Photooptical Properties of Polymethacrylates Having Cyanoazobenzene‐Containing Side Groups with Lateral Methyl Substituents and Different Spacer Length

New photochromic polymethacrylates with different spacer length having azobenzene side groups and lateral methyl substituents were synthesized. The phase behavior of polymethacrylates and their photooptical properties were studied and compared with unsubstituted analogues. It is shown that an introduction of lateral methyl substituents results in almost complete suppression of liquid crystalline (LC) phase formation and strong decrease of photoinduced dichroism values. It is found that rates of the photoinduced E‐Z isomerization and back thermal Z‐E isomerization are almost independent on spacer lengths. Due to the presence of lateral substituents, the photoinduced azobenzene Z‐form shows remarkable long lifetime, and back thermal conversion at room temperature takes more than 10 days. Specific peculiarities of the photoorientation process in polymer films under the polarized UV and visible light action were studied and their mechanism is suggested. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57, 1337–1342     

Polytriacetylenes bearing directly attached functional groups with tunable physical and electronic properties

We report the synthesis and characterization of a unique class of conjugated polymers, polytriacetyelenes (PTAs), from a set of trans‐enediyne (EDY) monomers bearing alkyl and aromatic substituents. Two different methods, i.e., Glaser‐Hay coupling and Pd‐catalyzed oxidative coupling, were employed depending on the nature of the side‐chains. Our methodology is highly versatile in that it allows direct attachment of aromatic substituents to the PTA main‐chains, allowing enhanced tunability in polymer electronic properties, which has not been achievable through previously reported methods. The newly synthesized PTAs displayed strong ability of quenching the fluorescence of poly(3‐hexylthiophene) (P3HT), a prototypical conjugated polymer in organic solar cells, indicating possible applications of these PTAs in optoelectronic devices. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 1391‐1395     

An Efficient Labelling Approach to Harness Backbone and Side‐Chain Protons in 1H‐Detected Solid‐State NMR Spectroscopy

¹H‐detection can greatly improve spectral sensitivity in biological solid‐state NMR (ssNMR), thus allowing the study of larger and more complex proteins. However, the general requirement to perdeuterate proteins critically curtails the potential of ¹H‐detection by the loss of aliphatic side‐chain protons, which are important probes for protein structure and function. Introduced herein is a labelling scheme for ¹H‐detected ssNMR, and it gives high quality spectra for both side‐chain and backbone protons, and allows quantitative assignments and aids in probing interresidual contacts. Excellent ¹H resolution in membrane proteins is obtained, the topology and dynamics of an ion channel were studied. This labelling scheme will open new avenues for the study of challenging proteins by ssNMR.     

增益导引-折射率反导引大模场光纤激光器抽运技术研究进展

介绍了一种新型增益导引-折射率反导引大模场光纤的结构、基本理论以及其在光纤激光器领域的重要应用. 在综合分析了不同抽运条件下的激光输出特性以及光纤的热效应特征后, 得出侧面抽运是增益导引-折射率反导引大模场光纤的最佳抽运方案的结论; 重点介绍了增益导引-折射率反导引大模场光纤侧面抽运的理论模拟以及基于V形槽技术的侧面抽运实验研究过程, 为相关领域的实验研究提供了参考; 最后分析了实验结果与理论差距较大的原因, 并提出了改进的方向.     

Side Information Generation Scheme Based on Coefficient Matrix Improvement Model in Transform Domain Distributed Video Coding

In order to effectively improve the quality of side information in distributed video coding, we propose a side information generation scheme based on a coefficient matrix improvement model. The discrete cosine transform coefficient bands of the Wyner–Ziv frame at the encoder side are divided into entropy coding coefficient bands and distributed video coding coefficient bands, and then the coefficients of entropy coding coefficient bands are sampled, which are divided into sampled coefficients and unsampled coefficients. For sampled coefficients, an adaptive arithmetic encoder is used for lossless compression. For unsampled coefficients and the coefficients of distributed video coding coefficient bands, the low density parity check accumulate encoder is used to calculate the parity bits, which are stored in the buffer and transmitted in small amount upon decoder request. At the decoder side, the optical flow method is used to generate the initial side information, and the initial side information is improved according to the sampled coefficients by using the coefficient matrix improvement model. The experimental results demonstrate that the proposed side information generation scheme based on the coefficient matrix improvement model can effectively improve the quality of side information, and the quality of the generated side information is improved by about 0.2–0.4 dB, thereby improving the overall performance of the distributed video coding system.     

Criss‐cross amphiphilic polymers and analogous model systems

A new class of amphiphilic polymers carrying two pendant docosyl (C22) chains, located at periodic intervals that are separated by PEG chains of varying lengths, was synthesized via a simple melt‐transesterification polymerization, using dimethyl, 2,5‐didocosyloxyterephthalate as one of the monomers. DSC, variable temperature FT‐IR, and WAXS studies demonstrated that immiscibility between the pendant docosyl units and the backbone PEG segments drives their self‐segregation; this results in the crystallization of the pendant docosyl segments and the generation of a lamellar morphology with the alkyl segments and the PEG chains occupying alternate layers. Based on the study of model criss‐cross amphiphiles that resemble the polymer repeat unit, it is postulated that the chains reconfigure such that both the docosyl chains fold to one side of the terephthalate unit while the PEG segments form a loop on the other side; these chains then organize in a bilayer to form the lamellar structure. The simplicity of the synthesis and the rather unique properties of these polymers suggests that such a design could be translated to develop other interesting functional materials that could exploit the immiscibility‐driven microphase separation for the generation of sub‐10 nm domains; these could have potential applications, such as in membranes, solid polymer electrolyte formulations, and so forth. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 1554–1563     

Synthesis and photovoltaic properties of conjugated side chains polymers with different electron‐withdrawing and donating end groups

A series of novel low band gap polymers containing conjugated side chains with 4,7‐dithien‐5‐yl‐2,1,3‐benzodiathiazole and different electron‐withdrawing end groups of aldehyde ( PT‐DTBTCHO ), 2‐ethylhexyl cyanoacetate ( PT‐DTBTCN ), 1,3‐diethyl‐2‐thiobarbituric acid ( PT‐DTBTDT ), and electron‐donating end group of 2‐methylthiophene ( PT‐DTBTMT ) have been designed and synthesized. All polymers exhibit good solubility in common organic solvents, film‐forming ability, and thermal stability. These conjugated polymers show the broad ultraviolet‐visible absorption and the narrow optical band gaps in the range of 1.65–1.90 eV. Through changing the end group of conjugated side chains, the photophysical properties and energy levels of the polymers were tuned effectively. Bulk heterojunction solar cells based on the blend of these polymers and (6,6)‐phenyl‐C₆₁‐butyric acid methyl ester (PC₆₁BM) reached the best power conversion efficiency (PCE) of 2.72%. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

与 Cauchy 微分中值定理相关的几个问题

根据Cauchy微分中值定理表达式的结构引入辅助函数 F（x ，c）＝ f （x）- f （c）g（x）- g（c）（a＜ c＜ b），通过讨论其可导性，得到相关的几个不等式，由此得出Cauchy微分中值定理存在唯一“中值点”的一个条件，并给出其逆定理的一个较弱表述。     

Synthesis of poly(isopropenylphenoxy propylene carbonate) and its facile side‐chain functionalization into hydroxy‐polyurethanes

4‐Isopropenyl phenol ( 4‐IPP ) is a versatile dual functional intermediate that can be prepared readily from bisphenol‐A ( BPA ). Through etherification with epichlorohydrin to the phenolic group of 4‐IPP , it can be converted into 4‐isopropenyl phenyl glycidyl ether ( IPGE ). On further reaction with carbon dioxide in the presence of tetra‐n‐butyl ammonium bromide ( TBAB ) as the catalyst, IPGE was transformed into 4‐isopropenylphenoxy propylene carbonate ( IPPC ) in 90% yield. Cationic polymerization of IPPC with strong acid such as trifluoromethanesulfonic acid or boron trifluoride diethyl etherate as the catalyst at ?40 °C gave a linear poly(isopropenylphenoxy propylene carbonate), poly( IPPC ), with multicyclic carbonate groups substituted uniformly at the side‐chains of the polymer. The cyclic carbonate groups of poly( IPPC ) were further reacted with different aliphatic amines and diamines resulting in formation of polymers with hydroxy‐polyurethane on side‐chains. Syntheses, characterizations of poly( IPPC ) and its conversion into hydroxy‐polyurethane crosslinked polymers were presented. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 802–808