含氨基,羟基吸附剂对胆红素的吸附

本文分别合成了含氨基和羟基的高分子吸附剂，并对它们对胆红素的吸附性能进行了研究。实验表明，经3小时的吸附后，含氨基和含羟基的吸附剂对胆红素的吸附率可达80％以上，对其吸附胆红素的性能和机理进行了探讨。     

Chiral susceptibility and chiral phase transition in Nambu–Jona-Lasinio model

We give a general relation between the chiral susceptibility and the thermodynamical potential and a relation between the chiral susceptibility and the condition for furcations to appear in the Wigner solution(s) in the Nambu–Jona-Lasinio (NJL) model. We find that the chiral susceptibility is a quantity able to represent the appearance of furcation in the solution(s) of the gap equation and the concavo–convexity of the thermodynamical potential in the NJL model. It indicates that the chiral susceptibility can identify the stability of the states and the chiral phase transition in NJL model. We propose that analyzing the chiral susceptibility may play an important role in studying the chiral phase transition in approaches superior to the NJL model.     

A bio‐safe cyclophosphazene derivative flame retardant for polylactic acid composites: Flammability and cytotoxicity

An efficient bio‐safe cyclophosphazene flame retardant, 1,5,9,13,16,20‐Hexaoxa‐7,14,21‐triaza‐6λ⁴,8λ⁴,5λ⁴‐triphosphatrispiro[5.1.5.1.5.1]heneicosa‐6,8(14),15(21)‐triene (HCPO), was synthesized, and then was incorporated into polylactic acid (PLA) to improve the fire safety. The chemical structure of HCPO was confirmed by Fourier‐transformed infrared spectroscopy, mass spectrometry, and nuclear magnetic resonance spectroscopy. The thermal stability of the compound was characterized by thermogravimetric (TG) analyzer. The cytotoxic effects of HCPO to cells were evaluated. Fire behavior and thermal stability of PLA composites were investigated by vertical burning, limiting oxygen index (LOI), TG analysis, and cone calorimeter. The morphology of residual charring was observed by scanning electron microscope. The results showed HCPO was bio‐safe, and highly effective to enhance the flame retardancy of PLA composites. The LOI value was increased from 18.4 to 27.5 and UL‐94 grade achieved V‐0 for the PLA composite containing only 2% HCPO and 2% pentaerythrotol. It was demonstrated that intermolecular cross‐linking reaction between pentaerythrotol and HCPO in high temperature range could accelerate the formation of compact char layers.     

Investigation on the growth of CaCu3Ti4O12 thin film and the origins of its dielectric relaxations

Using the radio frequency magnetron sputtering, CaCu₃Ti₄O₁₂ (CCTO) thin films were deposited on platinized silicon substrates. The influence of annealing temperature on structures and morphologies of the thin films was investigated. The high annealing temperature increased the crystallinity of the films. Temperature dependence of the dielectric constant revealed an amazing different characteristic of the dielectric relaxation at ∼10 MHz, whose characteristic frequency abnormally increased with the decrease of the measuring temperature unlike the relaxations due to extrinsic origins. Meanwhile, the dielectric constant at high frequencies was close to the value derived from the first principle calculation. All these gave the evidences to ascribe this relaxation to the intrinsic mechanism.     

A new synthetic approach to phosphatidylethanolamine

A new synthetic method for phosphatidylethanolamine head group was developed via ring-opening of cyclic dioxaphospholane 2 with sodium azide and subsequent hydrogenation.The advantage of this strategy included short reaction steps,readily available materials and good yields.     

Theory of absorption and emission of radiation in molecular collisions: Semiclassical model

A semiclassical transition amplitude is derived for electronically inelastic molecular collisions in the presence of an intense electromagnetic field. The calculation of this amplitude involves the integration of classical trajectories for nuclei moving on effective potential energy surfaces. These surfaces, which exhibit an avoided crossing due to the coupling through the dipole interaction around the resonance nuclear configuration, are analytically continued to their complex intersection points, where trajectories switch surfaces. Other parts of these surfaces are similar to the field-free adiabatic surfaces, where one is shifted by ?ω. Metastable states, formed at some collision energies, are suggested in the field which are absent in the field-free system.     

An intramolecular benzyl rearrangement of 1-(N-benzyloxycarbonylamino)alkylphosphonate diesters under electrospray ionization conditions

The mass spectrometric behavior of eleven 1-(N-benzyloxycarbonyl(Cbz)amino)alkylphosphonate diesters was studied under positive ion electrospray ionization (ESI) conditions. Their fragmentation pathways are depicted and supported by tandem mass spectrometry. Besides the common eliminations of ether, benzyl alcohol, phosphite and an ether plus benzyl alcohol from molecular ions, the title compounds show a tendency to undergo an interesting intramolecular benzyl rearrangement to yield benzylphosphonate ions. The fragmentation patterns do not depend on the substituent attached to the alpha-carbon atom.     

A new approach to highly electrooptically active materials using cross-linkable, hyperbranched chromophore-containing oligomers as a macromolecular dopant

A new, practical approach to a variety of highly electrooptically active polymers for device development is described. It involves the use of a new thermally cross-linkable, hyperbranched oligomer containing nonlinear optical (NLO) chromophores as a macromolecular dopant in a common host polymer. A series of NLO polymeric blends were readily formulated and showed large and stable electrooptic (EO) coefficients (up to 65 pm/V). In comparison with previously studied linear NLO polyimides and guest-host polymers doped with molecular chromophores and even linear NLO analogous oligomers, this new approach offers clear advantages for device development in terms of improved poling efficiency, larger EO coefficients, good temporal stability, and versatile material formulation.     

Helical supramolecular nanorods via sequential meticulous tailoring of noncovalent interaction and light irradiation

Polymers are widely recognized to entail random conformations in good solvent governed by the need for achieving the highest entropy to reach thermodynamic equilibrium. In this context, it remains grand challenging to directly arrange them into ordered conformation as building blocks for further self-assembling into hierarchal structures. Herein, we report a simple yet viable strategy to progressively assemble rationally designed azobenzene-containing alternating copolymer(i.e., poly(binaphthyls...     

Ultrafast and selective labeling of endogenous proteins using affinity-based benzotriazole chemistry

Chemical modification of proteins is enormously useful for characterizing protein function in complex biological systems and for drug development. Selective labeling of native or endogenous proteins is challenging owing to the existence of distinct functional groups in proteins and in living systems. Chemistry for rapid and selective labeling of proteins remains in high demand. Here we have developed novel affinity labeling probes using benzotriazole (BTA) chemistry. We showed that affinity-based BTA probes selectively and covalently label a lysine residue in the vicinity of the ligand binding site of a target protein with a reaction half-time of 28 s. The reaction rate constant is comparable to the fastest biorthogonal chemistry. This approach was used to selectively label different cytosolic and membrane proteins in vitro and in live cells. BTA chemistry could be widely useful for labeling of native/endogenous proteins, target identification and development of covalent inhibitors.

Affinity-based benzotriazole (BTA) probes selectively and covalently label native proteins or endogenous proteins in cells with a fast reaction rate. It is enormously useful for characterizing protein function in biological systems and for drug development.