Anhydride Moiety Research Articles

Polyanhydrides: Synthesis, Properties, and Applications

This review focusses on polyanhydrides, a fascinating class of degradable polymers that have been used in and investigated for many bio-related applications because of their degradability and capacity to undergo surface erosion. This latter phenomenon is driven by hydrolysis of the anhydride moieties at the surface and high hydrophobicity of the polymer such that degradation and mass loss (erosion) occur before water can penetrate deep within the bulk of the polymer. As such, when surface-eroding polymers are used as therapeutic delivery vehicles, the rate of delivery is often controlled by the rate of polymer erosion, providing predictable and controlled release rates that are often zero-order. These desirable attributes are heavily influenced by polymer composition and morphology, and therefore also monomer structure and polymerization method. This review examines approaches for polyanhydride synthesis, discusses their general thermomechanical properties, surveys their hydrolysis and degradation processes along with their biocompatibility, and looks at recent developments and uses of polyanhydrides in drug delivery, stimuli-responsive materials, and novel nanotechnologies.

Hydrothermal Synthesis and Processing of Barium Titanate Nanoparticles Embedded in Polymer Films.

Barium titanate nanoparticles embedded in flexible polymer films were synthesized using hydrothermal processing methods. The resulting films were characterized with respect to material composition, size distribution of nanoparticles, and spatial location of particles within the polymer film. Synthesis conditions were varied based on the mechanical properties of the polymer films, ratio of polymer to barium titanate precursors, and length of aging time between initial formulations of the solution to final processing of nanoparticles. Block copolymers of poly(styrene-co-maleic anhydride) (SMAh) were used to spatially separate titanium precursors based on specific chemical interactions with the maleic anhydride moiety. However, the glassy nature of this copolymer restricted mobility of the titanium precursors during hydrothermal processing. The addition of rubbery butadiene moieties, through mixing of the SMAh with poly(styrene-butadiene-styrene) (SBS) copolymer, increased the nanoparticle dispersion as a result of greater diffusivity of the titanium precursor via higher mobility of the polymer matrix. Additionally, an aminosilane was used as a means to retard cross-linking in polymer-metalorganic solutions, as the titanium precursor molecules were shown to react and form networks prior to hydrothermal processing. By adding small amounts of competing aminosilane, excessive cross-linking was prevented without significantly impacting the quality and composition of the final barium titanate nanoparticles. X-ray diffraction and X-ray photoelectron spectroscopy were used to verify nanoparticle compositions. Particle sizes within the polymer films were measured to be 108 ± 5 nm, 100 ± 6 nm, and 60 ± 5 nm under different synthetic conditions using electron microscopy. Flexibility of the films was assessed through measurement of the glass transition temperature using dynamic mechanical analysis. Dielectric permittivity was measured using an impedance analyzer.

Inhibition of carbonic anhydrase isoforms I, II, IV, VII and XII with carboxylates and sulfonamides incorporating phthalimide/phthalic anhydride scaffolds

We report a panel of carboxylates and sulfonamides incorporating phthalic anhydride and phthalimide moieties in their structure and their interaction with the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1). They were synthesized from substituted anthranilic acids and trimellitic anhydride chloride, followed by reaction with primary amines and were tested for the inhibition of five physiologically relevant CA isoforms, the human (h) hCA I, II, IV, VII and XII, some of which are involved in serious pathologies (CA II, IV and XII in glaucoma; CA VII in epilepsy; CA XII in some solid tumors). The carboxylic acids were generally poor inhibitors of isoforms hCA I, II and IV but were highly effective, low nanomolar inhibitors of hCA VII and XII. The sulfonamides inhibited all isoforms significantly, and some of them were sub-nanomolar hCA VII inhibitors, although their isoform selectivity was lower compared to the carboxylates. This study proves that carboxylic acids incorporating a phthalic anhydride/phthalimide based scaffold may lead to isoform-selective inhibitors by applying the tail approach, mostly used up until now for obtaining sulfonamide, sulfamide and sulfamate CA inhibitors.

Grafting of adipic anhydride to carbon nanotubes through a Diels-Alder cycloaddition/oxidation cascade reaction

Different reactions have been reported for the successful functionalization of carbon nanotubes (CNT). The Diels-Alder cycloaddition is recognized as a plausible chemical approach, but few reports are known where this strategy has been used. In this study, the functionalization was performed by 1,3-butadiene generated from 3-sulfolene under heating conditions in diglyme. This simple and easily scalable method resulted in functionalized CNT with mass losses of 10–23% by thermogravimetric analysis (nitrogen atmosphere). The functionalization was also supported by acid-base titration, elemental analysis, temperature programmed desorption and X-ray photoelectron spectroscopy. The high content in oxygen detected on the CNT surface was assigned to anhydride formation due to a cascade oxidation of the alkene groups generated in the cycloaddition reaction. The complete evolution of the alkene leads to a grafting density of 4.2 mmol g−1 for the anhydride moiety. Ab-initio calculations in CNT model systems indicate that the Diels-Alder addition of butadiene is a feasible process and that subsequent oxidation reactions may result in the formation of the anhydride moiety. The presence of the anhydride group is a valuable asset for grafting a multitude of complex molecules, namely through the nucleophilic addition of amines.

Rapid determination of anhydride content in trans-polyisoprene-graft-maleic anhydride by double-shot pyrolysis gas chromatography–mass spectrometry

A rapid method for determination of anhydride content in synthetic trans-polyisoprene-graft-maleic anhydride (sTPIgMA) by double-shot pyrolysis gas chromatography mass spectrometry (DS-PyGC/MS) has been developed. The sample preparation step was minimized and samples were easy to handle. Dissolution of the polymer in toxic solvents could be avoided, and solid specimens containing unreacted MA monomer could be analyzed without purification. Unreacted MA monomer, residual solvent, and other volatile substances were eliminated from sTPIgMA during the thermal desorption step. In the subsequent pyrolysis step, grafted anhydride moieties were thermally decomposed to carbon dioxide and quantified. The content of grafted anhydride, measured by the DS-PyGC/MS method, was compared with the values obtained from conventional titration and FTIR methods. The determination of grafted anhydride content in sTPIgMA by DS-PyGC/MS was shown to be fast, simple, accurate, and repeatable.

Succinate Functionalization of Hyperbranched Polyglycerol-Coated Magnetic Nanoparticles as a Draw Solute During Forward Osmosis.

Hyperbranched polyglycerol-coated magnetic nanoparticles (SHPG-MNPs) were functionalized with succinate groups to form a draw solute for use in a forward osmosis (FO). After the one-step synthesis of hyperbranched polyglycerol-coated magnetic nanoparticles (HPG-MNPs), the polyglycerol groups on the surfaces of the HPG-MNPs were functionalized with succinic anhydride moieties. The resulting SHPG-MNPs showed no change of size and magnetic property compared with HPG-MNPs and displayed excellent dispersibility in water up to the concentration of 400 g/L. SHPG-MNPs solution showed higher osmotic pressure than that of HPG-MNPs solution due to the presence of surface carboxyl groups in SHPG-MNPs and could draw water from a feed solution across an FO membrane without any reverse draw solute leakage during FO process. Moreover, the water flux remained nearly constant over several SHPG-MNP darw solute regeneration cycles applied to the ultrafiltration (UF) process. The SHPG-MNPs demonstrate strong potential for use as a draw solute in FO processes.

Chemical Modification of Polyisobutylene Succinimide Dispersants and Characterization of Their Associative Properties.

The secondary amines found in b-PIBSI dispersants prepared by attaching two polyisobutylene chains to a polyamine core via two succinimide moieties were reacted with ethylene carbonate (EC). The reaction generated urethane bonds on the polyamine core to yield the modified b-PIBSI dispersants (Mb-PIBSI). Five dispersants were prepared by reacting 2 molar equivalent (meq) of polyisobutylene terminated at one end with a succinic anhydride moiety (PIBSA) with 1 meq of hexamethylenediamine (HMDA), diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), and pentaethylenehexamine (PEHA) to yield the corresponding b-PIBSI dispersants. Characterization of the level of secondary amine modification for the Mb-PIBSI dispersants with traditional techniques such as FTIR and (1)H NMR spectroscopies was greatly complicated by interactions between the carbonyls of the succinimide groups and unreacted secondary amines of the Mb-PIBSI dispersants. Therefore, an alternative procedure was developed based on fluorescence quenching of the succinimides by secondary amines and urethane groups. The procedure took advantage of the fact that the succinimide fluorescence of the Mb-PIBSI dispersants was quenched much more efficiently by secondary amines than by the urethane groups that resulted from the EC modification of the amines. While EC modification did not proceed for b-PIBSI-DETA and b-PIBSI-TETA certainly due to steric hindrance, 60 and 70% of the secondary amines found in the longer polyamine core of b-PIBSI-TEPA and b-PIBSI-PEHA had reacted with EC as determined by the fluorescence quenching analysis. Furthermore, the ability of the Mb-PIBSI dispersants to adsorb at the surface of carbon black particles used as mimic of the carbonaceous particles typically found in engine oils was compared to that of their unmodified analogues.

In situ preparation of a magnetic composite during functionalization of poly[maleic anhydride-co-3,9-divinyl-2,4,8,10-tetraoxaspiro(5.5)undecane] with erythritol

New magnetic hybrid composites were prepared, in situ, during the functionalization of poly[maleic anhydride-co-3,9-divinyl-2,4,8,10-tetraoxaspiro(5.5)undecane] copolymer, by opening the anhydride ring with erythritol and by introducing magnetic nanoparticles into the polymeric matrix. The procedure allows for magnetic nanocomposite preparation. More than that, the new polymeric matrices owing to their suitable and specific functionalities are anticipated to be used for further link of biological molecules via the maleic anhydride moiety and the polyol presence. The hybrid composites are analyzed by infrared absorption spectrometry, dynamic light scattering (DLS), TG-DTG analysis, X-ray diffraction, SEM, TEM, and vibrating sample magnetometry. Examination of the magnetic composites by DLS analysis shows that the material consists mostly of particles with mean sizes between 295 and 342 nm, depending on the magnetite type in synthesis. The obtained results indicate the magnetite encapsulation and the interactions established with the polymeric matrix that lead to carbonyl band shifting in FTIR spectra, composite particle size decreasing, and influence on XRD and magnetic behavior data. The report of magnetization demonstrates that the prepared nanocomposites are superparamagnetic.

Gas Permeation Properties of Soluble Aromatic Polyimides Based on 4-Fluoro-4,4'-Diaminotriphenylmethane.

A series of new organic polyimides were synthesized from 4-fluoro-4'4"-diaminotriphenylmethane and four different aromatic dianhydrides through a one-step, high-temperature, direct polycondensation in m-cresol at 180–200 °C, resulting in the formation of high-molecular-weight polyimides (inherent viscosities ~ 1.0–1.3 dL/g). All the resulting polyimides exhibited good thermal stability with initial decomposition temperatures above 434 °C, glass-transition temperatures between 285 and 316 °C, and good solubility in polar aprotic solvents. Wide-angle X-ray scattering data indicated that the polyimides were amorphous. Dense membranes were prepared by solution casting and solvent evaporation to evaluate their gas transport properties (permeability, diffusivity, and solubility coefficients) toward pure hydrogen, helium, oxygen, nitrogen, methane, and carbon dioxide gases. In general, the gas permeability was increased as both the fractional free volume and d-spacing were also increased. A good combination of permeability and selectivity was promoted efficiently by the bulky hexafluoroisopropylidene and 4-fluoro-phenyl groups introduced into the polyimides. The results indicate that the gas transport properties of these films depend on both the structure of the anhydride moiety, which controls the intrinsic intramolecular rigidity, and the 4-fluoro-phenyl pendant group, which disrupts the intermolecular packing.

Structures and properties of polyimide fibers containing ether units

Copolyimide (co-PI) fibers containing 4,4′-oxydiphthalic anhydride (ODPA) moiety into the 3,3′,4,4′-biphenyltetracarboxylic dianhydride (BPDA)/p-phenylenediamine backbone were prepared via a two-step wet-spinning method. The processability and mechanical properties were improved significantly after the incorporation of ODPA, and the fibers exhibited an optimum tensile strength of 10.94 cN dtex−1 and modulus of 470.52 cN dtex−1 with elongation of 2.75 % at a BPDA/ODPA molar ratio of 7/3. Two-dimensional wide angle X-ray diffraction indicated that highly oriented structures and ordered molecular packing regions were formed in the fibers. Two-dimensional small angle X-ray scattering revealed that the incorporation of ODPA resulted in the reduction in radius, length, misorientation, and internal surface roughness of the microvoids in the fibers simultaneously, which was supposed to be mainly dominated for the drastically improved mechanical properties of PI fibers. Moreover, the co-PI fibers exhibited excellent thermal and thermal-oxidative stability, and the 5 % weight loss temperature was above 572 and 535 °C under nitrogen and air, respectively.

Upon synthesis of a polymeric matrix with pH and temperature responsiveness and antioxidant bioactivity based on poly(maleic anhydride-co-3,9-divinyl-2,4,8,10-tetraoxaspiro [5.5] undecane) derivatives

Poly(maleic anhydride-co-3,9-divinyl-2,4,8,10-tetraoxaspiro [5.5] undecane), acquired through radical polymerization, was synthesized with the aim to prepare an alternant copolymer with precise placement of functional groups along the polymer backbones. The new structure owing to the suitable and specific functionalities is anticipated to be used as reactive polymer to link bioactive compounds via maleic anhydride moiety. The copolymer was improved in its functionality by maleic anhydride ring opening with different amounts of erythritol in order to confer antioxidant characteristics to the polymeric structure. The chemical structure of the new prepared polymers was confirmed by FTIR and (1)H NMR spectra, and the polymers were also characterized from the viewpoint of their thermal stability. The dual sensitivity of the polymeric structure, at temperature and pH, was evaluated by determining the hydrodynamic radius and zeta potential in interdependence with the environment conditions. The polymer morphology was investigated by SEM. The antioxidant character was evaluated measuring the scavenger properties of the functionalized copolymer with erythritol against the 2,2-diphenyl-1-picrylhydrazyl radicals. The acute toxicity investigation, realized in vivo for the copolymer and the derivatives, allows the inclusion of the compounds into the group of moderately toxic accordingly to Hodge and Sterner toxicity scale owing to the lethal dose 50 determined values.

Synthesis of imidized nanoparticles containing soy oil under various reaction conditions

The imidization of poly(styrene-co-maleic anhydride) nanoparticles in presence of soy oil was studied, resulting in the formation of nanoparticles with 20–80nm diameter with a porous structure allowing to incorporate 50wt.% soy oil. The reaction efficiency strongly depends on the amount of ammonium hydroxide as imidizing agent, which ratio was varied between 1.01 and 1.60 relatively to the maleic anhydride moieties. Finally, stable aqueous dispersions are obtained with a higher solid content and somewhat higher Zetapotential compared to purely imidized nanoparticles. There are concurring reactions between imidization and coupling of the unsaturated double bonds in soy oil to the ammonolysed maleic anhydride. Therefore, a large amount of non-embedded oil was only observed when the imidization is favoured under high concentrations of ammonium hydroxide. Using spectroscopy and thermal analysis, it is concluded that a complex organized nanostructure is formed between the poly(styrene-co-maleimide) and soy oil, which results in a suppression of Tg evaluated by (temperature-modulated) differential scanning calorimetry.

Novel nonadride, heptadride and maleic acid metabolites from the byssochlamic acid producer Byssochlamys fulva IMI 40021 - an insight into the biosynthesis of maleidrides.

The filamentous fungus Byssochlamys fulva strain IMI 40021 produces (+)-byssochlamic acid 1, its novel dihydroanalogue 2 and four related secondary metabolites. Agnestadrides A, 17 and B, 18 constitute a novel class of seven-membered ring, maleic anhydride-containing (hence termed heptadride) natural products. The putative maleic anhydride precursor 5 for both nonadride and heptadride biosynthesis was isolated as a fermentation product for the first time and its structure confirmed by synthesis. Acid 5 undergoes facile decarboxylation to anhydride 6. The generic term maleidrides is proposed to encompass biosynthetically-related compounds containing maleic anhydride moieties fused to an alicyclic ring, varying in size and substituents.

Critical Analysis of Harmful Gases from Flue Gas

The invention provides a wet, regenerable scrubbing process using ammonium hydroxide (NH 4 OH) solution to remove acid anhydride moiety gases, and trace amounts of hydrogen chloride gas (HCl) and hydrogen fluoride (HF) gas in a gas-liquid contacting reactor. In particular, the invention uses “aqua ammonia” or an aqueous ammonia scrubbing liquor such as [NH 3 (aq)/ammonium hydroxide (NH 4 OH)] to extract certain effluent compounds via acid-base or neutralization reactions. Generally, an effluent gas is subjected to chemical scrubbing with aqueous ammonia or some other ammoniacontaining compound in a gas-liquid contactor reactor or a scrubber to remove gaseous acid anhydride moieties. The chemical scrubbing produces ammonium salts of the conjugate bases of the acid anhydride moieties. Thermal regeneration of the ammonia scrubbing liquor occurs in an adjacent vessel or remotely.

Radical Alternating Copolymerization of Twisted 1,3-Butadienes with Maleic Anhydride as a New Approach for Degradable Thermosetting Resin

We report a novel approach for the synthesis of a readily curable and degradable resin by the radical alternating copolymerization of 1,3-diene monomers with maleic anhydride. 2,4-Dimethyl-1,3-pentadiene predominantly produced an alternating copolymer rather than a Diels–Alder adduct during the reaction with maleic anhydride. We revealed the most stable conformation as a twisted diene structure of 2,4-dimethyl-1,3-pentadiene and the other methyl-substituted dienes by DFT calculations, while a completely planar structure was preferred for the s-cis and s-trans conformers of the nonsubstituted butadiene. The highly alternating repeating structure of the produced copolymers was revealed based on the NMR analysis and copolymerization reactivity ratios. The alternating copolymers including an anhydride moiety and a carbon-to-carbon double bond in each repeating unit was conveniently used for the thermosetting, subsequent degradation, and polymer–surface modification by postpolymerization reactions such as epox...

Enzymatic kinetic resolution of sec-alcohols using an ionic liquid anhydride as acylating agent

A task-specific ionic liquid bearing an anhydride moiety was synthesized for the first time in good yield (83%) through a carbodiimide-mediated coupling reaction. The enantiomeric separation of a series of sec-alcohols was performed via enzymatic kinetic resolution, employing an ionic anhydride as acylating agent and Candidaantarctica Lipase B as a biocatalyst. A fast and efficient recovery of both enantiomers was achieved separately due to the ionic nature of the acyl donor, combined with the possibility of carrying out the enzymatic step in an organic solvent.

The Biosynthesis and Catabolism of the Maleic Anhydride Moiety of Stipitatonic Acid

AbstractA series of directed knockout experiments, combined with an in vitro assay of pathway components, has elucidated for the first time the chemical steps involved in the biosynthesis of the tropolone class of fungal maleic anhydrides. The pathway involves the stepwise oxidation of aldehyde and methyl carbon atoms to form a 1,2‐dicarboxylate. A hydrolase‐catalyzed interconversion of this and the corresponding maleic anhydride, followed by decarboxylation of the diacid leads to the pathway’s final product of stipitatic acid.

The biosynthesis and catabolism of the maleic anhydride moiety of stipitatonic acid.

A series of directed knockout experiments, combined with an in vitro assay of pathway components, has elucidated for the first time the chemical steps involved in the biosynthesis of the tropolone class of fungal maleic anhydrides. The pathway involves the stepwise oxidation of aldehyde and methyl carbon atoms to form a 1,2-dicarboxylate. A hydrolase-catalyzed interconversion of this and the corresponding maleic anhydride, followed by decarboxylation of the diacid leads to the pathway's final product of stipitatic acid.

Synthesis and properties of hybrid alkyd–acrylic dispersions and their use in VOC-free waterborne coatings

Hybrid waterborne alkyd–acrylic dispersions with solid content of 40%, free from any surfactant and exempt of any organic solvent, were successfully synthesized by a melt co-condensation reaction between an acrylic prepolymer bearing carboxylic groups and a long-oil alkyd resin. Spontaneous emulsification of the ensuing hybrid resin was achieved by the addition of an aqueous ammonia solution that neutralized the carboxylic functions. The key role of the carboxylic groups on the stabilization process and on the storage stability of the dispersion was assessed and it was shown that the insertion of anhydride moieties within the acrylic prepolymer ensured the efficient coupling between the acrylic and the alkyd resin and prevented the phase separation. These dispersions are easy to implement and might be used to prepare high quality zero VOC coatings in terms of drying time, stability and gloss. The most stable dispersion was also used in the formulation of air-drying waterborne lacquers and their coating properties were evaluated.

Improving the properties of polylactic acid by blending with low molecular weight polylactic acid‐g‐natural rubber

The low molecular weight (Mw) polylactic acid‐g‐natural rubber (PLA‐g‐NR) was synthesized by grafting the maleated natural rubber (MNR) with low molecular weight PLA at a weight ratio of 1:1 in toluene at 80°C. Two types of MNR (MNR10 and MNR20) having anhydride moieties of 10 and 20 wt%, respectively, were prepared. The reaction was followed by IR analysis. Next, the obtained PLA‐g‐NR was blended with pristine PLA using a twin‐screw extruder at PLA to PLA‐g‐NR weight ratios of 90:10, 80:20, 70:30, and 60:40 followed by compression to obtain specimens for testing. In case of 10 wt% PLA‐g‐NR having MNR10, it was found that blending of PLA with PLA‐g‐NR resulted in a 200% improvement in impact strength and twofold percent elongation at break (flexibility). Further SEM analysis confirmed that PLA‐g‐NR was compatible with PLA matrix. In contrast, NR was present as disperse particles which exhibited poor adhesion to PLA. From these findings, it was also found that PLA‐g‐NR was capable of improving the properties of PLA more than NR due to the fact that it exhibited higher compatibility. POLYM. ENG. SCI., 54:2770–2776, 2014. © 2013 Society of Plastics Engineers