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Topology-Templated Synthesis of Crystalline Porous Covalent Organic Frameworks.
Jin, Enquan; Geng, Keyu; Lee, Ka Hung; Jiang, Weiming; Li, Juan; Jiang, Qiuhong; Irle, Stephan; Jiang, Donglin.
Affiliation
  • Jin E; Department of Chemistry, Faculty of Science, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore.
  • Geng K; Department of Chemistry, Faculty of Science, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore.
  • Lee KH; Computational Sciences and Engineering Division & Chemical Sciences Division, Oak Ridge National Laboratory, USA.
  • Jiang W; Department of Chemistry, Faculty of Science, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore.
  • Li J; Department of Chemistry, Faculty of Science, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore.
  • Jiang Q; Department of Chemistry, Faculty of Science, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore.
  • Irle S; Computational Sciences and Engineering Division & Chemical Sciences Division, Oak Ridge National Laboratory, USA.
  • Jiang D; Bredesen Centre for Interdisciplinary Research and Graduate Education, University of Tennessee, Knoxville, TN, 37996, USA.
Angew Chem Int Ed Engl ; 59(29): 12162-12169, 2020 Jul 13.
Article in En | MEDLINE | ID: mdl-32329936
ABSTRACT
A strategy is presented for the synthesis of crystalline porous covalent organic frameworks via topology-templated polymerization. The template is based on imine-linked frameworks and their (001) facets seed the C=C bond formation reaction to constitute 2D sp2 carbon-conjugated frameworks. This strategy is applicable to templates with different topologies, enables designed synthesis of frameworks that cannot be prepared via direct polymerization, and creates a series of sp2 carbon frameworks with tetragonal, hexagonal, and kagome topologies. The sp2 carbon frameworks are highly luminescent even in the solid state and exhibit topology-dependent π transmission and exciton migration; these key fundamental π functions are unique to sp2 carbon-conjugated frameworks and cannot be accessible by imine-linked frameworks, amorphous analogues, and 1D conjugated polymers. These results demonstrate an unprecedented strategy for structural and functional designs of covalent organic frameworks.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2020 Document type: Article Affiliation country: Singapore

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2020 Document type: Article Affiliation country: Singapore