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Zwitterionization of multiwalled carbon nanotubes (ZCNTs) is initially conducted by grafting poly(4-styrenesulfonic acid) and poly(4-vinylpyridine) copolymers via an atom transfer radical polymerization (ATRP) reaction, and the products obtained are further used as an aqueous additive to fabricate thin-film nanocomposite (TFN) nanofiltration (NF) membranes. The most optimal membrane with a ZCNT dosage of 0.01%, Z-TFN 0.01% shows nearly 31% enhancement in water permeability (14.9 ± 0.5 L m-2 h-1 bar-1), probably due to the shortened ZCNT, which could create a larger number of inorganic-organic interfaces in the barrier layers. Besides, it also exhibits MgSO4/NaCl selectivity (5.6 ± 0.8), 2.8 times higher than that of the pristine one (2.0 ± 0.2), which is attributed to the formation of ion-response channels and the stretching effect of the side chains. By using model brackish water as the feed solution and subjecting it to a two-stage NF process, the outstanding separation ability of the Z-TFN 0.01% membrane for the ions with the final Na+/Mg2+ concentration ratio in the permeate reaching as high as 589.2, as against only 111.7 for the control, is displayed. Furthermore, due to the strong bacteriostasis ability of quaternary ammonium compounds, Z-TFN 0.01% also shows excellent antibacterial properties, as evidenced by the mortality of Escherichia coli to 97% after remaining in contact with the membrane surface.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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The efficient synthesis of large-ring pseudopeptidic macrocycles through a multicomponent [2 + 2] reductive amination reaction is described. The reaction was entirely governed by the structural information contained in the corresponding open-chain pseudopeptidic bis(amidoamine) precursors, which have a rigid (R,R)-cyclohexane-1,2-diamine moiety. A remarkable match/mismatch relationship between the configurations of the chiral centers of the cyclic diamine and those of the peptidic frame was observed. The macrocyclic tetraimine intermediates have been studied in detail by NMR spectroscopy, circular dichroism (CD), and molecular modeling, and the results support the appropriate preorganization induced by the match combination of the chiral centers. We have also synthesized the corresponding open-chain bis(imine) model compounds. The structural studies (NMR spectroscopy, CD, modeling) of these systems showed an intrinsically lower reactivity of the mismatch combination, even when the product of the reaction was acyclic. In addition, a synergistic effect between the two chiral substructures for the correct folding of the molecules was observed. Finally, X-ray analysis of the HCl salt of one of the macrocycles showed an interesting pattern; the macrocyclic rings stack in columnar aggregates leaving large interstitial channels filled with water-solvated chloride anions.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Reference of 3030-47-5, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.3030-47-5, Name is N1-(2-(Dimethylamino)ethyl)-N1,N2,N2-trimethylethane-1,2-diamine, molecular formula is C9H23N3. In a Article,once mentioned of 3030-47-5

An efficient synthesis of 5-organotellanyl-1H-1,2,3-triazole compounds was accomplished through [3+2] cycloaddition reaction of organic azides and (organotellanyl)alkynes. Additionally, 5-organotellanyl-1H-1,2,3-triazoles were readily functionalized at the 5-position by using a Sonogashira cross-coupling reaction, leading to highly functionalised triazoles. The regiochemistry of the products was assessed by two-dimensional NMR spectroscopic experiments and X-ray crystallography. An efficient synthesis of 5-organotellanyl-1H-1,2,3-triazole compounds through [3+2] cycloaddition reaction of organic azides and (organotellanyl)alkynes is presented. The 5-organotellanyl-1H-1,2,3-triazoles were readily functionalized at the 5-position to give highly functionalized triazoles. Copyright

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

A new application about 6-Methyl-2,2′-bipyridine

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Synthetic Route of 56100-22-2, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.56100-22-2, Name is 6-Methyl-2,2′-bipyridine, molecular formula is C11H10N2. In a Article,once mentioned of 56100-22-2

Cobalt complexes have shown great promise as electrocatalysts in applications ranging from hydrogen evolution to C-H functionalization. However, the use of such complexes often requires polydentate, bulky ligands to stabilize the catalytically active Co(I) oxidation state from deleterious disproportionation reactions to enable the desired reactivity. Herein, we describe the use of bidentate electronically asymmetric ligands as an alternative approach to stabilizing transient Co(I) species. Using disproportionation rates of electrochemically generated Co(I) complexes as a model for stability, we measured the relative stability of complexes prepared with a series of N,N-bidentate ligands. While the stability of Co(I)Cl complexes demonstrates a correlation with experimentally measured thermodynamic properties, consistent with an outer-sphere electron transfer process, the set of ligated Co(I)Br complexes evaluated was found to be preferentially stabilized by electronically asymmetric ligands, demonstrating an alternative disproportionation mechanism. These results allow a greater understanding of the fundamental processes involved in the disproportionation of organometallic complexes and have allowed the identification of cobalt complexes that show promise for the development of novel electrocatalytic reactions.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Related Products of 4730-54-5, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 4730-54-5, Name is 1,4,7-Triazacyclononane, molecular formula is C6H15N3. In a Review,once mentioned of 4730-54-5

More than 2 million people fleeing conflict, persecution, and poverty applied for asylum between 2015 and 2016 in the European Union. Due to this, medical practitioners in recipient countries may be facing a broader spectrum of conditions and unusual presentations not previously encountered, including a wide range of infections with pulmonary involvement. Tuberculosis is known to be more common in migrants and has been covered broadly in other publications. The scope of this review was to provide an overview of exotic infections with pulmonary involvement that could be encountered in refugees and migrants and to briefly describe their epidemiology, diagnosis, and management. As refugees and migrants travel from numerous countries and continents, it is important to be aware of the various organisms that might cause disease according to the country of origin. Some of these diseases are very rare and geographically restricted to certain regions, while others have a more cosmopolitan distribution. Also, the spectrum of severity of these infections can vary from very benign to severe and even life-threatening. We will also describe infectious and noninfectious complications that can be associated with HIV infection as some migrants might originate from high HIV prevalence countries in sub-Saharan Africa. As the diagnosis and treatment of these diseases can be challenging in certain situations, patients with suspected infection might require referral to specialized centers with experience in their management. Additionally, a brief description of noncommunicable pulmonary diseases will be provided.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Properties and Exciting Facts About 2-(1H-1,2,4-Triazol-3-yl)pyridine

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Related Products of 23195-62-2, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 23195-62-2, Name is 2-(1H-1,2,4-Triazol-3-yl)pyridine, molecular formula is C7H6N4. In a Article,once mentioned of 23195-62-2

A new copper coordination polymer [Cu2I(C7H5N4)2]n (1) with the 3-(pyridin-2-yl)- 1,2,4-triazole (Hpt) and copper iodide was synthesized. It crystallizes in the triclinic space group P1 with a = 8.6380(9), b = 9.2434(9), c = 11.8588(12) A, alpha = 99.5890(10), beta = 109.0990(10)o, gamma = 105.2800(10)o, V = 829.25(15) A3, Dc = 2.180 g/cm3, Z = 2, F(000) = 522, GOOF = 1.046, the final R = 0.0245 and wR = 0.0598. The crystal structure shows that two copper ions are bridged by two mu2-n1:n0-3-(pyridin-2-yl)-1,2,4-triazole anions and two iodide ions. The coordination environments of the Cu ion are Cu(1)N5 and Cu(2)N2I2, giving distorted square pyramidal geometry and trigon pyramid geometry. The magnetic and fluorescent properties of 1 were studied.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Surface-initiated polymerizations were carried out from polymeric surfaces of commercially important polyester films, poly(ethylene terephthalate) (PET) and poly(ethylene naphthalate) (PEN). These plastic films were modified prior to polymerization by plasma oxidation, exposing surface hydroxyl groups, in order to immobilise patterned self assembled monolayers (SAMs) of trichlorosilane initiator, through the soft lithographic method of microcontact printing (muCP). Subsequently, polymerizations were initiated from the surface via controlled atom transfer radical polymerization (ATRP), under aqueous conditions, to create patterned brushes of the thermo-responsive polymer poly(N-isopropyl acrylamide) (PNIPAM). By creating patterned, rather than homogeneous brushes characterization was made possible by atomic force microscopy (AFM).

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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The invention discloses an inferior ethyl bridge – wuwu zirconium indene, Louis compound and its preparation method and application in the oligomerization of propylene. The invention of the ethylenedioxy-based hydrosilane – wuwu zirconium, Louis composition can be through the ethylenedioxy – fluorenylmethylchloroformate ligand compound hydrosilane-first with alkyl alkali metal in the organic medium reaction, then adding ZrCl4 Or HfCl4 Obtained by the method. The invention of the linen – wuwu zirconiumethyl bridge indene, Louis compound is a high-efficient catalyst, under a comparatively mild condition, used for catalytic oligomerization of propylene, with high catalytic activity, and of the untreated alkyl the alumina alkane helps can be high under the catalysis of the selectively containing the allyl group of acrylic oligomer; at the same time can be controlled by polymerization reaction conditions for the realization of aligned polymer molecular weight control, and has very high industrial application value. Its structure has the following general formula: (by machine translation)

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Rhombimines, chiral macrocyclic tetraimines, are preferentially formed because of the structural bias in the reaction of aromatic ether-linked dialdehydes with enantiomerically pure trans-1,2-diaminocyclohexane.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Chiral ordered mesoporous silica (COMS) was synthesized in basic media by combining tetraethyl orthosilicate and quaternized aminosilane (with a templating role) silica sources together with four different standard amino acids (arginine, histidine, isoleucine, and proline). Besides the hexagonal MCM-41-type structure, narrow pore size distribution, and high specific surface area, it was found that these solids have potential for enantiomeric separation because of the transference of chirality from the amino acid to the silica. This is illustrated by the resolution of several racemic mixtures (those of proline, isoleucine, trans-4-hydroxyproline, pipecolic acid, valine, leucine, and phenylglycine) with the calcined COMS prepared with l-proline. The opposite behavior observed in induced circular dichroism experiments with calcined COMS, obtained using both enantiomers of proline, confirmed their chiral nature. The high number and variety of existing amino acids, and chiral organic compounds in general, makes these ordered silicas attractive for the production of enantiopure substances.(Figure Presented)

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI