Tag: 600-700

On January 21, 2011, Cho, Hyun Chul; Lee, Han Sol; Chun, Jiseul; Lee, Sang Moon; Kim, Hae Jin; Son, Seung Uk published an article.Category: iodides-buliding-blocks The title of the article was Tubular microporous organic networks bearing imidazolium salts and their catalytic CO2 conversion to cyclic carbonates. And the article contained the following:

Tubular microporous organic networks bearing imidazolium salts (T-IM) were prepared by Sonogashira coupling of tetrakis(4-ethynylphenyl)methane and diiodoimidazolium salts, which showed promising catalytic activities in heterogeneous conversion of CO2 into cyclic carbonates. The experimental process involved the reaction of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)(cas: 934008-48-7).Category: iodides-buliding-blocks

The Article related to imidazolium tubular microporous network catalyst insertion carbon dioxide epoxide, cyclic carbonate preparation insertion carbon dioxide epoxide catalyst, Heterocyclic Compounds (More Than One Hetero Atom): Dioxoles, Oxathioles, Dithioles and other aspects.Category: iodides-buliding-blocks

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

On September 30, 2017, Inamori, Daiki; Miwa, Takuya; Fujihara, Tetsuaki; Tsuji, Yasushi; Terao, Jun published an article.Name: 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1) The title of the article was Thieme Chemistry Journals Awardees – Where Are They Now? Synthesis of a Dinuclear Copper NHC Complex Bearing a Rigid 蟺-Conjugated Cyclic Framework. And the article contained the following:

Macrocyclic dinuclear complexes have been gaining popularity in the design of homogeneous catalysts. Herein, we report the design of such a complex featuring catalytically active sites fixed inside the ring and its synthesis using a cross-coupling reaction. The experimental process involved the reaction of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)(cas: 934008-48-7).Name: 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)

The Article related to copper macrocycle heterocyclic carbene conjugation preparation optimized structure, Organometallic and Organometalloidal Compounds: Groups Ib, Iib – Cu, Ag, Au, Zn, Cd, Hg and other aspects.Name: 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)

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

On April 12, 2010, Chun, Jiseul; Lee, Han Sol; Jung, Il Gu; Lee, Soon Won; Kim, Hae Jin; Son, Seung Uk published an article.Quality Control of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1) The title of the article was Cu2O: A Versatile Reagent for Base-Free Direct Synthesis of NHC-Copper Complexes and Decoration of 3D-MOF with Coordinatively Unsaturated NHC-Copper Species. And the article contained the following:

A new and direct synthetic route for N-heterocyclic carbene (NHC)-copper complexes was disclosed by heating imidazolium halides with Cu2O. The related synthetic procedure was quite simple and the product easily separable from the reaction mixture by simple filtration. Ultimately, this reaction was successfully applied to decorate three-dimensional(3D)-metal organic framework (MOFs) with coordinatively unsaturated NHC-copper species. The experimental process involved the reaction of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)(cas: 934008-48-7).Quality Control of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)

The Article related to copper oxide versatile reagent nhc carbene complex, imidazolium halide reaction copper monoxide, crystal mol structure copper cerium imidazolidene carbene complex, Organometallic and Organometalloidal Compounds: Groups Ib, Iib – Cu, Ag, Au, Zn, Cd, Hg and other aspects.Quality Control of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)

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

On November 16, 2018, Ormerod, Dominic; Dorbec, Matthieu; Merkul, Eugen; Kaval, Nadya; Lefevre, Nicolas; Hostyn, Steven; Eykens, Lies; Lievens, Jo; Sergeyev, Sergey; Maes, Bert U. W. published an article.Recommanded Product: 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1) The title of the article was Synthesis of Pd Complexes Containing Tailed NHC Ligands and Their Use in a Semicontinuous Membrane-Assisted Suzuki Cross-Coupling Process. And the article contained the following:

Homogeneous catalysis has proved to be a reliable method for preparing numerous mol. entities, but catalysts can be expensive and difficult to remove. Because of this, industry targets catalysts that are easily separated and recovered and feature increased turnover numbers The ongoing shift from multipurpose batch reactors toward continuous manufacturing in fine chems. synthesis results in a new set of catalyst requirements. This paper reports the design and use of Pd complexes suitable for a semicontinuous Suzuki cross-coupling reaction based on a membrane-assisted reactor. These Pd complexes contain tailed N-heterocyclic carbene (NHC) ligands, allowing internal catalyst recovery by organic solvent nanofiltration with top-layer-modified ceramic membranes. These membranes give selective nanofiltration of the catalyst based on a combination of size exclusion and affinity separation (solvent-solute-membrane interactions). The semicontinuous system developed led to significantly improved turnover numbers, simplified product isolation, and consequently reduced mass intensity by simply adding more of the reactants and reagents to the reaction vessel. The experimental process involved the reaction of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)(cas: 934008-48-7).Recommanded Product: 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)

The Article related to palladium nitrogen heterocyclic carbene complex preparation catalyst, semicontinuous membrane assisted suzuki cross coupling palladium catalyst, Organometallic and Organometalloidal Compounds: Group Viii – Co, Ni, Ru, Rh, Pd, Os, Ir, Pt and other aspects.Recommanded Product: 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)

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

On April 12, 2007, Chung, Young-Keun; Jung, Il-Gu; Chun, Sung-Ho; Park, Young-Whan; Yoon, Sung-Cheol; Lim, Taesun; Lee, Jungmin; Choi, Dai-Seung published a patent.Recommanded Product: 934008-48-7 The title of the patent was Metal complex catalysts for polymerizing cyclic olefins. And the patent contained the following:

Cyclic olefin-based monomers are polymerized using a metal catalyst complex represented by: [M(L1)x(L’2)y(L3)z]a[Ani]b wherein M is a Group X metal; [M(L1)x (L’2)y(L3)z] is a cationic precatalyst; L1 is an anionic hydrocarbyl-containing ligand; L’2 is a neutral ligand; L3 is an N-heterocyclic carbene ligand; [Ani] is an anion capable of weakly coordinating with the metal M; x is 1 or 2; y is 0 to 4; z is 1 or 2; 2鈮+y+z鈮?; a and b are each 1 to 10. The metal catalyst complex has an N-heterocyclic carbene ligand, and thus, is excellent in thermal stability and reactivity. The experimental process involved the reaction of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)(cas: 934008-48-7).Recommanded Product: 934008-48-7

The Article related to cyclic olefin polymerization metal complex catalyst, Chemistry of Synthetic High Polymers: Polymerization Kinetics, Mechanisms, Thermodynamics, Catalysis, Catalysts and other aspects.Recommanded Product: 934008-48-7

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

On April 26, 2007, Chung, Young-Keun; Jung, Il-Gu; Chun, Sung-Ho; Park, Young-Whan; Choi, Dai-Seung; Yoon, Sung-Cheol; Lim, Taesun; Lee, Jungmin published a patent.Reference of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1) The title of the patent was Production of cyclic olefin polymer using a metal complex catalyst having an N-heterocyclic carbene ligand. And the patent contained the following:

The polymer is produced by addition polymerization of a cyclic olefin monomer in the presence of a metal complex catalyst represented by [M(L1)x(L2)y(L3)z]a[Ani]b, wherein M=a Group X metal; [M(L1)x(L2)y(L3)z]=a cationic complex; L1=an anionic hydrocarbyl-containing ligand; L2=a neutral ligand; L3=an N-heterocyclic carbene ligand; [Ani]=an anion capable of weakly coordinating with the metal M; x=1 or 2; y=0-4; z=1 or 2; 2鈮+y+z鈮?; a, b=number of 1-10 which is used to satisfy the net charge balance of the metal catalyst complex. Thus, 5.6 g 4-bromo-2,6-dimethyl aniline and 1.58 mL 40% glyoxal were reacted for 48 h to give 4.1 g N,N’-bis(4-bromo-2,6-dimethylphenyl)-1,2-ethanediimine, , 3 g of which was reacted with 0.22 g para-formaldehyde in the presence of 4M HCl to give 1.8 g gray powder, 1.5 g of which was added with 0.39 g potassium tert-butoxide, stirred for 4 h, to give 0.9 g carbene compound (A). Carbene compound A (0.9 g) and 0.38 g palladium allyl chloride were reacted in THF for 1 h to give 1.2 g palladium complex, which was combined with silver tetrafluoroborate to polymerize norbornene at 80掳 for 24 h to give a norbornene homopolymer with 99% yield. The experimental process involved the reaction of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)(cas: 934008-48-7).Reference of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)

The Article related to norbornene palladium heterocyclic carbene polymerization catalyst, Chemistry of Synthetic High Polymers: Polymerization Kinetics, Mechanisms, Thermodynamics, Catalysis, Catalysts and other aspects.Reference of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)

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

Wang, Chang-An; Li, Yan-Wei; Hou, Xian-Ming; Han, Yin-Feng; Nie, Kun; Zhang, Jian-Ping published an article in 2016, the title of the article was N-Heterocyclic Carbene-based Microporous Organic Polymer Supported Palladium Catalyst for Carbon-Carbon Coupling Reaction.SDS of cas: 934008-48-7 And the article contains the following content:

Highly dispersed Pd(0) nanoparticles were successfully immobilized into stable N-heterocyclic carbene-based microporous organic polymer (NHC-MOP) via a simple post-treatment. The microporous structure of the NHC-MOP polymer can efficiently prevent the aggregation of Pd nanoparticles and the NHC-MOP network embedding with N-heterocyclic carbene ligand can efficiently disperse Pd particles, which promoting the catalytic activity of the polymers. As-synthesized Pd@NHC-MOP catalyst shows excellent catalytic activity in catalyzing the Suzuki-Miyaura and Heck cross-coupling reactions. The superior utility of Pd@NHC-MOP in catalysis was elucidated by the broad scope of the reactants and the high yields of the reaction products, together with the high recyclability of the catalyst. The Pd@NHC-MOP catalyst can be reused at least eleven times for Suzuki-Miyaura coupling reaction or nine times for Heck coupling reaction without any significant loss of the catalytic activity. The experimental process involved the reaction of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)(cas: 934008-48-7).SDS of cas: 934008-48-7

The Article related to heterocyclic carbene microporous organic polymer supported palladium catalyst preparation, suzuki miyaura heck coupling catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.SDS of cas: 934008-48-7

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

Zhou, Hui; Zhang, Qing-Yong; Lu, Xiao-Bing published an article in 2016, the title of the article was Synthesis and catalytic application of N-heterocyclic carbene copper complex functionalized conjugated microporous polymer.HPLC of Formula: 934008-48-7 And the article contains the following content:

A N-heterocyclic carbene copper(I) complex functionalized conjugated microporous polymer (CMP-NHC-CuCl) was synthesized by palladium-catalyzed Sonogashira cross-coupling chem. The resulting CMP-NHC-CuCl proved to be a good heterogeneous catalyst in the hydrosilylation of functionalized terminal alkynes with boryldisiloxane to afford (β,β)-(E)-vinyldisiloxane with high stereoselectivity, and the catalyst could be used four times without obvious loss in catalytic activity. Moreover, CMP-NHC-CuCl was also efficient in catalyzing the hydrosilylation of CO2 with triethoxysilane to form silyl formate under mild conditions. The experimental process involved the reaction of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)(cas: 934008-48-7).HPLC of Formula: 934008-48-7

The Article related to heterocyclic carbene copper functionalized conjugated microporous polymer preparation catalyst, terminal alkyne hydrosilylation conjugated microporous polymer imidazolidene copper catalyzed and other aspects.HPLC of Formula: 934008-48-7

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

On July 20, 2009, Chun, Jiseul; Jung, Il Gu; Kim, Hae Jin; Park, Mira; Lah, Myoung Soo; Son, Seung Uk published an article.Formula: C27H35ClI2N2 The title of the article was Concomitant Formation of N-Heterocyclic Carbene-Copper Complexes within a Supramolecular Network in the Self-Assembly of Imidazolium Dicarboxylate with Metal Ions. And the article contained the following:

A new building block containing an imidazolium salt was synthesized and used for the construction of supramol. networks with cadmium and copper ions. The authors discovered the concomitant formation of an N-heterocyclic carbene-Cu complex (CN = 2) in the self-assembly of imidazolium dicarboxylates and Cu nitrates in DMF under heating. The proton in the 2 position of the imidazolium salt was abstracted, and CuII was reduced to CuI during the self-assembly process. The experimental process involved the reaction of 1H-Imidazolium, 1,3-bis[4-iodo-2,6-bis(1-methylethyl)phenyl]-, chloride (1:1)(cas: 934008-48-7).Formula: C27H35ClI2N2

The Article related to copper heterocyclic carbene complex preparation self assembly supramol structure, crystal structure copper heterocyclic carbene complex, mol structure copper heterocyclic carbene complex, imidazolium dicarboxylate self assembly copper nitrate and other aspects.Formula: C27H35ClI2N2

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

Application of 189518-78-3On May 9, 2018 ,《Aggregation-induced CPL response from chiral binaphthyl-based AIE-active polymers via supramolecular self-assembled helical nanowires》 appeared in Polymer. The author of the article were Ma, Jing; Wang, Yuxiang; Li, Xiaojing; Yang, Lan; Quan, Yiwu; Cheng, Yixiang. The article conveys some information:

In this paper chiral polymer R-P could be synthesized by click polymerization reaction of (R)-3,3′-diethynyl-2,2′-bis(octyloxy)-1,1′-binaphthalene (R-M-1) and 1,2-bis(4-azidophenyl)-1,2-diphenylethene (M-2), and S-P was obtained by click polymerization reaction of (S)-3,3′-diethynyl-2,2′-bis(octyloxy)-1,1′-binaphthalene (S-M-1) and M-2, resp. R-/S-P enantiomers can show strong aggregation-induced circularly polarized luminescence (AICPL) emission signals in the aggregate and cast-spin film, and the dissymmetry factors (glum) can be up to 6.97 × 10-3 and 1.45 × 10-2, resp. The SEM images further demonstrate that AICPL response behavior of R-/S-P can be attributed to the formation of the supramol. self-assembled helical nanowires in the aggregation state at 90% of the fraction of water (fw). The results came from multiple reactions, including the reaction of (R)-3,3′-Diiodo-2,2′-bis(methoxymethoxy)-1,1′-binaphthalene(cas: 189518-78-3Application of 189518-78-3)

(R)-3,3′-Diiodo-2,2′-bis(methoxymethoxy)-1,1′-binaphthalene(cas: 189518-78-3) belongs to organic iodides. Organic iodides are used in veterinary products (Organic Iodide Powder) as a nutritional source of iodine. In the chemical industry, alkyl iodides serve as excellent alkylating agents and, specifically, methyl iodide is used as a methylating agent in the synthesis of various pharmaceutical drugs.Application of 189518-78-3

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