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Synthetic Strategies to Extended Aromatic Covalent Organic Frameworks.
Prieto, Tania; Ponte, Clara; Guntermann, Roman; Medina, Dana D; Salonen, Laura M.
Afiliación
  • Prieto T; CINBIO, Universidade de Vigo, Department of Organic Chemistry, 36310, Vigo, Spain.
  • Ponte C; Nanochemistry Research Group, International Iberian Nanotechnology Laboratory (INL), Av. Mestre José Veiga, 4715-330, Braga, Portugal.
  • Guntermann R; CICECO-Aveiro Institute of Materials, University of Aveiro, Campus Universitário de Santiago, 3810-193, Aveiro, Portugal.
  • Medina DD; Department of Chemistry and Center for NanoScience (CeNS), Ludwig Maximilians University (LMU), Butenandtstraße 11 (E), 81377, Munich, Germany.
  • Salonen LM; Department of Chemistry and Center for NanoScience (CeNS), Ludwig Maximilians University (LMU), Butenandtstraße 11 (E), 81377, Munich, Germany.
Chemistry ; 30(45): e202401344, 2024 Aug 12.
Article en En | MEDLINE | ID: mdl-38771916
ABSTRACT
π-Conjugated materials are highly attractive owing to their unique optical and electronic properties. Covalent organic frameworks (COFs) offer a great opportunity for precise arrangement of building units in a π-conjugated crystalline matrix and tuning of the properties through choice of functionalities or post-synthetic modification. With this review, we aim at summarizing both the most representative as well as emerging strategies for the synthesis of π-conjugated COFs. We give examples of direct synthesis using large, π-extended building blocks. COFs featuring fully conjugated linkages such as vinylene, pyrazine, and azole are discussed. Then, post-synthetic modification methods that result in the extension of the COF π-system are reviewed. Throughout, mechanistic insights are presented when available. In the context of their utilization as film devices, we conduct a concise survey of the prominent COF layer deposition techniques reported and their aptness for the deposition of fused aromatic systems.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: España