Single-crystal x-ray diffraction structures of covalent organic frameworks

Author:

Ma Tianqiong12ORCID,Kapustin Eugene A.3,Yin Shawn X.4,Liang Lin1ORCID,Zhou Zhengyang2,Niu Jing1ORCID,Li Li-Hua1ORCID,Wang Yingying1,Su Jie2ORCID,Li Jian2,Wang Xiaoge2ORCID,Wang Wei David1ORCID,Wang Wei15ORCID,Sun Junliang2ORCID,Yaghi Omar M.36ORCID

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, Gansu 730000, China.

2. College of Chemistry and Molecular Engineering, Beijing National Laboratory for Molecular Sciences, Peking University, Beijing 100871, China.

3. Department of Chemistry, University of California-Berkeley; Materials Sciences Division, Lawrence Berkeley National Laboratory; Kavli Energy NanoSciences Institute at Berkeley; Berkeley Global Science Institute, Berkeley, CA 94720, USA.

4. Drug Product Science & Technology, Bristol-Myers Squibb Co., One Squibb Drive, New Brunswick, NJ 08903, USA.

5. Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300071, China.

6. King Abdulaziz City for Science and Technology, Riyadh 11442, Saudi Arabia.

Abstract

Covalent organic frameworks writ large Covalent organic framework (COF) materials have been difficult to characterize structurally and to exploit because they tend to form powders or amorphous materials. Ma et al. studied a variety of three-dimensional COFs based on imine linkages (see the Perspective by Navarro). They found that the addition of aniline inhibited nucleation and allowed the growth of crystals large enough for single-crystal x-ray diffraction studies. Evans et al. describe a two-step process in which nanoscale seeds of boronate ester–linked two-dimensional COFs can be grown into micrometer-scale single crystals by using a solvent that suppresses the nucleation of additional nanoparticles. Transient absorption spectroscopy revealed superior charge transport in these crystallites compared with that observed in conventional powders. Science , this issue p. 48 , p. 52 ; see also p. 35

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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