Enzyme-catalyzed transesterification of galactomannan extracted from mesquite seed () with vinyl carboxylate esters.

Galactomannans (GM) are hemicellulosic polysaccharides composed of D-mannopyranose chains linked by β (1 → 4) glycosidic linkages with branches of D-galactopyranose linked by α (1 → 6) linkages. This polysaccharide is recognized for its hydrophilic character, as it is rich in hydroxyl groups (-OH). This chemical characteristic, combined with the absence of ionic charges, enables structural modifications such as transesterification of the fatty acid chains (FA), which provides a strategy for obtaining amphiphilic structures.

Difluoroboron Complexes Based on Benzimidazole-Phenolates as Blue Emitters.

Novel four-coordinated boron complexes (-) were synthesized via a reaction between BF·CHOH and benzimidazole-phenolate ligands (-), which are N,O-donors. These complexes exhibit intense blue emission in the solution and solid states accompanied by notable fluorescence quantum yields (Φ). The study of the structure-property relation, through theoretical and experimental approaches, revealed a distinctive trend where compounds incorporating electron-donating substituents (methyl and ethoxy groups) in the phenolate moiety manifest shifts in emission wavelengths across the blue spectrum, concomitant with an increase in Φ.

Beryllium compounds for the carbon-halogen bond activation of phenyl halides: the role of non-innocent ligands.

Beryllium is a metallomimetic main-group element, , it behaves similarly to transition metals (TMs) in some bond activation processes. To investigate the ability of Be compounds to activate C-X bonds (X = F-I), we have computationally investigated, using DFT methods, the reaction of (CAAC)2Be (CAAC = 1-(2,6-diisopropylphenyl)-3,3,5,5-tetramethylpyrrolidin-2-ylidene) and a series of five-membered heterocyclic beryllium bidentate ligands with phenyl halides. We have analysed all plausible reaction mechanisms and our results show that, after the initial C-X oxidative addition, migration of the phenyl group occurs towards the less electronegative heteroatom.

Functionality and characterization of modified starch films with pineapple leaf fibers.

The objective of this work was to modify banana starch with pineapple leaf fibers (PALF) and its production of biodegradable films. The reaction conditions of the starch modification were a Starch/PALF mass ratio of 50, a time of 1 h and a temperature of 140 °C, to obtain a yield of 41.18 %.

Gel dressing based on type I collagen modified with oligourethane and silica for skin wound healing.

Cutaneous wound healing is a complex process that leads the skin reparation with the formation of scar tissue that typically lacks skin appendages. This fact drives us to find new strategies to improve regenerative healing of the skin. This study outlines, the contribution of colloidal silica particles and oligourethane crosslinking on the collagen material properties and the effect on skin wound healing in rats.

Oxidative Coordination versus C -C(O)Me Bond Cleavage in Acetylacetonate Iridium Complexes.

Iridabicycles [Ir{κ -N,C,O-(pyC(H)=C(C(O)Me) }(Cl)(L-L)](L-L=cod (cod=1,5-cyclooctadiene), 1 a; bipy (bipy=2,2'-bipyridine), 1 b) have been obtained by oxidative coordination of 3-(pyridine-2-yl-methylene)pentane-2,4-dione L1, to the complexes [{Ir(μ-Cl)(cod)} ] and [{Ir(μ-Cl)(coe) } ] (coe=cis-cyclooctene), the latter in the presence of bipy. Remarkably, cleavage of the C -C(O)Me bond of L1 has instead been achieved in the reaction with [Ir(Cl)(dmb) ] (dmb=2,3-dimethylbutadiene), yielding a compound formulated as [Ir{κ -N,C-(pyC(H)C(C(O)Me))}(CO)(μ-Cl)(Me)] , 2. Treatment of dimer 2 with DMSO or PMe produced the complexes[Ir{κ -N,C-(pyC(H)C(C(O)Me)}(CO)Cl(Me)L] (L=DMSO, 3 a; PMe , 3 b).

Thermal, morphological and structural characterization of a copolymer of starch and polyethylene.

The objective of this paper was to perform a copolymerization between polyethylene and starch in order to obtain new environmentally friendly materials. The copolymer obtained was characterized thermally, morphologically and structurally, including its pasting profile. The starch-g-PE copolymer showed lower thermal stability compared to the control materials.

Phytochemical profiles and classification of Agave syrups using H-NMR and chemometrics.

Background: Agave syrups are natural sweeteners that are highly desirable for human consumption because they have low glycemic index. In this work, we explored the potential of H-NMR-Chemometrics as a useful tool in the identification and differentiation of Agave syrups. Also, we evaluated the phytochemical screening and antioxidant capacity of Agave syrup compared to other natural sweeteners.

Design of Silica-Oligourethane-Collagen Membranes for Inflammatory Response Modulation: Characterization and Polarization of a Macrophage Cell Line.

The polarization of macrophages M0 to M1 or M2 using molecules embedded in matrices and hydrogels is an active field of study. The design of biomaterials capable of promoting polarization has become a paramount need nowadays, since in the healing process macrophages M1 and M2 modulate the inflammatory response. In this work, several immunocytochemistry and ELISA tests strongly suggest the achievement of polarization using collagen-based membranes crosslinked with tri-functionalized oligourethanes and coated with silica.

Crystal structure and Hirshfeld surface analysis of 3-cyano-phenyl-boronic acid.

In the title compound, CHBNO, the mean plane of the -B(OH) group is twisted by 21.28 (6)° relative to the cyano-phenyl ring mean plane. In the crystal, mol-ecules are linked by O-H⋯O and O-H⋯N hydrogen bonds, forming chains propagating along the [101] direction.

In vitro evaluation of apoptotic effect of bis(acetylacetonato-k O,O')(1,10-phenanthroline-k N,N')Zn(II) complex.

Phenanthroline derivatives have been reported as potential bioactive compounds because of their ability to interact with DNA. To evaluate the antiproliferative effect of bis(acetylacetonate-k O,O)(1,10-phenanthroline-k N,N)Zn(II) or Zn(acac) (phen) complex, the compound was obtained in a simple manner and further characterized to determine crystal structure, thermal behavior, morphology, and spectroscopic properties. The structure of the complex was confirmed by X-ray single structure as well as by 1H and 13C nuclear magnetic resonance (NMR) in dmso-d6 (dimethyl sulfoxide) solution and in the solid state by 13C CP/MAS.

Improved properties of composite collagen hydrogels: protected oligourethanes and silica particles as modulators.

This paper reports the structure-property relationship of novel biomedical hydrogels derived from collagen, water-soluble oligourethanes, and silica. The molecular weight (MW) of oligourethanes, synthesized from polyoxyethylene diol and hexamethylene, l-lysine, isophorone or trimethylhexamethylene diisocyanates (P(HDI), P(LDI), P(IPDI) and P(TMDI), respectively), is determined by the chemical structure of the starting aliphatic diisocyanate. Thus, the collagen polymerization process and both the characteristics and mechanics of the formed three-dimensional (3D) network had a direct relation with the oligourethane MW.

Quantum chemical characterization of zwitterionic structures: Supramolecular complexes for modifying the wettability of oil-water-limestone system.

In this work, we present a quantum chemical study pertaining to some supramolecular complexes acting as wettability modifiers of oil-water-limestone system. The complexes studied are derived from zwitterionic liquids of the types N'-alkyl-bis, N-alquenil, N-cycloalkyl, N-amyl-bis-beta amino acid or salts acting as sparkling agents. We studied two molecules of zwitterionic liquids (ZL10 and ZL13), HOMO and LUMO levels, and the energy gap between them, were calculated, as well as the electron affinity (EA) and ionization potential (IP), chemical potential, chemical hardness, chemical electrophilicity index and selectivity descriptors such Fukui indices.