Novel dyestuff polymers were successfully obtained through oxidative polymerization technique. The synthesized Schiff base and its polymer were soluble in alkaline'aqueous medium and they have various colors in different solutions. Also, it can be said that the synthesized compounds are suitable as coloring agent (dyestuff) for textile applications. Fluorescence properties of the compounds were determined in DMF with different concentrations (mg/L). Poly-tris(4- aminophenyl)methanol (P-TAPM) has quite high emission and excitation intensity values. Optical and electrochemical band gaps of the polymers were lower than those of the monomers indicating the more conjugated structure of the polymers. The oxidized states of the novel dyestuff compounds were examined by cyclic voltammetry (CV) technique. The solid state conductivity measurements showed that the synthesized polymers were semiconductors when exposed to the iodine vapour their conductivities could be increased. P-TAPM had the highest undoped conductivity. Thermal characterizations of the synthesized compounds were carried out by TG-DTA and DSC methods. 相似文献
Summary: Two new polymers containing 2‐pyrazoline units in the main chain were synthesized for the first time by a Suzuki polycondensation between a 2‐pyrazoline monomer and aryl diboronic esters. The polymers showed high photoluminescence (PL) in both the solution and the solid state; quantum yields of PL in toluene were higher than 76%. Thermogravimetric analysis and cyclic voltammetry showed that the polymers had high thermal stability and good reversibility under electrochemical oxidation.
New polymers ( 2 and 3 ) with strong photoluminescence and good reversibility under electrochemical oxidation were synthesized here. 相似文献
A series of ferrocene‐modified poly(glycidyl methacrylate) (PGMA‐Fc) compounds were synthesized and applied as burning rate catalysts in simulative solid propellant to overcome migration problems. 1H NMR and Fourier transform infrared spectroscopies and gel permeation chromatography were used to characterize the synthesized polymers. Their electrochemical behavior was evaluated using cyclic voltammetry. Their catalytic performance for the decomposition of ammonium perchlorate (AP) was investigated using thermogravimetric analysis. Anti‐migration studies were conducted in migration tubes under 50°C. The results show that PGMA‐Fc has a good catalytic effect on lowering the thermal decomposition temperature of AP. Anti‐migration studies show that PGMA‐Fc has better anti‐migration performance than ferrocene and catocene. 相似文献
A series of benzo[ghi]perylene (Bp) and coronene (Cor) derivatives substituted with electron‐withdrawing methoxycarbonyl (COOMe) or electron‐donating methoxyl (MeO) groups was synthesized. The electrochemical, spectroscopic, and photophysical properties of these compounds were investigated by cyclic voltammetry, steady‐state and time‐resolved spectroscopy, and quantum‐yield measurements. Introduction of suitable substituents onto the aromatic rings enabled control of electrochemical and spectroscopic behavior. Examination of excited‐state dynamics revealed that fluorescence quantum yields increased with increasing number of COOMe groups in both Bp and Cor derivatives, consistent with the findings of DFT calculations. Single‐crystal analysis allowed the performance of field‐effect transistors containing single crystals of the derivatives to be rationalized. 相似文献
Reaction between the NH groups in polybenzimidazole (PBI) and bisoxazoline compounds (1,3‐phenylene bisoxazoline, 1,3‐PBO) resulted in the successful preparation of novel network polymers. Adjusting the amount of the bisoxazoline compound, which is a cross‐linking agent for the preparation of network polymers, and obtaining dynamic mechanical measurements, electrical resistivity measurements, thermomechanical measurements, and tensile tests allowed the determination of the heat resistance and mechanical strength of these novel network polymers. Examination of the elementary reaction of PBI and the1,3‐PBO curing reaction by using model compounds revealed that the NH group in the PBI structure reacted with the oxazoline group of 1,3‐PBO. Comparison of noncross‐linked PBI with the PBI network polymers obtained through cross‐linking reaction with bisoxazoline compounds demonstrated improvements in heat resistance and mechanical strength of the PBI‐bisoxazoline network polymers. 相似文献
Poly(azomethine)s containing phosphor, silane and carbazole were synthesized with multiple stage and examined through different photophysical, electrochemical, and thermal behaviours. Following substances were synthesized as an initial step: N-hexyl-carbazole (CH) and N-hexyl-carbazolaldehyde (CHDA), via elimination reaction in argon media and N-hexyl-carbazole azomethine (CHA) via condensation reaction of CHDA with 4-aminophenol also poly(azomethine)s (P-Si-CHA, P-P-CHA) containing silane and phosphor via elimination reaction. The structures of synthesized compounds were confirmed by Fourier-transform infrared spectroscopy (FT-IR), Ultraviolet–visible spectroscopy (UV–Vis) and nuclear magnetic resonance spectroscopy (NMR). Electrochemical properties of compounds were examined with cyclic voltammetry (CV) technique. Fluorescence measurements were utilized to investigate the photochemical behaviors by photoluminescence (PL) analysis. CHA compound surprisingly presented multicolor emission behavior (when excited at 370, 420, 480, 540 and 580 nm, the solution emitted blue, green, yellow, orange and red lights, respectively) with relatively high quantum yield (19.9%) in DMF solvent. Additionally, thermal behaviors of all compounds were determined by TG and DSC techniques. Surface morphologies of polymers were imaged with scanning electron microscope (SEM). 相似文献
New ferrocenyl‐based valproic acid (VPA) ester derivatives were designed and synthesized according to the reaction of appropriate haloalkylferrocene derivatives with VPA in the presence of K2CO3 and a catalytic amount of 18‐crown‐6 ether. Elemental analyses and Fourier transform infrared, 1H NMR, 13C NMR and mass spectra all well confirmed the predicted molecular structure. This is the first report in which ferrocene has been applied in derivatization of VPA as a chromogenic group. The electrochemical properties of the synthesized compounds were studied using cyclic voltammetry measurements, and energies of the frontier molecular orbitals were determined. In addition, the solubilities of the final compounds were studied in distilled water, phosphate buffer (pH = 7.4) and 0.9% (w/v) NaCl solution. 相似文献
Various optically pure organosilicon compounds were synthesized or separated on HPLC. Stereoregular silicon‐containing polymers, poly(carbosilane)s, poly(carbosiloxane)s and poly(siloxane)s were synthesized from these compounds as monomer. Stereochemistry of the elementary reactions to give stereoregular polymers was elucidated. 相似文献
New nickel‐containing ionic liquids were synthesized, characterized and their electrochemistry was investigated. In addition, a mechanism for the electrochemical synthesis of nanoparticles from these compounds is proposed. In these so‐called liquid metal salts, the nickel(II) cation is octahedrally coordinated by six N‐alkylimidazole ligands. The different counter anions that were used are bis(trifluoromethanesulfonyl)imide (Tf2N?), trifluoromethanesulfonate (OTf?) and methanesulfonate (OMs?). Several different N‐alkylimidazoles were considered, with the alkyl sidechain ranging in length from methyl to dodecyl. The newly synthesized liquid metal salts were characterized by CHN analysis, FTIR, DSC, TGA and viscosity measurements. An odd‐even effect was observed for the melting temperatures and viscosities of the ionic liquids, with the complexes with an even number of carbon atoms in the alkyl chain of the imidazole having a higher melting temperature and a lower viscosity than the complexes with an odd number of carbons. The crystal structures of several of the nickel(II) complexes that are not liquid at room temperature were determined. The electrochemistry of the compounds with the lowest viscosities was investigated. The nickel(II) cation could be reduced but surprisingly no nickel deposits were obtained on the electrode. Instead, nickel nanoparticles were formed at 100 % selectivity, as confirmed by TEM. The magnetic properties of these nanoparticles were investigated by SQUID measurements. 相似文献