as follows:

The efficient transformation of CO2 into chems. and fuels is a key challenge for the decarbonisation of the synthetic production chain. Formic acid (FA) represents the first product of CO2 hydrogenation and can be a precursor of higher added value products or employed as a hydrogen storage vector. Bases are typically required to overcome thermodn. barriers in the synthesis of FA, generating waste and requiring post-processing of the formate salts. The employment of buffers can overcome these limitations, but their catalytic performance has so far been modest. Here, we present a methodol. utilizing IL as buffers to catalytically transform CO2 into FA with very high efficiency and comparable performance to the base-assisted systems. The combination of multifunctional basic ionic liquids and catalyst design enables the synthesis of FA with very high catalytic efficiency in TONs of >8*105 and TOFs > 2.1*104 h-1.2,6-Dibromopyridine(cas: 626-05-1Quality Control of 2,6-Dibromopyridine) was used in this study.

2,6-Dibromopyridine(cas: 626-05-1) belongs to pyridine. Pyridine is a relatively complex molecule and exhibits a number of different bands in IR spectra. Among others, the bands characterizing the ν8a and ν19b modes have been found to be sensitive to the coordination or protonation of the molecule. Note that the band that is diagnostic for the PyH+ ion at about 1545 cm− 1 (ν19b mode) does not overlap with any of the other bands.Quality Control of 2,6-Dibromopyridine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem