ORIGINAL RESEARCH article
Uncovering the Structural Diversity of Y(III) Naphthalene-2,6-Dicarboxylate MOFs Through Coordination Modulation
- 1WestCHEM School of Chemistry, University of Glasgow, Glasgow, United Kingdom
- 2EPSRC Centre for Innovative Manufacturing in Continuous Manufacturing and Crystallisation, University of Strathclyde Technology and Innovation Centre, Glasgow, United Kingdom
Metal-organic frameworks (MOFs)—network structures built from metal ions or clusters and connecting organic ligands—are typically synthesized by solvothermal self-assembly. For transition metal based MOFs, structural predictability is facilitated by control over coordination geometries and linker connectivity under the principles of isoreticular synthesis. For rare earth (RE) MOFs, coordination behavior is dominated by steric and electronic factors, leading to unpredictable structures, and poor control over self-assembly. Herein we show that coordination modulation—the addition of competing ligands into MOF syntheses—offers programmable access to six different Y(III) MOFs all connected by the same naphthalene-2,6-dicarboxylate ligand, despite controlled synthesis of multiple phases from the same metal-ligand combination often being challenging for rare earth MOFs. Four of the materials are isolable in bulk phase purity, three are amenable to rapid microwave synthesis, and the fluorescence sensing ability of one example toward metal cations is reported. The results show that a huge variety of structurally versatile MOFs can potentially be prepared from simple systems, and that coordination modulation is a powerful tool for systematic control of phase behavior in rare earth MOFs.
Research revolving around metal-organic frameworks (MOFs)—network structures wherein metal ions or clusters are connected by organic linkers into diverse topologies (Furukawa et al., 2013)—has rapidly increased in recent years following publication of landmark materials in the late 1990s (Chui et al., 1999; Li et al., 1999), with there being ~70,000 MOF structures reported in the Cambridge Structural database as of 2016 (Moghadam et al., 2017). The reason for this interest can be attributed to the permanent porosity and vast range of structural and chemical properties that can be imparted on MOFs, leading to an array of applications from gas storage and separation (Yang and Xu, 2017) to drug delivery and biosensing (Abánades Lázaro and Forgan, 2019). As more MOFs are discovered it is becoming apparent that there is a large range of fascinating topologies accessible, showing diversities in their coordination, solvation, and porosity.
A considerable amount of research focuses on the discovery and synthesis of new frameworks, utilizing a wide range of metals—most commonly transition metals—and organic linkers. We have studied the modulated self-assembly of Zr(IV) (Marshall et al., 2016) and Sc(III) (Marshall et al., 2018) MOFs in detail, yet studies into the synthesis of new yttrium materials appear to be somewhat limited. Whilst yttrium is a d block metal, it is considered as a rare earth (RE) metal and displays coordination chemistry similar to the lanthanides when in the Y(III) oxidation state. As such, there are several reports of lanthanide doped Y-MOFs, for example MIL-78 (Serre et al., 2004) and MIL-92 (Surblé et al., 2005), with the possibility of utilizing the inherent luminescence of europium and terbium to impart nitroaromatic detection and tunable photoluminescence properties on the otherwise non-luminescent materials (Singha et al., 2015; Zheng et al., 2015). Of the single metal Y-MOFs reported, several exhibit permanent porosity and high thermal and water stability, leading to a range of potential applications (Weng et al., 2006; Luo et al., 2008; Jiang et al., 2010; Gong et al., 2012; Duan et al., 2013; Kim et al., 2015; Bezrukov and Dietzel, 2017; Mohideen et al., 2018). For example, a 1,2,4,5-tetrakis(4-carboxyphenyl)benzene based Y-MOF has been utilized for indoor moisture control (Abdulhalim et al., 2017), whilst a framework based on a hexa-carboxylate linker showed selective adsorption of C2H2 and CO2 over CH4 (Liu et al., 2017).
Much like in the synthesis of many other MOFs, coordination modulation—the addition of monotopic linkers as capping agents or crystallization promotors (McGuire and Forgan, 2015)—has been used in the synthesis of Y-MOFs in order to achieve highly crystalline material. Coordination modulation is routinely implemented in the synthesis of MOFs, most commonly enhancing crystallinity and allowing the isolation of single crystals, although under certain conditions, coordination modulation can also control particle size, allowing for the synthesis of nanomaterials (Guo et al., 2012; Chen et al., 2018), or introduce defects throughout a structure whilst maintaining the overall topology (Wu et al., 2013). It should be noted that the use of different modulators in syntheses does not tend to have an effect on the topology of the resultant material. For example, in the case of Zr-MOFs of the UiO topology, the use of different modulators, such as L-proline, benzoic and acetic acid, still results in the formation of the UiO structure, merely with different physical or chemical properties (Schaate et al., 2011; Marshall et al., 2016). Unlike their transition element counter parts however, RE elements have less predictable coordination geometries, resulting in a greater variety of coordination geometries. As a result there is much more difficulty in the prediction of rare earth MOF structures compared to transition metal-based MOFs (Pagis et al., 2016), with coordination modulation potentially perturbing self-assembly to allow isolation of new structures (Decadt et al., 2012). For example, Eddaoudi et al. have introduced 2-fluorobenzoic acid as an efficient modulator of RE MOFs, isolating for example Y-MOFs containing hexanuclear (Figure 1A) (Xue et al., 2013, 2015; Luebke et al., 2015) and nonanuclear (Figure 1B) (Guillerm et al., 2014; Abdulhalim et al., 2017; Chen et al., 2017) secondary building units (SBUs).
Figure 1. Examples of 12-connected (A) [Y6(OH)8(RCO2)12(H2O)6]2− and (B) [Y9(O)2(OH)14 (RCO2)12(H2O)7]3− SBUs accessible through coordination modulation. (C) Chemical structure of the naphthalene-2,6-dicarboxylic acid (NDC-H2) linker.
Herein, we report an extensive study into the effects of coordination modulation on the crystallization of naphthalene-2,6-dicarboxylic acid (NDC-H2, Figure 1C) Y-MOFs. Contrary to many modulated syntheses in which modulation does not affect overall topology, in this case the use of different modulators led to the crystallization of a range of phases containing Y(III) and 2,6-NDC2−, each exhibiting different coordination, solvation, and void space. The selected modulators ranged in pH, size and functionality. Several of the Y-MOFs were synthesized in bulk with phase purity via solvothermal synthesis, with multiple syntheses also successfully being carried out via microwave assisted heating, considerably reducing synthesis time. The luminescent properties of one of the MOFs were also examined, studying the sensing abilities of the framework in the presence of a variety of metals ions.
Results and Discussion
Use of different modulators allowed isolation of six different framework structures wherein Y3+ cations are linked by 2,6-NDC2− units (see SI, section Synthesis). A summary of synthetic conditions is given in Table 1.
Subjecting YCl3 and 2,6-NDC-H2 to solvothermal synthesis in DMF at 120°C resulted in the isolation of [Y2(NDC)3(C3H7NO)2]n (1). 1 is a 3D coordination polymer, which crystallizes in the monoclinic space group P21/c. The asymmetric unit contains two crystallographically independent Y3+ ions having the same connectivity, three 2,6-NDC2− linkers and two DMF molecules. One dimensional chains of Y3+ cations running down the crystallographic c axis (Figure 2A) are connected by carboxylate units of the linkers, with three NDC2− units bridging adjacent metal ions in the (η1:η1:μ2) motif seen in the related Sc2(BDC)3 MOF (Miller et al., 2005; Perles et al., 2005). The larger size of Y3+ compared to Sc3+ leads to coordination of one DMF molecule, making the Y3+ molecules seven-coordinate (Figure 2B), and distancing them further from one another along the chain (Y···Y ~4.8 Å) than in Sc2(BDC)3 (Sc···Sc ~4.4 Å). The chains connect into a net with diamond-shaped pores into which the DMF molecules protrude (Figure 2C).
Figure 2. Crystal structure of 1. (A) The one-dimensional chain SBU. (B) The coordination sphere of Y1. (C) The overall packing structure showing potential porosity. (D) Stacked PXRD patterns of bulk samples of 1 and 2 compared to their predicted patterns, confirming crystals of 2 were isolated from material with bulk composition of 1. Crystal structure of 2. (E) One-dimensional chain SBU with coordinating nitrate (cyan) and DMF (magenta). (F) Packing structure showing structural relationship with 1. H atoms and disorder removed for clarity in all crystal structure images.
The synthesis of 1 can be successfully scaled up to produce the material in bulk with high crystallinity and phase purity, as shown by powder X-ray diffraction (PXRD), which was carried out on a washed and dried sample, showing a close match to the pattern predicted from the crystal structure (Figure 2D). Rapid microwave synthesis (Lin et al., 2012) of 1 is also possible. Yttrium chloride was used rather than yttrium nitrate in order to produce single crystals suitable for structure determination X-ray diffraction, however the same structure is produced when using yttrium nitrate (Figure S1).
In a synthesis using Y(NO3)·6H2O and NDC-H2 doped with two additional equivalents of water, it was possible to isolate crystals of [Y3(NDC)4(C3H7NO)4(NO3)]n (2), from a bulk solid that was shown by PXRD to comprise almost entirely 1 (Figure 2D and Figure S2). Structure 2 crystallizes in the triclinic space group , with the asymmetric unit containing one and a half Y3+ ions, two 2,6-NDC2− linkers, one and a half coordinated nitrate molecules and two coordinated DMF molecules. The unit cell contains two crystallographically independent Y3+ centers, one of which is disordered across two crystallographically equivalent positions through an inversion center. The structure is related to 1; it is comprised of 1D chains of single metal ions, repeating in a [Y1···Y1···Y2]n fashion over the independent Y3+ ions (Figure 2E). The Y1 centers are linked by four bridging NDC2− units with carboxylate groups in the (η1:η1:μ2) motif, with each Y1 linked to an adjacent Y2 by two carboxylates in the same (η1:η1:μ2) motif and the seven-coordinate geometry completed by a DMF solvent molecule. As such, the Y2 centers coordinate to four carboxylate oxygen atoms (two bridging from each Y1 center) with the coordination sphere filled by two DMF molecules and one bidentate nitrate anion, making it eight-coordinate. The Y2 ions are disordered across an inversion center, resulting in two distinct positions 1.3213(3) Å apart with associated disorder of the coordinated ligands. Along the chain, which has the sequence Y1Y1Y2Y1Y1Y2, the Y1···Y1 distance is 4.1635(1) Å, while the Y1···Y2 distances are longer and asymmetric, with one Y1···Y2 distance of 5.1434(2) Å and the other of 5.4725(2) Å, likely because Y1···Y1 are connected via four carboxylate groups from four linkers whereas Y1···Y2 are connected by only two carboxylate groups from two linkers. The overall structure looks similar to 1, with diamond-like pores containing DMF and nitrate ligands pointing into potential pore space (Figure 2F).
Attempts to produce phase pure samples of 2, by deliberate addition of 16 equivalents of nitric acid as a source of nitrate into solvothermal syntheses, resulted in the isolation of [Y2(NDC)3(C3H7NO)4]n (3), which has a significantly different structure but contains no nitrate. The structure, which crystallizes in the triclinic space group, has discrete dimeric SBUs (Figure 3A) rather than 1D chains of Y3+ ions. The asymmetric unit consists of a nine-coordinate Y3+ ion, one and a half 2,6-NDC2− linkers and two coordinated DMF molecules. Four NDC2− linkers bridge the binuclear SBU, two with the (η1:η1:μ2) motif and two with the (η1:η2:μ2) motif, with adjacent pairs of Y3+ ions in the SBU separated by 3.9933(2) Å and related by an inversion center. The Y3+ ions also coordinate to a linker in a terminal bidentate (η1:η2:μ1) motif (Figure 3B) and two DMF molecules, making them nine-coordinate. The bridging linkers form square grid-like sheets along the bc plane, with the terminal linkers connecting the sheets in an offset manner to form a 3D net with a calculated void space [N2 probe, Mercury 3.10.3 (Macrae et al., 2008)] of 31.9%, with continuous channels running through the framework along the a axis (Figure 3C). A discrete complex, [Y2(3,5-DHB)2(CH3CO2)4(H2O)4] (DHB = dihydroxybenzoate), with a closely related coordination arrangement to the dimeric SBU in 3, has been observed previously (Dan et al., 2006).
Figure 3. The crystal structure of 3. (A) The dimeric SBU. (B) The differing coordination modes of the crystallographically independent NDC2− ligands. (C) The packing structure viewed down the a axis. H atoms removed for clarity.
The synthesis of 3 differs from the others in that crystallization occurs at room temperature after the reaction solution has been heated to 120°C for 24 h. Upon removing the reaction jar from the oven, the clear yellow solution (previously colorless) was left undisturbed in a chilled room for a further 3 days, wherein crystallization of block crystals occurred. The reaction was successfully scaled up, proven both visually and by SCXRD, however the framework is not stable to solvent loss as demonstrated by a change in PXRD pattern, highlighting the decomposition (Figure S3). Structurally analogous MOFs have been prepared from Ce, Eu, and Tb, which also decompose in air (Wang et al., 2002), although a Nd derivative has shown sufficient stability to allow gas uptake, with SBET = 150 m2g−1 (Wang et al., 2015).
Subsequently, carboxylate-based modulators were examined. Incorporation of 40 equivalents of acetic acid into the synthesis resulted in the isolation of [Y(NDC)(CH3CO2)(C3H7NO)]n (4) as a phase pure material. 4 crystallizes in the triclinic space group , with the asymmetric unit containing an eight-coordinate Y3+ ion, one 2,6-NDC2− linker, a coordinated acetate and a DMF molecule. The structure is related to 1, with one-dimensional chains of Y3+ ions bridged by NDC2− linkers, but one NDC2− ligand is replaced by two acetate ligands (Figure 4A). The structure can be thought of as containing chains of dimers; two equivalent Y3+ ions, related by an inversion center, are bridged by carboxylate units from two NDC2− ligands in the (η1:η1:μ2) motif and two acetates in the (η1:η2:μ2) motif. These dimers are linked to one another by two further NDC2− carboxylates, also in the (η1:η1:μ2) motif, with the Y3+ coordination sphere being completed by a DMF molecule. The Y···Y distance within the “dimer” is 3.8689(9) Å, while the Y···Y distance to the adjacent “dimer” in the chain is 5.570(1) Å. 4 has a similar packing arrangement to 1, with diamond-shaped pores down the b axis filled with DMF molecules (Figure 4B). Unlike 2, the sample can be prepared in bulk, with phase purity confirmed by PXRD (Figure 4C).
Figure 4. Crystal structure of 4. (A) One dimensional chain SBU, with coordinated acetate (blue) and DMF (magenta). (B) Packing structure viewed down the b axis. (C) Stacked PXRD patterns of 4 and 5 compared to their predicted patterns. (D) Optical image of the hexagonal plates of 5, which give rise to preferred orientation related peak height discrepancies in the PXRD pattern of bulk samples. Scale bar 500 μm. Crystal structure of 5. (E) Trigonal SBU showing bridging formates. (F) Packing structure showing solvent inaccessible voids between SBUs. (G) Hexagonal packing arrangement viewed down the c axis.
The combination of 2-fluorobenzoic acid, nitric acid, and water as co-modulators for RE MOFs has previously resulted in isolation of MOFs with UiO-66 (Xue et al., 2013) and MIL-88 (Wei et al., 2017) nets, as well as novel topologies (Guillerm et al., 2014). With Y3+ and NDC2−, a structure related to MIL-88C is formed, (CH3)2NH2[Y3(NDC)3(HCOO)3(OH)]n (5). Structure 5 crystallizes as hexagonal plates (Figure 4D) in the space group, with the asymmetric unit containing one seven-coordinate Y3+ ion, one 2,6-NDC2− linker, one formate and one third of a dimethylammonium ion (both generated by decomposition of DMF), and one third of a hydroxyl ion. The framework is comprised of [Y3(μ3-OH)(RCO2)6] trimeric SBUs [Figure 4E, Y1···O1C = 2.2986(3) Å] linked by NDC2− linkers into the MIL-88C topology (Figure 4F). The SBUs, which lie in the ab plane, are further connected via two bridging formates per Y3+ ion to form a 2D sheet; the distance between neighboring clusters, measured between the oxygen atoms of adjacent bridging μ3-OH ligands (O1C), is 10.376(2) Å. Disordered dimethylammonium ions sit in the plane of the clusters, forming NH···O hydrogen bonds to oxygen atoms of the linking formates [N1S···O1F = 3.0180(5) Å] and NDC2− linkers [N1S···O1 = 3.0100(3) Å]. The overall structural formula can be confirmed by 1H NMR spectroscopic analysis of digested samples, clearly showing the presence of dimethylammonium cations and formate anions with integral ratios consistent with the overall formula (Figure S6). The structure has pockets of void space totaling 20.3% of the framework, with the bridging formates preventing a continuous solvent accessible pore (Figure 4G). Whilst similar to MIL-88C type structures, the higher coordination number of Y compared to transition metals results in the additional coordination of the formate groups to link the SBUs, expected to limit the breathing nature of 5, a property associated with transition metal linked MIL-88C materials (Horcajada et al., 2011). The crystal structure of the analogous Er-MOF has recently been reported, with the Y-MOF identified by PXRD (Wei et al., 2017).
Tartaric acid has previously been shown to be an efficient modulator in the synthesis of a mixed metal Y-BDC MOF in a mixed EtOH/water solvent system (Abdelbaky et al., 2014), and so conditions (heating to 80°C for 24 h) inspired by this were implemented with Y3+ and NDC2−. Single crystals of [Y2(NDC)3(C2H5OH)(H2O)3]n·3(C3H7NO) (6) could be isolated from the resulting gel. 6 crystallizes in the triclinic space group ; the crystal structure was determined from a selected crystal and does not represent the bulk material, which, after washing and drying, PXRD analysis confirms to be predominantly 1 (Figure S7). The asymmetric unit of 6 contains two Y3+ ions, three 2,6-NDC2− linkers, a coordinated ethanol molecule and three coordinated water molecules. Chains of single Y3+ ions run along the bc plane throughout the framework (Figure 5A), alternating in a -Y1-Y1-Y2-Y2- fashion. Each Y3+ is bridged by two NDC2− carboxylates in the (η1:η1:μ2) motif and is also bridged by a bidentate NDC2− carboxylate in a (η1:η1:μ1) arrangement. The difference between Y1 and Y2 lies in coordinated solvents; Y1 is coordinated to one water molecule and one ethanol molecule, whilst Y2 is coordinated to two water molecules. Within the linear metal chain there are three different but similar Y-Y distances—Y1···Y1 = 4.742(2) Å, Y2···Y2 = 4.731(2) Å, and Y1···Y2 = 4.8846(2) Å,—highlighting the similarity of the eight-coordinate Y3+ ions.
Figure 5. The crystal structure of 6. (A) One dimensional chain SBU, with coordinating ethanol colored blue. (B) Packing structure showing significant void space, with ordered DMF guests removed for clarity.
The chains are connected in an approximately hexagonal manner by the NDC2− ligands to form a framework with a 29% void space [N2 probe, Mercury 3.10.3 (Macrae et al., 2008)], running in disconnected sheets along the bc plane (Figure 5B) and containing ordered DMF solvent molecules. It was unfortunately not possible to prepare a phase-pure sample of 6.
By simple modification of synthetic conditions, six different MOFs have been characterized from a single metal-ligand system, with counterions, solvents, and most importantly modulators playing key roles in directing structure formation. Of the six, the syntheses of frameworks 1, 4, and 5 were successfully scaled up to produce the materials in bulk with high crystallinity and phase purity, as shown by PXRD which was carried out on washed and dried samples. The predicted and experimental powder patterns show good overlap, while minor discrepancies in peak intensities can be attributed to preferential orientation of the packed powder samples. These three frameworks were also successfully produced through microwave-assisted synthesis. Each was carried out on the same scale as that of the bulk solvothermal synthesis and produced crystalline, phase pure material in 2 h and under compared to 24 h solvothermally (Figures S4 and S5). Compounds 2 and 6 crystallize alongside 1 under specific conditions, while 3 can also be scaled up, but appears to be unstable to drying.
1, 4, and 5 can be produced in bulk and have potential voids if solvents can be successfully removed. As such, thermogravimetric analysis was carried out on bulk samples (Figures S8 and S9), along with an undried sample of 3, which is unstable to solvent removal, to assess its bulk composition (Figure 6). The TGA profile of 1 shows the stepwise loss of its two DMF molecules, with a mass loss of 8.6% followed by another of 7.5% between 115°C and 290°C. The final weight loss of 66.2% between 525°C and 618°C can be attributed to the organic linkers. Analysis of 4 shows a similar initial loss of coordinated DMF between 154°C and 214°C, followed by a stepped 55.3% mass loss between 340°C and 670°C arising from the loss of acetate and linkers. 5 shows a first weight loss of 16.2% between 287°C and 336°C which closely correlates with the loss of dimethylammonium cations and formate anions. The following two-step loss of 55.5% can be attributed to the loss of NDC2− linkers and hydroxide. Due to decomposition of 3 on solvent removal, the material was not fully dried before analysis. As such, the initial 22.1% weight loss between 55°C and 126°C arises from encapsulated DMF. The subsequent mass loss of 20.2% correlates with the loss of coordinated DMF, and is followed by a 43.7% mass loss due to organic linkers, confirming the bulk composition suggested by the single crystal structure.
Despite the ability to remove solvent molecules from the materials, none were found to be porous to N2 at 77 K. Removal of coordinated DMF from 1 and 4 presumably results in framework collapse, although it is noted that during the peer review period, a Ce(III) analog of 1 was reported which could be desolvated at 300°C to a phase that was porous to CO2 (Atzori et al., in press). For 5, whilst the framework does show void space, it is possible that access to the void channels is blocked due to charge-balancing dimethylammonium ions lying in the cluster layer of the framework.
The luminescence properties of 5 were investigated in DMF solution in the presence of a variety of metal nitrates, with differing extents of cation exchange with the dimethylammonium ions a possible mechanism for fluorescent sensing. The excitation of the free NDC-H2 linker at λ = 287 nm leads to an emission maximum at λ = 375 nm, with a shoulder at λ = 364 nm, dictating the excitation wavelength for 5. Finely ground framework 5 (2 mg) was immersed in 5 ml of 5 mM DMF solutions of Mx+(NO3)x (M = Ag+, Al3+, Cd2+, Ca2+, Cr3+, Co2+, Cu2+, Fe3+, Mn2+, Mg2+, Ni2+, K+, Na+, Zn2+) and sonicated for 30 min. The luminescence of 5 can be seen to vary to some degree in the presence of all the metal nitrates (Figure 7A). Soaking in Fe3+ and Cu2+ solutions led to complete quenching of luminescence, whereas Al3+ and Zn2+ solutions gave rise to a considerable increase in luminescence. The presence of Cd2+ and Zn2+ notably leads to a shift in the intensity ratio between the 364 and 375 nm peaks, along with the appearance of a new shoulder peak at 350 nm (Figure S10).
Figure 7. (A) Changes in luminescence of samples of 5 when contacted with 5 mM DMF solutions of metal nitrates. (B) Concentration dependence of turn-off sensing of Cu2+. Experiments carried out in triplicate, typical spectra for Cu2+ sensing shown as an inset.
To examine any potential structural changes, the crystallinity of 5 was examined via PXRD after soaking of the samples for 3 days in the metal nitrate solutions. The crystallinity of 5 is retained in the presence of all metals except Fe3+, where the sample becomes completely amorphous (Figure S11). The concentration dependence of Cu2+ turn-off sensing was examined, with significant quenching still observed at 0.1 mM concentrations of Cu2+ (Figure 7B).
Through the use of a range of different modulators, a series of six yttrium frameworks with the naphthalene-2,6-dicarboxylate linker have been synthesized, each exhibiting different coordination, solvation, and void space. Unlike transition metal frameworks in which coordination modulation can be used to enhance crystallinity or impart structural properties whilst maintaining topology, the same technique when used with yttrium leads to a range of polymorphs, with the modulator instead acting as a structural director. The resultant frameworks show considerable structural diversity and high thermal stabilities, with framework 5 presenting interesting luminescence properties in the presence of metal nitrate solutions. This technique could unlock a vast myriad of new yttrium frameworks, with this work generating six structures resulting from just one linker, and a seventh recently published using 2,6-difluorobenzoic acid as modulator (Liu et al., 2018). The combination of modulation along with alternative linkers, varying in their functionality, length, and connectivity, could lead to diverse further interesting frameworks.
Data Availability Statement
The data which underpin this work are available at http://dx.doi.org/10.5525/gla.researchdata.728.
RSF and SLG devised the Project. SLG carried out the research, CW carried out crystallographic analysis, and RSF supervised the project. All authors contributed to the writing of the manuscript.
RSF thanks the Royal Society for receipt of a URF. We thank EPSRC (EP/K503058, EP/L50497X, EP/M506539, and EP/M508056/1) and the EPSRC Centre for Innovative Manufacturing in Continuous Manufacturing and Crystallisation (EP/K503289/1) for funding this work.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We thank the EPSRC National Crystallographic Service for single crystal data collections (Coles and Gale, 2012). We thank Dr. Ross Marshall for his early contribution to the project, conducting preliminary syntheses and providing useful discussion.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fchem.2019.00036/full#supplementary-material
Abdelbaky, M. S. M., Amghouz, Z., García-Granda, S., and García, J. R. (2014). A metal–organic framework assembled from Y(III), Li(I), and terephthalate: hydrothermal synthesis, crystal structure, thermal decomposition and topological studies. Dalton Trans. 43, 5739–5746. doi: 10.1039/c3dt53415d
Abdulhalim, R. G., Bhatt, P. M., Belmabkhout, Y., Shkurenko, A., Adil, K., Barbour, L. J., et al. (2017). A fine-tuned metal–organic framework for autonomous indoor moisture control. J. Am. Chem. Soc. 139, 10715–10722. doi: 10.1021/jacs.7b04132
Atzori, C., Lomachenko, K. A., Øien-Ødegaard, S., Lamberti, C., Stock, N., Barolo, C., and Bonino, F (in press). Disclosing the Properties of a New Ce(III)-Based MOF: Ce2(NDC)3(DMF)2. Cryst. Growth Des. doi: 10.1021/acs.cgd.8b01369
Bezrukov, A. A., and Dietzel, P. D. C. (2017). A permanently porous yttrium–organic framework based on an extended tridentate phosphine containing linker. Inorg. Chem. 56, 12830–12838. doi: 10.1021/acs.inorgchem.7b01574
Chen, Y., Zhang, S., Chen, F., Cao, S., Cai, Y., Li, S., et al. (2018). Defect engineering of highly stable lanthanide metal-organic frameworks by particle modulation for coating catalysis. J. Mater. Chem. A 6, 342–348. doi: 10.1039/C7TA09036F
Chen, Z., Weseliński, Ł. J., Adil, K., Belmabkhout, Y., Shkurenko, A., Jiang, H., et al. (2017). Applying the power of reticular chemistry to finding the missing alb-MOF platform based on the (6,12)-coordinated edge-transitive net. J. Am. Chem. Soc. 139, 3265–3274. doi: 10.1021/jacs.7b00219
Chui, S. S. Y., Lo, S. M. F., Charmant, J. P. H., Orpen, A. G., and Williams, I. D. (1999). A chemically functionalizable nanoporous material [Cu3(TMA)2(H2O)3]n. Science 283, 1148–1150. doi: 10.1126/science.283.5405.1148
Dan, M., Cheetham, A. K., and Rao, C. N. (2006). Diverse structures and dimensionalities in hybrid frameworks of strontium and lanthanum with isomeric dihydroxybenzoates. Inorg. Chem. 45, 8227–8238. doi: 10.1021/ic060917k
Decadt, R., Van Hecke, K., Depla, D., Leus, K., Weinberger, D., Van Driessche, I., et al. (2012). Synthesis, crystal structures, and luminescence properties of carboxylate based rare-earth coordination polymers. Inorg. Chem. 51, 11623–11634. doi: 10.1021/ic301544q
Duan, J., Higuchi, M., Foo, M. L., Horike, S., Rao, K. P., and Kitagawa, S. (2013). A family of rare earth porous coordination polymers with different flexibility for CO2/C2H4 and CO2/C2H6 separation. Inorg. Chem. 52, 8244–8249. doi: 10.1021/ic401157n
Gong, H. Y., Rambo, B. M., Nelson, C. A., Cho, W., Lynch, V. M., Zhu, X., et al. (2012). Multi component self-assembly: supramolecular organic frameworks containing metal–rotaxane subunits (RSOFs). Dalton Trans. 41, 1134–1137. doi: 10.1039/C1DT11495F
Guillerm, V., Weselinski, Ł. J., Belmabkhout, Y., Cairns, A. J., D'elia, V., Wojtas, Ł., et al. (2014). Discovery and introduction of a (3,18)-connected net as an ideal blueprint for the design of metal–organic frameworks. Nat. Chem. 6, 673–680. doi: 10.1038/nchem.1982
Guo, H., Zhu, Y., Wang, S., Su, S., Zhou, L., and Zhang, H. (2012). Combining coordination modulation with acid–base adjustment for the control over size of metal–organic frameworks. Chem. Mater. 24, 444–450. doi: 10.1021/cm202593h
Horcajada, P., Salles, F., Wuttke, S., Devic, T., Heurtaux, D., Maurin, G., et al. (2011). How linker's modification controls swelling properties of highly flexible iron(III) dicarboxylates MIL-88. J. Am. Chem. Soc. 133, 17839–17847. doi: 10.1021/ja206936e
Jiang, H. L., Tsumori, N., and Xu, Q. (2010). A series of (6,6)-connected porous lanthanide–organic framework enantiomers with high thermostability and exposed metal sites: scalable syntheses, structures, and sorption properties. Inorg. Chem. 49, 10001–10006. doi: 10.1021/ic101294s
Kim, Y., Yang, T., Yun, G., Ghasemian, M. B., Koo, J., Lee, E., et al. (2015). Hydrolytic transformation of microporous metal–organic frameworks to hierarchical micro- and mesoporous MOFs. Angew. Chem. Int. Ed. 54, 13273–13278. doi: 10.1002/anie.201506391
Lin, Z. J., Yang, Z., Liu, T. F., Huang, Y. B., and Cao, R. (2012). Microwave-assisted synthesis of a series of lanthanide metal–organic frameworks and gas sorption properties. Inorg. Chem. 51, 1813–1820. doi: 10.1021/ic202082w
Liu, C., Eliseeva, S. V., Luo, T. Y., Muldoon, P. F., Petoud, S., and Rosi, N. L. (2018). Near infrared excitation and emission in rare earth MOFs via encapsulation of organic dyes. Chem. Sci. 9, 8099–8102. doi: 10.1039/C8SC03168A
Liu, K., Li, X., Ma, D., Han, Y., Li, B., Shi, Z., et al. (2017). A microporous yttrium metal-organic framework of an unusual nia topology for high adsorption selectivity of C2H2 and CO2 over CH4 at room temperature. Mater. Chem. Front. 1, 1982–1988. doi: 10.1039/C7QM00164A
Luebke, R., Belmabkhout, Y., Weselin^ski, L. J., Cairns, A. J., Alkordi, M., Norton, G., et al. (2015). Versatile rare earth hexanuclear clusters for the design and synthesis of highly-connected ftw-MOFs. Chem. Sci. 6, 4095–4102. doi: 10.1039/C5SC00614G
Luo, J., Xu, H., Liu, Y., Zhao, Y., Daemen, L. L., Brown, C., et al. (2008). Hydrogen adsorption in a highly stable porous rare-earth metal-organic framework: sorption properties and neutron diffraction studies. J. Am. Chem. Soc. 130, 9626–9627. doi: 10.1021/ja801411f
Macrae, C. F., Bruno, I. J., Chisholm, J. A., Edgington, P. R., Mccabe, P., Pidcock, E., et al. (2008). Mercury CSD 2.0 - new features for the visualization and investigation of crystal structures. J. Appl. Cryst. 41, 466–470. doi: 10.1107/S0021889807067908
Marshall, R. J., Hobday, C. L., Murphie, C. F., Griffin, S. L., Morrison, C. A., Moggach, S. A., et al. (2016). Amino acids as highly efficient modulators for single crystals of zirconium and hafnium metal-organic frameworks. J. Mater. Chem. A 4, 6955–6963. doi: 10.1039/C5TA10401G
Marshall, R. J., Lennon, C. T., Tao, A., Senn, H. M., Wilson, C., Fairen-Jimenez, D., et al. (2018). Controlling interpenetration through linker conformation in the modulated synthesis of Sc metal–organic frameworks. J. Mater. Chem. A 6, 1181–1187. doi: 10.1039/C7TA09699B
Miller, S. R., Wright, P. A., Serre, C., Loiseau, T., Marrot, J., and Férey, G. (2005). A microporous scandium terephthalate, Sc2(O2CC6H4CO2)3, with high thermal stability. Chem. Commun. 30, 3850–3852. doi: 10.1039/b506677h
Moghadam, P. Z., Li, A., Wiggin, S. B., Tao, A., Maloney, A. G. P., Wood, P. A., et al. (2017). Development of a cambridge structural database subset: a collection of metal–organic frameworks for past, present, and future. Chem. Mater. 29, 2618–2625. doi: 10.1021/acs.chemmater.7b00441
Mohideen, M. I. H., Belmabkhout, Y., Bhatt, P. M., Shkurenko, A., Chen, Z., Adil, K., et al. (2018). Upgrading gasoline to high octane numbers using a zeolite-like metal–organic framework molecular sieve with ana-topology. Chem. Commun. 54, 9414–9417. doi: 10.1039/C8CC04824J
Pagis, C., Ferbinteanu, M., Rothenberg, G., and Tanase, S. (2016). Lanthanide-based metal organic frameworks: synthetic strategies and catalytic applications. ACS Catal. 6, 6063–6072. doi: 10.1021/acscatal.6b01935
Perles, J., Iglesias, M., Martín-Luengo, M. Á., Monge, M. Á., Ruiz-Valero, C., and Snejko, N. (2005). Metal–organic scandium framework: useful material for hydrogen storage and catalysis. Chem. Mater. 17, 5837–5842. doi: 10.1021/cm051362e
Schaate, A., Roy, P., Godt, A., Lippke, J., Waltz, F., Wiebcke, M., et al. (2011). Modulated synthesis of zr-based metal–organic frameworks: from nano to single crystals. Chem. Eur. J. 17, 6643–6651. doi: 10.1002/chem.201003211
Serre, C., Millange, F., Thouvenot, C., Gardant, N., Pellé, F., and Férey, G. (2004). Synthesis, characterisation and luminescent properties of a new three-dimensional lanthanide trimesate: M((C6H3)–(CO2)3) (M = Y, Ln) or MIL-78. J. Mater. Chem. 14, 1540–1543. doi: 10.1039/B312425H
Singha, D. K., Majee, P., Mondal, S. K., and Mahata, P. (2015). Visible detection of explosive nitroaromatics facilitated by a large stokes shift of luminescence using europium and terbium doped yttrium based MOFs. RSC Adv. 5, 102076–102084. doi: 10.1039/C5RA22599J
Surblé, S., Serre, C., Millange, F., Pelle, F., and Férey, G. (2005). Synthesis, characterisation and properties of a new three-dimensional Yttrium–Europium coordination polymer. Solid State Sci. 7, 1074–1082. doi: 10.1016/j.solidstatesciences.2005.04.015
Wang, C. C., Yeh, C. T., Ke, S. Y., Cheng, Y. T., Yang, C. C., Lee, G. H., et al. (2015). Assembly of three Nd(III) 2,6-naphthalenedicarboxylates (ndc2−) 3D coordination polymers based on various secondary building units (SBUs): structural diversity and gas sorption properties. RSC Adv. 5, 92378–92386. doi: 10.1039/C5RA10799G
Wang, Z., Jin, C. M., Shao, T., Li, Y. Z., Zhang, K. L., Zhang, H. T., et al. (2002). Syntheses, structures, and luminescence properties of a new family of three-dimensional open-framework lanthanide coordination polymers. Inorg. Chem. Commun. 5, 642–648. doi: 10.1016/S1387-7003(02)00515-4
Wei, N., Zuo, R. X., Zhang, Y. Y., Han, Z. B., and Gu, X. J. (2017). Robust high-connected rare-earth MOFs as efficient heterogeneous catalysts for CO2 conversion. Chem. Commun. 53, 3224–3227. doi: 10.1039/C7CC00363C
Weng, D., Zheng, X., and Jin, L. (2006). Assembly and upconversion properties of lanthanide coordination polymers based on hexanuclear building blocks with (μ3-OH) bridges. Eur. J. Inorg. Chem. 2006, 4184–4190. doi: 10.1002/ejic.200600491
Wu, H., Chua, Y. S., Krungleviciute, V., Tyagi, M., Chen, P., Yildirim, T., et al. (2013). Unusual and highly tunable missing-linker defects in zirconium metal–organic framework UiO-66 and their important effects on gas adsorption. J. Am. Chem. Soc. 135, 10525–10532. doi: 10.1021/ja404514r
Xue, D. X., Belmabkhout, Y., Shekhah, O., Jiang, H., Adil, K., Cairns, A. J., et al. (2015). Tunable rare earth fcu-MOF platform: access to adsorption kinetics driven gas/vapor separations via pore size contraction. J. Am. Chem. Soc. 137, 5034–5040. doi: 10.1021/ja5131403
Xue, D. X., Cairns, A. J., Belmabkhout, Y., Wojtas, L., Liu, Y., Alkordi, M. H., and Eddaoudi, M. (2013). Tunable rare-earth fcu-MOFs: a platform for systematic enhancement of CO2 adsorption energetics and uptake. J. Am. Chem. Soc.135, 7660–7667. doi: 10.1021/ja401429x
Keywords: metal-organic frameworks, yttrium, coordination modulation, microwave synthesis, fluorescent sensing
Citation: Griffin SL, Wilson C and Forgan RS (2019) Uncovering the Structural Diversity of Y(III) Naphthalene-2,6-Dicarboxylate MOFs Through Coordination Modulation. Front. Chem. 7:36. doi: 10.3389/fchem.2019.00036
Received: 27 November 2018; Accepted: 14 January 2019;
Published: 31 January 2019.
Edited by:Tony D. James, University of Bath, United Kingdom
Reviewed by:Guzman Gil-Ramirez, University of Lincoln, United Kingdom
Adam Charles Sedgwick, University of Texas at Austin, United States
Copyright © 2019 Griffin, Wilson and Forgan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ross S. Forgan, Ross.Forgan@glasgow.ac.uk