Borys Osmialowski
Shared posts
[ASAP] Synthesis of Aza[n]helicenes up to n = 19: Hydrogen-Bond-Assisted Solubility and Benzannulation Strategy
[ASAP] Ni-Catalyzed Mild Synthesis of Sulfonylurea via Tandem Coupling of Sulfonyl Azide, Isocyanide, and Water
[ASAP] Synthesis, Photophysical Properties, and Aromaticity of Pyrazine-Fused Tetrazapentalenes
High efficiency branched thermal activated delayed fluorescent probe based on cyanogroup for detecting Fe3+ with low limit of detection
Publication date: February 2022
Source: Dyes and Pigments, Volume 198
Author(s): Suyu Qiu, Kaizhi Zhang, Tao Zhou, Hui Xu, Jianmin Yu, Xinxin Ban, Fengjie Ge, Dongbao Jia, Qingzheng Zhu, Aiyun zhu
[ASAP] Band Gap Engineering in Acceptor-Donor-Acceptor Boron Difluoride Formazanates
[ASAP] One-Pot Synthesis of Triazatriphenylene Using the Povarov Reaction
MgO‐Template Synthesis of Extremely High Capacity Hard Carbon for Na‐Ion Battery
Mg‐templated hard carbon as an extremely high capacity negative electrode material for Na‐ion batteries is successfully synthesized by heating a freeze‐dried mixture of magnesium gluconate and glucose. The hard carbon demonstrates an extraordinarily large reversible capacity of 478 mAh g−1 with a high Coulombic efficiency of 88 % at the first cycle. Owing to the low potential operation, estimated energy density of the full cell is very high.
Abstract
Extremely high capacity hard carbon for Na‐ion battery, delivering 478 mAh g−1, is successfully synthesized by heating a freeze‐dried mixture of magnesium gluconate and glucose by a MgO‐template technique. Influences of synthetic conditions and nano‐structures on electrochemical Na storage properties in the hard carbon are systematically studied to maximize the reversible capacity. Nano‐sized MgO particles are formed in a carbon matrix prepared by pre‐treatment of the mixture at 600 °C. Through acid leaching of MgO and carbonization at 1500 °C, resultant hard carbon demonstrates an extraordinarily large reversible capacity of 478 mAh g−1 with a high Coulombic efficiency of 88 % at the first cycle.
[ASAP] Palladium-Catalyzed C-4 Selective Coupling of 2,4-Dichloropyridines and Synthesis of Pyridine-Based Dyes for Live-Cell Imaging
[ASAP] Computationally Assisted Design of Polarizing Agents for Dynamic Nuclear Polarization Enhanced NMR: The AsymPol Family
[ASAP] Thermal E/Z Isomerization in First Generation Molecular Motors
Synthesis, Properties, and Semiconducting Characteristics of BF2 Complexes of β,β-Bisphenanthrene-Fused Azadipyrromethenes
Porphyrin–Azobenzene–Bodipy Triads: Syntheses, Structures, and Photophysical Properties
Fluorescent Molecular Rotors of Organoboron Compounds from Schiff Bases: Synthesis, Viscosity, Reversible Thermochromism, Cytotoxicity, and Bioimaging Cells
Concurrent Covalent and Supramolecular Polymerization
Abstract
Covalent and supramolecular polymerizations, both of which offer their own unique advantages, have emerged as popular strategies for making artificial materials. Herein, we describe a concurrent covalent and supramolecular polymerization strategy—namely, one which utilizes 1) a bis-azide-functionalized diazaperopyrenium dication that undergoes polymeriation covalently with a bis-alkyne-functionalized biphenyl derivative in one dimension as a result of a rapid and efficient β-cyclodextrin(CD)-accelerated, cucurbit[6]uril(CB)-templated azide–alkyne cycloaddition, while 2) the aromatic core of the dication is able to dimerize in a criss-cross fashion by dint of π–π interactions, enabling simultaneous supramolecular assembly, resulting in an extended polymer network in an orthogonal dimension.
Pushing out the polymers: A concurrent covalent and supramolecular polymerization strategy has been developed. It utilizes a rapid and efficient β-cyclodextrin-accelerated, cucurbit[6]uril-templated azide–alkyne polymerization concurrently with the supramolecular assembly of diazaperopyrenium dications, which are located periodically along the polymer backbone, by dint of π–π dimerization.