Poly(N-isopropylacrylamide)-b-poly{6-[4-(4-methylphenyl-azo)phenoxy]hexylmethacrylate} (PNIPAM32-b-PAzoMM8) and poly(N-isopropylacrylamide)-b-poly{6-[methyl(4-nitrophenyldiazenyl)phenyl]aminohexylmethacrylate} (PNIPAM32-b-PAzoNO10) were prepared by reversible addition–fragmentation chain transfer (RAFT) radical polymerization. The optical properties of Eu(DBM)3Phen (Eu, Europium; DBM, dibenzoylmethide; Phen, 1,10-phenanthroline)-doped azobenzene-containing copolymer vesicle solutions were studied by UV–vis and fluorescence spectroscopy. When the electronic transition bands of azobenzene and Eu(DBM)3Phen overlapped at about 350 nm in PNIPAM32-b-PAzoMM8, the fluorescent emission intensity at 612 nm of Eu(DBM)3Phen could be modulated by irradiation with UV and visible light. However, when the absorption of the azobenzene-moiety red-shifted to 477 nm in PNIPAM32-b-PAzoNO10, the luminescence intensity of Eu(DBM)3Phen was not affected any longer. The difference between these two systems was possibly caused by the energy allocation in the luminescence process, which was discussed in detail. 相似文献
AB diblock copolymers of poly(2-(dimethylamino)ethyl metharylate-block-potassiurn acrylate) were prepared via reversible addition-fragmentation chain transfer (RAFT) polymerization. The structure of the block polymer was determined by the nuclear magnetic resonance (NMR) spectroscopy and the gel permeation chromatography. Moreover, it has also been shown that the diblock copolymers exhibit aggregate as function of the pH according to the result of 1H-NMR spectroscopy, FT-IR absorption spectra, UV-vis transmittance spectroscopy, transmission electron microscopy and ultrasonic particle size analyzer. The result was attributed that such AB diblock copolymers were tailored to undergo pH-induced self-assembly. Furthermore, the aggregate can be as template of metal nanoparticles preparation, and the sizes of the aggregate, in turn, strongly control nanoparticle sizes. 相似文献
Bathochromic shift in excitation spectrum was observed during emission measurement of Eu(DBM)(3)Phen containing dilute solution in methyl methacrylate (MMA). Detailed analysis shows that the reason of bathochromic shift is not the formation of molecule aggregation. It is caused by the intense absorption of ligands in the complex. Based on this model, a new method has been established to rectify excitation spectra before emission measurement of systems with different concentration. There exists a critical value of the absorption strength, which is 0.87 from calculation. Higher absorption than this value will cause the bathochromic shift of excitation peak. The wavelength whose absorbance is 0.87 will be the position of the strongest excitation peak. With 200 ppm and 500 ppm Eu(DBM)(3)Phen as the standard sample, relations between relative concentration and wavelength of excitation peak in Eu(DBM)(3)Phen system were deduced and plotted. Theoretical curves are in good agreement with experiment data except extra-dilute concentration, for partial decomplexation of the beta-diketonate and phenanthroline ligands. 相似文献
Diacetylene monomer containing p-nitrophenyl azobenzene moiety (NADA) was synthesized. Silver nanoparticles with different
concentrations were adulterated in the above polymerized NADA (PNADA) films and the third-order nonlinear optical properties
were investigated in detail. UV–vis spectra and transmission electron microscopy were used to confirm the formation of PNADA/Ag
nanocomposite films. The silver nanoparticles (average size of 10 nm) were well dispersed in the polymer films. The value
of the nonlinear refractive index n2 for PNADA films (8.48×10−15 cm2/W) was much higher than that of pure polydiacetylene films. Further, the introduction of silver nanoparticles into the PNADA
polymer films led to the further enhancement of nonlinear optical properties. The maximum value of n2 for PNADA/Ag nanocomposite films could be 11.6×10−15 cm2/W. This enhancement should be ascribed to the surface plasmon resonance of silver nanoparticles. 相似文献
Herein, we synthesize a coumarin‐substituted diacetylene monomer (CODA) and report the novel photo‐controlled reversible assembly and disassembly behavior of the polymerized CODA (PCODA) vesicles. The photo‐triggered dimerization and cleavage reactions of the coumarin groups within the surface of the adjacent PCODA vesicles can be utilized as the driving force to induce assembly and disassembly of PCODA vesicles. Moreover, the boundary of PCODA vesicles in the aggregates becomes more obscure when the irradiation time exceeds 30 min. Fusion occurs upon close docking of target membranes, driven by sufficient dimerization of the coumarin groups within the surface of PCODA vesicles. 相似文献
Poly(N‐isopropylacrylamide)‐block‐poly{6‐[4‐(4‐pyridyazo)phenoxy] hexylmethacrylate} (PNIPAM‐b‐PAzPy) was synthesized by successive reversible addition‐fragmentation chain transfer (RAFT) polymerization. In a water/tetrahydrofuran (H2O/THF) mixture, amphiphilic PNIPAM‐b‐PAzPy self‐assembles into giant micro‐vesicles. Upon alternate ultraviolet (UV) and visible light irradiation, obvious reversible swelling‐shrinking of the vesicles was observed directly under an optical microscope. The maximum percentage increase in volume, caused by the UV light, reached 17%. Moreover, the swelling could be adjusted using the UV light power density. The derivation of this effect is due to photoinduced reversible isomerization of azopyridine units in the vesicles.