Sugar-based micro/mesoporous hypercross-linked polymers with in situ embedded silver nanoparticles for catalytic reduction

Qing Yin, Qi Chen, Li-Can Lu and Bao-Hang Han

Beilstein J. Org. Chem. 2017, 13, 1212–1221. doi:10.3762/bjoc.13.120

Supporting Information

Supporting Information File 1: Additional spectra.
IR spectra of the SugPOP-1–3; 13C CP/MAS NMR spectra of SugPOP-1 and SugPOP-2; TGA curves of polymers SugPOP-1–3 under nitrogen atmosphere; CO2 adsorption isotherms of SugPOP-1–3 with pressure up to 1.13 bar; X-ray diffraction patterns of SugPOP-1 and AgNPs/SugPOP-1 composite; TGA plot of the AgNPs/SugPOP-1 composite under air atmosphere; 1H NMR, 13C NMR, and MS spectra of new monomers are provided.
Format: PDF Size: 532.1 KB Download

Presentation Graphic

Picture with graphical abstract, title and authors for social media postings and presentations.

Format: PNG Size: 259.5 KB Download
Back To Article

Article is part of the issue

Stefan Bräse

Latest Articles

Two new aromatic polyketides from a sponge-derived Fusarium

  1. Mada Triandala Sibero,
  2. Tao Zhou,
  3. Keisuke Fukaya,
  4. Daisuke Urabe,
  5. Ocky K. Karna Radjasa,
  6. Agus Sabdono,
  7. Agus Trianto and
  8. Yasuhiro Igarashi
  • Full Research Paper
  • Published 09 Dec 2019

Beilstein J. Org. Chem. 2019, 15, 2941–2947, doi:10.3762/bjoc.15.289

Automated glycan assembly of arabinomannan oligosaccharides from Mycobacterium tuberculosis

  1. Alonso Pardo-Vargas,
  2. Priya Bharate,
  3. Martina Delbianco and
  4. Peter H. Seeberger
  • Full Research Paper
  • Published 06 Dec 2019

Beilstein J. Org. Chem. 2019, 15, 2936–2940, doi:10.3762/bjoc.15.288

A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones

  1. Daniel P. Pienaar,
  2. Kamogelo R. Butsi,
  3. Amanda L. Rousseau and
  4. Dean Brady
  • Letter
  • Published 06 Dec 2019

Beilstein J. Org. Chem. 2019, 15, 2930–2935, doi:10.3762/bjoc.15.287

Chemical synthesis of tripeptide thioesters for the biotechnological incorporation into the myxobacterial secondary metabolite argyrin via mutasynthesis

  1. David C. B. Siebert,
  2. Roman Sommer,
  3. Domen Pogorevc,
  4. Michael Hoffmann,
  5. Silke C. Wenzel,
  6. Rolf Müller and
  7. Alexander Titz
  • Full Research Paper
  • Published 05 Dec 2019

Beilstein J. Org. Chem. 2019, 15, 2922–2929, doi:10.3762/bjoc.15.286

Synthesis and optoelectronic properties of benzoquinone-based donor–acceptor compounds

  1. Daniel R. Sutherland,
  2. Nidhi Sharma,
  3. Georgina M. Rosair,
  4. Ifor D. W. Samuel,
  5. Ai-Lan Lee and
  6. Eli Zysman-Colman
  • Full Research Paper
  • Published 04 Dec 2019

Beilstein J. Org. Chem. 2019, 15, 2914–2921, doi:10.3762/bjoc.15.285

Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids

  1. László Orha,
  2. József M. Tukacs,
  3. László Kollár and
  4. László T. Mika
  • Full Research Paper
  • Published 03 Dec 2019

Beilstein J. Org. Chem. 2019, 15, 2907–2913, doi:10.3762/bjoc.15.284

Bacterial terpene biosynthesis: challenges and opportunities for pathway engineering

  1. Eric J. N. Helfrich,
  2. Geng-Min Lin,
  3. Christopher A. Voigt and
  4. Jon Clardy
  • Review
  • Published 29 Nov 2019

Beilstein J. Org. Chem. 2019, 15, 2889–2906, doi:10.3762/bjoc.15.283

Influence of the cis/trans configuration on the supramolecular aggregation of aryltriazoles

  1. Sara Tejera,
  2. Giada Caniglia,
  3. Rosa L. Dorta,
  4. Andrea Favero,
  5. Javier González-Platas and
  6. Jesús T. Vázquez
  • Full Research Paper
  • Published 28 Nov 2019

Beilstein J. Org. Chem. 2019, 15, 2881–2888, doi:10.3762/bjoc.15.282

Emission and biosynthesis of volatile terpenoids from the plasmodial slime mold Physarum polycephalum

  1. Xinlu Chen,
  2. Tobias G. Köllner,
  3. Wangdan Xiong,
  4. Guo Wei and
  5. Feng Chen
  • Full Research Paper
  • Published 28 Nov 2019

Beilstein J. Org. Chem. 2019, 15, 2872–2880, doi:10.3762/bjoc.15.281

Facile regiodivergent synthesis of spiro pyrrole-substituted pseudothiohydantoins and thiohydantoins via reaction of [e]-fused 1H-pyrrole-2,3-diones with thiourea

  1. Aleksandr I. Kobelev,
  2. Nikita A. Tretyakov,
  3. Ekaterina E. Stepanova,
  4. Maksim V. Dmitriev,
  5. Michael Rubin and
  6. Andrey N. Maslivets
  • Full Research Paper
  • Published 27 Nov 2019

Beilstein J. Org. Chem. 2019, 15, 2864–2871, doi:10.3762/bjoc.15.280

Latest Thematic Issues

Molecular switches

Wiktor Szymanski and Stefan Hecht


Jeroen S. Dickschat

Reactive intermediates – carbocations

Dean J. Tantillo and Stephanie R. Hare

2018 Show Issue

Novel macrocycles – and old ones doing new tricks

Wei Jiang and Christoph A. Schalley

2018 Show Issue

Mechanochemistry II

José G. Hernández

2018 Show Issue

Multicomponent reactions III

Thomas J. J. Müller

2018 Show Issue

Keep Informed

RSS Feed

Subscribe to our Latest Articles RSS Feed.


Follow the Beilstein-Institut


Twitter: @BeilsteinInst