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Photoconductivity of novel poly(N-vinyl)-3-[p-nitrophenylazo]carbazole/CdS-nanoparticle polymer composite
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作者 丁莉芸 姜德生 +4 位作者 黄俊 戴磊 刘诚 王军涛 李斌 《中国有色金属学会会刊:英文版》 CSCD 2006年第B01期191-194,共4页
The photoconductive characteristic of the inorganic/organic hybridized polymer system is reported, in which a novel bi-functional photorefractive (PR) poly(N-vinyl)-3-[p-nitrophenylazo]carbazole (PVNPAK) serves as a p... The photoconductive characteristic of the inorganic/organic hybridized polymer system is reported, in which a novel bi-functional photorefractive (PR) poly(N-vinyl)-3-[p-nitrophenylazo]carbazole (PVNPAK) serves as a polymeric charge-transporting and second-order nonliner optical matrix and quantum dots composed of surface passivated cadmium sulfide serve as a charge-generation sensitizer. The hybrid PVNPAK/CdS-nanoparticles polymer composites with different mass ratio of CdS to PVNPAK were prepared. The generation of photocurrent on illumination and photoconductive properties of the PVNPAK/CdS-nanoparticles polymer composites were studied. The results show that the addition of CdS nanoparticle as a photosensitizer can enhance the photoconductivity of the PVNPAK significantly because of the properties of the high quantum efficiency of photosensitization and high charge transport to conducting polymer. 展开更多
关键词 光电导性 聚乙烯基对硝基苯偶氮咔唑 CDS纳米粒子 无机/有机杂化聚合物体系 复合材料
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Preparation and Characterization of Fullerene C_(60) and Phthalocyanine Co-grafted Poly(epoxy propyl carbazole)
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作者 Jian Ming XU Wei Xiang CHEN Zhu De XU 《Chinese Chemical Letters》 SCIE CAS CSCD 2001年第8期679-682,共4页
The fullerene C-60 and phthatocyanine co-grafted poly (epoxy propyl carbazole) (C-60-CuPC-PEPC) was synthesized by Friedel-Crafts reaction. It was found that C-60-CuPc-PEPC had good UV-Vis absorption property, whose a... The fullerene C-60 and phthatocyanine co-grafted poly (epoxy propyl carbazole) (C-60-CuPC-PEPC) was synthesized by Friedel-Crafts reaction. It was found that C-60-CuPc-PEPC had good UV-Vis absorption property, whose active spectral range was expanded from UV to visible spectrum region, and exhibited better photoconductivity than CuPc-PEPC and PEPC. These improvements could be attributed to the interaction between C-60, phthalocyanine and PEPC. 展开更多
关键词 FULLERENE PHTHALOCYANINE poly (epoxy propyl carbazole) UV-VIS photocondivity
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DFT Study on the Thermodynamic Properties of Poly-bromine Carbazole
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作者 徐松 刘辉 +2 位作者 柳红霞 杨郭英 王遵尧 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2010年第4期535-542,共8页
The molecular structures of 135 poly-bromine carbazole (PBCZs) compounds were fully optimized at the B3LYP/6-31G* level, and their thermodynamic properties at 98.15 K, 1.013 ×105 Pa were consequently obtained.... The molecular structures of 135 poly-bromine carbazole (PBCZs) compounds were fully optimized at the B3LYP/6-31G* level, and their thermodynamic properties at 98.15 K, 1.013 ×105 Pa were consequently obtained. Based on our isodesmic reaction, standard formation heat (ΔfHθ) and standard formation free energy (ΔfGθ) of PBCZs were calculated. Furthermore, the relationship between thermodynamic parameters and the position and number (NPBS) of Brsubstitution were also discussed. To our interest, a good dependence can be observed among entro- py (Sθ), ΔfHθ, ΔfGθ and NPBS. Ultimately, the theoretical stability order of isomers can be decided judging from the ΔfGθ value. 展开更多
关键词 poly-bromine carbazole (PBCZs) position of Br-substitution method (NPBS) thermodynamic properties relative stability
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Optical Properties of Fullerenated Poly(epoxy propyl carbazole)
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作者 Tao GU Wan Xi CHEN Zhu De XU (Department of Chemistry, Zhejiang University, Hangzhou 310027) 《Chinese Chemical Letters》 SCIE CAS CSCD 1998年第9期835-837,共3页
The optical properties of the fullerenated poly(epoxy propyl carbazole) (PEPC) have been investigated. Compared with pure PEPC, fullerenated PEPC has the same structure in the UV region of the absorption spectrum, and... The optical properties of the fullerenated poly(epoxy propyl carbazole) (PEPC) have been investigated. Compared with pure PEPC, fullerenated PEPC has the same structure in the UV region of the absorption spectrum, and extends the active range to a longer wavelength. The apparent quenching of PEPC fluorescence was observed in the fullerenated polymer and it can be attributed to intramolecular excited state energy transfer. 展开更多
关键词 fullerene (fullerenated) PEPC (poly(epoxy propyl carbazole)) optical properties
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Efficient and stable organic solar cells enabled by a poly(carbazole phosphonic acid)hole transporter
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作者 Zhijun Ren Siwei Luo +12 位作者 Xiaoyu Shi Yunjie Dou Tianxiao Liu Lingyuan Wang Kwok Kiu Tsang Feifei Wang Yu Zhao Yangyang Liu Xiaodong Hu Xiaoxiao Peng Wei Liu He Yan Shangshang Chen 《Science China Chemistry》 SCIE EI CAS CSCD 2024年第6期1941-1945,共5页
Conventional self-assembled monolayer(SAM)hole transporters in organic solar cells(OSCs)generally suffer from poor uniformity and limited thickness tolerance,hindering their large-scale production.To overcome these li... Conventional self-assembled monolayer(SAM)hole transporters in organic solar cells(OSCs)generally suffer from poor uniformity and limited thickness tolerance,hindering their large-scale production.To overcome these limitations,we introduce a novel polymeric hole transporter synthesized by polymerizing carbazole phosphonic acid(PACz).The resultant Poly-2PACz material exhibits exceptional conductivity,high tolerance for variations in layer thickness,and improved film uniformity compared with conventional SAMs.Consequently,the OSCs utilizing Poly-2PACz achieve a remarkable power conversion efficiency of 19.1%and a high fill factor of 81.2%,surpassing the devices based on 2PACz.Moreover,Poly-2PACz-based OSCs demonstrate excellent operational stability,retaining over 80%of their initial efficiency after 1,400 h of continuous light exposure in ambient conditions.This work presents a novel strategy for designing hole transporters,paving the way for more efficient and stable OSCs. 展开更多
关键词 organic solar cells hole transporters poly(carbazole phosphonic acid) STABILITY
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Synthesis and evaluation of poly(N-vinyl caprolactam)-co-tert-butyl acrylate as kinetic hydrate inhibitor
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作者 Xing Huang Ran Zhu +10 位作者 Liwei Cheng Yijian Zhu Peng Xiao Xiaohui Wang Bei Liu Changyu Sun Weixin Pang Qingping Li Guangjin Chen Xinjing Xu Jinfeng Ji 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2022年第10期317-325,共9页
Low dosage kinetic hydrate inhibitors(KHIs)are a kind of alternative chemical additives to high dosage thermodynamic inhibitors for preventing gas hydrate formation in oil&gas production wells and transportation p... Low dosage kinetic hydrate inhibitors(KHIs)are a kind of alternative chemical additives to high dosage thermodynamic inhibitors for preventing gas hydrate formation in oil&gas production wells and transportation pipelines.In this paper,a new KHI,poly(N-vinyl caprolactam)-co-tert-butyl acrylate(PVCapco-TBA),was successfully synthesized with N-vinyl caprolactam(NVCap)and tert-butyl acrylate.The kinetic inhibition performances of PVCap-co-TBA on the formations of both structureⅠmethane hydrate and structureⅡnatural gas hydrate were investigated by measuring the onset times of hydrate formation under different conditions and compared with commercial KHIs such as PVP,PVCap and inhibex 501.The results indicated that PVCap-co-TBA outperformed these widely applied inhibitors for both structureⅠand structureⅡhydrates.At the same dosage of KHI,the maximum tolerable degree of subcooling under which the onset time of hydrate formation exceeded 24 hours for structureⅠhydrate was much lower than that for structureⅡhydrate.The inhibition strength increased with the increasing dosage of PVCap-co-TBA;The maximum tolerable degree of subcooling for the natural gas hydrate is more than10 K when the dosage was higher than 0.5%(mass)while it achieved 12 K when that dosage rose to0.75%(mass).Additionally,we found polypropylene glycol could be used as synergist at the dosage of 1.0%(mass)or so,under which the kinetic inhibition performance of PVCap-co-TBA could be improved significantly.All evaluation results demonstrated that PVCap-co-TBA was a very promising KHI and a competitive alternative to the existing commercial KHIs. 展开更多
关键词 Hydrate Kinetics Inhibitor poly(n-vinyl aprolactam)–co-tert-butyl acrylate SYNERGIST SYNTHESIS
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Synthesis, Characterization and in vitro Degradation Properties of Poly(Propylene Fumarate-co-Propylene Sebacate) Networks 被引量:1
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作者 张娜 杨德安 +1 位作者 蔡仲雨 常俊标 《Transactions of Tianjin University》 EI CAS 2007年第4期254-262,共9页
Poly(propylene fumarate-co-propylene sebacate) (P(PF-co-PS)) was crosslinked with Nvinyl pyrrolidone (N-VP) to form networks. It was investigated as biodegradable bone cement. In this paper, P(PF-co-PS) was ... Poly(propylene fumarate-co-propylene sebacate) (P(PF-co-PS)) was crosslinked with Nvinyl pyrrolidone (N-VP) to form networks. It was investigated as biodegradable bone cement. In this paper, P(PF-co-PS) was synthesized and characterized by ^1H-NMR, FTIR and GPC. The effects of the amount of sebacate segments in P(PF-co-PS) main chains and the quantity of N-vinyl pyrrolidone on the in vitro degradation of the polymer networks were examined. Cylindrical specimens were submerged in phosphate buffered saline (PBS) at 37 ℃ and the pH value of PBS is 7.4 for 10 weeks. The gravimetry and compressive mechanical properties were tested over the degradation period. Networks formed by P(PF-oo-PS)8020/N-VP exhibited higher weight loss and better mechanical properties when compared with poly(propylene fumarate)/N-VP networks. The mechanical properties of P(PF-co-PS)/N-VP can be maintained for a very long time, even for 70 days, the yield strength, fracture strength and compressive modulus are (51.78 ± 2.01) MPa, (52.331 ± 1.84) MPa and (957.78 ± 24.40) MPa, respectively. The results demonstrate that the compressive mechanical properties and degradation velocity can be modulated by the amount of crosslinking agents and sebacate segments along the main chains of copolymers. 展开更多
关键词 biodegradation in vitro degradation polyester poly(propylene fumarate-co-propylene sebacate) n-vinyl pyrrolidone
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Photorefractive Effect in an Azobenzene Chromophore Side Groups Polymer
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作者 方华 LI Mingtian 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2014年第6期1290-1293,共4页
We have analyzed the photorefractive(PR) effect of a polymer composite was reported which combines a novel bi-functional poly(N-vinyl)-3-[p-nitrophenylazo]carbazolyl(PVNPAK) and 2,4,7-trinitro-9-fluorenone(TNF... We have analyzed the photorefractive(PR) effect of a polymer composite was reported which combines a novel bi-functional poly(N-vinyl)-3-[p-nitrophenylazo]carbazolyl(PVNPAK) and 2,4,7-trinitro-9-fluorenone(TNF). PVNPAK was synthesized by a post-azo-coupling reaction, with an azo derivative as the electrooptic chromophore and carbazolyl as photoconductive moiety. The asymmetric two-beam coupling gain of 13.9 cm-1 and diffraction efficiency of 1.2% for poled polymer film fabricated using a corona poling are obtained at the wavelength of 647.1 nm, confirming photorefractivity. We interpreted this result as the orientational enhancement, in which the spatial charge field may enhance the modulated orientation of the azobenzen chromophore. It is unexpected that the photorefractive gain of 9.5 cm-1 for the unpoled polymer film also was observed without external field in two-beam coupling(TBC) experiment. This phenomenon is attributed to a light-induced orientational grating when the azobenzene groups are illuminated by polarized light. 展开更多
关键词 photorefractive (PR) effect poly(n-vinyl)-3-[p-nitrophenylazo]carbazolyl orientational enhancement
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含偶氮苯生色团聚乙烯咔唑的全光光开关效应 被引量:4
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作者 姚胜兰 吴水珠 +2 位作者 佘卫龙 罗锻斌 严琨 《华南理工大学学报(自然科学版)》 EI CAS CSCD 北大核心 2004年第1期61-64,共4页
应用物理掺杂方法成功制得了以聚乙烯咔唑为主体材料 ,以偶氮苯生色团染料分散红 1、分散红 1 3和分散黄 7(DR- 1、DR- 1 3、DY- 7)为客体材料的全光光开关器件 .通过光响应测试发现其在低功率光强 (1 2 .5~ 30mW ,51 4nm)的激发光驱... 应用物理掺杂方法成功制得了以聚乙烯咔唑为主体材料 ,以偶氮苯生色团染料分散红 1、分散红 1 3和分散黄 7(DR- 1、DR- 1 3、DY- 7)为客体材料的全光光开关器件 .通过光响应测试发现其在低功率光强 (1 2 .5~ 30mW ,51 4nm)的激发光驱动下具有优良的全光光开关效应 .同时从激发光调制频率、生色团含量和染料分子结构等方面进行了比较分析 ,发现同等实验条件下开关效应随着染料分子极性增大而增强 ,而生色团掺杂含量较高的 (2 0 % )薄膜全光光开关效应较优 ,较低的调制频率 (30Hz) 展开更多
关键词 生色团 聚乙烯咔唑 全光光开关效应 光致异构
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聚乙烯咔唑侧基含有偶氮发色基团的制备研究 被引量:2
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作者 张文龙 赵洪 +2 位作者 王暄 温玉萍 白永平 《材料科学与工艺》 EI CAS CSCD 北大核心 2006年第6期657-660,共4页
本文研究了聚乙烯咔唑侧基含偶氮发色基团的制备及合成工艺.我们以聚乙烯咔唑为偶合组分,和发色基团对硝基苯重氮盐在相转移催化剂存在下,采用后重氮偶合方法,制备出偶氮化聚乙烯咔唑.聚乙烯咔唑和重氮盐摩尔质量比1:4,重氮盐按分批加... 本文研究了聚乙烯咔唑侧基含偶氮发色基团的制备及合成工艺.我们以聚乙烯咔唑为偶合组分,和发色基团对硝基苯重氮盐在相转移催化剂存在下,采用后重氮偶合方法,制备出偶氮化聚乙烯咔唑.聚乙烯咔唑和重氮盐摩尔质量比1:4,重氮盐按分批加入方式加入到反应液中,反应时间96小时,反应温度室温.通过红外光谱和紫外光谱分析确定了重氮基团已接入到聚乙烯咔唑上. 展开更多
关键词 聚乙烯咔唑 重氮盐 发色基团
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聚乙烯咔唑侧基含偶氮对硝基苯非线性光生色基团的合成及表征 被引量:2
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作者 张文龙 赵洪 +2 位作者 王暄 温玉萍 白永平 《高分子材料科学与工程》 EI CAS CSCD 北大核心 2007年第1期80-83,共4页
研究了一种可作为聚合物类光折变材料中半功能型的基体材料——聚乙烯侧基含偶氮对硝基苯。以聚乙烯咔唑和偶氮盐为原料,以十二烷基苯磺酸钠为相转移催化剂,通过后重氮偶合方法,制备出聚乙烯咔唑侧基含生色团偶氮对硝基苯。用IR、UV-v i... 研究了一种可作为聚合物类光折变材料中半功能型的基体材料——聚乙烯侧基含偶氮对硝基苯。以聚乙烯咔唑和偶氮盐为原料,以十二烷基苯磺酸钠为相转移催化剂,通过后重氮偶合方法,制备出聚乙烯咔唑侧基含生色团偶氮对硝基苯。用IR、UV-v is、1H-NM R、GPC对聚合物偶合前后进行了分析和表征。IR、UV-v is、1H-NM R测试表明了偶氮苯已经接到咔唑环上。UV-v is结果表明偶合反应时间对聚合物的偶氮含量有很大的影响。GPC结果表明,聚合物与重氮盐偶合后,分子量增大。 展开更多
关键词 聚乙烯咔唑 偶氮盐 后重氮偶合
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聚(聚(N-乙烯基咔唑))的电化学合成及表征 被引量:2
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作者 周卫强 彭花萍 徐景坤 《应用化学》 CAS CSCD 北大核心 2008年第4期396-400,共5页
用电化学阳极氧化法一步合成具有电致变色的自支撑导电聚(聚(N-乙烯基咔唑))(PPVK)膜,电导率为0.012S/cm。循环伏安研究表明,PPVK膜具有良好的氧化还原可逆性,且在三氟化硼乙醚溶液中PPVK膜的电化学活性非常稳定。红外光谱... 用电化学阳极氧化法一步合成具有电致变色的自支撑导电聚(聚(N-乙烯基咔唑))(PPVK)膜,电导率为0.012S/cm。循环伏安研究表明,PPVK膜具有良好的氧化还原可逆性,且在三氟化硼乙醚溶液中PPVK膜的电化学活性非常稳定。红外光谱分析结果表明,PVK二次聚合发生在苯环上。荧光光谱分析结果表明,PPVK膜是一种良好的蓝色荧光物质。交流阻抗谱研究表明,PPVK的阳极氧化过程(0.5~1.9V)可以分为P掺杂区(0.5—1.3V)、过渡区(1.4~1.5V)和过氧化区(1.6~1.9V)3个电位区域。 展开更多
关键词 导电高分子 电化学聚合 聚(聚(N-乙烯基咔唑))膜 荧光光谱 阻抗谱
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富勒烯化聚环氧丙基咔唑的合成与表征 被引量:1
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作者 顾涛 陈万喜 徐铸德 《功能高分子学报》 CAS CSCD 1998年第4期473-477,共5页
通过Friedel-Crafts反应制备了富勒烯化的聚环氧丙基咔唑,聚合物中C60的含量最高可达7.6wt%。通过凝胶渗透色谱法测定了聚合物分子量,并采用1H和13CNMR,IR,热分析及光谱等手段对其结构进行了分... 通过Friedel-Crafts反应制备了富勒烯化的聚环氧丙基咔唑,聚合物中C60的含量最高可达7.6wt%。通过凝胶渗透色谱法测定了聚合物分子量,并采用1H和13CNMR,IR,热分析及光谱等手段对其结构进行了分析与表征。 展开更多
关键词 聚环氧丙基咔唑 光导体 富勒烯化 碳60
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新型含咔唑基聚芳亚胺的合成与性能研究
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作者 徐真 苗鲁滨 +3 位作者 徐艺 胡红菊 张林 林润雄 《合成化学》 CAS CSCD 北大核心 2011年第4期476-479,共4页
以3,6-二氨基-N-(2-乙基己烷基)咔唑和二溴化芳香酮为单体,经钯催化的胺基化缩聚反应合成了三种新型的含咔唑基的聚芳亚胺[PAI-C(a)~PAI-C(c)],其结构经1H NMR,IR和元素分析表征。用DSC和TG对PAI-C的热性能进行了研究;用UV和荧光... 以3,6-二氨基-N-(2-乙基己烷基)咔唑和二溴化芳香酮为单体,经钯催化的胺基化缩聚反应合成了三种新型的含咔唑基的聚芳亚胺[PAI-C(a)~PAI-C(c)],其结构经1H NMR,IR和元素分析表征。用DSC和TG对PAI-C的热性能进行了研究;用UV和荧光光谱对PAI-C的光学性能进行了研究。结果表明,PAI-C均具有较高的玻璃化转变温度(Tg〉240℃)和良好的热稳定性(Td〉480℃);PAI-C具有一定的光学性能。 展开更多
关键词 聚芳亚胺 钯催化剂 咔唑 合成 热性能 热性能 光学性能
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聚甲基丙烯酸乙基咔唑酯后重氮化的研究
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作者 张文龙 于亚洲 +2 位作者 戴亚杰 张新 王暄 《塑料助剂》 2009年第2期43-46,共4页
通过后重氮偶合方法,以聚甲基丙烯酸乙基咔唑酯(PACE)和重氮盐为原料,以十二烷基苯磺酸钠为相转移催化剂,制备了聚甲基丙烯乙基咔唑酯接枝偶氮硝基苯。讨论了时间、催化剂用量、不同溶剂对合成工艺的影响。用IR﹑UV-vis方法表征偶合后... 通过后重氮偶合方法,以聚甲基丙烯酸乙基咔唑酯(PACE)和重氮盐为原料,以十二烷基苯磺酸钠为相转移催化剂,制备了聚甲基丙烯乙基咔唑酯接枝偶氮硝基苯。讨论了时间、催化剂用量、不同溶剂对合成工艺的影响。用IR﹑UV-vis方法表征偶合后聚合物结构。 展开更多
关键词 聚甲基丙烯酸乙基咔唑酯 后重氮偶合 合成工艺 相转移
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C_(60)接枝聚(N-乙烯基咔唑)的合成、表征及光电导性能 被引量:7
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作者 李浪 陶征洪 +2 位作者 汪长春 杨武利 府寿宽 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2000年第5期816-818,共3页
The C60 grafted poly(N-vinyl carbazole) (PVK) polymer(CGP) was prepared by simple radical polymerization initiated by BPO at 90℃.The products were characterized by UV-Vis, FTIR, GPC and fluorescence and it was proven... The C60 grafted poly(N-vinyl carbazole) (PVK) polymer(CGP) was prepared by simple radical polymerization initiated by BPO at 90℃.The products were characterized by UV-Vis, FTIR, GPC and fluorescence and it was proven that C60 was grafted covalently to the PVK. The C60 moiety in the product was about 1. 2% (mass fraction). The photoconductlvity study revealed that the photoconductivity of PVK was improved obviously through grafting C60.The half time of light decaying (t1/2) of CGP reached 0. 35 s. 展开更多
关键词 C60接枝聚(N-乙烯基咔唑) 光电导性能 合成 碳60
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聚对苯撑乙炔咔唑薄膜对TNT挥发物的检测 被引量:2
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作者 刘暘 支俊格 +2 位作者 石建兵 佟斌 董宇平 《发光学报》 EI CAS CSCD 北大核心 2012年第1期102-108,共7页
以3,6-二溴-9-辛基咔唑和2,5-二戊烷氧基-1,4-二乙炔基苯为单体,通过Pd催化的Sonogashira偶联反应合成了聚对苯撑乙炔咔唑衍生物PPECz。PPECz的溶液和固体薄膜都具有较好的发光性能,并且均对2,4,6-三硝基甲苯(TNT)有明显的响应。在常温... 以3,6-二溴-9-辛基咔唑和2,5-二戊烷氧基-1,4-二乙炔基苯为单体,通过Pd催化的Sonogashira偶联反应合成了聚对苯撑乙炔咔唑衍生物PPECz。PPECz的溶液和固体薄膜都具有较好的发光性能,并且均对2,4,6-三硝基甲苯(TNT)有明显的响应。在常温常压条件下,微量(40μg)的TNT挥发物在60 s内就能使聚合物PPECz薄膜的荧光强度被猝灭56%,可作为一种潜在的硝基苯类爆炸物的荧光检测材料。 展开更多
关键词 聚对苯撑乙炔 咔唑 TNT挥发物检测 荧光猝灭
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掺杂聚乙烯基咔唑的螺噁嗪光致变色的性能 被引量:2
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作者 许劼 田晓慧 +1 位作者 元以中 孙海涛 《化学试剂》 CAS CSCD 北大核心 2011年第7期607-608,659,共3页
将PVK(聚乙烯基咔唑)以不同的比例掺杂至螺噁嗪光致变色化合物的体系中,通过对螺噁嗪开环体紫外-可见光谱和聚乙基咔唑荧光光谱的分析可以得出,掺杂体系中聚乙烯基咔唑中的电子空穴可容纳螺噁嗪光致变色过程中迁移的电子,从而提高了螺... 将PVK(聚乙烯基咔唑)以不同的比例掺杂至螺噁嗪光致变色化合物的体系中,通过对螺噁嗪开环体紫外-可见光谱和聚乙基咔唑荧光光谱的分析可以得出,掺杂体系中聚乙烯基咔唑中的电子空穴可容纳螺噁嗪光致变色过程中迁移的电子,从而提高了螺噁嗪开环的效率。 展开更多
关键词 螺噁嗪 聚乙烯基咔唑 掺杂 光致变色
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主链含N-烷基咔唑环结构聚芳醚酮的性能表征 被引量:3
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作者 王菲菲 王志鹏 +1 位作者 王红华 周光远 《应用化学》 CAS CSCD 北大核心 2015年第4期379-385,共7页
对含N-烷基咔唑环结构的聚芳醚酮(PPCz E、PPCz B和PPCz H)进行基本物理性能方面的表征,并与商业化酚酞基聚芳醚酮(PEK-C)进行比较。咔唑环结构的引入使聚合物在345 nm附近有强紫外光吸收并表现出发蓝光能力。由于疏水性烷基侧链的... 对含N-烷基咔唑环结构的聚芳醚酮(PPCz E、PPCz B和PPCz H)进行基本物理性能方面的表征,并与商业化酚酞基聚芳醚酮(PEK-C)进行比较。咔唑环结构的引入使聚合物在345 nm附近有强紫外光吸收并表现出发蓝光能力。由于疏水性烷基侧链的存在,聚合物薄膜的水接触角(87°-103°)大于PEK-C(76°),但同时烷基侧链所引起的聚合物链间距的增大导致聚合物的吸水率(0.65%-0.86%)高于PEK-C(0.56%)。此外,聚合物表现出较好的尺寸稳定性(平均线膨胀系数6.4×10^-5℃^-1)和电绝缘性能(体积电阻率1016Ω·cm)。聚合物的拉伸模量在1.9-2.0 GPa之间,拉伸强度在72.5-75.0 MPa之间以及断裂伸长率在6.5%-7.2%之间。高温条件下(≤225℃),PPCz E仍具有良好的拉伸性能。 展开更多
关键词 聚芳醚酮 咔唑 侧链烷基 荧光 接触角 拉伸性能
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模板法制备聚乙烯咔唑及其复合物纳米管有序阵列 被引量:3
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作者 姜源 徐正 《无机化学学报》 SCIE CAS CSCD 北大核心 2005年第9期1389-1391,共3页
PVK or PVK-C60 solution was dropped onto the alumina membrane and the solution was filled into the channel of the membrane due to the capillary action. As the solvent evaporation, the nanotubes were formed. The morpho... PVK or PVK-C60 solution was dropped onto the alumina membrane and the solution was filled into the channel of the membrane due to the capillary action. As the solvent evaporation, the nanotubes were formed. The morphology of the sample was examined by SEM and fluorescence of PVK and PVK-C60 was determined. Emis- sion intensity of PVK was weakened by C60, indicating that C60 improved the conductive property of PVK nan- otubes. 展开更多
关键词 聚乙烯基咔唑 纳米管 C60
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