Tag: M.W=100-200

Name: (2S)-(+)-3-Chloropropane-1,2-diol. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: (2S)-(+)-3-Chloropropane-1,2-diol, is researched, Molecular C3H7ClO2, CAS is 60827-45-4, about Porphyrin with circularly polarized luminescence in aggregated states. Author is Wang, Rongqiao; Chen, Shibing; Chen, Qiaoru; Guo, Hongyu; Yang, Fafu.

Porphyrin with circularly polarized luminescence (CPL) in aggregated state was seldom presented due to the strong aggregation-caused quenching (ACQ) effect at aggregation. This work designed and synthesized a novel porphyrin derivative (CPL-P) with good CPL behavior in aggregated states based on the strong AIE-FRET effect and good chirality transfer of liquid crystalline porphyrin, which was constructed by using porphyrin unit as core with four AIE cyanostilbene groups bearing peripheral chiral alkyl chains. CPL-P exhibited orderly hexagonal columnar mesophase between 62.5°C and 113.2°C. It displayed excellent fluorescence emission at 640-760 nm in aggregated states due to the AIE-FRET effect between cyanostilbene unit and porphyrin moiety. Moreover, CPL-P showed the strong CD and CPL properties in aggregated states based on the effective chiral transfer of the spiral liquid crystalline self-assembly. The |glum| value for mesophase attained 6.6 x 10-3 based on the combining effect of AIE-FRET and chiral transfer. This research supplied a new strategy for transferring typical achiral porphyrin with ACQ effect to luminescent mol. with good CPL behavior in aggregated state.

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Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Electric Literature of C9H11Cu. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Mesitylcopper(I), is researched, Molecular C9H11Cu, CAS is 75732-01-3, about Unusual structurally characterized pyridine carbinoxide copper(II) coordination compounds, isolated from organic solvents. Author is Boyle, Timothy J.; Ottley, Leighanna M.; Raymond, Rebecca.

The coordination behavior of pyridine-2-methanol (H-OPy) with copper in organic solvents was crystallog. determined Initial attempts to generate the Cu(II) OPy derivatives from an alcoholysis exchange of Cu(OCH3)2, with H-OPy in toluene, gave [Cu(μc-OPy)(OcPy)]2 (1, c indicates chelation). The square-based pyramidal geometries noted for each Cu center resulted from one OcPy and two μc-OPy ligands, generating an unusual Ci symmetry. From the reaction of H-OPy and the Cu(I) species Cu(C6H2(CH3)3-2,4,6), mononuclear Cu(II) complex Cu(OcPy)2(H-OPy)2 (2) was isolated. Compound 2 is unusual in that it adopts a square planar arrangement around the Cu metal center using two OcPy ligands; however, the metal center also coordinates with two H-OPy mols. forming an octahedral geometry. Upon dissolution in water, both 1 and 2 react to form the previously reported Cu(OcPy)2·2H2O (3). Attempts to add a Lewis base through dissolution of 1 in selected solvents (i.e., THF, pyridine, 1-methylimidazole) led to [Cu(μc-OPy)(OcPy)]2·H2O (4), which possesses a C2 symmetry. The water was believed to be extracted from the dry solvents. A Cl derivative was also solved for the Cu(II)/Cu(I) species [Cu(OPy)2]2[CuCl(H-OPy)2]2 (5) from THF dried over apparently contaminated sieves. 1-5 Were characterized by x-ray crystallog.

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Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Models for the reactive states of homocuprates: syntheses, structures and reactivities of [Cu2Li2Mes4] and [Cu3LiMes4], published in 2007-01-21, which mentions a compound: 75732-01-3, mainly applied to copper lithium tetranuclear mesityl metallacycle preparation structure; crystal structure copper lithium tetranuclear mesityl metallacycle; mol structure copper lithium tetranuclear mesityl metallacycle; enone regioselective addition reaction copper lithium mesityl metallacycle promotion; DFT structure copper lithium tetranuclear mesityl metallacycle, Related Products of 75732-01-3.

The synthesis and characterization (including x-ray crystallog.) of two novel tetranuclear and thermally-stable Li arylcuprates, [Cu2Li2Mes4] and [Cu3LiMes4], are reported. [Cu3LiMes4] is a highly active regioselective promoter for the 1,4-addition of organolithiums to enones (e.g. ≤96% conversion of cyclohex-2-enone to 3-butylcyclohexanone). DFT studies of 3 isomeric forms of [Cu2Li2Mes4] are reported.

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Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

The reaction of an aromatic heterocycle with a proton is called a protonation. One of articles about this theory is 《Oligomers. XVI. Oligomers of acrylonitrile. II. Polymerization and degradation investigations》. Authors are Zahn, Helmut; Schafer, Paul.The article about the compound:2-Methylglutaronitrilecas:4553-62-2,SMILESS:N#CC(C)CCC#N).Application of 4553-62-2. Through the article, more information about this compound (cas:4553-62-2) is conveyed.

cf. C.A. 53, 13993c. The polymerization of acrylonitrile with dodecyl mercaptan in the presence of pyridine resulted in a polymer of average mol. weight 950. From 170° on, melting oligomers with mol. weights from 280 were obtained by fractional precipitation Some HCN has been split off during thermal degradation of polyacrylonitrile. The liquid products formed at 550° were shown to be mainly nitriles which could be separated into 4 fractions. Acrylonitrile and a dimer could be found, the latter was identical with synthetic 1,3-dicyanobutane. 33 references.

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Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (2S)-(+)-3-Chloropropane-1,2-diol( cas:60827-45-4 ) is researched.Product Details of 60827-45-4.Bredikhina, Zemfira A.; Kurenkov, Alexey V.; Zakharychev, Dmitry V.; Krivolapov, Dmitry B.; Bredikhin, Alexander A. published the article 《New example of spontaneous resolution among aryl glycerol ethers: 3-(2,6-dichlorophenoxy)propane-1,2-diol》 about this compound( cas:60827-45-4 ) in Journal of Molecular Structure. Keywords: crystallization spontaneous resolution dichlorophenoxypropanediol. Let’s learn more about this compound (cas:60827-45-4).

Using a set of simple tests, based on the properties of ideal conglomerate phase diagrams, it was suggested to the conglomerate-formative nature of 3-(2,6-dichlorophenoxy)propane-1,2-diol 1. Addnl. arguments were drawn during the study of a single crystal x-ray diffraction study of the compound The crystal packing details were evaluated and discussed. Racemic 1 were resolved into individual (S)- and (R)-components by a preferential crystallization procedure.

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Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Optimizing organic electrosynthesis through controlled voltage dosing and artificial intelligence, published in 2019-09-03, which mentions a compound: 4553-62-2, Name is 2-Methylglutaronitrile, Molecular C6H8N2, Quality Control of 2-Methylglutaronitrile.

Organic electrosynthesis can transform the chem. industry by introducing electricity-driven processes that are more energy efficient and that can be easily integrated with renewable energy sources. However, their deployment is severely hindered by the difficulties of controlling selectivity and achieving a large energy conversion efficiency at high c.d. due to the low solubility of organic reactants in practical electrolytes. This control can be improved by carefully balancing the mass transport processes and electrocatalytic reaction rates at the electrode diffusion layer through pulsed electrochem. methods. The authors explore these methods in the context of the electrosynthesis of adiponitrile (ADN), the largest organic electrochem. process in industry. Systematically exploring voltage pulses in the timescale between 5 and 150 ms led to a 20% increase in production of ADN and a 250% increase in relative selectivity with respect to the state-of-the-art constant voltage process. Also, combining this systematic exptl. study with artificial intelligence (AI) tools allowed the authors to rapidly discover drastically improved electrosynthetic conditions, reaching improvements of 30 and 325% in ADN production rates and selectivity, resp. This powerful AI-enhanced exptl. approach represents a paradigm shift in the design of electrified chem. transformations, which can accelerate the deployment of more sustainable electrochem. manufacturing processes.

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Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Preparation and characterization of copper(I) amides, published in 1981, which mentions a compound: 75732-01-3, Name is Mesitylcopper(I), Molecular C9H11Cu, Synthetic Route of C9H11Cu.

Cu(I) amides, CuNRR’, were prepared by the reaction of mesitylcopper(I) with RR’NH and characterized by chem. and thermal analyses. CuNRR’ react with CO2 in C6H6 in presence of tert-BuNC to give RR’NCO2Cu.(tert-Bu-NC)n, which with MeI give RR’NCO2Me.

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Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Oligonuclear Homoleptic Copper(I) Pyrazolates with Multinucleating Ligand Scaffolds: High Structural Diversity in Solid-State and Solution, published in 2009-11-02, which mentions a compound: 75732-01-3, Name is Mesitylcopper(I), Molecular C9H11Cu, Synthetic Route of C9H11Cu.

The synthesis of three pyrazole-based, potentially binucleating ligands 3,5-bis(R1NMeCH2)-4-R2pyrazole (L1H: R1 = pyridyl-2-methyl-, R2 = Ph; L2H: R1 = 8-quinolyl-, R2 = H; L3H: R1 = 8-quinolyl-, R2 = Ph) is described. Reaction of L1-3H with 1 equiv of mesitylcopper affords oligonuclear homoleptic complexes [CuL]n (1-3). The single crystal x-ray structure of 2 shows a tetranuclear assembly of linear coordinated Cu(I)-centers bridged by pyrazolato ligands that alternate above and below the Cu4 plane, with addnl. weak interactions from some of the ligand side arms. As the single crystal X-ray structure of 3 reveals, Ph substitution at the 4-position of the pyrazolato framework leads to significant structural modification of the Cu4 array, giving a rhombical tetranuclear complex with two linear coordinated Cu(I) centers that exhibit a short intramol. Cu···Cu contact (2.8212(10) Å) and two peripheral Cu(I) centers in a distorted tetrahedral coordination mode. Thus, 3 represents a very rare example of an inorganic pyrazolato cuprate which can also be viewed as a partly rearranged structural isomer of 2. Also, the crystal lattice of 3 shows an extended network of intra- and intermol. π-π stacking interactions between the aromatic rings. In solution, 1-3 each form two types of oligomers a and b that slowly (<1 s-1) equilibrate at room temperature Using Diffusion Ordered Spectroscopy (DOSY) and variable temperature 1H NMR spectroscopy, a and b correspond to a tetrameric and a (planar) trimeric species. Coordination of the pyridyl/quinolyl side arms that is observed in the solid state seems to be only transient in solution This literature about this compound(75732-01-3)Synthetic Route of C9H11Cuhas given us a lot of inspiration, and I hope that the research on this compound(Mesitylcopper(I)) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Related Products of 75732-01-3. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: Mesitylcopper(I), is researched, Molecular C9H11Cu, CAS is 75732-01-3, about A heteroleptic tetranuclear copper amide/aryl complex: 1,4:2,3-bis(μ-2,4,6-trimethylphenyl-C,C)-1,2:3,4-bis[μ-bis(trimethylsilyl)amido-N,N]tetracopper(I). Author is Niemeyer, Mark.

The title compound, [1,2:3,4-(CuBtsa)2-1,4:2,3-(CuMes)2] [Btsa is N(SiMe3)2; Mes is 2,4,6-Me3C6H2], was obtained as the product of a ligand redistribution between the GeII amide, GeBtsa2, and the CuI aryl, CuMes. The compound is triclinic, space group P1̅, with a 9.171(2), b 11.353(2), c 20.314(4) Å, α 101.98(1), β 94.56(2), γ 107.28(2)°; Z = 2, dc = 1.383; R = 0.037, Rw(F2) = 0.101 for 8527 reflections. It contains an almost planar eight-membered central ring, Cu4C2N2, with two-coordinate Cu atoms (average Cu-C 1.986, average Cu-N 1.936, average C-Cu-N 169.97°).

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Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Product Details of 75732-01-3. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: Mesitylcopper(I), is researched, Molecular C9H11Cu, CAS is 75732-01-3, about Organoborane substituted polythiophenes. Author is Li, Haiyan; Sundararaman, Anand; Venkatasubbaiah, Krishnan; Jakle, Frieder.

Side group diarylboryl substituted polythiophenes through silicon-boron exchange were synthesized. It was found that all the synthesized polymers are strongly colored. Varying the aryl substitution on boron can tailor the photophys. behavior. Thus, their potential applications in electronic devices and as sensor materials are under investigation.

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Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com