Flexibility in metal-organic framework materials: Impact on sorption properties

Recent years have seen the development of a new class of porous coordination polymers known collectively as metal organic framework materials (MOFs). This review outlines recent progress in understanding how adsorption characteristics of these systems differ from rigid classical sorbents such as activated carbon and zeolites. Gas/vapor adsorption studies for characterization of the porous structures of MOF materials are reviewed and differences in adsorption characteristics based on detailed measurement of equilibrium and dynamical sorption behavior, compared with previous generations of sorbents, are highlighted. The role of framework flexibility and specific structural features, such as windows and pore cavities, within the MOF porous structures are discussed in relation to adsorption mechanisms.     

Total synthesis of (-)-hennoxazole A

An enantioselective, convergent total synthesis of the antiviral marine natural product (-)-hennoxazole A is completed in 14 steps (longest linear sequence) from commercially available 4-methyloxazole-2-carboxylic acid. Synthesis of the C(1)-C(15) pyran/bisoxazole fragment takes advantage of an aldol-like coupling between a dimethyl acetal and an N-acetylthiazolidinethione for the direct, stereoselective installation of the C(8)-methoxy-bearing stereocenter. A one-pot acetoacetate acylation/decarboxylation/cyclodehydration of another elaborate thiazolidinethione allows for rapid assembly of the pyran-based ring system. Synthesis of the C(15)-C(25) skipped triene side chain fragment makes use of a [2,3]-Wittig-Still rearrangement for efficient installation of the trisubstituted Z-double bond. Key late-stage coupling of the two fragments is effected by deprotonation of the methyl group on the bisoxazole system using lithium diethylamide, followed by alkylation with an allylic bromide side chain segment to form the C(15)-C(16) bond.     

Surface interactions and quantum kinetic molecular sieving for H2 and D2 adsorption on a mixed metal-organic framework material

A rational strategy has been used to immobilize open metal sites in ultramicroporosity for stronger binding of multiple H 2 molecules per unsaturated metal site for H 2 storage applications. The synthesis and structure of a mixed zinc/copper metal-organic framework material Zn 3(BDC) 3[Cu(Pyen)] .(DMF) 5(H 2O) 5 (H 2BDC = 1,4 benzenedicarboxylic acid and PyenH 2 = 5-methyl-4-oxo-1,4-dihydro-pyridine-3-carbaldehyde) is reported. Desolvation provides a bimodal porous structure Zn 3(BDC) 3[Cu(Pyen)] (M'MOF 1) with narrow porosity (<0.56 nm) and an array of pores in the bc crystallographic plane where the adsorbate-adsorbent interactions are maximized by both the presence of open copper centers and overlap of the potential energy fields from pore walls. The H 2 and D 2 adsorption isotherms for M'MOF 1 at 77.3 and 87.3 K were reversible with virtually no hysteresis. Methods for determination of the isosteric enthalpies of H 2 and D 2 adsorption were compared. A virial model gave the best agreement (average deviation <1 standard deviation) with the isotherm data. This was used in conjunction with the van't Hoff isochore giving isosteric enthalpies at zero surface coverage of 12.29 +/- 0.53 and 12.44 +/- 0.50 kJ mol (-1) for H 2 and D 2 adsorption, respectively. This is the highest value so far observed for hydrogen adsorption on a porous material. The enthalpy of adsorption, decreases with increasing amount adsorbed to 9.5 kJ mol (-1) at approximately 1.9 mmol g (-1) (2 H 2 or D 2 molecules per Cu corresponding to adsorption on both sides of planar Cu open centers) and is virtually unchanged in the range 1.9-3.6 mmol g (-1). Virial analysis of isotherms at 87.3 K is also consistent with two H 2 or D 2 molecules being bound to each open Cu center. The adsorption kinetics follow a double exponential model, corresponding to diffusion along two types of pores, a slow component with high activation energy (13.35 +/- 0.59 kJ mol (-1)) for the narrow pores and a faster component with low activation energy (8.56 +/- 0.41 kJ mol (-1)). The D 2 adsorption kinetic constants for both components were significantly faster than the corresponding H 2 kinetics for specific pressure increments and had slightly lower activation energies than the corresponding values for H 2 adsorption. The kD 2/ kH 2 ratio for the slow component was 1.62 +/- 0.07, while the fast component was 1.38 +/- 0.04 at 77.3 K, and the corresponding ratios were smaller at 87.3 K. These observations of kinetic isotope quantum molecular sieving in porous materials are due to the larger zero-point energy for the lighter H 2, resulting in slower adsorption kinetics compared with the heavier D 2. The results show that a combination of open metal centers and confinement in ultramicroporosity leads to a high enthalpy for H 2 adsorption over a wide range of surface coverage and quantum effects influence diffusion of H 2 and D 2 in pores in M'MOF 1.     

Parametric study of factors affecting melamine-resorcinol-formaldehyde xerogels properties

Resorcinol-formaldehyde (RF) xerogels are organic materials have been widely studied due to their industrially relevant characteristics, through which, RF gels have significant potential to be tailored to specific applications. Xerogel properties have been tailored, within this study, by altering the synthesis procedure with a focus on monomer concentrations, catalyst to monomer ratio, and the introduction of a nitrogen-rich precursor, thereby incorporating nitrogen into the structure to additionally affect the chemical properties of the final gel. Melamine (M) is used as the source of nitrogen, partially replacing the resorcinol (R) typically used, and resulting in a melamine-resorcinol-formaldehyde (MRF) gel; synthesis was facilitated by a sodium carbonate catalyst (C), as often used in RF gel production. R/C and R/F molar ratios, and M concentration ([M]), were chosen as parameters to study in-depth, as they have previously been shown to markedly influence sol-gel formation. The MRF gels produced were subsequently characterized to determine porous structure and chemical functionality. The results indicate that, texturally, increasing [M] produces a similar effect as increasing R/C values: increasing pore size, while decreasing surface area. Pore volume tends to increase when R/C or M increase individually but pore volume and surface area decrease drastically when both variables increase concurrently. Microporosity also tends to increase as R/C decreases, and as the concentration of M is decreased. Altering the gel matrix, by replacing M for R, results in a weakening of the gel structure, as the bridges formed during curing are reduced in quantity, which indicates a maximum level of substitution that can occur within these materials. Combined, these results suggest that nitrogen can be successfully incorporated into organic gel structures but that the interplay between process variables is crucial in determining final gel characteristics for specific applications.     

Nonparametric estimation of the spectral measure,and associated dependence measures,for multivariate extreme values using a limiting conditional representation

The traditional approach to multivariate extreme values has been through the multivariate extreme value distribution G, characterised by its spectral measure H and associated Pickands’ dependence function A. More generally, for all asymptotically dependent variables, H determines the probability of all multivariate extreme events. When the variables are asymptotically dependent and under the assumption of unit Fréchet margins, several methods exist for the estimation of G, H and A which use variables with radial component exceeding some high threshold. For each of these characteristics, we propose new asymptotically consistent nonparametric estimators which arise from Heffernan and Tawn’s approach to multivariate extremes that conditions on variables with marginal values exceeding some high marginal threshold. The proposed estimators improve on existing estimators in three ways. First, under asymptotic dependence, they give self-consistent estimators of G, H and A; existing estimators are not self-consistent. Second, these existing estimators focus on the bivariate case, whereas our estimators extend easily to describe dependence in the multivariate case. Finally, for asymptotically independent cases, our estimators can model the level of asymptotic independence; whereas existing estimators for the spectral measure treat the variables as either being independent, or asymptotically dependent. For asymptotically dependent bivariate random variables, the new estimators are found to compare favourably with existing estimators, particularly for weak dependence. The method is illustrated with an application to finance data.     

High resolution proton magnetic resonance of selenophene

The high resolution proton magnetic resonance of selenophene has been studied at 100 Mc/s. The spectrum was analysed as an A₂X₂ system and the following coupling constants were obtained: J ₂₃ = 5·35, J ₂₄ = 1·05, J ₃₄ = 3·56, J ₂₅ = 2·47 c.p.s. Coupling was also observed between ⁷⁷Se and the α and β protons and coupling constants of 48 c.p.s. (α) and 9·5 c.p.s. (β) were obtained. The τ values were 2·30 (α) and 2·88 (β). The results are compared with values available for furan, pyrrole and thiophene and the conclusion is drawn that selenophene is probably a planar molecule.