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一种两步后合成修饰策略:将短链多胺连接到Zn-NH-BDC金属有机框架上以增强CO吸附

A Two Step Postsynthetic Modification Strategy: Appending Short Chain Polyamines to Zn-NH-BDC MOF for Enhanced CO Adsorption.

作者信息

Justin Anita, Espín Jordi, Kochetygov Ilia, Asgari Mehrdad, Trukhina Olga, Queen Wendy L

机构信息

Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), CH-1951 Sion, Switzerland.

出版信息

Inorg Chem. 2021 Aug 16;60(16):11720-11729. doi: 10.1021/acs.inorgchem.1c01216. Epub 2021 Jul 15.

Abstract

Functionalizing metal-organic frameworks (MOFs) with amines is a commonly used strategy to enhance their performance in CO capture applications. As such, in this work, a two-step strategy to covalently functionalize NH-containing MOFs with short chain polyamines was developed. In the first step, the parent MOF, ZnO(NH-BDC), was exposed to bromoacetyl bromide (BrAcBr), which readily reacts with pendant -NH groups on the 2-amino-1,4-benzenedicarboxylate (NH-BDC) ligand. H NMR of the digested MOF sample revealed that as much as 90% of the MOF ligands could be functionalized in the first step. Next, the MOF samples 60% of the ligands functionalized with acetyl bromide, ZnO(NH-BDC)(BrAcNH-BDC), was exposed to several short chain amines including ethylenediamine (ED), diethylenetriamine (DETA), and tris(2-aminoethyl)amine (TAEA). Subsequent digested H NMR analysis indicated that a total of 30%, 28%, and 19% of the MOF ligands were successfully grafted to ED, DETA, and TAEA, respectively. Next, the CO adsorption properties of the amine grafted MOFs were studied. The best performing material, TAEA-appended-ZnO(NH-BDC)(BrAcNH-BDC), exhibits a zero-coverage isosteric heat of CO adsorption of -62.5 kJ/mol, a value that is considerably higher than the one observed for the parent framework, -21 kJ/mol. Although the boosted CO affinity only leads to a slight increase in the CO adsorption capacity in the low-pressure regime (0.15 bar), which is of interest in postcombustion carbon dioxide capture, the CO/N (15/85) selectivity at 313 K is 143, a value that is ∼35 times higher than the one observed for ZnO(NH-BDC), 4.1. Such enhancements are attributed to accessible primary amines, which were grafted to the MOF ligand. This hypothesis was further supported via DRIFTS measurements of TAEA-Ac-ZnO(NH-BDC)(BrAcNH-BDC) after exposure to CO, which revealed the chemisorption of CO via the formation of hydrogen bonded carbamates/carbamic acid and CO species; the latter are adducts formed between CO and [amineH]Br salts that are produced during the amine grafting step.

摘要

用胺对金属有机框架(MOF)进行功能化是提高其在CO捕获应用中性能的常用策略。因此,在本工作中,开发了一种用短链多胺对含NH的MOF进行共价功能化的两步策略。第一步,将母体MOF,即ZnO(NH-BDC),暴露于溴乙酰溴(BrAcBr)中,其很容易与2-氨基-1,4-苯二甲酸酯(NH-BDC)配体上的侧链-NH基团发生反应。对消化后的MOF样品进行的¹H NMR分析表明,在第一步中高达90%的MOF配体可以被功能化。接下来,将60%的配体用乙酰溴功能化后的MOF样品,即ZnO(NH-BDC)(BrAcNH-BDC),暴露于几种短链胺中,包括乙二胺(ED)、二亚乙基三胺(DETA)和三(2-氨基乙基)胺(TAEA)。随后的消化¹H NMR分析表明,分别有30%、28%和19%的MOF配体成功接枝到ED、DETA和TAEA上。接下来,研究了胺接枝MOF的CO吸附性能。性能最佳的材料,即TAEA连接的-ZnO(NH-BDC)(BrAcNH-BDC),表现出CO吸附的零覆盖等压热为-62.5 kJ/mol,该值远高于母体框架所观察到的值,即-21 kJ/mol。尽管增强的CO亲和力在低压范围(0.15 bar)仅导致CO吸附容量略有增加,这在燃烧后二氧化碳捕获中是令人感兴趣的,但在313 K时的CO/N₂(15/85)选择性为143,该值约为ZnO(NH-BDC)所观察到的值4.1的35倍。这种增强归因于接枝到MOF配体上的可及伯胺。通过对暴露于CO后的TAEA-Ac-ZnO(NH-BDC)(BrAcNH-BDC)进行DRIFTS测量,进一步支持了这一假设,该测量揭示了通过形成氢键氨基甲酸盐/氨基甲酸和CO物种实现的CO化学吸附;后者是在胺接枝步骤中产生的CO与[胺H]Br盐之间形成的加合物。

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