Fast and efficient synthesis of microporous polymer nanomembranes via light-induced click reaction; Beilstein Journal of Organic Chemistry; Vol. 13
| Parent link: | Beilstein Journal of Organic Chemistry.— , 20015- Vol. 13.— 2017.— [P. 558-563] |
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| Korporacja: | |
| Kolejni autorzy: | , , , , , , |
| Streszczenie: | Title screen Conjugated microporous polymers (CMPs) are materials of low density and high intrinsic porosity. This is due to the use of rigid building blocks consisting only of lightweight elements. These materials are usually stable up to temperatures of 400 °C and are chemically inert, since the networks are highly crosslinked via strong covalent bonds, making them ideal candidates for demanding applications in hostile environments. However, the high stability and chemical inertness pose problems in the processing of the CMP materials and their integration in functional devices. Especially the application of these materials for membrane separation has been limited due to their insoluble nature when synthesized as bulk material. To make full use of the beneficial properties of CMPs for membrane applications, their synthesis and functionalization on surfaces become increasingly important. In this respect, we recently introduced the solid liquid interfacial layer-by-layer (LbL) synthesis of CMP-nanomembranes via Cu catalyzed azide–alkyne cycloaddition (CuAAC). However, this process featured very long reaction times and limited scalability. Herein we present the synthesis of surface grown CMP thin films and nanomembranes via light 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. |
| Język: | angielski |
| Wydane: |
2017
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| Hasła przedmiotowe: | |
| Dostęp online: | http://dx.doi.org/10.3762/bjoc.13.54 |
| Format: | Elektroniczne Rozdział |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=656352 |
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| 200 | 1 | |a Fast and efficient synthesis of microporous polymer nanomembranes via light-induced click reaction |f An Qi [et al.] | |
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| 300 | |a Title screen | ||
| 320 | |a [References: 33 tit.] | ||
| 330 | |a Conjugated microporous polymers (CMPs) are materials of low density and high intrinsic porosity. This is due to the use of rigid building blocks consisting only of lightweight elements. These materials are usually stable up to temperatures of 400 °C and are chemically inert, since the networks are highly crosslinked via strong covalent bonds, making them ideal candidates for demanding applications in hostile environments. However, the high stability and chemical inertness pose problems in the processing of the CMP materials and their integration in functional devices. Especially the application of these materials for membrane separation has been limited due to their insoluble nature when synthesized as bulk material. To make full use of the beneficial properties of CMPs for membrane applications, their synthesis and functionalization on surfaces become increasingly important. In this respect, we recently introduced the solid liquid interfacial layer-by-layer (LbL) synthesis of CMP-nanomembranes via Cu catalyzed azide–alkyne cycloaddition (CuAAC). However, this process featured very long reaction times and limited scalability. Herein we present the synthesis of surface grown CMP thin films and nanomembranes via light 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. | ||
| 461 | |t Beilstein Journal of Organic Chemistry |d 20015- | ||
| 463 | |t Vol. 13 |v [P. 558-563] |d 2017 | ||
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| 701 | 0 | |a An Qi | |
| 701 | 1 | |a Hassan |b Yo. |g Youssef | |
| 701 | 0 | |a Yan Xiaotong | |
| 701 | 0 | |a Mokhamed Takhid Khashim Abdelrazek |c chemist |c Associate Scientist of Tomsk Polytechnic University |f 1981- |3 (RuTPU)RU\TPU\pers\36807 | |
| 701 | 1 | |a Lang |b M. |g Mathias | |
| 701 | 1 | |a Brase |b S. |g Stefan | |
| 701 | 1 | |a Tsotsalas |b M. |g Manuel | |
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