19 Sep 1 3 5 triazine aromatic
5 Related Records Expand this section. Synthesis of a soluble poly(fluorenone). The mechanical properties of the films were excellent, and their tensile strength, elongation at break, and tensile moduli were in the ranges of 48–72 MPa, 5–7%, and 1.3–1.9 GPa, respectively. The Hole Blocking Effect of 4,4′,4″-trifluorotriazine (tfTZ) in Electroluminescent Devices. If you do not receive an email within 10 minutes, your email address may not be registered, Meta-Activated Nucleophilic Aromatic Substitution Reaction: Poly(biphenylene oxide)s with Trifluoromethyl Pendent Groups via Nitro Displacement. Synthesis and characterization of poly(arylene ether Chae Kyu Kim, Eun Seok Song, Hyung Joo Kim, Chiyoung Park, Jai Kyeong Kim, Young Chul Kim, Jae Woong Yu, Chulhee Kim. Makromolekulare Chemie I and Bayreuther Institut für Makromolekülforschung (BIMF), Universität Bayreuth, Universitätsstr. Nickel-catalysed Kumada polycondensation of di-functionalized Grignard reagent with aryl fluoride. 1 Structures Expand this section. Probing ultrafast excited state dynamics and nonlinear absorption properties of three star-shaped conjugated oligomers with 1,3,5-triazine core. Synthesis and characterization of novel poly[4-phenyl-3-(thiophen-3-ylmethyl)-1 In order to examine the potential application these polymers may possess for use in organic electroluminescent devices, the redox properties were studied by cyclic voltammetry. Synthesis and Properties of the Derivatives of 2,4,6-Tris(Phenoxy)-1,3,5-Triazine, All copolymers are amorphous except PAEP9010 as evidenced by WAXD. Datum: 11. Hyperbranched triazine-containing polyfluorenes: Efficient blue emitters for polymer light-emitting diodes (PLEDs). https://doi.org/10.1007/s11426-020-9714-0Appending triphenyltriazine to 1,10-phenanthroline: a robust electron-transport material for stable organic light-emitting diodes.
Photosensitizing porphyrin–triazine compound for bulk heterojunction solar cells. Jiwon Shin, Sungtack Lim, Dong-Myung Shin, Donsoo Choi, Chulhee Kim, Byungnam Kim. and you may need to create a new Wiley Online Library account.Synthesis and characterization of soluble copoly(arylene ether sulfone phenyl-s-triazine)s containing phthalazinone moieties in the main chain, Two bipolar blue-emitting fluorescent materials based on 1,3,5-triazine and peripheral pyrene for organic light-emitting diodes, I have read and accept the Wiley Online Library Terms and Conditions of UseNumber of times cited according to CrossRef: Shijie Ren, Robert Dawson, Andrea Laybourn, Jia-xing Jiang, Yaroslav Khimyak, Dave J. Adams, Andrew I. Cooper.
NEW USER Synthesis and Characterization of Aromatic Poly(1,3,5-triazine−ether)s for Electroluminescent DevicesSynthesis and luminescence characteristics of conjugated dendrimers with 2,4,6-triaryl-1,3,5-triazine periphery. Rafael Juárez, Rafael Gómez, José L. Segura, Carlos Seoane. Returning user Ganesh D. Sharma, Galateia E. Zervaki, Panagiotis Angaridis, Athanassios G. Coutsolelos. Lianpeng Xia, Yuyuan Xue, Kang Xiong, Chaosheng Cai, Zuosheng Peng, Ying Wu, Yuan Li, Jingsheng Miao, Dongcheng Chen, Zhanhao Hu, Jianbin Wang, Xiaobin Peng, Yueqi Mo, and Lintao Hou . The polymers showed optical properties in solution that were mainly dependant on the properties of the substituting R groups, on the triazine ring.
Such polymer exhibits glass transition temperature ( T g ) up to 315°C ,and possesses excellent thermal and thermo-oxidative stability without significant weight loss up to temperatures of approximately 500°C. Novel thermally stable and organosoluble aromatic polyamides with main chain phenyl-1,3,5-triazine moieties. The polymers have excellent thermal stability and are amorphous with glass transition temperatures in the range 190−250 °C. A series low molar mass and poly- (1,3,5-triazine)-ethers were synthesized by a condensation reaction. Its decomposition temperature for 5% mass-loss is in excess of 493°c in nitrogen and it retains 90% weight at round 520°C. https://doi.org/10.1007/s00289-014-1216-0Synthesis and characterization of 1,3,4-oxadiazole derivatives containing alkoxy chains with different lengths. https://doi.org/10.1021/acs.jpclett.9b01140Hiroko Inomata,, Kenichi Goushi,, Takuma Masuko,, Tohru Konno,, Toshiro Imai,, Hiroyuki Sasabe,, Julie J. Abhishek P. Kulkarni,, Christopher J. Tonzola,, Amit Babel, and, Star-Shaped Donor-π-Acceptor Conjugated Oligomers with 1,3,5-Triazine Cores: Convergent Synthesis and Multifunctional Properties. Author to whom correspondence should be addressed.https://doi.org/10.1080/15685551.2017.1281786Synthesis and optical and electrochemical properties of new π-conjugated 1,3,5-triazine-containing polymers. A series of poly(1,3,5-triazine−ether)s was synthesized by polycondensation with 4,4‘-hexafluoroisopropylidenebis[phenol]. The polycondensation reaction was also affected by monomer concentration, solvents, and tertiary amines like pyridine. Symmetrical 1,3,5-triazine is the common. https://doi.org/10.1016/j.orgel.2009.09.016You have to login with your ACS ID befor you can login with your Mendeley account.A novel straightforward synthesis of 2,4,6-triaryl-1,3,5-triazines via copper-catalyzed cyclization of N-benzylbenzamidines. Hence, Pa and Pb (R=H and -OCH3, respectively) showed blue photoluminescent (PL) emission with high quantum yields (QY) even in polar solvents, whereas Pc (R=N,N-dimethylamino) gave green-blue PL emission with very low QY The PL spectra of the polymers in solution were concentration and polarity dependent, which suggested the formation of an exciplex. Dengxia Wang, Bin Li, Yaoheng Zhang, Zaijun Lu. 3% . And they exhibit excellent thermal stability with 5% weight loss temperature up to 522-532°C, 10% weight loss temperature ranging from 556°C to 567°C and the carbonized residue values at 800°C in the range of 69%-74%. 2% and initial moduli of 2. b
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