A new strategy, a post coupling method to develop the polyphosphazene (P2) functionalized with carbazolyl groups and nonlinear optical (NLO) chromophores, has been ex-plored. P2 exhibits good solubility in common organic solvents. The poled film of P2 exhibits a resonant d33 value of 42 pm/V by second harmonic generation (SHG) measurements. 相似文献
Two types of polysiloxanes,which contain both C60 moieties and carbazolyl groups in the side chains with a difference in the numbers of the reacting site on C60 molecules,were synthesized and their fluorescent properties were studied to distinguish the role of C60 in the luminescent polymers.Our results demonstrated that when C60 moieties are bonded to the polymers as multisubstituents but not linked to the luminescent moieties directly,the luminescence of the resultant polymers were still very strong instead of quenching,even the substituted degree is only 1.01. 相似文献
Development of an innovative strategy to prepare hyperbranched polysiloxanes (HBPS) is highly desirable due to the significant shortcomings of conventional fabrication approaches: the precursors need pre‐synthesis, the hydrosilylation reaction is conducted using costly catalysts, and hydrolysis of organosiloxanes easily results in gelation. Here, novel HBPS containing acetoacetyl groups (HBPS‐Ac) are synthesized through a cost‐efficient and easily controllable transesterification reaction. It is shown by gel permeation chromatography (GPC), Fourier transform infrared spectroscopy (FTIR), 1H NMR, and gas chromatography (GC) measurements that the polymerization process is a straightforward technique to prepare new HBPS. The polymers are capable to remove formaldehyde due to the highly efficient reaction of the active methylene in the acetoacetyl group with formaldehyde at room temperature. Notably, coatings incorporating 4 wt% of the polymers allow for formaldehyde absorption, while integrated performances are kept almost unaffected. Therefore, HBPS‐Ac are promising as scavengers for formaldehyde.
Vinyl‐terminated isotactic polystyrene macromonomers were copolymerized with ethylene and 1‐octene to new polyolefin graft copolymers with crystallizable polystyrene side chains. The iPS content was varied from 4 to 78 wt.‐% using different metallocene and halfsandwich catalysts. No solubility problems of the stereoregular macromonomer occured, because iPS does not crystallize during polymerization. In addition the polymers show nanophase separation of the polyolefin backbone and the iPS side chains. The crystallization of iPS, having a melting point of about 200 °C, can be achieved by annealing. This synthesis strategy allows the fabrication of a new class of thermoplastic elastomers with improved heat distortion temperatures.
A series of novel thiochromanone derivatives containing a sulfonyl hydrazone moiety were designed and synthesized. Their structures were determined by 1H-NMR, 13C-NMR, and HRMS. Bioassay results showed that most of the target compounds revealed moderate to good antibacterial activities against Xanthomonas oryzae pv. oryzae, Xanthomonas oryzae pv. oryzicolaby, and Xanthomonas axonopodis pv. citri. Compound 4i had the best inhibitory activity against Xanthomonas oryzae pv. oryzae, Xanthomonas oryzae pv. oryzicolaby, and Xanthomonas axonopodis pv. citri, with the EC50 values of 8.67, 12.65, and 10.62 μg/mL, which were superior to those of Bismerthiazol and Thiodiazole-copper. Meanwhile, bioassay results showed that all of the target compounds proved to have lower antifungal activities against Sclerotinia sclerotiorum, Fusarium oxysporum, Gibberella zeae, Rhizoctonia solani, Verticillium dahlia, and Botrytis cinerea than those of Carbendazim. 相似文献
Two functional polyurethanes (P1 and P2) bearing a large π electron conjugated chromophoric pendant were synthesized and characterized by FT‐IR, 1H‐NMR and UV‐Vis absorption spectra. Their optical limiting properties were evaluated. The results show that P1 and P2 show novel optical limiting properties, which are assigned to a long π electron conjugated chromophoric pendant. It was found that their optical limiting properties were affected simultaneously by solution concentration and P2 displays a better optical limiting property than P1 at the same solution transmittance, although that P1 has larger χ(3) (4.28×10?11 esu) than P2 (0.87×10?11 esu), and their optical limiting mechanism is investigated. 相似文献
Orthogonal syntheses of 4-, 5-, 6-, and 7-chloro substituted tryptamine derivatives were performed under the Grandberg–Zuyanova-modified Fisher indole-synthesis conditions. In the 4- and 6-substituted tryptamine cases, a bromine atom was utilized as an easily cleavable protecting group, which allowed complete regiocontrol. In addition, a chlorine substituent was preserved in the debromination step and could be utilized as a synthetic handle for late-stage diversification under modern Pd(0) catalysis conditions. 相似文献
For diethylenetriamino-trioxo-molybdenum(VI), density functional theory (DFT) method calculations of the structure, atomic charge distributions, electronic spectra, natural po- pulation analyses and thermodynamic properties at different temperatures have been performed by B3LYP method using LANL2DZ, CEP-121G and CEP-31G basis sets, respectively. The calculated results show that B3LYP/LANL2DZ method can best reproduce the molecular structure. The atomic charge distribution analyses indicate that during forming the complex, the ligand of diethyl- enetriamine donates negative charges to MoO3 and these charges are accepted by molybdenum(VI) atom as well as three oxygen atoms. The electronic spectra calculations indicate that B3LYP/ LANL2DZ results are nearest to experimental data among the three methods and electronic tran- sitions are mainly derived from the contribution of bands π→π*. The calculation of the second order optical nonlinearity was carried out, and the molecular hyperpolarizability was 0.7881*10-30 esu. 相似文献
