Sequential double click reactions: a highly efficient post-functionalization method for optoelectronic polymers‡
文献信息
Yongrong Li
A new post-functionalization method based on the Huisgen's 1,3-dipolar cycloaddition between azides and alkynes, followed by the atom-economic addition reaction between electron-rich alkynes and tetracyanoethylene (TCNE) was developed to introduce the donor–acceptor chromophores into polystyrene derivatives in remarkably high yields.
相关文献
Coronene-based metal–organic framework: a theoretical exploration
Chandrima Chakravarty, Bikash Mandal, Pranab Sarkar
DOI: 10.1039/C6CP05495A
In situ S-K XANES study of polymer electrolyte fuel cells: changes in the chemical states of sulfonic groups depending on humidity
Kazuhisa Isegawa, Tetsuo Nagami, Shinji Jomori, Masaaki Yoshida, Hiroshi Kondoh
DOI: 10.1039/C6CP04052G
Rational selection of amorphous or crystalline V2O5 cathode for sodium-ion batteries
Shikun Liu, Zhongqiu Tong, Jiupeng Zhao, Xusong Liu, Jing wang, Xiaoxuan Ma, Caixia Chi, Yu Yang, Yao Li
DOI: 10.1039/C6CP04064K
Observation of nanotwinning and room temperature ferromagnetism in sub-5 nm BiFeO3 nanoparticles: a combined experimental and theoretical study
Mandar M. Shirolkar, Xiaolei Dong, Jieni Li, Shiliu Yin, Ming Li, Haiqian Wang
DOI: 10.1039/C6CP04369K
C96H30 tailored single-layer and single-crystalline graphene quantum dots
Xingming Sun, Jun Yan, Zheng Xie, Ping Chen, Shuyun Zhou
DOI: 10.1039/C6CP03453E
Encapsulation of spherical nanoparticles by colloidal dimers
Gianmarco Munaò, Dino Costa, Carlo Caccamo
DOI: 10.1039/C6CP04704A
Pushing up the magnetisation values for iron oxide nanoparticles via zinc doping: X-ray studies on the particle's sub-nano structure of different synthesis routes
Jan Żukrowski, Marcin Sikora, Olga Safonova, Aleksey Shmeliov, Valeria Nicolosi, Tim Granath, Maximilian Oppmann, Marion Straßer
DOI: 10.1039/C6CP04221J
Electron spin dynamics and spin–lattice relaxation of trityl radicals in frozen solutions
Hanjiao Chen, Alexander G. Maryasov, Michael K. Bowman
DOI: 10.1039/C6CP02649D
Tuning the structure and mechanical property of polymer nanocomposites by employing anisotropic nanoparticles as netpoints
Jianxiang Shen, Wenchuan Wang
DOI: 10.1039/C6CP04460C
Ultra-weak interlayer coupling in two-dimensional gallium selenide
R. Longuinhos, J. Ribeiro-Soares
DOI: 10.1039/C6CP03806A
您可能还喜欢
什么是2,6-二溴-4,8-双[(2-乙基己基)氧基]苯并[1,2-b:4,5-b']二噻吩(CAS号:1226782-13-3)?
2,6-二溴-4,8-双[(2-乙基己基)氧基]苯并[1,2-b:4,5-b']二噻吩是一种有机化合物,分子式为C23H32Br2O2S2。该化合物具有芳香性和...
木聚硫钠(CAS号:37319-17-8)的物理化学性质是什么?
木聚硫钠通常为无色或白色结晶性粉末,具有吸湿性。其分子量约为121.11 g/mol。木聚硫钠易溶于水,不溶于醇类和其他非极性溶剂。在酸性或碱性溶液中,木聚硫钠...
2-甲氧基-4-(三氟甲基)苄溴, JRD(CAS号:886500-59-0)适用哪些法规指南?
该化合物在合成、储存和运输过程中需遵循《全球化学品统一分类和标签制度》(GHS)的健康、环境和物理危险分类。在欧洲还需符合《化学品注册、评估、授权和限制》(RE...
1,4-Diazoniabicyclo[2.2.2]octane-1,4-disulfinate(CAS号:119752-83-9)的主要用途是什么?
1,4-二氮杂双环[2.2.2]辛烷-1,4-二硫酸二酯主要用于有机合成中的保护基团,特别是在保护胺基和硫醇基方面具有广泛应用。此外,它还用于一些特殊化学反应的...
如何处理含有4-(Bromomethyl)-2-fluorobenzenesulphonamide(CAS号:1645275-47-3)的废料?
含有4-(Bromomethyl)-2-fluorobenzenesulphonamide的废液应首先进行中和处理,以降低pH值,避免对环境造成腐蚀性影响。随后...
Loureiriol(CAS号:479195-44-3)的物理化学性质是什么?
Loureiriol是一种天然化合物,其分子式为C15H22O4。Loureiriol为无色结晶性粉末,具有较高的熔点和良好的热稳定性。其相对分子质量为262....
在合成中是否有3-氨基苯甲酰苯胺(CAS号:14315-16-3)的替代品?
在合成过程中,可以考虑使用类似结构的化合物作为3-氨基苯甲酰苯胺的替代品,例如N-苯基-3-氰基苯胺或N-苯基-3-硝基苯胺等,这些化合物具有相似的化学性质,可...
4-异氰酰苯基硼酸频哪醇酯(CAS号:380430-64-8)的市场或研究趋势如何?
4-异氰酰苯基硼酸频哪醇酯主要应用于有机合成、药物化学和材料科学领域。随着绿色化学的发展,该化合物因其高效的官能团转化能力和环境友好性而受到越来越多的关注。近年...
如何储存3β-乙酰氧基-7,25-甘遂二烯-24(R)-醇(CAS号:1352001-09-2)?
3β-乙酰氧基-7,25-甘遂二烯-24(R)-醇应储存在阴凉、干燥、通风良好的地方,避免直接光照。储存容器应密封,防止空气中的水分和氧气影响化合物的稳定性。建...
如何储存4-氟-2-甲基-1H-吲哚(CAS号:1260383-51-4)?
应将4-氟-2-甲基-1H-吲哚存放在阴凉、干燥、通风良好的地方,避免直接暴露在光照下。容器应密封,避免与空气中的水蒸气接触。建议在避光、温度不超过25℃的环境...
来源期刊
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.












![6-(Benzyloxy)-8-(2-bromoacetyl)-2H-benzo[b][1,4]oxazin-3(4H)-one structure 6-(Benzyloxy)-8-(2-bromoacetyl)-2H-benzo[b][1,4]oxazin-3(4H)-one structure](https://cnstatic.chemtradehub.com/structs/926/926319-53-1-2287.webp)
![6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde structure 6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde structure](https://cnstatic.chemtradehub.com/structs/564/564-94-3-e746.webp)
