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LiBH4 doped with 1.6 mol % well-dispersed C60 is studied with solid-state nuclear magnetic resonance (NMR). Variable-temperature hydrogen NMR shows large changes between the data upon first heating and after exposure to 300 °C. After heating, a large fraction on the order of 50% of the hydrogen signal appears in a motionally narrowed peak, similar to a previous report of LiBH4 in a porous carbon aerogel nanoscaffold. Magic-angle spinning (MAS) NMR of 13C in a 13C-enriched sample finds the C60 has reacted already in the as-mixed (unheated) material. Dehydriding and rehydriding result in further 13C spectral changes, with nearly all intensity being found in a broad peak corresponding to aromatic carbons. It thus appears that the previously reported improved dehydriding and rehydriding kinetics of this material at least partially result from in situ formation of a carbon framework. The method may offer a new route to dispersal of hydrides in carbon support structures.

The phase evolution and electrical characteristics of In_2O_3(ZnO)_3 were examined when (Zn_(0.5)Sn_(0.5))_(1.5) (Zn:Sn = 1.1 ratio) was substituted for InO_(1.5) in In_2O_3(ZnO)_3. As the amount of (Zn_(0.5)Sn_(0.5))_(1.5) substitution increased up to 8 at%, a single phase of In_2O_3(ZnO)_3 was maintained with a homogeneous grain size distribution, constant electrical characteristics and decreasing lattice constants. When the amount of (Zn_(0.5)Sn_(0.5))_(1.5) is increased over the solubility limit (about 8 at%), the second phases of In_2O_3(ZnO)_4 and Zn_2SnO_4 appeared and the volume fraction of the In_2O_3(ZnO)_3 matrix decreased, while lattice constants remained unchanged. When 16 at% of (Zn0_5Sn_(0.5))_(1.5) was substituted, the In_2O_3(ZnO)_3 phase disappeared and three phases of In_2O_3(ZnO)_4, Zn_2SnO_4 and unreacted In_2O_3 coexisted. Because of the precipitation of the second phases, grain size decreased greatly. Carrier mobility and electrical conductivity were also decreased due to the disappearance of the In_2O_3(ZnO)_3 phase and the decrease of grain size.

The NaAlH4 system remains the archetype of hydrogen storage solids. However, the detailed mechanisms of the hydrogen reactions of NaAlH4 remain unknown. We report 27Al in situ nuclear magnetic resonance (NMR) spectroscopic data revealing an Al-bearing mobile species that could provide the large scale metal-atom transport needed for rehydriding. This new species forms under reaction conditions but can be captured at ambient temperature using excess H2 pressure. The NMR measurements demonstrate that the species is highly mobile (at 20 °C) and carries both Al and H atoms. On the basis of the 27Al shift (close to NaAlH4) and the disorder evident in X-ray diffraction, the species is identified as highly defective NaAlH4, likely having a large AlH3 vacancy concentration.

An unusual case of a diquaternary ammonium dication, with large bulky end groups built from the tropane moiety and connected by a C4 methylene chain, is found to reside in zeolite SSZ-35 (STF). The structure of the guest/host product is such that the tropane bicylic entities reside in the shallow cavities of the cages of the STF structure and the C4 methylene chain runs through the 10-ring (~5.5 Å) window that connects the cages. This is a most unusual (and energy-intensive) templating of a zeolite structure with the guest molecule spanning two unit cells. The unusual result was found by single crystal studies with the addition of the use of the SQUEEZE program to show a consistent fit for the guest molecule following from measured electron densities in the crystal structure work. These analyses were followed with MAS NMR studies to confirm the integrity of the diquaternary guest molecule in the host sieve. A few comparative diquaternary guest molecules in MFI zeolite are also studied.

By in situ X-ray diffraction (XRD) and nuclear magnetic resonance (NMR) spectroscopy, the role of Li2B12H12 for the sorption of LiBH4 is analyzed. We demonstrate that Li2B12H12 and an amorphous Li2B10H10 phase are formed by the reaction of LiBH4 with diborane (B2H6) at 200 °C. Based on our present results, we propose that the Li2B12H12 formation in the desorption of LiBH4 can be explained as a result of reaction of diborane and LiBH4. This reaction of the borohydride with diborane may also be observed for other borohydrides, where B12H12 phases are found during decomposition.

Desorption and subsequent rehydrogenation of Mg(BH_4)_2 with and without 5 mol % TiF_3 and ScCl_3 have been investigated. Temperature programmed desorption (TPD) experiments revealed a significant increase in the rate of desorption as well as the weight percentage of hydrogen released with additives upon heating to 300 °C. Stable Mg(B_xH_y)_n intermediates were formed at 300 °C, whereas MgB_2 was the major product when heated to 600 °C. These samples were then rehydrogenated and subsequently characterized with powder X-ray diffraction (pXRD), Raman, and NMR spectroscopy. We confirmed significant conversion of MgB_2 to fully hydrogenated Mg(BH_4)_2 for the sample with and without additives. TPD and NMR studies revealed that the additives have a significant effect on the reaction pathway during both dehydrogenation and rehydrogenation reactions. This work suggests that the use of additives may provide a valid pathway for improving intrinsic hydrogen storage properties of magnesium borohydride.

A lithium salt of anionic scandium tetraborohydride complex, LiSc(BH_4)_4, was studied both experimentally and theoretically as a potential hydrogen storage medium. Ball milling mixtures of LiBH_4 and ScCl_3 produced LiCl and a unique crystalline hydride, which has been unequivocally identified via multinuclear solid-state nuclear magnetic resonance (NMR) to be LiSc(BH_4)_4. Under the present reaction conditions, there was no evidence for the formation of binary Sc(BH_4)_3. These observations are in agreement with our first-principles calculations of the relative stabilities of these phases. A tetragonal structure in space group I (#82) is predicted to be the lowest energy state for LiSc(BH_4)_4, which does not correspond to structures obtained to date on the crystalline ternary borohydride phases made by ball milling. Perhaps reaction conditions are resulting in formation of other polymorphs, which should be investigated in future studies via neutron scattering on deuterides. Hydrogen desorption while heating these Li−Sc−B−H materials up to 400 °C yielded only amorphous phases (besides the virtually unchanged LiCl) that were determined by NMR to be primarily ScB_2 and [B_(12)H_(12)]^(−2) anion containing (e.g., Li_2B_(12)H_(12)) along with residual LiBH_4. Reaction of a desorbed LiSc(BH_4)_4 + 4LiCl mixture (from 4LiBH_4/ScCl_3 sample) with hydrogen gas at 70 bar resulted only in an increase in the contents of Li_2B_(12)H_(12) and LiBH_4. Full reversibility to reform the LiSc(BH_4)_4 was not found. Overall, the Li−Sc−B−H system is not a favorable candidate for hydrogen storage applications.

The detemplation process in Me-SBE (Me = Co^2+, Mg^2+, and Mn^2+) aluminophosphates was studied to elucidate materials stability and framework characteristics. In addition, the hydrothermal synthesis conditions were optimized to obtain materials with minimal phase impurities. This was accomplished by means of decreasing reaction temperature and increasing aging periods. Scanning electron microscopy analysis of the Mg- and Mn-SBE as-synthesized samples revealed square plates with truncated corner morphologies grown in aggregated fashion and contrasting with the previously reported hexagonal platelike morphology of Co-SBE. Cautious detemplation in vacuum, using an evacuation rate of 10 mmHg/s and a temperature of 648 K, resulted in surface areas of about 700, 500, and 130 m^2/g for Mg-, Co-, and Mn-SBE, respectively. Thermal gravimetric analysis and in situ high-temperature powder X-ray diffraction analyses indicate the frameworks for all of the SBE variants experienced collapse upon treatment with helium at temperatures above 700 K and subsequently formed an aluminophosphate trydimite dense phase. Detemplation in air at all times resulted in framework destruction during detemplation. In situ differential scanning calorimetry−powder X-ray diffraction data showed that the SBE frameworks experience breathing modes related to specific endothermic and exothermic scenarios during air treatment. Decomposition and elimination of the organic template during vacuum treatment was verified by Fourier transform infrared spectroscopy. X-ray photoelectron spectroscopy revealed that most of the Co atoms in vacuum-treated samples are in tetrahedral coordination, while the Mn atoms exhibit various coordination states. Ultraviolet-visible, electron paramagnetic resonance, and magic-angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy corroborated the latter result in addition to providing evidence for the formation of Mn extra framework species. ^(27)Al MAS NMR spectra for vacuum-detemplated Mg-SBE samples prior to and after dehydration confirmed the reversible formation of aluminum octahedral sites. This, however, did not affect the porous nature of detemplated Mg-SBE samples as these are capable of adsorbing 19 water molecules per super cage at 298 K.

Grafted V(V)−calixarene complexes that are 1,3-disubstituted at the lower rim have been synthesized using an extraordinarily mild procedure, using the V(III)−calixarene precursor p-But−calix[4]−(OMe)2(O)2V−Cl (1c), which is subsequently grafted onto silica and, afterward, oxidized to yield material 2c. The calixarene acts as a sterically bulky chelating ligand and enforces isolated pseudo-octahedral vanadium centers on silica, as ascertained by 51V NMR spectroscopy and analysis of the UV/vis spectrum of materials after calixarene removal via calcination. 13C CP/MAS NMR spectroscopy of 2c reveals lack of a downfield-shifted ipso carbon resonance, which is strongly indicative of a high d-orbital electron density for the V metal centers in 2c, a result that is expected on the basis of a proposed simple geometric model that is consistent with single-crystal X-ray crystallographic data of early transition metal metallocalixarenes. This result motivates future programming of grafted metal centers with chemical ...

An additional dimension has been added to our long-standing studies in high silica zeolite synthesis via a guest/host synergism. We have created and studied the impact of making symmetric diquaternary ammonium compounds, by varying the chain length between nitrogen charge centers, and the heterocycle size and geometry containing the nitrogen. This allows the introduction of a second spatial parameter in the use of the charged organo-cation guest in the zeolite synthesis. The series of 15 diquaternary ammonium compounds (5 heterocycles synthesized onto chain lengths of C4-C6) were tested in a total of 135 zeolite syntheses reactions. Nine screening reactions were employed for each guest molecule, and the conditions built upon past successes in finding novel high silica zeolites via introduction of boron, aluminum, or germanium as substituting tetrahedral framework atoms for silicon. Eighteen different zeolite structures emerged from the studies. The use of specific chain lengths for derivatives of the pyrrolidine ring system produced novel zeolite materials SSZ-74 and 75.

The decomposition of crystalline magnesium borohydride upon heating was studied using thermal desorption, calorimetry, in situ X-ray diffraction, and solid state NMR. Hydrogen release from Mg(BH4)2 occurs in at least four steps via formation of several polyborane intermediate species and includes an exothermic reaction yielding crystalline MgH2 as an intermediate. The decomposition products may be only partially recharged after the very first step and also via hydrogenation of Mg metal. The intermediate formation of amorphous MgB12H12, was confirmed by 11B NMR. A four-stage pathway for the thermal decomposition of Mg(BH4)2 is proposed.

Aluminoborane compounds AlB_4H_(11), AlB_5H_(12), and AlB_6H_(13) were reported by Himpsl and Bond in 1981, but they have eluded the attention of the worldwide hydrogen storage research community for more than a quarter of a century. These aluminoborane compounds have very attractive properties for hydrogen storage: high hydrogen capacity (i.e., 13.5, 12.9, and 12.4 wt % H, respectively) and attractive hydrogen desorption temperature (i.e., AlB_4H_(11) decomposes at ~125 °C). We have synthesized AlB_4H_(11) and studied its thermal desorption behavior using temperature-programmed desorption with mass spectrometry, gas volumetric (Sieverts) measurement, infrared (IR) spectroscopy, and solid state nuclear magnetic resonance (NMR). Rehydrogenation of hydrogen-desorbed products was performed and encouraging evidence of at least partial reversibility for hydrogenation at relatively mild conditions is observed. Our chemical analysis indicates that the formula for the compound is closer to AlB_4H_(12) than AlB_4H_(11).

Reversible dehydrogenation and hydrogenation reactions have been reported for a number of reactions based on lithium alanate and lithium amide materials. The dehydrogenation and hydrogenation reactions involving these materials are, however, usually very complex. Significant discrepancies exist among different studies published in literature. Understanding the reaction mechanism and the dependence of the reaction pathway on material preparation processes and processing parameters is critical. In this paper, the hydrogenation reactions of the mixture of 3Li2NH/Al/4 wt%TiCl3 were investigated as a function of the heating rate. The hydrogenated products were characterized by means of TGA, XRD and solid-state NMR. These new results showed that the re-formation of Li3AlH6 depends strongly on the heating rate during the hydrogenation process. The dehydrogenation and rehydrogenation reaction pathways and possible mechanisms of the combined system are, however, still under investigation.

In an effort to develop reversible metal borohydrides with high hydrogen storage capacities and low dehydriding temperature, doping LiBH4 with various metal halides and hydrides has been conducted. Several metal halides such as TiCl3, TiF3, and ZnF2 effectively reduced the dehydriding temperature through a cation exchange interaction. Some of the halide doped LiBH4 are partially reversible. The LiBH4 + 0.1TiF3 desorbed 3.5 wt % and 8.5 wt % hydrogen at 150 and 450 °C, respectively, with subsequent reabsorption of 6 wt % hydrogen at 500 °C and 70 bar observed. XRD and NMR analysis of the rehydrided samples confirmed the reformation of LiBH4. The existence of the (B12H12)−2 species in dehydrided and rehydrided samples gives insight into the resultant partial reversibility. A number of other halides, MgF2, MgCl2, CaCl2, SrCl2, and FeCl3, did not reduce the dehydriding temperature of LiBH4 significantly. XRD and TGA-RGA analyses indicated that an increasing proportion of halides such as TiCl3, TiF3, and ZnCl2 from 0.1 to 0.5 mol makes lithium borohydrides less stable and volatile. Although the less stable borohydrides such as LiBH4 + 0.5TiCl3, LiBH4 + 0.5TiF3, and LiBH4 + 0.5ZnCl2 release hydrogen at room temperature, they are not reversible due to unrecoverable boron loss caused by diborane emission. In most cases, doping that produced less stable borohydrides also reduced the reversible hydrogen uptake. It was also observed that halide doping changed the melting points and reduced air sensitivity of lithium borohydrides.

Solid aluminum hydride, AlH 3 , has been proposed and studied for applications in hydrogen storage. In some samples, a comparatively narrow feature in the proton NMR spectrum is observed; we demonstrate here that this peak is due to molecular hydrogen (H 2 ) trapped within the solid, presumably from earlier processing procedures or partial decomposition. Static and magic-angle spinning NMR show that the responsible species is highly mobile, even at 11 K. Neutron-energy-gain spectra obtained at 3.5 K yield a feature at or near the free-rotor H 2 energy difference between the J = 1 and J = 0 states. Both NMR and neutron scattering demonstrate ortho – para conversion at low temperatures. Similar NMR signatures in other hydrogen-storage solids such as NaAlH 4 may also be due to trapped H 2 .

Small-angle neutron scattering (SANS), nuclear magnetic resonance (NMR), wide-angle and small-angle X-ray scattering (WAXS and SAXS) measurements were carried out to investigate the three morphological forms of polyaniline emeraldine base (PANI-EB): unstructured, microtubes, and nanofibers. Although the chemical backbone between these two materials is quite similar, their solid structures are quite different, showing differences in the molecular conformation and supramolecular packing. Detailed solid-state 13C and 15N NMR characterization of PANI nanofibers (compared to the unstructured, granular form) revealed a slight variation in the structural features of the polymer that led to some differences in the chemical environments of the respective nuclei. The presence of two extra-sharp peaks at 96.5 and 179.8 ppm is a distinct feature found exclusively in the nanofiber spectra. Moreover, the crosspolarization (CP) dynamics study disclosed the presence of a complete set of sharp NMR peaks that are responsible for the presence of a more ordered morphology in the nanofiber. Small-angle neutron scattering indicated very sharp interfaces in the PANI fibers, which are well organized and have extremely sharp domains within the length scales probed (not, vert, similar10–1 nm). Overall, the X-ray scattering and spectroscopy data suggest that the nanofiber form is structurally different from the unstructured, PANI-EB powder. These differences are manifested, in part, by the additional chemistry occurring during the synthesis of the nanofibers.

Physico-chemical characterization of the high-silica zeolite catalyst SSZ-74 (ref. 1) suggested that it, like the related materials TNU-9 (ref. 2) and IM-5 (ref. 3), has a multidimensional 10-ring channel system. Such pore systems are ideal for many petrochemical applications, and indeed SSZ-74 has been shown to be a good catalyst for a wide variety of reactions. The elucidation of its framework structure, however, proved to be difficult. Comparable problems were encountered with TNU-9 and IM-5, which were synthesized with related structure-directing agents. Their framework structures, which are the two most complex ones known, both have 24 Si atoms in the asymmetric unit, and were finally solved by combining high-resolution powder diffraction data with information derived from high-resolution electron microscopy images. Therefore, a similar approach, using the powder charge-flipping algorithm to combine the two types of data and molecular modelling to help to locate the structure-directing agent, was applied to SSZ-74. This procedure eventually revealed a most unusual 23-Si-atom framework structure (|(C(16)H(34)N(2))(4)Si(92)(4)O(184)(OH)(8)]) with ordered Si vacancies.

A new molecular sieve topology has been determined from a multistage Monte Carlo computer simulation procedure using the program ZEFSAII. The material, SSZ-77, consists of alternating layers present in the RUT and AST topologies, and intergrowths may be possible in the way that this material grows. The product first arose from a synthesis where it appears that the degradation of the quaternary ammonium structure directing agent (SDA) produced the viable organo-guest molecule in the structure formation. The synthesis requires the use of Ge as well as Si as lattice components. In the absence of Ge, only RUT forms. An additional study was carried out to determine the suitable size of guest molecules in a series spanning trimethylamine to tetraethylammonium in the presence of benzyltrimethylammonium. It is found from NMR investigations that none of the larger molecules are occluded within the cages of the SSZ-77 structure, and that the primary occluded species is trimethylamine or tetramethylammonium.

The hydrogen storage reaction ScH_2 + 2LiBH_4 → ScB_2 + 2LiH + 4H_2 (8.91 wt %), based on the thermodynamic destabilization of LiBH_4, is predicted to have a reaction enthalpy of ΔH_(300K) = 34.1 kJ/mol H_2. The isothermal kinetic desorption behavior in this system was measured. At temperatures up to 450 °C, less than 5 wt % H_2 is released, which is only half of the theoretical capacity. Powder X-ray diffraction data indicate that LiBH_4 has decomposed into LiH in the final desorption product, but the data provide no evidence that ScH_2 has participated in the reaction. Magic angle spinning NMR (MAS NMR) results do not show that the expected ScB_2 equilibrium product phase has formed during desorption. While the addition of 2 mol % TiCl_3 catalyst does improve desorption kinetics at 280 °C, it does not otherwise assist the destabilization reaction. The calculated reaction enthalpy suggests that this system should be of interest at moderate temperatures, but the large heats of formation of the reactant phases in this system appear to play a critical role in determining overall kinetics. Furthermore, the formation of a Li_2B_(12)H_(12) intermediate phase was determined by MAS NMR, which is an undesirable stable product if reaction reversibility is to be accomplished.

^(11)B NMR spectroscopy has been employed to identify the reaction intermediates and products formed in the amorphous phase during the thermal hydrogen desorption of metal tetrahydroborates (borohydrides) LiBH_4, Mg(BH_4)_2, LiSc(BH_4)_4, and the mixed Ca(AlH_4)_(2-)LiBH_4 system. The ^(11)B magic angle spinning (MAS) and cross polarization magic angle spinning (CPMAS) spectral features of the amorphous intermediate species closely coincide with those of a model compound, closo-borane K2B_(12)H_(12) that contains the [B_(12)H_(12)]^(2-) anion. The presence of [B_(12)H_(12)]^(2-) in the partially decomposed borohydrides was further confirmed by high-resolution solution ^(11)B and ^1H NMR spectra after dissolution of the intermediate desorption powders in water. The formation of the closo-borane structure is observed as a major intermediate species in all of the metal borohydride systems we have examined.

Complex metal hydrides are attracting much attention as a class of candidate materials for hydrogen storage. Lithium-based complex hydrides, including lithium aluminum hydrides (LiAlH_4 and Li_3AlH_6), are among the most promising materials, owing to their high hydrogen contents. In the present work, we investigated the dehydrogenation/rehydrogenation reactions of a combined system of Li_3AlH_6 and Mg(NH_2)_2, which has a theoretical hydrogen capacity of 6.5 wt %. Thermogravimetric analysis of hydrogenated 2/3Al−Li_2Mg(NH)2 (doped with 4 wt % TiCl_3) indicated that a large amount of hydrogen (∼6.2 wt %) can be stored under 300 °C and 172 bar of hydrogen pressure. The FT-IR and NMR results showed that the reaction between Li_3AlH_6 and Mg(NH_2)_2 is reversible. Further, a short-cycle experiment has demonstrated that the new combined material system of alanates and amides can maintain its hydrogen storage capacity upon cycling of the dehydrogenation/rehydrogenation reactions.

Multinuclear and multidimensional solid state NMR techniques including magic-angle-spinning (MAS) and multiple-quantum (MQ) MAS experiments have been used to characterize various AlH_3 samples. At least three distinct polymorphic AlH_3 phases have been prepared by desolvating the alane etherate product from its organometallic synthesis. MAS-NMR spectra for the ^(1)H and ^(27)Al nuclei have been obtained on a variety of AlH_3 samples that include the β- and γ-phases as well as the α-phase. ^(27)Al MAS NMR was found to respond with high sensitivity for showing differences in spatial arrangements of AlH_6 octahedra in the three polymorphs studied. Based on the characteristic NMR signatures determined, phase transition of the γ-AlH_3 to the α-AlH_3 was studied at room and high temperatures. Direct decomposition of the γ-AlH_3 to aluminum metal at room temperature was also unambiguously confirmed by NMR studies.

The crystalline structure of a 7 Li and 11 B labeled lithium borohydride has been investigated using neutron powder diffraction at 3.5, 360, and 400 K. The B–H bond lengths and H–B–H angles for the [BH4] � tetrahedra indicated that the tetrahedra maintained a nearly ideal configuration throughout the temperature range investigated. The atomic displacement parameters at 360 K suggest that the [BH4] � tetrahedra become increasingly disordered as a result of large amplitude librational and reorientational motions as the orthorhombic to hexagonal phase transition (T ¼ 384 K) is approached. In the high-temperature hexagonal phase, the [BH4] � tetrahedra displayed extreme disorder about the trigonal axis along which they are aligned. Neutron vibrational spectroscopy data were collected at 5 K over an energy range of 10–170 meV, and were found to be in good agreement with prior Raman and low-resolution neutron spectroscopy studies.

Metal dodecaborates M_2/_nB_(12)H_(12) (n denotes the valence of the metal M), containing icosahedral polyatomic anion [B_(12)H_(12)]^(2−), have been attracting increasing interest as potential energy materials, especially in the context of hydrogen storage and superionic conductivity. M_2/_nB_(12)H_(12) are commonly formed as dehydrogenation intermediates from metal borohydrides M(BH_4)_n, like LiBH_4 and Mg(BH_4)_2, which are well-known as potential high-density hydrogen storage materials. The strong B−B bond in the icosahedral [B_(12)H_(12)]^(2−), however, is regarded to be the key factor that prevents the rehydrogenation of dodecaborates. In order to elucidate the mechanism as well as to provide effective solutions to this problem, a novel solvent-free synthesis route of anhydrous M_2/nB_(12)H_(12) (here M means Li, Na, and K) has been developed. Thermal stability and transformations of the anhydrous single phase Li_2B_(12)H_(12) suggested the formation of the high temperature polymorph of Li_2B_(12)H_(12) during the dehydrogenation of LiBH_4, while concurrently emphasized the importance of further investigation on the decomposition mechanism of metal borohydrides and metal dodecaborates. The high stability of icosahedral [B_(12)H_(12)]^(2−), on the other hand, favors its potential application as solid electrolyte. Recently, Na^+ conductivity of Na_2B_(12)H_(12) was reported to be 0.1 S/cm above its order−disorder phase transition at ∼529 K, which is comparable to that of a polycrystalline β”-Al_2O_3 (0.24 S/cm at 573 K) solid state Na-electrolyte. Mechanistic understanding on the diffusion behavior of cation and further improvement of ionic conductivity at a lower temperature, however, are important in order to facilitate the practical application of metal dodecaborates as superionic conductors.

We discuss the use of nuclear magnetic resonance (NMR) spectroscopy to investigate the physical state of the eutectic composition of LiBH_(4)–Ca(BH_4)_2 (LC) infiltrated into mesoporous scaffolds and the interface effect of various scaffolds. Eutectic melting and the melt infiltration of mixed borohydrides were observed through in situ NMR. In situ and ex situ NMR results for LC mixed with mesoporous scaffolds indicate that LiBH_4 and Ca(BH_4)_2 exist as an amorphous mixture inside of the pores after infiltration. Surprisingly, the confinement of the eutectic LC mixture within the mesopores is initiated below the melting temperature, which indicates a certain interaction between the borohydrides and the mesoporous scaffolds. The confined borohydrides remain inside of the pores after cooling. These phenomena were not observed in microporous or nonporous materials, and this observation highlights the importance of the pore structure of the scaffolds. Such surface interactions may be associated with a faster dehydrogenation of the nanoconfined borohydrides.

A highly electrophilic cationic PdII complex, [Pd(MeCN)_4][BF_4]_2 (1), brings about the preferential activation of the B–H bond in ammonia-borane (NH3·BH3, AB). At room temperature, the reaction between 1 in CH_3NO_2 and AB in tetraglyme leads to Pd nanoparticles and formation of spent fuels of the general formula MeNH_xBO_y as reaction byproducts, while 2 equiv. of H_2 is efficiently released per AB equiv. at room temperature within 60 seconds. For a mechanistic understanding of dehydrogenation by 1, the chemical structures of spent fuels were intensely characterized by a series of analyses such as elemental analysis (EA), X-ray photoelectron spectroscopy (XPS), solid state magic-angle-spinning (MAS) NMR spectra (^2H, ^(13)C, ^(15)N, and ^(11)B), and cross polarization (CP) MAS methods. During AB dehydrogenation, the involvement of MeNO2 in the spent fuels showed that the mechanism of dehydrogenation catalyzed by 1 is different from that found in the previously reported results. This AB dehydrogenation derived from MeNO_2 is supported by a subsequent digestion experiment of the AB spent fuel: B(OMe)_3 and N-methylhydroxylamine ([Me(OH)N]_2CH_2), which are formed by the methanolysis of the AB spent fuel (MeNH_xBO_y), were identified by means of ^(11)B NMR and single crystal structural analysis, respectively. A similar catalytic behavior was also observed in the AB dehydrogenation catalyzed by a nickel catalyst, [Ni(MeCN)_6][BF_4]_2 (2).

The germanosilicate ITQ-24 (IWR framework type) was synthesized in fluoride medium using 1,3,5-tris(1,2-dimethylimidazolium) benzene as the structure directing agent (SDA). A structure analysis of the as-synthesized ITQ-24 material using synchrotron powder diffraction data and difference electron density calculations have allowed the fluoride ions and the germanium atoms to be located and the conformation of the SDA to be determined. The benzyl ring is perpendicular to the b axis with the three imidazolium moieties forming a “T-shaped” arrangement. Ge atoms replace some of the Si in the double-4-ring (d4r) and in one of the single-4-rings (s4r). The other s4r contains only Si. Fluoride ions are in the d4r units. Initially, the space group Cmmm (highest possible symmetry) was assumed, but the framework geometry was strained. An independent evaluation of the symmetry using the powder charge flipping algorithm in Superflip led to a successful refinement with reasonable geometry and a refined composition of |[(C_6H_3)(C_7H_(10)N_2)_3]_2F_2|[Si_(40.2)Ge_(15.8)O_(112)] in the space group Pban.

A new method for the excitation and detection of high-order 13 C multiple-quantum (MQ) nuclear magnetic resonance (NMR) signals in solids under magic-angle spinning (MAS) condition is presented. In this experimental scheme, high-order 13 C MQ coherences are generated by relaying several sequentially generated 13 C double-quantum (DQ) coherences in dipolar coupled networks. Numerical simulations and experimental implementations are presented to demonstrate the efficiency of this method under a moderate MAS frequency regime. 13 C MQ signals up to 10-quantum coherences are observed experimentally on the model compound 1- 13 C-labeled glycine, at an MAS frequency of 12 kHz.

Achieving high degrees of molecular confinement in materials is a difficult synthetic challenge that is critical for understanding supramolecular chemistry on solid surfaces and control of host-guest complexation for selective adsorption and heterogeneous catalysis. In this Article, using 2H MAS NMR spectroscopy of tethered carbamates as a molecular probe, we systematically investigate the degree of steric confinement within three types of materials: two-dimensional silica surface, bulk amorphous microporous silica, and bulk amorphous mesoporous silica. The resulting NMR spectra are described with a simple two-site hopping model for motion and prove that the bulk silica network severely limits the molecular mobility of the immobilized carbamate at room temperature to the same degree as surface-functionalized materials at low-temperatures (approximately 210 K). Raising the temperature of the bulk materials to 413 K still demonstrates the effect of confinement, as manifested in significantly longer characteristic times for the immobilized carbamate relative to surface-functionalized materials at room temperature. The environment surrounding the carbonyl functionality of the immobilized carbamate is investigated using FT-IR spectroscopy, which shows the carbonyl stretching band to be equally shifted for all materials to lower wavenumbers relative to its noninteracting value in carbon tetrachloride solvent. These results suggest that electrostatic interactions between the carbonyl of the immobilized carbamate and silica surface may play an important role in confining the immobilized carbamate and nucleating the formation of a pore wall close to the immobilized carbamate during bulk materials synthesis.

The objective of this study is to prepare sulfonic acid functionalized zeolite BEA nanocrystals, and determine the bulk proton conductivity of this new material. Phenethyl functionalized zeolite BEA nanocrystals are synthesized using a mixture of fumed silica and phenethyltrimethoxysilane as silica sources. Contact of the phenethyl zeolite BEA nanocrystals with concentrated sulfuric acid removes the organic structure-directing agent (SDA) and simultaneously sulfonates the phenethyl moieties. Detailed characterizations of the zeolite BEA nanocrystals are performed using dynamic light scattering (DLS), Fourier transform Raman spectroscopy (FT-Raman), 29Si cross-polarization magic angle spinning nuclear magnetic resonance spectroscopy (29Si CPMAS NMR), 13C CPMAS NMR, 1H MAS NMR, thermogravimetric (TGA) analyses, transmission electron microscopy (TEM) and powder X-ray diffraction (XRD). Sulfonic acid functionalized zeolite BEA nanocrystals have proton conductivities in the range of 1.2 × 10−3–1.2 × 10−2 S/cm compared to 1.5 × 10−4 S/cm for unfunctionalizated zeolite BEA.

This study surveys the use of a range of structure-directing agents (SDA) in zeolite synthesis experiments under the conditions using HF. The studies made are all for systems containing only silica as the inorganic component. Key points to emerge from the study are a reinforcement of the concept of more open-framework host structures forming when the reactions are more concentrated (lower H2O/SiO2 ratios). This discovery had been reported previously from the research group at ITQ in Valencia, Spain. Our studies show that some novel all-silica compositions have been achieved using this route for synthesis. Two new relationships we explore are whether the use of fluoride anion in synthesis has different nucleation selectivities as a function of dilution, and whether guest molecules can achieve tighter packing in the host structures using the fluoride route as contrasted with the hydroxide route. We explore this with MAS NMR studies. We find that some large organo-cations, which produce no products in alkaline media, give interesting host structure in the fluoride reactions. To cite this article: S.I. Zones et al., C. R. Chimie 8 (2005).

This work is an experimental response to an intriguing paper recently published by Catlow and co-workers, which looked at the computational feasibility of fluorine location in three different all-silica zeotypes (Attfield, M. P.; Catlow, C. R. A.; Sokol, A. A. Chem. Mater. 2001, 13, 4708). The materials were chosen as representative of three unique host locations. Our present work examined the synthesis of zeotypes AST, IFR, and MTT using organo-cations with a strong preference for crystallizing these structures. We studied the effect of reaction time and the H(2)O/SiO(2) reactant ratio. The latter is probably the most important function in these zeolite crystallizations that use HF. As reaction conditions became more dilute, AST gave way to SGT and IFR to MTW as host structures, while the MTT synthesis was invariant. Our reactions were studied in terms of product yield vs time, product organo-cation content, fluorine content, and the representative (29)Si and (19)F NMR spectra for certain samples. A single crystal study was carried out for a sample of MTT. Our results showed that, consistent with other recent studies, low H(2)O/SiO(2) reactant ratios lead to more open framework host structures (i.e., IFR vs MTW), and there is typically a higher uptake of organo-cation and fluorine. The structure may well contain a higher population of 4-rings within the silicate substructure. While MTT that contains no 4-rings was chosen as the best possible candidate to achieve an ion-pair for the organo-cation and fluoride anion within the silicate host, both NMR and single crystal work confirm that fluoride is bonded to a 5-coordinate silica center within the lattice.

A comparison of two zeolite systems was made with trivalent element substitution for the use of N-benzyl-DABCO as the structure-directing agent (SDA). Boron and aluminum were used at the same initial concentrations. One reason for the study was awareness that a higher number of new zeolite structures are being found when researching borosilicate reaction mixtures. The borosilicate system studied produces SSZ-42 (IFR) while the aluminosilicate system yields beta zeolite (BEA). We focused on comparisons of the kinetics and found that the borosilicate system crystallized more rapidly, kept most of the boron in solution before incorporation into the crystal, and added mass even at the point where all solids were crystalline. In contrast, the aluminosilicate gel remained almost entirely in the solid phase through a long induction period and the mass of solids was relatively constant. The kinetics were followed by using a variety of techniques including powder XRD, pH changes, elemental analyses, partitioning in centrifugation and effects of dilution. The reaction systems were followed via NMR techniques. The transformation to crystalline could be seen by NMR for both the aluminosilicate and borosilicate reactions. Proton NMR changes were followed for both sets of solids. In addition, a profile for removal of boron from solution and towards the growing SSZ-42 was quantified by NMR. An unusual tetrahedral doublet for 11B was found in the SSZ-42 product. No such doublet was observed for tetrahedral aluminum in the case of beta zeolite formation.

Neutral Ni(II) salicylaldimine catalysts (pendant ligand NCMe or PPh3) were used to copolymerize ethylene with monomers containing esters, alcohols, anhydrides, and amides and yielded linear functionalized polyethylene in a single step. -Olefins and polycyclic olefin comonomers carrying functionality were directly incorporated into the polyethylene backbone by the catalysts without any cocatalyst, catalyst initiator, or other disturber compounds. The degree of comonomer incorporation was related to the monomer structure: tricyclononenes norbornenes -olefins. A wide range of comonomer incorporation, up to 30 mol %, was achieved while a linear polyethylene structure was maintained under mild conditions (40 °C, 100 psi ethylene). Results from the characterization of the copolymers by solution and solid-state NMR techniques, thermal analysis, and molecular weight demonstrated that the materials contained a relatively pure microstructure for a functionalized polyethylene that was prepared in one step with no catalyst additive. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2842–2854, 2002

SSZ-43 and SSZ-48 are new high-silica molecular sieves prepared with organic structure-directing agents (SDAs) derived from the decahydroquinolinium cation. SSZ-48 has a related theoretical 14 member-ring (MR) net, and computer modeling with energy minimization has been used to predict SDAs suitable for stablilizing this theoretical 14MR structure. Three SDAs derived from decahydroquinolinium cation were indicated as plausible candidates for the synthesis of the 14MR material. These SDAs are investigated here using several reaction chemistries. The results show that in addition to SSZ-43 and SSZ-48, other materials including known, large-pore, high-silica molecular sieves such as SSZ-31, CIT-6 and zeolite beta can be synthesized with these SDAs. 29 Si NMR data show that some of the newly synthesized materials contain a significant amount of Q3 sites. The removal of the SDAs through calcination converts these Q3 sites to Q4 silicons, and generates microporosity.

Attempts to synthesize solvent-free MgB_(12)H_(12) by heating various solvated forms (H_2O, NH_3, and CH_3OH) of the salt failed because of the competition between desolvation and dehydrogenation. This competition has been studied by thermogravimetric analysis (TGA) and temperature-programmed desorption (TPD). Products were characterized by IR, solution- and solid-state NMR spectroscopy, elemental analysis, and single-crystal or powder X-ray diffraction analysis. For hydrated salts, thermal decomposition proceeded in three stages, loss of water to form first hexahydrated then trihydrated, and finally loss of water and hydrogen to form polyhydroxylated complexes. For partially ammoniated salts, two stages of thermal decomposition were observed as ammonia and hydrogen were released with weight loss first of 14 % and then 5.5 %. Thermal decomposition of methanolated salts proceeded through a single step with a total weight loss of 32 % with the release of methanol, methane, and hydrogen. All the gaseous products of thermal decomposition were characterized by using mass spectrometry. Residual solid materials were characterized by solid-state 11B magic-angle spinning (MAS) NMR spectroscopy and X-ray powder diffraction analysis by which the molecular structures of hexahydrated and trihydrated complexes were solved. Both hydrogen and dihydrogen bonds were observed in structures of [Mg(H_2O_6B_(12)H_(12)]⋅6 H_2O and [Mg(CH_3OH)_(6)B_(12)H_(12)]⋅6 CH_3OH, which were determined by single-crystal X-ray diffraction analysis. The structural factors influencing thermal decomposition behavior are identified and discussed. The dependence of dehydrogenation on the formation of dihydrogen bonds may be an important consideration in the design of solid-state hydrogen storage materials.

The active sites of enzymes are contained within nanoscale environments that exhibit exquisite levels of specificity to particular molecules. The development of such nanoscale environments on synthetic surfaces, which would be capable of discriminating between molecules that would nominally bind in a similar way to the surface, could be of use in nanosensing, selective catalysis and gas separation. However, mimicking such subtle behaviour, even crudely, with a synthetic system remains a significant challenge. Here, we show that the reactive sites on the surface of a tetrairidium cluster can be controlled by using three calixarene–phosphine ligands to create a selective nanoscale environment at the metal surface. Each ligand is 1.4 nm in length and envelopes the cluster core in a manner that discriminates between the reactivities of the basal-plane and apical iridium atoms. CO ligands are initially present on the clusters and can be selectively removed from the basal-plane sites by thermal dissociation and from the apical sites by reactive decarbonylation with the bulky reactant trimethylamine-N-oxide. Both steps lead to the creation of metal sites that can bind CO molecules, but only the reactive decarbonylation step creates vacancies that are also able to bond to ethylene, and catalyse its hydrogenation.

A novel one-pot process that can produce freestanding reduced graphene oxide (RGO) sheets in large scale through a mechanochemical method is presented, which is based on a 1:1 adduct of hydrazine and carbon dioxide (H_3N^+NHCO_2^−, solid hydrazine). We were able to synthesize RGO sheets by grinding solid hydrazine with graphene oxide (GO), followed by storing the mixed powder at 50 °C for 10 min. No solvents, nor large vessels, nor post-annealing at high temperatures are required. The resulting RGO sample was characterized by elemental analysis, X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, Brunauer–Emmett–Teller measurement, thermo gravimetric analysis, Fourier transform infrared spectroscopy, solid state nuclear magnetic resonance spectroscopy, and conductivity measurement. It exhibits excellent conductivity and possesses a high specific surface area. This reduction method was successfully applied for the fabrication of inkjet-printed RGO devices on a flexible substrate.

Layered borosilicate zeolite precursor ERB-1P (Si/B = 11) is delaminated via simultaneous deboronation and SDA removal, to yield material DZ-1 consisting of silanol nests, using a simple aqueous Zn(NO_3)_2 treatment. Characterization of this synthesis process by PXRD shows loss of long-range order, and transmission electron microscopy (TEM) demonstrates transformation of rectilinear layers in the layered zeolite precursor to single and curved layers in the delaminated material. N_2 physisorption confirms the expected decrease of micropore volume and increase in external surface area for delaminated materials relative to their calcined 3D zeolite counterpart. Elemental analysis shows loss of B and absence of Zn in the delaminated material. Resonances corresponding to silanol nests are evident via^(29)Si solid-state NMR spectroscopy in DZ-1, which should be located within 12-MR pockets near the external surface. We have successfully utilized these nests as tetrahedral recognition sites for incorporation of Ti within an isolated framework coordination environment in material Ti-DZ-1. Diffuse-reflectance ultraviolet (DR-UV) spectroscopy of Ti-DZ-1 confirms isolated framework Ti sites, which are assigned to bands in the range of 210 nm–230 nm. Infrared spectra of Ti-DZ-1 consist of a distinct absorption band at 960 cm^(−1), which is absent in DZ-1 prior to Ti incorporation and has been previously correlated with the presence of framework Ti species. Infrared spectra after pyridine adsorption demonstrate bands consistent with Lewis-acid sites in the resulting Ti-substituted delaminated zeolite. The accessibility of these Lewis-acid sites is confirmed when using Ti-DZ-1 as a catalyst for cyclohexene epoxidation using tert-butyl hydroperoxide as the organic oxidant – a reaction for which both DZ-1 and TS-1 are inactive.

A zeolite synthesis system is described in which a minor amount of structure-directing agent is used to specify the nucleation product, and then a larger amount of an amine is used to provide both pore filling and basicity capacities in the synthesis. A number of syntheses of different zeolite products are described for reactions in the SiO2/Al2O3 range of 35, which are conditions which yield high silica zeolites but are toward the more catalytically active end of the SiO2/Al2O3 spectrum. There are a number of cost-saving benefits described for this synthesis route including reduced structure-directing agent cost, waste stream cleanup costs, and time in reactor and reagent flexibility. Some details of the reaction are shown for this route to zeolite SSZ-25. The reaction was also used as a way to screen a new structure-directing agent, and zeolite SSZ-47 was discovered in this manner. The surprisingly high inorganic cation uptake in some of the zeolite products also may indicate that they play an important...

The synthesis of aluminosilicate zeolite, SSZ-25, is described using a two-component organic guest molecule strategy. This method has been recently described by us and is quite effective in crystallizing a variety of aluminosilicate zeolites with reduction in template cost. In this instance the original organic guest component used in the discovery of SSZ-25, N',N',N'-trimethyl-2-adamantammonium cation, is used in conjunction with a variety of smaller amines. The amine is the major organic component in the synthesis and the quaternary ammonium compound, while a minor component, is essential for structure direction to the desired zeolite product. Studies here show that the adamantyl component is preferentially taken up during crystal growth. Our studies showed that the use of the multi-organic component approach to synthesis resulted in a faster and cheaper route to crystallizing SSZ-25. The SSZ-25 has been described in the literature as having the MWW topology and as such has two different channel systems accessed by 10-ring openings; the channel systems do not intersect. One set of 10-rings open into large cavities. In this study we used NMR spectroscopy to examine the as-made materials and to see if the two organic components are used in different capacities in the synthesis, probing if the admantyl component is only found in these larger cavities. The crystalline products could be affected by solvent extraction with polar solvents like dimethylformamide: the X-ray powder patterns and elemental analyses changed with solvent treatment. The solvent-treated crystals were studied by NMR spectroscopy, elemental analysis, and argon adsorption. The two-component organic guest approach was also found to be quite flexible not only with regard to the amine, but also towards the quaternary ammonium compounds. Non-adamantyl polycyclic templates could be used, and polar but non-quaternized adamantyl derivatives also succeeded in directing towards SSZ-25 formation. On the other hand. in one instance it was shown that the two-component approach favors SSZ-25 as the kinetic product but at longer run times Ostwald ripening was observed, leading to the disappearance of SSZ-25 and formation of ferrierite zeolite and quartz.

A new method for synthesizing ∗BEA-type molecular sieves that involves the use of mesoporous materials as reagents is presented. Si-Beta (pure-silica, ∗BEA-type molecular sieve) is synthesized by heating TEAOH-impregnated Si-MCM-41 to 150°C for several days. The Si-Beta obtained has a small number of Q3 sites that are mostly siloxy groups that balance the charge of TEA cations. TEA cations can easily be removed by contacting the Si-Beta with acetic acid solution, and as a result, a highly hydrophobic Si-Beta is formed. Ti-Beta is synthesized from Ti-containing mesoporous silica or Ti-impregnated Si-MCM-41 without adding Al3+, alkali-metal cations and seeds. The incorporation of Ti into the ∗BEA structure is confirmed by UV–vis data. ∗BEA-type materials that contain other species such as Al, B, V, Zr and Zn can also be prepared.

In situ solid-state NMR methodologies have been employed to investigate the photocatalytic oxidation of ethanol (C2H5OH) over a TiO2-coated optical microfiber catalyst and two other TiO2-based catalysts. Adsorption of ethanol on the surface of the TiO2/optical microfiber catalyst formed a strongly hydrogen-bonded species and a Ti ethoxide species. In situ UV irradiation experiments under 13C magic angle spinning (MAS) conditions reveal the formation of two main reaction intermediates, 1,1-diethoxyethane (CH3CH(OC2H5)2) and acetic acid, under dry conditions. The catalyst was shown to be highly effective for the degradation of ethanol as complete photooxidation of ethanol was observed to form acetic acid and CO2. These results were compared to those using a monolayer catalyst supported on porous Vycor glass and powdered TiO2. Solid-state NMR investigations on TiO2 powder modeled after temperature-programmed desorption experiments confirm the identities of the hydrogen-bonded and Ti ethoxide species and show...

In situ solid-state NMR methodologies have been employed to investigate the photocatalytic oxidation of ethanol (C2H5OH) over two TiO2-based catalysts, Degussa P-25 powder and a monolayer TiO2 catalyst dispersed on porous Vycor glass. Two adsorption sites were observed for ethanol, a chemisorbed species identified as an ethoxide species, and a hydrogen-bonded species. The Ti-bound ethoxide was found to be the more photocatalytically reactive species. 13 C magic-angle spinning (MAS) experiments revealed that long-lived intermediates, including acetaldehyde (CH3CHO), acetic acid, formic acid, and acetate were observed under dry conditions and in the presence of molecular oxygen. Similar reaction intermediates form on the surfaces of both catalysts. 13 C cross-polarization MAS experiments allowed us to identify and follow the evolution of surface-bound species during UV irradiation. Acetate, which forms from mobile acetic acid, appears to be bound to the non-irradiated surfaces of the powdered TiO2 catalyst, and was also observed on the surface of TiO2/PVG catalyst, and further degradation was not possible. The presence of molecular oxygen was found to be essential for photooxidation to proceed.

The crystal structure of solvent-free Li2B12H12 has been determined by powder X-ray diffraction and confirmed by a combination of neutron vibrational spectroscopy and first-principles calculations. This compound is a possible intermediate in the dehydrogenation of LiBH4, and its structural characterization is crucial for understanding the decomposition and regeneration of LiBH4. Our results reveal that the structure of Li2B12H12 differs from other known alkali-metal (K, Rb, and Cs) derivatives.

In situ solid-state NMR methodologies have been employed to investigate the photocatalytic oxidation of trichloroethylene (TCE) over two TiO2-based catalysts, Degussa P-25 powder and a monolayer Ti...

Molecular-level interactions at organic–inorganic interfaces play crucial roles in many fields including catalysis, drug delivery, and geological mineral precipitation in the presence of organic matter. To seek insights into organic–inorganic interactions in porous framework materials, we investigated the phase evolution and energetics of confinement of a rigid organic guest, N,N,N-trimethyl-1-adamantammonium iodide (TMAAI), in inorganic porous silica frameworks (SSZ-24, MCM-41, and SBA-15) as a function of pore size (0.8 nm to 20.0 nm). We used hydrofluoric acid solution calorimetry to obtain the enthalpies of interaction between silica framework materials and TMAAI, and the values range from −56 to −177 kJ per mole of TMAAI. The phase evolution as a function of pore size was investigated by X-ray diffraction, IR, thermogravimetric differential scanning calorimetry, and solid-state NMR. The results suggest the existence of three types of inclusion depending on the pore size of the framework: single-molecule confinement in a small pore, multiple-molecule confinement/adsorption of an amorphous and possibly mobile assemblage of molecules near the pore walls, and nanocrystal confinement in the pore interior. These changes in structure probably represent equilibrium and minimize the free energy of the system for each pore size, as indicated by trends in the enthalpy of interaction and differential scanning calorimetry profiles, as well as the reversible changes in structure and mobility seen by variable temperature NMR.

Layered borosilicate zeolite precursor ERB-1P (Si/B = 11) is delaminated via isomorphous substitution of Al for B using a simple aqueous Al(NO_3)_3 treatment. Characterization by PXRD shows loss of long-range order, and TEM demonstrates transformation of rectilinear layers in the precursor to single and curved layers in the delaminated material. N_2 physisorption and base titration confirm the expected decrease of micropore volume and increase in external surface area for delaminated materials relative to their calcined 3D zeolite counterpart, whereas FTIR and multinuclear NMR spectroscopies demonstrate synthesis of Brønsted acid sites upon delamination. Comparative synthetic studies demonstrate that this new delamination method requires (i) a borosilicate layered zeolite precursor, in which boron atoms can be isomorphously substituted by aluminum, (ii) neutral amine pore fillers instead of rigid and large quaternary amine SDAs, and (iii) careful temperature control, with the preferred temperature window being around 135 °C for ERB-1P delamination. Acylation of 2-methoxynaphthalene was used as a model reaction to investigate the catalytic benefits of delamination. A partially dealuminated delaminated material displays a 2.3-fold enhancement in its initial rate of catalysis relative to the 3D calcined material, which is nearly equal to its 2.5-fold measured increase in external surface area. This simple, surfactant- and sonication-free, mild delamination method is expected to find broad implementation for the synthesis of delaminated zeolite catalysts.