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81.
Synthesis and thermal properties of the thermosetting resin based on cyano functionalized benzoxazine 总被引:2,自引:0,他引:2
G.P. Cao 《Polymer Degradation and Stability》2008,93(3):739-744
A novel thermosetting resin based on cyano functionalized benzoxazine (BZCN) has been synthesized from 2,6-bis(4-diaminobenzoxy)benzonitrile phenol and formaldehyde by solution reaction. The structure of the monomer is supported by FTIR, 1H NMR and 13C NMR spectra, which have exhibited that the reactive benzoxazine rings and cyano group exist in the molecular structure of BZCN. The curing reactions of BZCN are monitored by the disappearance of the nitrile peak and the tri-substituted benzene ring that is attached with oxazine ring peak at 2231 and 930 cm−1, respectively. The complete cured materials could achieve char yields up to 70% at 800 °C in nitrogen atmosphere, above 64% at 600 °C in air (20% oxygen) environments and the glass transition temperature up to 250 °C. The thermally activated curing polymerization reaction of BZCN follows multiple polymerization mechanisms via the ring-opening polymerization of oxazine rings and the triazine ring-formation of cyano groups, which contribute to the stability of the polymer. 相似文献
82.
Ultra-high molecular weight polyethylene (UHMWPE) with a microporous structure was prepared via thermally induced phase separation (TIPS).Liquid paraffin (LP) was used as a diluent in the preparation of microporous UHMWPE. Small angle laser light scattering (SALLS) and differential scanning calorimetry (DSC) were used to determine the phase separation temperatures,i.e.the cloud points and the dynamic crystallization temperatures,respectively.It was found that the cloudI points were coincident with the cr... 相似文献
83.
Jiahui Liu Junjie Liu Prof. Dr. Haoyuan Li Prof. Dr. Zhengyang Bin Prof. Dr. Jingsong You 《Angewandte Chemie (International ed. in English)》2023,62(31):e202306471
Narrowband organic light-emitting diodes (OLEDs) are receiving significant attention and have demonstrated impressive performance in blue and green OLEDs. However, developing high-performance narrowband red OLEDs remains a highly desired yet challenging task. Herein, we have developed narrowband red fluorescent emitters by utilizing a boron-dipyrromethene (BODIPY) skeleton in combination with a methyl-shield strategy. These emitters exhibit small full-width at half-maxima (FWHM) ranging from 21 nm (0.068 eV) to 25 nm (0.081 eV) and high photoluminescence quantum yields (ΦPL) ranging from 88.5 % to 99.0 % in toluene solution. Using BODIPY-based luminescent materials as emitters, high-performance narrowband red OLEDs have been assembled with external quantum efficiency as high as 18.3 % at 623 nm and 21.1 % at 604 nm. This work represents, to our knowledge, the first successful case of achieving NTSC pure-red OLEDs with the Commission Internationale de l’Éclairage (CIE) coordinates of [0.67, 0.33] based on conventional fluorescent emitters. 相似文献
84.
Sheng Jun Luo ;Wan Long Pan ;Ying Nan Chi ;Yan Qing Xu ;Kun Lin Huang ;Chang Wen Hu 《中国化学快报》2008,19(10):1147-1150
1-(1-Adamantylamino)-2,4,6-trinitrobenzene (1) as a potential energy material has been synthesized in excellent yield and characterized by FT-IR, 1H NMR and single crystallographic methods, and is thermally stable, decomposed in the range of 215- 72℃. 相似文献
85.
Dr. Bo Zhou Zhenhong Qi Meiqi Dai Chang Xing Prof. Dr. Dongpeng Yan 《Angewandte Chemie (International ed. in English)》2023,62(39):e202309913
Harnessing the potential of thermally activated delayed fluorescence (TADF) and room temperature phosphorescence (RTP) is crucial for developing light-emitting diodes (LEDs), lasers, sensors, and many others. However, effective strategies in this domain are still relatively scarce. This study presents a new approach to achieving highly efficient deep-blue TADF (with a PLQY of 25 %) and low-energy orange RTP (with a PLQY of 90 %) through the fabrication of lead-free hybrid halides. This new class of monomeric and dimeric 0D antimony halides can be facilely synthesized using a bottom-up solution process, requiring only a few seconds to minutes, which offer exceptional stability and nontoxicity. By leveraging the highly adaptable molecular arrangement and crystal packing modes, the hybrid antimony halides demonstrate the ability to self-assemble into regular 1D microrod and 2D microplate morphologies. This self-assembly is facilitated by multiple non-covalent interactions between the inorganic cores and organic shells. Notably, these microstructures exhibit outstanding polarized luminescence and function as low-dimensional optical waveguides with remarkably low optical-loss coefficients. Therefore, this work not only presents a pioneering demonstration of deep-blue TADF in hybrid antimony halides, but also introduces 1D and 2D micro/nanostructures that hold promising potential for applications in white LEDs and low-dimensional photonic systems. 相似文献
86.
Justina Jovaišaitė Sven Kirschner Steponas Raišys Gediminas Kreiza Paulius Baronas Saulius Juršėnas Matthias Wagner 《Angewandte Chemie (International ed. in English)》2023,62(4):e202215071
Organic ultralong room temperature phosphorescence (RTP), or organic afterglow, is a unique phenomenon, gaining widespread attention due to its far-reaching application potential and fundamental interest. Here, two laterally expanded 9,10-dimesityl-dihydro-9,10-diboraanthracene (DBA) derivatives are demonstrated as excellent afterglow materials for red and blue-green light emission, which is traced back to persistent thermally activated delayed fluorescence and RTP. The lateral substitution of polycyclic DBA scaffold, together with weak transversal electron-donating mesityl groups, ensures the optimal molecular properties for (reverse) intersystem crossing and long-lived triplet states in a rigid poly(methyl methacrylate) matrix. The achieved afterglow emission quantum yields of up to 3 % and 15 %, afterglow lifetimes up to 0.8 s and 3.2 s and afterglow durations up to 5 s and 25 s (for red and blue-green emitters, respectively) are attributed to the properties of single molecules. 相似文献
87.
This paper discusses the effects of adding particulate filler to a system undergoing liquid–liquid thermally induced phase separation (L–L TIPS). While much is known about the growth of droplets in L–L TIPS, little is known about the effect particular fillers have on droplet growth and the final cell size in the resulting microporous membranes. In this work, zeolite particles are shown to have a significant effect on the final cell size of these microporous membranes, the extent of which depends on the particle loading and processing conditions used to form the membrane. Two polymer–diluent–zeolite systems are reported: isotactic polypropylene–diphenyl ether and poly(methyl methacrylate)–cyclohexanol, both with zeolite 4A particles. 相似文献
88.
Low dielectric constant (low-k) porous films of high density polyethylene-grafted-maleic anhydride were prepared via thermally induced phase separation (TIPS) using di-n-octyl phthalate as the solvent and methanol as the extractant. The results show that, for the process of TIPS, cellular structures of spherical pores were obtained. Lower polymer concentration and lower cooling rate induced larger pores and higher porosity. For the dielectric constant, the introduction of pores considerably reduced the dielectric constant from 2.60 to 1.56 at most. Pore size showed little effect on dielectric constant in our experiment, but porosity was found to be the key influential factor. The relationship between dielectric constant and porosity was found to be best fit to Rayleigh model. 相似文献
89.
Dr. Shuangyan Hu Lijun Liu Dr. Heng Li Dr. David Pahovnik Prof. Dr. Nikos Hadjichristidis Prof. Dr. Xuechang Zhou Prof. Dr. Junpeng Zhao 《化学:亚洲杂志》2023,18(1):e202201097
A series of ester-ether copolymers were obtained via the reaction between α,ω-dihydroxyl poly(ϵ-caprolactone) (PCL) and ethylene oxide (EO) or monosubstituted epoxides catalyzed by strong phosphazene bases. The two types of monomeric units were distributed in highly random manners due to the concurrence of epoxide ring-opening and fast transesterification reactions. The substituent of epoxide showed an interesting bidirectional effect on the enzymatic degradability of the copolymer. Compared with PCL, copolymers derived from EO exhibited enhanced hydrophilicity and decreased crystallinity which then resulted in higher degradability. For the copolymers derived from propylene oxide and 1,2-butylene oxide, the hydrophobic alkyl pendant groups also allowed lower crystallinity of the copolymers thus higher degradation rates. However, further enlarging the pendant groups by using styrene oxide or 2-ethylhexyl glycidyl ether caused a decrease in the degradation rate, which might be ascribed to the higher bulkiness hindering the contact of ester groups with lipase. 相似文献
90.
Jaroslav Mosná?ek Monica Bertoldo Chiara Cappelli Ivan Luká? 《Polymer Degradation and Stability》2007,92(5):849-858
Various diazo-compounds, 1,2,2,6,6-pentamethylpiperidin-4-yl diazoacetate (PMPDA), 2,2,6,6-tetramethylpiperidin-4-yl diazoacetate (TMPDA), methyl diazoacetate (MDA), 1,2,2,6,6-pentamethylpiperidin-4-yl 2-diazo-3-methyloxycarbonylpropionate (PMPMDS), 1,2,2,6,6-pentamethylpiperidin-4-yl 2-diazo-4-methyloxycarbonylbutanoate (PMPMDP), and one azide, methyl azidocarboxylate (MAC), were successfully prepared and grafted on polyethylene films by UV light (λ > 210 nm) activation. The treated films were characterised by FT-IR spectroscopy and contact angle measurements. Ab-initio quantum mechanical calculations allowed simulating the IR absorption spectra of the polymer grafted species. These last and the related grafting yields are discussed with reference to the diazo-compound structure and concentration. Up to 8.6 mol% of bonded groups (grafted groups/ethylene monomeric unit) were found without affecting the polymer molecular weight distribution, as shown by GPC analysis. All modified films bearing HAS groups showed very high photo-stability. 相似文献