surface modification of uio-66 with cat-ddmat for the synthesis of self-assembled metal-organic framework monolayers

Self-Assembly of Polymer-Grafted Metal Organic Framework Monolayers

Metal-organic frameworks (MOFs) are crystalline, porous materials that offer large surface areas while being readily tunable through modifications of the organic ligands or metal nodes1,2. MOFs are constructed from two components: an organic ligand and metal ions (or metal ion clusters referred to as secondary building units, SBUs). MOFs have been investigated for chemical (e.g., gas) storage, separations, catalysis, sensing, and drug delivery. Generally, MOFs are synthesized in the form of crystalline powders; however, for ease of handling in many applications, formulation into other form factors is desirable if not necessary3,4. For example, mixed matrix membranes (MMMs) of MOFs with polymers have been reported as one particularly useful composite of MOFs and polymers5. However, in some cases, MMMs may have limitations due to the incompatibility/immiscibility between MOF and polymer components5,6. Therefore, strategies have been explored to incorporate polymer grafting directly onto MOF particles to form polymer-grafted MOFs.
Inorganic and metallic nanoparticles exhibit unique behavior in terms of optical, magnetic, catalytic, and mechanical properties7,8. However, they tend to aggregate easily after synthesis, which can hinder their processability. To enhance their processability, polymer chains can be grafted onto the particle surface9. Nanoparticles with high grafting density offer excellent dispersion and stability due to favorable enthalpic interactions between surface polymers and the solvent and entropic repulsion interactions between the particles10. Grafting of polymers onto particle surfaces can be achieved through a variety of strategies11. The most straightforward approach is the &#39;grafting to&#39; particle strategy, where functional groups, such as thiols or carboxylic acids, are introduced at the ends of polymer chains to directly bind to the nanoparticle. When complementary chemical groups, such as hydroxyls or epoxides, are present on the particle surface, polymer chains can be grafted onto these groups via covalent chemical approaches12,13. The &#39;grafting from&#39; particle or surface-initiated polymerization method involves anchoring initiators or chain transfer agents (CTAs) to the surface of nanoparticles and then growing polymer chains on the particle surface through surface-initiated polymerization. This method often achieves higher grafting density than the &#39;grafting to&#39; approach. Furthermore, grafting from enables the synthesis of block copolymers, thereby expanding the diversity of polymer structures that can be immobilized on a particle surface.
Examples of polymer grafting onto MOF particles have begun to emerge, largely focused on installing polymerization sites on the organic ligands of the MOF. In a recent study published by Shojaei and coworkers, vinyl groups were covalently attached to the ligands of Zr(IV)-based MOF UiO-66-NH2 (UiO = Universitetet i Oslo, where the terephthalic acid ligand contains an amino substituent), followed by methyl methacrylate (MMA) polymerization to create polymer-grafted MOFs with a high grafting density (Figure 1A)14. Similarly, Matzger and coworkers functionalized the amine groups on a core-shell MOF-5 (a.k.a., IRMOF-3@MOF-5) particles with 2-bromo-iso-butyl groups. Using polymerization initiated by the 2-bromo-iso-butyl groups, they created poly(methyl methacrylate) (PMMA)-grafted PMMA@IRMOF-3@MOF-515.
In addition to functionalizing the ligand of the MOF for grafting from polymerization, new methods that create sites for polymer grafting via coordination to the metal centers (a.k.a., SBUs) of the MOF have also been explored. For example, a ligand that can bind to the MOF metal centers, such as catechol (Figure 1B), can be used to coordinate to exposed metal sites on the MOF surface. Using a catechol-functionalized chain-transfer agent (cat-CTA, Figure 1B) the MOF surface can be functionalized and made suitable for a grafting from polymerization.
Recently, the aforementioned strategy for synthesizing MOFs-polymer composites has also been used for the creation of free-standing MOF monolayers16,17,18. MOFs such as UiO-66 and MIL-88B-NH2 (MIL = Materials of Institute Lavoisier) were surface-functionalized with pMMA using a ligand-CTA strategy (Figure 1B). The polymer-grafted MOF particles were self-assembled at an air-water interface to form self-supporting, self-assembled metal-organic framework monolayers (SAMMs) with a thickness of ~250 nm. The polymer content in these composites was ~20 wt%, indicating that SAMMs contained ~80 wt% MOF loading. Followup studies showed that different vinyl polymers could be grafted onto UiO-66 to produce SAMMs with different characteristics19. Analytical techniques such as thermogravimetric analysis (TGA), dynamic light scattering (DLS), and gel permeation chromatography (GPC) were used to calculate polymer brush height and grafting density of the surface-grafted MOF-polymer composites.
Herein, the preparation of SAMMs from UiO-66-pMA (pMA = poly(methyl acrylate)) is presented. For the polymerization of methyl acrylate (MA), 2-(dodecylthiocarbonothioylthio)-2-methylpropionic acid (DDMAT, Figure 1B) is used as the CTA19. The functionalization of the UiO-66 particles with cat-DDMAT is essential for the grafting of pMA. Cat-DDMAT can be synthesized through a two-step acylation procedure from a commercially available CTA&#160;and dopamine hydrochloride19. It is also crucial to use UiO-66 particles of uniform size for the successful formation of SAMMs19; therefore, the UiO-66 used in this study was prepared using the continuous addition method20. The polymerization method employed for forming the polymer-grafted MOF particles is photoinduced reversible addition-fragmentation chain transfer (RAFT) conducted under blue LED light (using an in-house-built photoreactor, Figure 2) with a tris(2-phenylpyridine)iridium (Ir(ppy)3) photocatalyst. RAFT polymerization gives exceptionally narrow polymer dispersity that can be finely controlled. Free CTA is included during the polymerization reaction because the ratio of transfer agent to monomer allows for control over the molecular weight during polymerization. The amount of cat-DDMAT transfer agent on the surface of the MOF particles is small; therefore, excess free CTA is added and the amount of monomer to be used is calculated based off of the amount of free CTA present21. After polymerization, the free polymer produced from the free CTA is removed by washing, leaving only the polymer-grafted UiO-66-pMA. Subsequently, this composite is dispersed in toluene at a high concentration and used to form SAMMs at an air-water interface.

저자 스포트라이트: 자체 조립된 MOF-폴리머 복합재 탐색

Synthesis and Characterization of Self-Assembled Metal-Organic Framework Monolayers Using Polymer-coated Particles(고분자 코팅 입자를 사용한 자체 조립된 금속-유기 프레임워크 단층의 합성 및 특성 분석)

Our laboratory is interested at the intersection of porous solids, specifically metal organic frameworks and organic polymers. We're really interested in understanding the interface between these two materials and how we can make composites that have new emergent properties that are characteristic of both the porous solid as well as the polymer component. Recently, we found that grafting polymer onto the surface of MOF, we could produce composite MOF polymer particle that's self-assembled into ultrathin films.We call this film self-assembled MOF monolayer, or SAMs. We are now interested in understanding how SAMs vary depending on polymer length, particle size, and other characteristics. I've begun to explore the role of polymer molecular weight, polymer composition, and polymer grafting density, as well as particle size and shape on SAM formation and stability.I believe this study will be very important for understanding and controlling SAM formation, stability, and future applications. One interesting feature of SAMs is that they can be made ultra thin, just one particle layer thick. We are unaware of other particle films this thin that are unsupported by another substrate and freestanding.This unique property may give SAMs advantages as cross-membrane over other films or particle assemblies. We're really interested in continuing to study SAMs, their self-assembly, and what unique properties make them so stable as ultra thin films. In particular, we're really interested in studying SAMs as coatings and membranes and their use in challenging separations.Ultimately, we think SAMs provide a number of avenues for research that have yet to be explored.

자체 조립된 금속-유기 프레임워크 단층의 합성을 위해 cat-DDMAT를 사용한 UiO-66의 표면 개질

먼저 10mg의 카테콜-DDMAT를 20밀리리터 바이알에 옮깁니다. 눈금이 매겨진 실린더를 사용하여 바이알에 클로로포름 5ml를 조심스럽게 추가합니다. UiO-66 물 분산액을 40밀리리터 원추형 원심분리기 튜브에 옮긴 다음 카테콜-DDMAT 용액을 동일한 튜브에 추가합니다.철저한 혼합을 위해 3분 동안 용액을 소용돌이치십시오. 다음으로, 눈금이 매겨진 실린더를 사용하여 결합 된 혼합물에 20 밀리리터의 에탄올을 첨가하십시오. 튜브를 잘 흔들어 용액을 고르게 섞습니다.대략 10에 혼합물을 분리하십시오, 10 분 동안 000 G. 상층액을 제거합니다. 그런 다음 약 40ml의 신선한 에탄올을 추가하여 펠릿을 세척합니다.입자를 적절하게 재분산시키기 위해 용액을 초음파 처리합니다. 다시 원심분리한 후 튜브에 DMSO 5mL를 추가합니다. 최적의 분산을 위해 입자를 다시 초음파 처리합니다.보관을 위해 용액을 15밀리리터 원뿔형 원심분리기 튜브로 옮깁니다.

surface-modification-uio-66-with-cat-ddmat-for-synthesis-self

Research

JoVE Journal

Chemistry

Surface Modification of UiO-66 with cat-DDMAT for the Synthesis of Self-Assembled Metal-Organic Framework Monolayers

365 조회수.  University of California, San Diego. 먼저 10mg의 카테콜-DDMAT를 20밀리리터 바이알에 옮깁니다. 눈금이 매겨진 실린더를 사용하여 바이알에 클로로포름 5ml를 조심스럽게 추가합니다. UiO-66 물 분산액을 40밀리리터 원추형 원심분리기 튜브에 옮긴 다음 카테콜-DDMAT 용액을 동일한 튜브에 추가합니다.철저한 혼합을 위해 3분 동안 용액을 소용돌이치십시오. 다음으로, 눈금이 매겨진 실린더를 사용하여 결합 된 ?...

비디오: 자체 조립된 금속-유기 프레임워크 단층의 합성을 위해 cat-DDMAT를 사용한 UiO-66의 표면 개질

Synthesis and Characterization of Self-Assembled Metal-Organic Framework Monolayers Using Polymer-Coated Particles

Metal-organic frameworks (MOFs) are materials with potential applications in fields such as gas adsorption and separation, catalysis, and biomedicine. Attempts to enhance the utility of MOFs have involved the preparation of various composites, including polymer-grafted MOFs. By directly grafting polymers to the external surface of MOFs, issues of incompatibility between polymers and MOFs can be overcome. Polymer brushes grafted from the surface of MOFs can serve to stabilize the MOF while enabling particle assembly into self-assembled metal-organic framework monolayers (SAMMs) via polymer-polymer interactions.
Control over the chemical composition and molecular weight of the grafted polymer can allow for tuning of the SAMM characteristics. In this work, instructions are provided on how to immobilize a chain transfer agent (CTA) onto the surface of the MOF UiO-66 (UiO = Universitetet i Oslo). The CTA&#160;serves as initiation sites for the growth of polymers. Once polymer chains are grown from the MOF surface, the formation of SAMMs is achieved through self-assembly at an air-water interface. The resulting SAMMs are characterized and shown to be freestanding by scanning electron microscopy imaging. The methods presented in this paper are expected to make the preparation of SAMMs more accessible to the research community and thereby expand their potential use as a&#160;MOF-polymer composite.

A protocol for the synthesis and characterization of self-assembled metal-organic framework monolayers is provided using polymer-grafted, metal-organic framework (MOF) crystals. The procedure shows that polymer-grafted MOF particles can be self-assembled at an air-water interface resulting in well-formed, free-standing, monolayer structures as evidenced by scanning electron microscopy imaging.

Metal-organic frameworks (MOFs) are materials with potential applications in fields such as gas adsorption and separation, catalysis, and biomedicine. ...