4.8 Article

Troger?s Base Chemistry in Solution and in Zr(IV)-Based Metal-Organic Frameworks

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c08623

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资金

  1. U.S. Department of Energy (DOE) Office of Science, Basic Energy Sciences Program for Separation [DE-FG02-08ER15967, HDTRA1-18-1-0003]
  2. Department of Defense (DoD) through the National Defense Science & Engineering Graduate (NDSEG) Fellowship Program
  3. NSF Graduate Research Fellowship [DGE-1842165]
  4. Ryan Fellowship
  5. International Institute for Nanotechnology at Northwestern University
  6. National Key R & D Program of China [2021YFA1200402, 2022YFA1503302, 2021YFA1501501, 2021YFA1200302]
  7. National Natural Science Foundation of China [91856204]
  8. Key Project of Basic Research of Shanghai [22JC14021000]

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The study focuses on the strap elimination of a carboxylate-carrying TB in solution and Zr(IV)-based MOFs, revealing different reactions depending on solvent used. In the MOF synthetic system, the derivatization process is topology-guided and dependent on local acid concentration, resulting in the formation of Zr-MOFs with different topologies. Additionally, a novel post-synthetically water-induced in situ linker formylation process was discovered in one of the MOFs.
Tro''ger's base (TB) and its derivatives have been studied extensively due to their unique concave shape stemming from the endomethylene strap. However, the strap-clipped TB chemistry has been largely overlooked in metal-organic framework (MOF) solids, leading to a gap in our knowledge within this field. In this work, we report the in situ strap elimination of a carboxylate-carrying TB in the presence of formic acid, both in solution and in Zr(IV)-based MOFs. In the solution system, the methanodiazocine nucleus can be exclusively transformed into an N,N '-diformyl-decorated phenhomazine derivative, regardless of the solvent used (DMF, DMA, or DEF), as unambiguously uncovered by single crystal X-ray crystallography. In contrast, while in the MOF synthetic system, the degree of derivatization reaction can be effectively controlled to give either the secondary diamine or formyl-decorated diamine, depending on the solvent used (DMF or DEF), resulting in the formation of two Zr-MOFs with 8 connected bcu (NU-1900) and 12-connected fcu (NU-407) topologies, respectively. The derivatization mechanism is proposed to be topology-guided and dependent on the local acid concentration during the MOF formation processes. Moreover, we discovered a novel post-synthetically water-induced in situ linker formylation process in NU-1900 through sequential formic acid elimination, migration, and condensation processes, affording an isostructural framework with the same linker as in NU-407, which further corroborates our proposed mechanism. Additionally, the highly defective NU-1900 with abundant accessible Zr sites was demonstrated to be an outstanding catalyst for the detoxification of a nerve agent simulant with a half-life of less than 1 min.

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