Tag: M.W=150-200

Liu, Xin published the artcilePillared Metal-Organic Framework Initiating Intermolecular Atom-Transfer Radical Addition via Visible-Light-Induced Electron Transfer Activation of Haloalkanes, Recommanded Product: Ethylbromofluoroacetate, the publication is ACS Applied Materials & Interfaces (2021), 13(29), 34114-34123, database is CAplus and MEDLINE.

Herein, a novel metal-organic framework (MOF) with a pillared-layer structure was rationally synthesized to initiate intermol. atom-transfer radical addition (ATRA) via photoinduced electron transfer activation of haloalkanes. The MOF synthesized via the controllable pillared-layer method is of excellent visible-light absorption and high chem. stability. Photocatalytic experiments show the atom transfer of various alkyl halides (R-X, X = Cl/Br/I) onto diverse olefins was successfully achieved to produce functional ATRA products. The mechanism and exptl. investigations reveal the prepared MOF serves as an efficient photocatalyst with strong reduction potential to activate haloalkane substrates via photoinduced electron transfer, generating a highly reactive alkyl radical to trigger the ATRA reaction. Key events in the ATRA reaction, including alkyl radical photogeneration as well as halide transfer, have been further regulated to achieve preferable photocatalytic performance with higher yields, shorter reaction time, and desirable cycling capability. It is notable that the work is the first report on photoinduced electron transfer activation of halides by a MOF photocatalyst for the ATRA reaction, providing a new blueprint for MOFs to develop photoinduced radical reactions.

ACS Applied Materials & Interfaces published new progress about 401-55-8. 401-55-8 belongs to bromides-buliding-blocks, auxiliary class Fluoride,Bromide,Aliphatic hydrocarbon chain,Ester, name is Ethylbromofluoroacetate, and the molecular formula is C4H6BrFO2, Recommanded Product: Ethylbromofluoroacetate.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Armstrong, Megan K. published the artcileDiastereodivergent Reductive Cross Coupling of Alkynes through Tandem Catalysis: Z- and E-Selective Hydroarylation of Terminal Alkynes, Category: bromides-buliding-blocks, the publication is Journal of the American Chemical Society (2018), 140(32), 10233-10241, database is CAplus and MEDLINE.

A diastereodivergent hydroarylation of terminal alkynes is accomplished using tandem catalysis. The hydroarylation allows highly selective synthesis of both E and Z diastereoisomers of aryl alkenes, from the same set of starting materials, using the same combination of palladium and copper catalysts. The selectivity is controlled by simple changes in the stoichiometry of the alc. additive. The hydroarylation has excellent substrate scope and can be accomplished in the presence of various classes of compounds, including esters, nitriles, alkyl halides, epoxides, carbamates, acetals, ethers, silyl ethers, and thioethers. The Z-selective hydroarylation is accomplished using a new approach based on tandem Sonogashira coupling and catalytic semiredn. The E-selective hydroarylation involves an addnl. catalytic isomerization of the Z-alkene. Our explorations of the reaction mechanism explain the role of individual reaction components and how the subtle changes in the reaction conditions influence the rates of specific steps of the hydroarylation. Our studies also show that, although the Z- and E-selective hydroarylation reactions are mechanistically closely related, the roles of the palladium and copper catalysts in the two reactions are different.

Journal of the American Chemical Society published new progress about 81216-14-0. 81216-14-0 belongs to bromides-buliding-blocks, auxiliary class Linker,PROTAC Linker, name is 7-Bromohept-1-yne, and the molecular formula is C7H11Br, Category: bromides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Lee, Mitchell T. published the artcileSynthesis of Isomerically Pure (Z)-Alkenes from Terminal Alkynes and Terminal Alkenes: Silver-Catalyzed Hydroalkylation of Alkynes, Application of 7-Bromohept-1-yne, the publication is Journal of the American Chemical Society (2019), 141(43), 17086-17091, database is CAplus and MEDLINE.

Here, an efficient synthesis of diastereopure Z-alkenes (Z:E > 300:1) through a silver-catalyzed hydroalkylation of terminal alkynes using alkylboranes as coupling partners is demonstrated. The exploration of the substrate scope, which reveals the broad functional group compatibility of the new method, is also described. Preliminary mechanistic studies suggest that a 1,2-metalate rearrangement of the silver borate intermediate is the key step responsible for the stereochem. outcome of the reaction.

Journal of the American Chemical Society published new progress about 81216-14-0. 81216-14-0 belongs to bromides-buliding-blocks, auxiliary class Linker,PROTAC Linker, name is 7-Bromohept-1-yne, and the molecular formula is C7H11Br, Application of 7-Bromohept-1-yne.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Derince, Betul published the artcileArchitectural design of new conjugated systems carrying donor-π-acceptor groups (carbazole-CF₃): Characterizations, optical, photophysical properties and DSSC′s applications, SDS of cas: 111-83-1, the publication is Journal of Molecular Structure (2022), 1250(Part_2), 131689, database is CAplus.

In this study, two new organic dyes containing substituted N-octyl carbazole as electron donor and -CF₃ units as electron acceptor group were designed and synthesized for ZnO-based dye sensitized solar cells (DSSCs). The synthesized carbazole derivatized compounds 3,6-bis(3,5-bis(trifluoromethyl)phenyl)-9-octyl-9H-carbazole (IVa) and 3,6-bis(4-(trifluoromethyl)phenyl)-9-octyl-9H-carbazole (IVb) were characterized by FT-IR, ¹H NMR, ¹³C NMR, HMBC and CHN analyses. The spectroscopic (UV-Vis and FL) and thermal properties (TGA-DTA) of these compounds were also investigated. The produced (IVa and IVb) ZnO films were used as photoanodes in all DSSCs. Microwave-assisted hydrothermal method was used to synthesize ZnO nanopowders with different morphologies which are used as photoanodes in DSSCs. The structural and morphol. properties of ZnO nanopowders were investigated using X-ray diffraction (XRD) and field emission SEM (FESEM). ZnO-DSSCs were produced through coating ZnO nanopowders on transparent conductive fluorine-doped tin oxide (FTO) coated glass substrate using the Doctor Blade method. Current-voltage measurements of all produced DSSCs were carried out under a solar simulator with AM 1.5 G filter having an irradiance of 100 mW/cm². Solar cell performances of all DSSCs such as; open-circuit voltage (V_oc), short circuit current (J_sc), fill factor (FF) and power conversion efficiency (PCE) were analyzed.

Journal of Molecular Structure published new progress about 111-83-1. 111-83-1 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 1-Bromooctane, and the molecular formula is C8H17Br, SDS of cas: 111-83-1.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Luan, Yu-Yong published the artcileThree-Component Ruthenium-Catalyzed meta-C-H Alkylation of Phenol Derivatives, Synthetic Route of 401-55-8, the publication is Organic Letters (2022), 24(5), 1136-1140, database is CAplus and MEDLINE.

Herein, synthesis of phenyl-(pyrimidinyloxyphenyl)butanoates I [R¹ = H, Me, Cl, etc.; R² = H, Me, F, etc; R³ = Me, F; R⁴ = Ph, 4-FC₆H₄, 4-BrC₆H₄, etc.; R² = R³ = Me, F; R⁵ = OEt, piperidin-1-yl, N(n-Bu)₂] via three-component ruthenium catalyzed C-H alkylation of phenoxypyrimidines and vinylbenzene and ethyl-bromo-difluoroacetates/alkyl bromides was reported. This strategy exhibited good substrates suitability and functional group tolerance with various phenol derivatives, which provided a synthetic potential drug approach. Mechanistic studies showed that a radical process might be involved in this process. In addition, the meta alkylated phenol was obtained by further removal of the directing group.

Organic Letters published new progress about 401-55-8. 401-55-8 belongs to bromides-buliding-blocks, auxiliary class Fluoride,Bromide,Aliphatic hydrocarbon chain,Ester, name is Ethylbromofluoroacetate, and the molecular formula is C4H6BrFO2, Synthetic Route of 401-55-8.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Blake, Matthew R. published the artcileSmall Molecules Targeting PTPσ-Trk Interactions Promote Sympathetic Nerve Regeneration, Category: bromides-buliding-blocks, the publication is ACS Chemical Neuroscience (2022), 13(5), 688-699, database is CAplus and MEDLINE.

Chondroitin sulfate proteoglycans (CSPGs) prevent sympathetic nerve regeneration in the heart after myocardial infarction and prevent central nerve regrowth after traumatic brain injury and spinal cord injury. Currently, there are no small-mol. therapeutics to promote nerve regeneration through CSPG-containing scars. CSPGs bind to monomers of receptor protein tyrosine phosphatase sigma (PTPσ) on the surface of neurons, enhancing the ability of PTPσ to bind and dephosphorylate tropomyosin receptor kinases (Trks), inhibiting their activity and preventing axon outgrowth. Targeting PTPσ-Trk interactions is thus a potential therapeutic target. Here, we describe the development and synthesis of small mols. (HJ-01 and HJ-02) that disrupt PTPσ interactions with Trks, enhance Trk signaling, and promote sympathetic nerve regeneration over CSPGs.

ACS Chemical Neuroscience published new progress about 111-83-1. 111-83-1 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 1-Bromooctane, and the molecular formula is C8H17Br, Category: bromides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Tang, Wei-Ke published the artcileVisible-Light-Enabled Decarboxylative Mono- and Difluoromethylation of Cinnamic Acids under Metal-Free Conditions, Category: bromides-buliding-blocks, the publication is Organic Letters (2017), 19(20), 5501-5504, database is CAplus and MEDLINE.

Several new mono- and difluoromethylation reactions of cinnamic acids using an Eosin Y catalytic system are reported. An efficient alkene fluoromethylation of α,β-unsaturated carboxylic acids, e.g., I, II, and III, was accomplished under ambient temperature and metal-free conditions, with a wide range of functional group tolerance. A mechanism that involves a radical process is proposed for this reaction.

Organic Letters published new progress about 401-55-8. 401-55-8 belongs to bromides-buliding-blocks, auxiliary class Fluoride,Bromide,Aliphatic hydrocarbon chain,Ester, name is Ethylbromofluoroacetate, and the molecular formula is C14H10O4S2, Category: bromides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Riente, Paola published the artcileShedding light on the nature of the catalytically active species in photocatalytic reactions using Bi₂O₃ semiconductor, COA of Formula: C4H6BrFO2, the publication is Nature Communications (2021), 12(1), 625, database is CAplus and MEDLINE.

The importance of discovering the true catalytically active species involved in photocatalytic systems allows for a better and more general understanding of photocatalytic processes, which eventually may help to improve their efficiency. Bi₂O₃ has been used as a heterogeneous photocatalyst and is able to catalyze several synthetically important visible-light-driven organic transformations. However, insight into the operative catalyst involved in the photocatalytic process is hitherto missing. Herein, we show through a combination of theor. and exptl. studies that the perceived heterogeneous photocatalysis with Bi₂O₃ in the presence of alkyl bromides involves a homogeneous BinBrm species, which is the true photocatalyst operative in the reaction. Hence, Bi₂O₃ can be regarded as a precatalyst which is slowly converted in an active homogeneous photocatalyst. This work can also be of importance to mechanistic studies involving other semiconductor-based photocatalytic processes.

Nature Communications published new progress about 401-55-8. 401-55-8 belongs to bromides-buliding-blocks, auxiliary class Fluoride,Bromide,Aliphatic hydrocarbon chain,Ester, name is Ethylbromofluoroacetate, and the molecular formula is C4H6BrFO2, COA of Formula: C4H6BrFO2.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

El-Saeed, H. M. published the artcileSynthesis and characterization of novel ionic liquids based on imidazolium for acid corrosion inhibition of aluminum: Experimental, spectral, and computational study, Recommanded Product: 1-Bromooctane, the publication is Journal of Molecular Liquids (2022), 119177, database is CAplus.

Three newly ionic liquids I [R = C₈H₁₇, C₁₀H₂₁, C₁₂H₂₅] were synthesized and their chem. structures characterized via different spectra techniques (FT-IR, elemental anal., and ¹H NMR). The corrosion inhibition of newly ionic liquids was evaluated on aluminum alloy in 1 M HCl at varied exposure temperatures (298-318 K) and varied concentrations via various exptl. and theor. methods for example mass loss, electrochem., spectral, and computational calculations The results illustrate that these types of ionic liquids inhibit corrosion of aluminum in acid solution with maximum inhibition efficiency was reached 83.2% at 298 K. The inhibition efficiency increases with the addition of zinc sulfate which had a synergistic impact which was reached to 92.7%. Also, the concentration of ionic liquids and the kind of cation have an impact on the obtained results. The existence of these inhibitors in the acidic solution improves the charge transfer resistance and lessens the double-layer capacitance. The Langmuir adsorption isotherm governs the adsorption of these inhibitors’ mols. on the aluminum alloy surface, and they behave as mixed-type inhibitors. The outputs reveal that the computational calculations match the exptl. data rather well.

Journal of Molecular Liquids published new progress about 111-83-1. 111-83-1 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 1-Bromooctane, and the molecular formula is C8H17Br, Recommanded Product: 1-Bromooctane.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Lerch, Swantje published the artcileThe Mizoroki-Heck Reaction in Tunable Aryl Alkyl Ionic Liquids, Application of 1-Bromooctane, the publication is European Journal of Organic Chemistry (2022), 2022(6), e202200008, database is CAplus.

Authors report the use of imidazolium based tunable aryl alkyl ionic liquids (TAAILs) as solvents in the Mizoroki-Heck reaction. Different com. available palladium sources, inorganic bases, TAAILs and reaction conditions were tested for the synthesis of trans-stilbene using bromobenzene and styrene. A variety of different stilbene derivatives were synthesized with exclusive formation of the (E)-isomers and isolated yields up to 97%. Author’s were able to optimize the reaction conditions using only 0.25 mol% of Pd(OAc)₂ as the catalyst and a reaction time of 4 h. No addnl. ligands or additives are used in the reaction. The catalytic system using TAAILs achieved higher yields than com. available imidazolium and phosphonium ionic liquids, demonstrating the potential of tailored ionic liquids as a reaction medium for the Mizoroki-Heck reaction.

European Journal of Organic Chemistry published new progress about 111-83-1. 111-83-1 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 1-Bromooctane, and the molecular formula is C8H17Br, Application of 1-Bromooctane.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary