Phenanthroline-Mediated Photoelectrical Enhancement in Calix[4]arene-Functionalized Titanium-Oxo Clusters.

Incorporating two organic ligands with different functionalities into a titanium-oxo cluster entity simultaneously can endow the material with their respective properties and provide synergistic performance enhancement, which is of great significance for enriching the structure and properties of titanium-oxo clusters (TOCs). However, the synthesis of such TOCs is highly challenging. In this work, we successfully synthesized a TBC4A-functionalized TOC, [Ti2(TBC4A)2(MeO)2] (Ti2; MeOH = methanol, TBC4A = tert-butylcalix[4]arene). By adjusting the solvent system, we successfully introduced 1,10-phenanthroline (Phen) and prepared TBC4A and Phen co-protected [Ti2(TBC4A)2(Phen)2] (Ti2-Phen). Moreover, when Phen was replaced with bulky 4,7-diphenyl-1,10-phenanthroline (Bphen), [Ti2(TBC4A)2(Bphen)2] (Ti2-Bphen), which is isostructural with Ti2-Phen, was obtained, demonstrating the generality of the synthetic method. Remarkably, Ti2-Phen demonstrates good stability and stronger light absorption, as well as superior photoelectric performance compared to Ti2. Density functional theory (DFT) calculations reveal that there exists ligand-to-core charge transfer (LCCT) in Ti2, while an unusual ligand-to-ligand charge transfer (LLCT) is present in Ti2-Phen, accompanied by partial LCCT. Therefore, the superior light absorption and photoelectric properties of Ti2-Phen are attributed to the existence of the unusual LLCT phenomenon. This study not only deeply explores the influence of Phen on the performance of the material but also provides a reference for the preparation of materials with excellent photoelectric performance.

Covalent Bonding Enhanced Polypropylene Based T-ZIF-8 Masterbatch with Superior Photocatalytic and Antibacterial Performances.

In order to solve the problem of poor compatibility between modified-ZIF-8 nanoparticles and mask matrix polypropylene (PP) and melt-blown materials, in this work, PP based modified-ZIF-8 antibacterial masterbatch was prepared employing surface modification and torque blending method. IR, SEM, XRD, XPS, DSC results confirm that the antibacterial masterbatch maintains the chemical and crystal structure of modified-ZIF-8 and the thermal stability of PP. Photocatalytic performance indicates that the antibacterial masterbatch basically maintains the photoresponse range of modified-ZIF-8, has narrower band gap and the superior photocatalytic performance than that of modified-ZIF-8. The photocatalytic antibacterial mechanism of ·O2- and h+ as antibacterial active species is revealed according to the energy band structure and free radical capture experiment. The photocatalytic antibacterial activity of the antibacterial masterbatch against Staphylococcus aureus and Escherichia coli under different dosage holds that the relationship between antibacterial rate and antibacterial agent concentration conforms to Beta distribution, demonstrating second-order kinetic behavior. The antibacterial properties reach the maximum when the loading of modified-ZIF-8 is 2% of the total weight of PP and melt-blown materials. S. aureus and E. coli could be completely killed when the simulated sunlight is irradiated for 30 min. These results indicate that PP based modified-ZIF-8 antibacterial masterbatch has potential application in photocatalytic antibacterial masks.

Mechanistic insight into homogeneous catalytic crosslinking behavior between cellulose and epoxide by explicit solvent models.

Inspired by recent advances on functional modification of cellulosic materials, the crosslinking behaviors of epoxide with cellulose under the catalysis of different homogeneous catalysts including H2O, Brønsted acid, Brønsted base, Lewis acid and neutral salt were systematically investigated using density functional theory (DFT) methods with hybrid micro-solvation-continuum approach. The results showed that catalytic activity, reaction mechanism and regioselectivity are determined by the combined effect of catalyst type, electronic effect and steric hindrance. All the homogeneous catalysts have catalytic activity for the crosslinking reaction, which decreases in the order of NaOH > HCl > NCl3 > MCl2 > CH3COOH > NaCl (N = Fe3+, Al3+; M = Zn2+, Ca2+). Upon the catalysis of NaOH, hydroxyl group of cellulose is firstly deprotonated to form a carbanion-like intermediate which will further attack the less sterically hindered C atom of epoxide showing excellent regioselectivity. Acidic catalysts readily cause epoxide protonated, which suffers from nucleophilic attack of cellulose and forms the carbocation-like intermediate. Brønsted acid exhibits poor regioselectivity, however, Lewis acid shows an interesting balance between catalytic activity and regioselectivity for the crosslinking reaction, which may be attributed to the unique catalysis and stabilization effects of its coordinated H2O on the transition state structure.

Synthesis, characterization and excellent antibacterial property of cellulose acetate reverse osmosis membrane via a two-step reaction.

In order to improve the antibacterial efficiency and spectrum of cellulose acetate reverse osmosis membrane (CA-RO), both quaternary ammonium and bromoacetyl groups were introduced into cellulose diacetate under mild conditions forming CA-RO with bi-antibacterial groups for seawater desalination. Bromoacetyl bromide and a series of tertiary amine were chosen as the modification agents respectively. The characterization results showed that both two antibacterial groups were successfully introduced with a certain density. The obtaining membrane had a less hydrophilic but more electronegative surface as well as improved mechanical property. The flux values increased firstly and decreased subsequently after twice modifications while the salt rejection rose. The membrane modified with N,N-dimethyloctylamine (DMOA) had the optimal comprehensive performance of flux and salt rejection. The antibacterial testing results indicated that the resulting RO membranes showed high antibacterial efficiency and broad-spectrum. Their bactericidal rates against gram-negative Escherichia coli (E. coli) and gram-positive Staphylococcus aureus (S. aureus) were more than 99.9%.

Non-leaching antibacterial cellulose triacetate reverse osmosis membrane via covalent immobilization of quaternary ammonium cations.

A novel procedure to fabricate quaternized cellulose triacetate reverse osmosis (QCTA-RO) membranes via the etherification procedure between partially hydrolyzed CTA-RO membrane and 3-chloro-2-hydroxypropyl-trimethyl ammonium chloride (CHPTAC) in alkaline solutions (pH=9-11) for different reaction time (1, 2, 3 and 4h) was proposed. The structure and performances of the obtained QCTA-RO membranes were characterized and their antibacterial performances against E. coli and S. aureus were evaluated through colony counting method. The results showed that quaternary amine group was successfully grafted on the surface of membrane via covalently bond without significant damage to morphology, mechanical performance and thermal stability. The permeation flux values increased with prolonging modification time to 3h, while the salt rejection decreased slightly but remained above 92%. QCTA-RO membranes displayed good antibacterial activity against Gram-negative E. coli and Gram-positive S. aureus and their bactericidal rates were 78.7-89.0% and 64.7-76.6% respectively at the optimized modification time of 2-3h.