Pickering emulsifiers are significant for organic reactions in an aqueous medium because they have the ability of emulsifying water-oil biphasic systems. For this reason, 2,5-bis[()-2-(triethoxysilyl)vinyl]pyridine [BTOSVP] containing a pyridine bridging group was selected as a precursor to prepare a novel salt of organosilicon framework (SOF), an amphiphilic mesoporous pyridine hydrobromide nanosphere. We first synthesized a mesoporous organosilicon framework made up of organic groups containing vinyl groups, pyridine groups, and so forth. Then, hydrobromic acid was added to protonate the pyridine groups in the mesoporous organosilicon framework. Eventually, pyridine hydrobromide salt was formed on the surfaces of channels, and the SOF was successfully prepared for the first time. Pyridine hydrobromide salt can be ionized in water into protonated pyridine cations located on the SOF surfaces and free Br-anions swimming around the protonated pyridine cations because of the electrostatic interaction. In the water-oil biphasic systems, hydrophilicity of SOF originates from the protonated pyridine cations and the lipophilicity of SOF comes from organic groups in the framework; thus, this new kind of SOF can be used as a new generation of solid Pickering emulsifiers. Most importantly, the mesoporous SOF nanosphere can also be used as a catalyst for significantly improved dibromination of olefins in an aqueous medium.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.1c08799DOI Listing

Publication Analysis

Top Keywords

organosilicon framework
16
water-oil biphasic
12
biphasic systems
12
aqueous medium
12
pyridine hydrobromide
12
protonated pyridine
12
pyridine cations
12
pyridine
9
salt organosilicon
8
dibromination olefins
8

Similar Publications

Photoredox/Nickel Dual-Catalytic Asymmetric Silylarylation of Alkenes.

Org Lett

January 2025

Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, Shanghai Key Laboratory of New Drug Design, and School of Pharmacy, East China University of Science and Technology, Shanghai 200237, P. R. China.

The efficient construction of chiral aryl-containing organosilicon frameworks via catalytic enantioselective three-component silylarylation of alkenes remains a great challenge. Herein, a photoredox/nickel dual-catalytic asymmetric protocol has been disclosed by using a chiral biimidazoline (BiIM) as the ligand, silylboranes as the silyl radical precursors, aryl bromides as the coupling partners, and morpholine as the promoter. Remarkably, the reaction features mild and green conditions, high reaction efficiency, and excellent enantioselectivity, enabling the facile synthesis of valuable chiral tropic acid and sila-isoflavanone structures.

View Article and Find Full Text PDF

Effective prediction of organosilicon molecular structures and risks in aquatic environment with machine learning.

Sci Total Environ

January 2025

State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; School of Environment, Hangzhou Institute for Advanced Study, UCAS, Hangzhou 330106, China.

Until now, mass spectrometry databases lack molecular information of most organosilicon oligomers, and risk models needing accurate molecular descriptors are unavailable for these emerging contaminants with thousands of monomers. To address this issue, based on molecular/fragment ions and relative abundance from GC-Orbitrap-MS, this study developed appropriate classification (accuracies = 0.750-0.

View Article and Find Full Text PDF

Synthesis of 3-Substituted Indoles by Yonemitsu Three-Component Reactions Accelerated in Microdroplet/Thin Film.

J Org Chem

December 2024

College of Material, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, 2318 Yuhangtang Road, Hangzhou 311121, China.

3-Substituted indoles are an important framework of many drugs, agricultural chemicals, functional materials, and bioactive compounds. Malononitrile-based three-component Yonemitsu reactions are attractive choices for the synthesis of 3-substituted indole derivatives but suffered from long reaction time and harsh conditions (e.g.

View Article and Find Full Text PDF

Chemical Synthesis and Multihybridization of Small-Sized Hollow Mesoporous Organosilica Nanoparticles Toward Advanced Theranostics.

Acc Chem Res

December 2024

State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Drug Discovery for Metabolic Diseases, Center of Advanced Pharmaceuticals and Biomaterials, China Pharmaceutical University, Nanjing 211198, China.

Article Synopsis
  • * Incorporating organic moieties into these nanoparticles creates mesoporous organosilica nanoparticles (MONs), which provide better biocompatibility, stimuli-responsive properties, and improved therapeutic effects.
  • * Recent research has concentrated on hollow-structured MONs (HMONs), particularly smaller sub-50 nm variants, which show advantages in drug delivery, but the synthesis and structural regulation of these small HMONs remain poorly understood.
View Article and Find Full Text PDF

Efforts toward the Total Synthesis of Thuggacin A.

Org Lett

November 2024

State Key Laboratory of Environmental Chemistry and Eco-toxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.

Thuggacin A () is a 17-membered-ring-polyketide antibiotic compound with excellent antituberculosis activity. The total synthesis of thuggacin A has not yet been reported so far. Herein, we disclose our efforts toward the convergent total synthesis of thuggacin A.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!