Oligothiophene-Bridged Conjugated Covalent Organic Frameworks
Author(s) -
Niklas Keller,
Derya Bessinger,
Stephan Reuter,
Mona Calik,
Laura Ascherl,
Fabian C. Hanusch,
Florian Auras,
Thomas Bein
Publication year - 2017
Publication title -
journal of the american chemical society
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.7b01631
Subject(s) - covalent bond , imine , conjugated system , chemistry , organic electronics , covalent organic framework , molecule , block (permutation group theory) , nanotechnology , dynamic covalent chemistry , realization (probability) , polymer , transistor , materials science , organic chemistry , supramolecular chemistry , physics , geometry , mathematics , quantum mechanics , voltage , catalysis , statistics
Two-dimensional covalent organic frameworks (2D-COFs) are crystalline, porous materials comprising aligned columns of π-stacked building blocks. With a view toward the application of these materials in organic electronics and optoelectronics, the construction of oligothiophene-based COFs would be highly desirable. The realization of such materials, however, has remained a challenge, in particular with respect to laterally conjugated imine-linked COFs. We have developed a new building block design employing an asymmetric modification on an otherwise symmetric backbone that allows us to construct a series of highly crystalline quaterthiophene-derived COFs with tunable electronic properties. Studying the optical response of these materials, we have observed for the first time the formation of a charge transfer state between the COF subunits across the imine bond. We believe that our new building block design provides a general strategy for the construction of well-ordered COFs from various extended building blocks, thus greatly expanding the range of applicable molecules.
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