Literature DB >> 30253016

Modification of Carbon Fibre Surfaces by Sulfur-Fluoride Exchange Click Chemistry.

James D Randall1, Daniel J Eyckens1, Filip Stojcevski1, Paul S Francis1, Egan H Doeven1, Anders J Barlow2, Andrew S Barrow3, Chantelle L Arnold1, John E Moses3, Luke C Henderson1.   

Abstract

Technologies that enable surface modification are in high demand and are critical for the implementation of new functional materials and devices. Here, we describe the first modification of a carbon surface (in this case carbon fiber) using the sulfur-fluoride exchange (SuFEx) reaction. The parent sulfur (VI) fluoride moiety can be installed directly to the surface via electrochemical deposition of the fluorosulfate phenyldiazonium tetrafluoroborate salt, or by 'SuFExing' a phenol on the carbon surface followed by treatment of the material with SO2 F2 ; similar to a 'graft to' or 'graft from' functionalization approach. We demonstrate that these SuFEx-able surfaces readily undergo exchange with aryl silyl ethers, and that the subsequent sulfate linkages are themselves stable under electrochemical redox conditions. Finally, we showcase the utility of the SuFEx chemistry by installing a pendant amino group to the fiber surface resulting in interfacial shear strength improvements of up to 130 % in epoxy resin.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Carbon; click chemistry; fiber-matrix adhesion; interfacial adhesion; surface science

Year:  2018        PMID: 30253016     DOI: 10.1002/cphc.201800789

Source DB:  PubMed          Journal:  Chemphyschem        ISSN: 1439-4235            Impact factor:   3.102


  5 in total

1.  SuFExable polymers with helical structures derived from thionyl tetrafluoride.

Authors:  Suhua Li; Gencheng Li; Bing Gao; Sidharam P Pujari; Xiaoyan Chen; Hyunseok Kim; Feng Zhou; Liana M Klivansky; Yi Liu; Hafedh Driss; Dong-Dong Liang; Jianmei Lu; Peng Wu; Han Zuilhof; John Moses; K Barry Sharpless
Journal:  Nat Chem       Date:  2021-08-16       Impact factor: 24.274

2.  A practical fluorosulfonylating platform via photocatalytic imidazolium-based SO2F radical reagent.

Authors:  Weigang Zhang; Heyin Li; Xiaojuan Li; Zhenlei Zou; Mengjun Huang; Jiyang Liu; Xiaochen Wang; Shengyang Ni; Yi Pan; Yi Wang
Journal:  Nat Commun       Date:  2022-06-18       Impact factor: 17.694

3.  A regio- and stereoselective Heck-Matsuda process for construction of γ-aryl allylsulfonyl fluorides.

Authors:  Hao-Yong Qin; Houying Gui; Zai-Wei Zhang; Tao Shu; Hua-Li Qin
Journal:  RSC Adv       Date:  2022-07-04       Impact factor: 4.036

4.  Complementary Base Lowers the Barrier in SuFEx Click Chemistry for Primary Amine Nucleophiles.

Authors:  Jan-Niclas Luy; Ralf Tonner
Journal:  ACS Omega       Date:  2020-11-23

5.  SuFEx-enabled, chemoselective synthesis of triflates, triflamides and triflimidates.

Authors:  Bing-Yu Li; Lauren Voets; Ruben Van Lommel; Fien Hoppenbrouwers; Mercedes Alonso; Steven H L Verhelst; Wim M De Borggraeve; Joachim Demaerel
Journal:  Chem Sci       Date:  2022-01-05       Impact factor: 9.825

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.