On-water surface synthesis of crystalline, few-layer two-dimensional polymers assisted by surfactant monolayers

Despite rapid progress in recent years, it has remained challenging to prepare crystalline two-dimensional polymers. Here, we report the controlled synthesis of few-layer two-dimensional polyimide crystals on the surface of water through reaction between amine and anhydride monomers, assisted by sur...

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Published inNature chemistry Vol. 11; no. 11; pp. 994 - 1000
Main Authors Liu, Kejun, Qi, Haoyuan, Dong, Renhao, Shivhare, Rishi, Addicoat, Matthew, Zhang, Tao, Sahabudeen, Hafeesudeen, Heine, Thomas, Mannsfeld, Stefan, Kaiser, Ute, Zheng, Zhikun, Feng, Xinliang
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.11.2019
Nature Publishing Group
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Abstract Despite rapid progress in recent years, it has remained challenging to prepare crystalline two-dimensional polymers. Here, we report the controlled synthesis of few-layer two-dimensional polyimide crystals on the surface of water through reaction between amine and anhydride monomers, assisted by surfactant monolayers. We obtained polymers with high crystallinity, thickness of ~2 nm and an average crystal domain size of ~3.5 μm 2 . The molecular structure of the materials, their grain boundaries and their edge structures were characterized using X-ray scattering and transmission electron microscopy techniques. These characterizations were supported by computations. The formation of crystalline polymers is attributed to the pre-organization of monomers at the water–surfactant interface. The surfactant, depending on its polar head, promoted the arrangement of the monomers—and in turn their polymerization—either horizontally or vertically with respect to the water surface. The latter was observed with a surfactant bearing a carboxylic acid group, which anchored amine monomers vertically through a condensation reaction. In both instances, micrometre-sized, few-layer two-dimensional polyamide crystals were grown. It is difficult to prepare 2D polymers that are crystalline over large areas. Now, few-layer 2D polyimides and polyamides with good crystallinity on the micrometre scale have been synthesized on a water surface. A surfactant monolayer is used to organize amine monomers before their polymerization with anhydride moieties.
AbstractList Despite rapid progress in recent years, it has remained challenging to prepare crystalline two-dimensional polymers. Here, we report the controlled synthesis of few-layer two-dimensional polyimide crystals on the surface of water through reaction between amine and anhydride monomers, assisted by surfactant monolayers. We obtained polymers with high crystallinity, thickness of ~2 nm and an average crystal domain size of ~3.5 μm2. The molecular structure of the materials, their grain boundaries and their edge structures were characterized using X-ray scattering and transmission electron microscopy techniques. These characterizations were supported by computations. The formation of crystalline polymers is attributed to the pre-organization of monomers at the water–surfactant interface. The surfactant, depending on its polar head, promoted the arrangement of the monomers—and in turn their polymerization—either horizontally or vertically with respect to the water surface. The latter was observed with a surfactant bearing a carboxylic acid group, which anchored amine monomers vertically through a condensation reaction. In both instances, micrometre-sized, few-layer two-dimensional polyamide crystals were grown.
Despite rapid progress in recent years, it has remained challenging to prepare crystalline two-dimensional polymers. Here, we report the controlled synthesis of few-layer two-dimensional polyimide crystals on the surface of water through reaction between amine and anhydride monomers, assisted by surfactant monolayers. We obtained polymers with high crystallinity, thickness of ~2 nm and an average crystal domain size of ~3.5 μm . The molecular structure of the materials, their grain boundaries and their edge structures were characterized using X-ray scattering and transmission electron microscopy techniques. These characterizations were supported by computations. The formation of crystalline polymers is attributed to the pre-organization of monomers at the water-surfactant interface. The surfactant, depending on its polar head, promoted the arrangement of the monomers-and in turn their polymerization-either horizontally or vertically with respect to the water surface. The latter was observed with a surfactant bearing a carboxylic acid group, which anchored amine monomers vertically through a condensation reaction. In both instances, micrometre-sized, few-layer two-dimensional polyamide crystals were grown.
Despite rapid progress in recent years, it has remained challenging to prepare crystalline two-dimensional polymers. Here, we report the controlled synthesis of few-layer two-dimensional polyimide crystals on the surface of water through reaction between amine and anhydride monomers, assisted by surfactant monolayers. We obtained polymers with high crystallinity, thickness of ~2 nm and an average crystal domain size of ~3.5 μm2. The molecular structure of the materials, their grain boundaries and their edge structures were characterized using X-ray scattering and transmission electron microscopy techniques. These characterizations were supported by computations. The formation of crystalline polymers is attributed to the pre-organization of monomers at the water-surfactant interface. The surfactant, depending on its polar head, promoted the arrangement of the monomers-and in turn their polymerization-either horizontally or vertically with respect to the water surface. The latter was observed with a surfactant bearing a carboxylic acid group, which anchored amine monomers vertically through a condensation reaction. In both instances, micrometre-sized, few-layer two-dimensional polyamide crystals were grown.Despite rapid progress in recent years, it has remained challenging to prepare crystalline two-dimensional polymers. Here, we report the controlled synthesis of few-layer two-dimensional polyimide crystals on the surface of water through reaction between amine and anhydride monomers, assisted by surfactant monolayers. We obtained polymers with high crystallinity, thickness of ~2 nm and an average crystal domain size of ~3.5 μm2. The molecular structure of the materials, their grain boundaries and their edge structures were characterized using X-ray scattering and transmission electron microscopy techniques. These characterizations were supported by computations. The formation of crystalline polymers is attributed to the pre-organization of monomers at the water-surfactant interface. The surfactant, depending on its polar head, promoted the arrangement of the monomers-and in turn their polymerization-either horizontally or vertically with respect to the water surface. The latter was observed with a surfactant bearing a carboxylic acid group, which anchored amine monomers vertically through a condensation reaction. In both instances, micrometre-sized, few-layer two-dimensional polyamide crystals were grown.
Despite rapid progress in recent years, it has remained challenging to prepare crystalline two-dimensional polymers. Here, we report the controlled synthesis of few-layer two-dimensional polyimide crystals on the surface of water through reaction between amine and anhydride monomers, assisted by surfactant monolayers. We obtained polymers with high crystallinity, thickness of ~2 nm and an average crystal domain size of ~3.5 μm 2 . The molecular structure of the materials, their grain boundaries and their edge structures were characterized using X-ray scattering and transmission electron microscopy techniques. These characterizations were supported by computations. The formation of crystalline polymers is attributed to the pre-organization of monomers at the water–surfactant interface. The surfactant, depending on its polar head, promoted the arrangement of the monomers—and in turn their polymerization—either horizontally or vertically with respect to the water surface. The latter was observed with a surfactant bearing a carboxylic acid group, which anchored amine monomers vertically through a condensation reaction. In both instances, micrometre-sized, few-layer two-dimensional polyamide crystals were grown. It is difficult to prepare 2D polymers that are crystalline over large areas. Now, few-layer 2D polyimides and polyamides with good crystallinity on the micrometre scale have been synthesized on a water surface. A surfactant monolayer is used to organize amine monomers before their polymerization with anhydride moieties.
Author Heine, Thomas
Qi, Haoyuan
Kaiser, Ute
Feng, Xinliang
Shivhare, Rishi
Addicoat, Matthew
Zheng, Zhikun
Liu, Kejun
Dong, Renhao
Zhang, Tao
Sahabudeen, Hafeesudeen
Mannsfeld, Stefan
Author_xml – sequence: 1
  givenname: Kejun
  orcidid: 0000-0001-9464-5421
  surname: Liu
  fullname: Liu, Kejun
  organization: Center for Advancing Electronics Dresden & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden
– sequence: 2
  givenname: Haoyuan
  orcidid: 0000-0002-6684-7074
  surname: Qi
  fullname: Qi, Haoyuan
  organization: Central Facility of Electron Microscopy, Electron Microscopy Group of Materials Science, Universität Ulm
– sequence: 3
  givenname: Renhao
  orcidid: 0000-0002-4125-9284
  surname: Dong
  fullname: Dong, Renhao
  organization: Center for Advancing Electronics Dresden & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden
– sequence: 4
  givenname: Rishi
  surname: Shivhare
  fullname: Shivhare, Rishi
  organization: Center for Advancing Electronics Dresden & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden
– sequence: 5
  givenname: Matthew
  orcidid: 0000-0002-5406-7927
  surname: Addicoat
  fullname: Addicoat, Matthew
  organization: School of Science and Technology, Nottingham Trent University
– sequence: 6
  givenname: Tao
  orcidid: 0000-0003-3218-0571
  surname: Zhang
  fullname: Zhang, Tao
  organization: Center for Advancing Electronics Dresden & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden
– sequence: 7
  givenname: Hafeesudeen
  surname: Sahabudeen
  fullname: Sahabudeen, Hafeesudeen
  organization: Center for Advancing Electronics Dresden & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden
– sequence: 8
  givenname: Thomas
  orcidid: 0000-0003-2379-6251
  surname: Heine
  fullname: Heine, Thomas
  organization: Center for Advancing Electronics Dresden & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Wilhelm-Ostwald-Institute for Physical and Theoretical Chemistry, Universität Leipzig
– sequence: 9
  givenname: Stefan
  orcidid: 0000-0003-0268-519X
  surname: Mannsfeld
  fullname: Mannsfeld, Stefan
  organization: Center for Advancing Electronics Dresden & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden
– sequence: 10
  givenname: Ute
  surname: Kaiser
  fullname: Kaiser, Ute
  email: ute.kaiser@uni-ulm.de
  organization: Central Facility of Electron Microscopy, Electron Microscopy Group of Materials Science, Universität Ulm
– sequence: 11
  givenname: Zhikun
  orcidid: 0000-0001-6127-7044
  surname: Zheng
  fullname: Zheng, Zhikun
  email: zhengzhikun@mail.sysu.edu.cn
  organization: Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Guangdong Engineering Technology Research Center for High-performance Organic and Polymer Photoelectric Functional Films, School of Chemistry, Sun Yat-sen University
– sequence: 12
  givenname: Xinliang
  surname: Feng
  fullname: Feng, Xinliang
  email: xinliang.feng@tu-dresden.de
  organization: Center for Advancing Electronics Dresden & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31548668$$D View this record in MEDLINE/PubMed
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Snippet Despite rapid progress in recent years, it has remained challenging to prepare crystalline two-dimensional polymers. Here, we report the controlled synthesis...
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SubjectTerms 639/638/298/923/1028
639/638/455/941
639/638/542/970
639/925/930/328/2082
Analytical Chemistry
Biochemistry
Carboxylic acids
Chemical synthesis
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Crystal growth
Crystal structure
Crystallinity
Crystals
Grain boundaries
Inorganic Chemistry
Molecular structure
Monolayers
Monomers
Organic Chemistry
Physical Chemistry
Polyamide resins
Polyamides
Polymerization
Polymers
Surfactants
Transmission electron microscopy
X-ray scattering
Title On-water surface synthesis of crystalline, few-layer two-dimensional polymers assisted by surfactant monolayers
URI https://link.springer.com/article/10.1038/s41557-019-0327-5
https://www.ncbi.nlm.nih.gov/pubmed/31548668
https://www.proquest.com/docview/2309515505
https://www.proquest.com/docview/2296666855
Volume 11
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