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Search for "microporous materials" in Full Text gives 7 result(s) in Beilstein Journal of Organic Chemistry.

Preparation of β-cyclodextrin/polysaccharide foams using saponin

  • Max Petitjean and
  • José Ramón Isasi

Beilstein J. Org. Chem. 2023, 19, 78–88, doi:10.3762/bjoc.19.7

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  • 15 mg/g of matrix. Similar results are found for the liquid path in the absence of saponin. The favourable influence of saponin to produce a more efficient matrix is confirmed. The freeze drying of solutions permits to produce microporous materials, as seen in the SEM images of Figure 2, where the
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Published 24 Jan 2023

Carbazole-functionalized hyper-cross-linked polymers for CO2 uptake based on Friedel–Crafts polymerization on 9-phenylcarbazole

  • Dandan Fang,
  • Xiaodong Li,
  • Meishuai Zou,
  • Xiaoyan Guo and
  • Aijuan Zhang

Beilstein J. Org. Chem. 2019, 15, 2856–2863, doi:10.3762/bjoc.15.279

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  • microporous HCPs and came to the conclusion that 2D and 3D-conjugated architectures with nonplanar rigid conformation and dendritic building blocks were favorable for getting a high BET specific surface area [6][19][20][21][23][24][25]. Qiao synthesized five microporous materials using carbazole with
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Published 26 Nov 2019

Mechanochemical synthesis of hyper-crosslinked polymers: influences on their pore structure and adsorption behaviour for organic vapors

  • Sven Grätz,
  • Sebastian Zink,
  • Hanna Kraffczyk,
  • Marcus Rose and
  • Lars Borchardt

Beilstein J. Org. Chem. 2019, 15, 1154–1161, doi:10.3762/bjoc.15.112

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  • sorption experiments with benzene and cyclohexane. Keywords: hyper-crosslinked polymers; mechanochemistry; microporous; solvent-free; vapor sorption; Introduction The widespread use of microporous materials in areas like gas storage, gas separation, and catalysis has led to the development of a wide
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Published 24 May 2019

Novel approach to hydroxy-group-containing porous organic polymers from bisphenol A

  • Tao Wang,
  • Yan-Chao Zhao,
  • Li-Min Zhang,
  • Yi Cui,
  • Chang-Shan Zhang and
  • Bao-Hang Han

Beilstein J. Org. Chem. 2017, 13, 2131–2137, doi:10.3762/bjoc.13.211

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  • voids associated with the pack of small particles of about 4 μm adhered to the external surface of spherical particles (Supporting Information File 1, Figure S5). The BET specific surface area values are calculated in the relative pressure range P/P0 = 0.01–0.10 for the microporous materials [31] for
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Published 12 Oct 2017

Fast and efficient synthesis of microporous polymer nanomembranes via light-induced click reaction

  • Qi An,
  • Youssef Hassan,
  • Xiaotong Yan,
  • Peter Krolla-Sidenstein,
  • Tawheed Mohammed,
  • Mathias Lang,
  • Stefan Bräse and
  • Manuel Tsotsalas

Beilstein J. Org. Chem. 2017, 13, 558–563, doi:10.3762/bjoc.13.54

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  • induced thiol–yne click reaction. Using this reaction, we could greatly enhance the CMP nanomembrane synthesis and further broaden the variability of the LbL approach. Keywords: click chemistry; conjugated microporous polymers (CMPs); microporous materials; nanomembranes; thin films; thiol–yne coupling
  • storage and separation as well as in organic electronics [8]. Among the microporous materials, conjugated microporous polymers (CMPs) [9][10] or porous aromatic frameworks (PAF) [11] have favorable properties for many applications, since they combine a high chemical and thermal stability, which is
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Published 17 Mar 2017

Robust C–C bonded porous networks with chemically designed functionalities for improved CO2 capture from flue gas

  • Damien Thirion,
  • Joo S. Lee,
  • Ercan Özdemir and
  • Cafer T. Yavuz

Beilstein J. Org. Chem. 2016, 12, 2274–2279, doi:10.3762/bjoc.12.220

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  • COP-156-amine showed fast and increased CO2 uptake under simulated moist flue gas conditions compared to the starting network and usual industrial CO2 solvents, reaching up to 7.8 wt % uptake at 40 °C. Keywords: C–C bond; CO2 capture; microporous materials; porous polymers; postmodification
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Published 28 Oct 2016

Diels–Alder reactions in confined spaces: the influence of catalyst structure and the nature of active sites for the retro-Diels–Alder reaction

  • Ángel Cantín,
  • M. Victoria Gomez and
  • Antonio de la Hoz

Beilstein J. Org. Chem. 2016, 12, 2181–2188, doi:10.3762/bjoc.12.208

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  • selectivity and atom economy. Moreover, Diels–Alder cycloadditions in combination with heterogeneous catalysts (i.e. doped-microporous materials) represent an interesting approach for the conversion of biomass feedstock into stable chemicals such as furfural derivatives, platform molecules which can be
  • and selectivity is the special confinement of the reactants and the presence of catalytic active sites, [15][16] by use of microporous materials doped with metals. While pore dimensions and topology of the microporous materials can affect the selectivity of the reaction, their activity can be strongly
  • the kinetically controlled endo-endo isomer rises after recycling. Conclusion In this work the DAR between cyclopentadiene and p-benzoquinone has been proved to take place on the catalyst surface when the reaction is carried out in presence of microporous materials, obtaining better results when a
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Published 13 Oct 2016
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