Surfactant-directed syntheses of mesostructured zinc imidazolates: formation mechanism and structural insights †

Supramolecular templating techniques have been widely used to direct the formation of porous materials with the goal of introducing permanent mesoporosity. While surfactant-directed self-assembly has been exploited for inorganic materials such as titania, silica, organosilica, and zeolites, it has rarely been applied to metal – organic frameworks (MOFs) and coordination polymers. Here we introduce a new family of gemini surfactant-directed zinc imidazolates, referred to as mesostructured imidazolate frameworks (MIFs), and present a detailed study on the influence of different gemini-type surfactants on the formation mechanism and structures of the resulting zinc imidazolates. The proposed formation mechanism for MIF-type materials involves co-assembly and crystallization processes that yield lamellar mesostructured imidazolate frameworks. Understanding and controlling such processes also has implications for the syntheses of microporous zinc imidazolate framework (ZIF) materials, whose formation can be suppressed in surfactant-rich solutions, whereas formation of MIF materials is favored in the presence of surfactants and triggered by the addition of halogenides. Solid-state 2D 13 C{ 1 H} HETCOR NMR measurements on prototypic CTAB-directed MIF-1 establish that the head group moieties of the surfactant molecules interact strongly with the zinc-imidazolate-bromide sheets. Additionally, the NMR analyses suggest that MIF-1 has a significant fraction of surfactant molecules that are interdigitated between the zinc-imidazolate-bromide sheets with an antiparallel stacking arrangement, consistent with the high thermal and chemical stability of the MIF hybrid materials.


Introduction
In recent years, metal-organic frameworks (MOFs) have received considerable attention due to their modularity and versatility, such as tunable pore sizes, 1,2 high specific surface areas [3][4][5] and the possibility to alter their properties via post-synthetic modification of the organic linkers. 6,7These desirable properties render MOFs multi-purpose scaffolds in a number of applications such as catalysis, 8,9 sensing, 10,11 gas storage 12,13 and drug delivery. 14,157][18] With interpenetration effects limiting the possibility of using larger linkers to increase the pore size, other routes such as the use of more complex connection motifs 17 or templating techniques have been utilized. 19The latter provide additional benefits by creating a hierarchical structure with bi-or multimodal pore-size distributions, including both micro-and mesopores, which facilitate the diffusion of bulky molecules and widen the potential applications in catalysis and drug delivery.
While exploring synthetic approaches to hierarchical ZIFs by soft templating, we have recently discovered the class of mesostructured imidazolate frameworks (MIFs), which combine structural elements of both coordination polymers and liquid crystalline mesophases to form hierarchical structures ordered on both the atomic-and nanoscale. 20MIFs are composed of zinc imidazolate chains or layers sandwiched between surfactant slabs, forming a mesoscopic layered hybrid structure similar to MCM-type lamellar silica or metal oxide mesophases. 20,21Therefore, the well-known structural analogies between zeolitic imidazolate frameworksa subclass of metalorganic frameworksand zeolites can also be extended mesophase materials, where surfactant-directed lamellar zinc imidazolate mesophases find their analogue in MCM-50-type silica mesostructures (Fig. 1a).Lamellar MIFs have previously been obtained under reverse microemulsion conditions in the presence of the surfactant cetyltrimethylammonium bromide (CTAB).Given the structural similarities between MIFs and MCM-50both on the molecular level (Zn-Im-Zn vs. Si-O-Si bonding angles) and on the mesoscale (mesoscopic phase segregation into organic and inorganic lamellar domains)design principles associated with mesostructured silica materials may ultimately enable the syntheses of MIFs with non-lamellar 3D hexagonal or cubic mesostructures.
Previous work on mesostructured silica materials has revealed the dominant role of the surfactant and its amphiphilic architecture and colloidal properties on the resulting mesostructures.3][24] Gemini surfactants can be described by the general structure n-m-n, with n being a terminal aliphatic carbon chain and m being a linker between two quaternary nitrogen ions (Fig. 1b).6][27][28] Earlier work on the influence of these surfactants on the formation of periodic mesoporous organosilica (PMO) has shown that n-6-n gemini surfactants (n = 12-22) can form multiple mesostructures, depending on the length of the terminal carbon chains.For example, shorter chains (n = 12-14) result in cubic phases, while longer chains often lead to 3D and 2D hexagonal (n = 16-20) or lamellar (n = 22) structures. 29In this work, we use gemini surfactants with different lengths of their alkyl chains (from 14 to 18 carbon atoms) and spacer lengths (4 to 10 carbon atoms) to synthesize a homologous series of mesostructured imidazolate frameworks.To develop a better understanding of the mechanisms underlying MIF formation, we rely on a combination of spectroscopic analyses that provide complementary information across multiple length scales.In particular, two-dimensional (2D) solid-state nuclear magnetic resonance (NMR) spectra establish specific surfactant-framework interactions in zinc methylimidazolate -CTAB hybrid materials.The detailed insights provided by this work are expected to aid in the design of MIFs with a broader range of mesostructured compositions, topologies, and hierarchical structural ordering.

Reagents & instruments
All reagents were commercially available and used as purchased without further purification.
Powder X-ray diffraction (PXRD) measurements were performed using a STOE Stadi P powder X-ray diffraction instrument, operated in Guinier geometry using a Mythen1K or an imaging plate detector.Infrared measurements were performed on a Perkin Elmer Spektrum BX II with an attenuated total reflectance unit.Elemental analysis was done in a thermal conductivity measurement cell of an Elementar vario EL.Analysis of halogenide content was done by titration with AgĲNO 3 ) on a Titroprocessor 672 by Metrohm.To determine the amount of zinc and other metal ions, the samples were analyzed based on optical emission of the elements in an Ar-plasma (ICP).Measurements were done on a VARIAN VISTA simultaneous spectrometer with autosampler and recorded with a CCD-detector.TEM measurements were performed on a Philips CM 30 ST microscope (LaB 6 cathode, 300 kV, C S = 1.15 mm).Sample preparation was done by drop casting highly diluted samples (~50 μg mL −1 ) on a carbon coated copper grid, followed by evaporation of the solvent.Solid-state NMR experiments were conducted at 11.7 T using Bruker AVANCE II and DSX-500 NMR spectrometers, both operating at frequencies of 500.24MHz for 1 H, 125.78 MHz for 13 C, and 50.70 MHz for 15 N.The experiments were performed at room temperature under magic-angle-spinning (MAS) conditions using a 4 mm Bruker H-X double-resonance probehead and zirconia rotors.For the solid-state 2D 13 C{ 1 H} HETeronuclear CORrelation (HETCOR) NMR experiments, high-power homonuclear 1 H-1 H decoupling was applied during the 1 H evolution period to enhance the resolution in the 1 H dimension, using the eDUMBO-1 pulse sequence 30 with a phase-modulated radio frequency pulse of constant amplitude (100 kHz).The 2D 13 C{ 1 H} HETCOR spectra were acquired with cross-polarization (CP) contact times of 1 ms or 5 ms, a recycle delay of 1 s, and SPINAL-64 1 H heteronuclear decoupling (80 kHz).128 transients (t 2 ) were signal-averaged for each of the 400 t 1 increments, resulting in a total experimental time of approximately 14 h for each spectrum.Thermogravimetric and differential thermal analysis measurements were performed on a combined DTA-TG-thermobalance (type 92-2400, Setaram).The samples were transferred into an aluminum oxide crucible and heated from room temperature to 700 °C at a rate of 5 °C min −1 .

Synthesis of gemini surfactants
The gemini surfactants were synthesized by dissolving 3 mmol of the respective N,N-dimethylamine in 75 mL of acetone and adding 1.5 mmol of the respective α,ω-dibromoalkane to the solution (for details on all chemicals used see Table S1 †).The solution was refluxed for 4 days, leading to the formation of a white precipitate that was obtained by centrifugation at 15 000 rpm for 10 minutes.The product was dried at room temperature overnight and yielded a white, waxy substance.Purity of the obtained surfactants was confirmed by elemental analysis, IR spectroscopy and solution-state NMR.

Results and discussion
MIFs were obtained in the presence of n-m-n gemini surfactants (n = 14-18, m = 4-10, see Fig. 1b) as structure directing agents in a variety of solvents ranging from methanol to inverse microemulsion systems such as n-heptane/1-hexanol/ water mixtures and THF.The materials could be obtained with imidazole (IM) and 2-methylimidazole (MeIM) as linkers, at room temperature as well as under reflux conditions.In order to obtain differently mesostructured materials, the ratio of IM to Zn(NO 3 ) 2 was altered between 8 : 1 and 1 : 4 and the surfactant concentration was varied between 0.01 M and 0.5 M.Although n-m-n gemini surfactants were reported to direct the formation of 3D cubic (n = 16-18, m = 10-12) and hexagonal (n = 16-18, m = 6-10) mesostructures in the MCM-type system, 31 we found the signature of lamellar MIF mesophases in all cases, irrespective of the type of gemini surfactant/solvent combination used, over the whole range of surfactant concentrations tested.The stacking parameters varied slightly depending on the solvent used (Table S2, 2), which is in principle agreement with the powder data.The doubled stacking parameter along b that can be observed in the Pawley fit may be rationalized by a superstructure, which prominently was observed for MIFs based on gemini-surfactants with m ≤ 8.The absence of higher order stacking reflections at around 2θ = 5°in hybrid materials with shorter linkers may be due to the discussed superstructure effects or accidental extinction. 22,32lemental analysis revealed a composition of all hybrid materials of zinc : IM/MeIM : bromine : surfactant of 1 : 1 : 2 : 0.5, corresponding for example to the empirical formula Zn 2 Br 4 ĲC 3 H 3 N 2 ) 2 ĲC 46 H 96 N 2 ) for the 16-10-16 imidazolate MIF (Table S3 †).The synthesized materials show good thermal stability up to ≈320 °C (Fig. S3 †), as well as chemical stability, withstanding even surfactant extraction procedures with supercritical CO 2 , yet showing the typical sensitivity of MOFs towards acids.Upon acid-induced decomposition of the material, the pristine surfactants and imidazolates were recovered, proving that all MIF constituents stay intact during the entire synthesis process.
Our data therefore suggest that all gemini-directed materials are composed of the same principal building units like the prototypic MIF-1, 20 as sketched in Fig. 2. The formerly proposed structure model consists of one-dimensional zinc-imidazolate chains with additional coordination of two bromine ions to the metal center.These chains of corner sharing tetrahedra are interleaved with surfactant layers, thus forming quasi twodimensional layered assemblies.This structural motif for the zinc imidazolate subunit has previously been reported by Lin et al. in a coordination polymer without incorporated surfactant molecules. 33,34Combination of the developed structure model with the metrics obtained from the Pawley fit shows good accordance between both (Fig. 2).
For the 14-6-14 IM MIF material, additional signals are observed in the 13 C MAS NMR spectrum, revealing the presence of different 13 C local environments.As shown in Fig. 3c, two different pairs of well-resolved 13 C signals are observed for the imidazolate carbon atoms (143.1 and 141.6 ppm, 126.1 and 124.4 ppm).These distinct pairs of 13 C signal intensities are consistent with two inequivalent 13 C local environments for the imidazolate species, likely due to superstructure effects, such as ABA-type stacking of the surfactantinorganic slabs.Such a stacking arrangement would also give rise to a doubled b-axis as found for other hybrid materials 35 and for pure CTAB. 36Interestingly, similar experiments on CTAB-directed MIF-1 (Fig. 3a) also exhibit two distinct 13 C signals (149.0 and 151.0 ppm) for the sp 2 carbon atom bonded to the nitrogen atoms of the methylimidazole moieties.These results, along with a detailed 2D NMR analysis of MIF-1, are discussed below.
Subtle but distinct differences are also observed in the 15 N local environments of the 14-6-14 IM MIF, as evidenced by 15 N MAS NMR (Fig. 3e) and consistent with the 13 C NMR analyses above.Two well-resolved and equally intense 15 N signals associated with the imidazolate nitrogen atoms are observed at −166.4 and −168.9 ppm for the 14-6-14 IM MIF, whereas only one corresponding 15 N signal (−166.2ppm) is observed for the 16-10-16 MeIM MIF (Fig. 3d).These results indicate that the local environments of the imidazolate species are highly sensitive to surfactant architecture, such as spacer length, leading to inequivalent imidazolate and surfactant interactions predominantly for materials synthesized using surfactants with shorter spacers (m ≤ 8).
The gemini MIFs obtained by syntheses with n-m-n gemini surfactants (n = 14, 16, 18; m = 4-10) all exhibit similar layered zinc-imidazolate structures separated by surfactant molecules, while the stacking parameter of the mesostructures differs for the surfactants used.All synthesized materials exhibit a lamellar mesostructure, with layer stacking distances varying between 25.4 Å and 35.6 Å for IM bridged systems and between 25.3 Å and 35.9 Å for MeIM bridged systems, respectively, depending on the used surfactants (Fig. 4).We find that the stacking of the material depends on both the surfactant tail length (n) as well as on the length of the spacer (m), indicating a tilted arrangement of the surfactants with respect to the zinc-imidazolate slabs.Our data show a direct correlation between the d-spacing and the tail length, with an increase in d-spacing by 1.7 ± 0.3 Å for an increase of the tail length by two carbon atoms (Fig. 4, S4 and Table S4 †).The observable lamellar stacking also increases with longer spacer lengths, but by a variable amount depending on the used spacer.Whilst the stacking distance increases by 4.6 Å when switching from m = 9 to m = 10 in 18-m-18 IM MIFs, the lamellar stacking decreases by ≈0.1 Å when switching from m = 7 to m = 8 in the same MIF system.
A closer look at the proposed structure of the MIF materials provides an explanation for this phenomenon.The distance between two ĳZnBr 2 ] − -units is roughly 6 Å, which is in good agreement with the distance between the two quartenary nitrogen ion headgroups of a m = 5 gemini surfactant.Up to a linker length of m = 9, we see that the surfactants appear to gradually tilt further away from the neighbouring [Zn(Me)IMBr 2 ] − -units in order to comply with the charge density of the inorganic slabs (Scheme S5 †).The sudden increase in stacking distance at m = 10 for IM (Fig. 4, left) is likely accompanied by a more abrupt structural rearrangement, such as an increase in the tilt angle α, leading to a more perpendicular alignment of the surfactants with respect to the layers and, hence, increased d-spacing.
The tilted arrangement of the gemini surfactants seems contradictory to our previous observations, as this asymmetric arrangement of the surfactants is expected to manifest distinct 15 N NMR signals for the two nitrogen atoms of the gemini head groups due to differences in local environments of the two alkylammonium ions.However, the alkyl-groups surrounding  the nitrogen atoms may well "screen" them and provide an overall similar local environment, rendering them less susceptible to direct interactions with the coordination polymer chains.
To complete our structural model of gemini-directed MIFs, we assume that the two surfactant carbon tails are oriented in a close-to-parallel conformation, in agreement with previous work on gemini-surfactants with spacer sizes m > 3. 37 This leads us to propose a model of the surfactant location in the material with both carbon tails parallel to each other with a fixed angle α of about 43°between the surfactant tail and the zinc imidazolate layers (Fig. S6 †).
Previously synthesized prototypic MIFs differ from the materials presented in this work only with respect to the type of surfactant used (alkyl ammonium vs. gemini alkyl ammonium), the resulting d-spacings and the apparent structural order, as indicated by the presence of high-angle reflections in the PXRD data of the gemini surfactants as opposed to those of CTAB-directed MIF-1.Despite their similar composition (ratio of inorganic and organic building blocks) and mesostructure, we assume a more rigid anchoring of the doubly cationic ammonium head groups of the gemini surfactants to the inorganic slabs as compared to CTAB-directed MIFs, stabilized by multiple hydrophobic interactions of the antiparallel interdigitated surfactant layers. 38o gain additional insights about the locations and interactions of the surfactants within MIF-type materials, solidstate 2D 13 C{ 1 H} HETeronuclear CORrelation (HETCOR) NMR measurements were performed on a CTAB-directed MIF material (MIF-1).MIF-1 was used instead of the gemini-directed MIFs because the CTAB-based system is less complicated and exhibits similar molecular-level interactions between different organic and inorganic moieties.Interactions among chemically distinct species in heterogeneous zinc imidazolate materials can be established by solid-state 2D NMR techniques that are sensitive to dipole-dipole couplings between molecularly proximate moieties.Here, solid-state 2D 13 C{ 1 H} HETCOR NMR spectra provide specific local and molecular-level information on CTA + -framework interactions in as-synthesized MIF-1.Furthermore, the intra-and intermolecular interactions are be distinguished by experimentally varying the 13 C-1 H cross-polarization contact time from short (e.g., 1 ms) to long (e.g., 5 ms) durations, respectively.
The solid-state 2D 13 C{ 1 H} HETCOR NMR spectra in Fig. 5a of as-synthesized MIF-1 exhibit strong and distinct intensity correlations between 13 C and 1 H nuclei associated with the CTA + surfactant molecules and the zinc-imidazolate-bromide sheets.A 1D 13 C{ 1 H} CPMAS NMR spectrum is shown above the horizontal axis, along with 13 C signal assignments corresponding to the various 13 C species of the CTA + surfactant and the methylimidazole moieties.Two 2D NMR spectra conducted with short (1 ms) and long (5 ms) CP contact times are shown in red and blue, respectively, for comparison.The 2D signal intensities observed for the short contact time arise from strongly dipolar-coupled nuclei that are associated principally with intramolecular interactions from covalently bonded 13 C and 1 H nuclei. Strong intensity correlations are observed between the 13 C signal of the methylimidazole aromatic carbon atoms (C 1 /C 2 ) at 126 ppm and the 1 H signals at 6.6 ppm and 7.3 ppm corresponding to their aromatic protons, as expected.Similarly, correlated signal intensity is observed at 16 ppm (C 17′ ), 17 ppm (C 4 ), and 53 ppm (C 1′ ) in the 13 C dimension associated with distinct methyl groups at 1.3 ppm, 2.55 ppm, and 2.45 ppm in the 1 H dimension from their respective covalently bonded hydrogen atoms.Additionally, 2D intensity correlations are observed at 67 ppm (C 2′ ) and 25-35 ppm (C 3′ -C 16′ ) from alkyl chain 13 C atoms with the 1 H signals at 3.35 ppm and 1.5 ppm, associated with the alkyl protons of the CTA + molecules.Together, these intramolecular 2D intensity correlations allow the numerous partially resolved 13 C and 1 H signals to be unambiguously assigned to as-synthesized MIF-1.
More interestingly, correlated signal intensity from intermolecular interactions between 13 C and 1 H nuclei on different molecular species provide complementary information concerning the proximities of the CTA + surfactant and the methylimidazole framework moieties.Correlated signal intensity is observed for a short cross-polarization contact time (1 ms, Fig. 5a, red) at 17 ppm (C 4 ) and 126 ppm ĲC 1 /C 2 ) in the 13 C dimension from the anionic zinc methylimidazolate chains and at 2.45 ppm in the 1 H dimension associated with the cationic CTA + head group; these results are consistent with the expected chargebalancing electrostatic interactions between the surfactant species and the MIF-1 framework.In the accompanying 1D 13 C{ 1 H} CPMAS spectrum, the two well-resolved 13  C environments (C 3a and C 3b ) associated with the sp 2 carbon atom bonded to the nitrogen atoms of the methylimidazole moieties.This is clearly evidenced in the 2D HETCOR spectrum, in which different intensity correlations are observed for these 13 C signals: while they both are correlated with the 1 H signal at 2.55 ppm from the methyl protons of the methylimidazole group (C 4 ), only the 13 C signal at 151 ppm (C 3b ) is correlated with the 1 H signal at 2.45 ppm from the CTA + head groups.This indicates that there are two distinct types of methylimidazole C 3 moieties, which differ according to their respective proximities to the CTA + head groups.Interestingly, the 1 H signal at 2.45 ppm from the CTA + head groups is also correlated with the alkyl 13 C signals at 16 ppm (C 17′ ), 24 ppm (C 16′ ), and 31 ppm (C 15′ ) associated with the ends of the CTA + alkyl chains; these specific intensity correlations reflect an interdigitated arrangement of a fraction of CTA + molecules where the head group and tail are in close proximity to each other, an arrangement known from the surfactant crystal structure.For this short contact time, correlated signal intensity is also observed between the 1 H signal at 2.55 ppm from the methyl protons of the methylimidazole moiety (C 4 ) and the 13 C signal at 24 ppm (C 16′ ) from the penultimate carbon atom on the end of the CTA + alkyl chain, which corroborates the interdigitated arrangement of some of the surfactant species.The molecular-level insights provided by these short-range intermolecular correlations (red arrows) are depicted in the schematic diagram in Fig. 5b.
For a longer contact time (5 ms), the 2D 13 C{ 1 H} HETCOR NMR spectrum (Fig. 5a, blue) acquired under otherwise identical conditions yields correlated signal intensity from more weakly coupled 13 C and 1 H nuclei (for reasons of internuclear distance or molecular mobilities).Intensity correlations are observed for the 13 C signal at 126 ppm (C 1 /C 2 ) with the 1 H signal at 1.3 ppm, revealing that the aromatic carbons (C 1 /C 2 ) of the methylimidazole are also molecularly proximate to the methyl protons of the CTA + tail.As observed and discussed above, the blue spectrum also reveals 2D signal intensity between both of the 13 C signals at 149 ppm (C 3a ) and 151 ppm (C 3b ) and the 1 H signal at 1.5 ppm associated with the CTA + alkyl protons, while only the C 3b carbon atom is molecularly close to the CTA + tail, based on the intensity correlation between the 13 C signal at 151 ppm and the 1 H signal at 1.3 ppm.This difference between the two distinct signals for C 3 indicates a high degree of order in the material if the antiparallel arrangement of the surfactant chains is taken into account.These longer-range intermolecular correlations are depicted by the blue arrows in the schematic diagram of Fig. 5b.
Collectively, the NMR results offer complementary and additional insights to previous X-ray diffraction analyses of MIF-1, which characterize the long-range order of the materials, though are insensitive to structural disorder or order that is present only locally (e.g., several nm).In particular, the absence of XRD reflections at high 2θ valuesas opposed to the gemini-type MIFsis consistent with a rather high degree of surfactant disorder commonly observed for other CTA + -directed mesostructured oxide materials. 39,40Nevertheless, the 2D 13 C{ 1 H} HETCOR NMR spectra establish that the head group moieties of the cationic CTA + surfactants interact strongly with the anionic zinc imidazolate framework, as previously observed for closely related CTA + -directed silicates with lamellar mesoscopic ordering. 39,40However, whereas the surfactant chains are highly disordered in the layered CTA + -silicate materials, MIF-1 has a significant fraction of its CTA + molecules that appear to be interdigitated between the zinc methylimidazolate chains with an anti-parallel stacking arrangement (Fig. 5b), as likewise inferred for the gemini-directed MIFs.Similar interdigitated, antiparallel arrangements of alkyl side chains on supramolecular assemblies of (linear) semiconducting polymers in bulk heterojunction materials have been observed, where the degree of ordering of the domains has a significant influence on the charge transfer properties. 41,42The discrepancy between the order observed in the 2D NMR experiments and apparent absence of order at the molecular level in the PXRD experiments can be explained in two ways: First, CTA + is an organic species that exhibits lower scattering factors compared to the inorganic layers, thus resulting in low scattering intensity especially at higher angles in the PXRD patterns.Secondly, the antiparallel arrangements of the alkyl side chains may be confined to small domains and broken up by significant conformational disorder, and therefore not detected by XRD methods.
To assess the importance of the halogenide counter-ions on the formation of lamellar MIF mesophases, the syntheses were conducted with gemini surfactant molecules without halogenide counter-ions (the bromine counter-ions were exchanged by nitrate ions via treatment with AgNO 3 ).For all combinations of solvents and surfactant concentrations tested, no mesostructured products were formed in the absence of the halogenide counter-ions, under otherwise identical conditions.By comparison, syntheses conducted with chlorine counterions yielded MIF products (Fig. S7 †).These results corroborate the important role of the halogenide counter-ions in syntheses of the MIF materials.In addition, the presence of the surfactant molecules appears to hinder the formation of ZIF structures, such as ZIF-8, which are typically obtained by mixing zinc nitrate and imidazole in methanol. 43However, adding halogenide ions to a reaction mixture containing methanol, zinc acetate, imidazole and surfactants with nitrate counter-ions led to the formation and rapid precipitation of a MIF product.Collectively, these observations underscore the importance of halogenide ions in the MIF syntheses.
Previously, a liquid crystal templating mechanism was proposed for the formation of MIF materials, according to which the mesostructure is directed by the surfactant molecules, while the coordination polymer nucleates and grows within the water reservoirs of the lamellar surfactant mesophase. 20s the curvature of the micellar structure formed by gemini surfactants is strongly dependent on the lengths of the tail and linker chains and is highly sensitive to the surfactant concentration and solvent composition, 27,44 this formation mechanism should in principle result in a wide variety of mesostructures, which is not observed in the present case where exclusively lamellar nanomorphologies are obtained.We therefore propose a formation mechanism in which the one-dimensional structure composed of negatively charged ĳZnĲMe)IMBr 2 ] − chains is formed first.These then assemble with the positively charged gemini surfactants by an electrostatically driven cooperative assembly process that is similarly observed with various MCM-type systems, 45 resulting in the 2D slab-like structures of the final lamellar mesostructured material (Fig. 6).Since the quasi-linear geometry of the zinc bromide imidazolate chains with vanishing curvature seems to direct and drive the mesostructure assembly, the formation of exclusively lamellar mesostructures with zero curvature is hence expected.

Conclusions
The solid-state NMR analyses yield detailed atomic-level insights on the structures of metal imidazolate framework materials, which support previously proposed structural models.Specifically, surfactant bilayers between the layers of one-dimensional zinc-imidazolate chains charge-compensate the chain structure.Although our efforts to obtain cubic or hexagonal mesostructured MIFs have so far been unsuccessful, the proposed formation mechanism of the gemini-directed MIFselectrostatically driven co-assembly governed by the formation of linear zinc bromide imidazolate chainssheds light on why exclusively lamellar structures have been found so far in the MIF system.The roles of halogenide counterions in surfactant-assisted syntheses of MIF and ZIF materials are established, along with their influences on the selectivity and nanoscale morphologies of MIF versus ZIF products.These results have general implications for syntheses of mesostructured imidazolate framework materials and the molecular-level interactions that are responsible for the assembly and crystallization of their ordered frameworks.

Fig. 1
Fig. 1 (a) Schematic diagram showing the similarities between ZIFs and zeolites on the one hand, and MIFs and MCM-type materials on the other hand.(b) Molecular structure of a representative gemini surfactant (here n = 15, m = 3).The spacer length m and the carbon tail length n can be altered to tune the properties of the surfactant.
Fig. S1 †), yet could not be correlated to specific solvent properties such as boiling point or dielectric constant.The obtained MIF phases exhibited varying degrees of crystallinity, and only a small fraction of the materials yielded powder patterns of suitable quality for indexing.Pawley refinement of the XRD pattern of 16-8-16 imidazolate MIF yielded metrics consistent with monoclinic symmetry (C2, a = 11.5829Å, b = 58.253Å, c = 9.2415 Å, β = 88.94°,wR = 7.57, GoF = 1.286,Fig. S2 †).Similar metrics were determined for gemini-directed MIFs with m ≤ 8.Although all samples are highly sensitive to the electron beam, transmission electron microscopy selected area diffraction (TEM SAED) data obtained for the 16-10-16 sample revealed a rectangular pattern with a = 11.5 Å and c = 9.2 Å and a lamellar stacking of 29 Å along [0k0] (Fig.

Fig. 4
Fig. 4 Graphical presentation of the d-values corresponding to the first observable stacking reflection in the PXRD measurements of all synthesized MIF materials as a function of spacer length (top) and tail length (bottom).Left: IM bridged MIFs, right: MeIM bridged MIFs.
C signals at 149 ppm and 151 ppm indicate the presence of two inequivalent13

Fig. 5
Fig.5(a) Solid-state 2D13 C{ 1 H} HETCOR NMR spectra acquired at room temperature for as-synthesized MIF-1 under MAS conditions of 12.5 kHz with 1 ms (red) or 5 ms (blue) cross-polarization (CP) contact times.For comparison, 1D single-pulse 1 H MAS and 1D 13 C{ 1 H} CPMAS spectra are shown along the vertical and horizontal axes, respectively, of the 2D spectra.Schematic diagrams of the CTA + surfactant and methylimidazole molecules are shown and their corresponding13 C and 1 H signal assignments are indicated in the 1D spectra.(b) Schematic diagram of MIF-1 (Zn/MeIM/CTAB) showing interactions between the zinc imidazolate chains and the CTA + molecules that are consistent with the 2D 13 C{ 1 H} HETCOR NMR analyses.Carbon and hydrogen atoms are labeled according to the assignments in Fig.1.Red and blue arrows indicate13 C-1 H dipolar interactions at short (1 ms) and long (5 ms) contact times, respectively.Note that Zn and Br atoms oriented into the page are colored gray.A fraction of the CTA + molecules are thought to be interdigitated with an antiparallel stacking arrangement.