Poly(4\|vinyl phenol) (PVPh) was synthesized from anisaldehyde via Perkin Doebner and decarboxyl reactions to form 4 methoxy styrene.It was then polymerized by free radical polymerization following dealkylation to for...Poly(4\|vinyl phenol) (PVPh) was synthesized from anisaldehyde via Perkin Doebner and decarboxyl reactions to form 4 methoxy styrene.It was then polymerized by free radical polymerization following dealkylation to form PVPh.A kind of stable multilayer utra thin film was successfully fabricated via self assembly technique from PVPh and diazoresin (DR) followed by UV irradiation.The driving force of self assembly was confirmed to be the hydrogen bonding attraction from diazonium group(—N + 2)of DR and phenolic hydroxy group(—Ph—OH)of PVPh.The film becomes very stable towards polar solvents after UV irradiation and it is believed that the H bonds between the layers of the film converts to covalent bonds following the decomposition of —N + 2 groups when the multilayer film underwent UV irradiation.展开更多
Through self assembly technique, a new type of layer by layer ultra thin film was fabricated based on water soluble substituted polyaniline and photosensitive diazoresin through electrostatic attraction. Under UV irra...Through self assembly technique, a new type of layer by layer ultra thin film was fabricated based on water soluble substituted polyaniline and photosensitive diazoresin through electrostatic attraction. Under UV irradiation, the bond nature between layers turns from ionic to covalent following the decomposition of diazonium group, and the film gets very stable. The photoelectric conversion property of substituted polyaniline containing self assembled film has also been investigated in this article.展开更多
On the substrate of modified quartz, two kinds of self assembled ultra thin films were fabricated through layer by layer electrostatic deposition with diazoresin′s sulfonate(DRS) as the polyanion, and chitosan(CS) as...On the substrate of modified quartz, two kinds of self assembled ultra thin films were fabricated through layer by layer electrostatic deposition with diazoresin′s sulfonate(DRS) as the polyanion, and chitosan(CS) as the polycation. The self assembly process was monitored by UV Vis spectra and confirmed that the layer by layer deposition takes place regularly. The films obtained both from DRS, CS(CS/DRS film) and from DR, DRS, CS(DR/DRS/CS/DRS film) were photo sensitive. Under irradiation of ultraviolet light, the stability of the films towards polar solvents increases significantly. The kinetic study shows that the rate of the photodecomposition reaction of DR/DRS/CS/DRS films is higher than that of CS/DRS films and doesnt show the first order reaction for both films.展开更多
A novel multiplayer film was assembled from poly[(4 carboxyphenyl)acetylene](PCPA) and diazoresin(DR) in aqueous solution via electrostatic attraction. Under UV irradiation, following the decomposition of diazonium gr...A novel multiplayer film was assembled from poly[(4 carboxyphenyl)acetylene](PCPA) and diazoresin(DR) in aqueous solution via electrostatic attraction. Under UV irradiation, following the decomposition of diazonium group between the adjacent interfaces of the multiplayers, the ionic bonds of the self assembly film convert to covalent bonds and the film becomes very stable toward electrolyte solutions. Thus the photoelectric conversion property of poly[(4 carboxyphenyl)acetylene] containing film can be measured in conventional three electrode photoelectrochemical cell, and 0.5 mol/L KCl solution can be used as the supporting electrolyte. The photocurrent spectroscopy responses coincide with the absorption spectrum of the irradiated self assembly film, which indicates that the irradiated DR/PCPA film is responsible for the photocurrent generation.展开更多
The self assembly between diazoresin(DR) and the homopolymer or copolymers of 4 N hydroxyphenyl acrylamide(NHPA) has been investigated.It was confirmed that the driven force of the assembly is H bonding attraction, in...The self assembly between diazoresin(DR) and the homopolymer or copolymers of 4 N hydroxyphenyl acrylamide(NHPA) has been investigated.It was confirmed that the driven force of the assembly is H bonding attraction, in which the DR plays a role of H acceptor, while the NHPA polymers act as a H donor, Under UV, the multiayer films become very stable towards polar solvents. For example, no any change was observed when the irradiated film was immersed in DMF at 20 ℃ for 12 h, but the unirradiated film was destroyled completely when it was immersed in DMF at the same temperature for 20 min. The dramatically improvement for the stability of the film towards polar solvents should be attributed to the bond conversion of the layers from H bond to covalent bond under UV irradiation.展开更多
文摘Poly(4\|vinyl phenol) (PVPh) was synthesized from anisaldehyde via Perkin Doebner and decarboxyl reactions to form 4 methoxy styrene.It was then polymerized by free radical polymerization following dealkylation to form PVPh.A kind of stable multilayer utra thin film was successfully fabricated via self assembly technique from PVPh and diazoresin (DR) followed by UV irradiation.The driving force of self assembly was confirmed to be the hydrogen bonding attraction from diazonium group(—N + 2)of DR and phenolic hydroxy group(—Ph—OH)of PVPh.The film becomes very stable towards polar solvents after UV irradiation and it is believed that the H bonds between the layers of the film converts to covalent bonds following the decomposition of —N + 2 groups when the multilayer film underwent UV irradiation.
文摘Through self assembly technique, a new type of layer by layer ultra thin film was fabricated based on water soluble substituted polyaniline and photosensitive diazoresin through electrostatic attraction. Under UV irradiation, the bond nature between layers turns from ionic to covalent following the decomposition of diazonium group, and the film gets very stable. The photoelectric conversion property of substituted polyaniline containing self assembled film has also been investigated in this article.
文摘On the substrate of modified quartz, two kinds of self assembled ultra thin films were fabricated through layer by layer electrostatic deposition with diazoresin′s sulfonate(DRS) as the polyanion, and chitosan(CS) as the polycation. The self assembly process was monitored by UV Vis spectra and confirmed that the layer by layer deposition takes place regularly. The films obtained both from DRS, CS(CS/DRS film) and from DR, DRS, CS(DR/DRS/CS/DRS film) were photo sensitive. Under irradiation of ultraviolet light, the stability of the films towards polar solvents increases significantly. The kinetic study shows that the rate of the photodecomposition reaction of DR/DRS/CS/DRS films is higher than that of CS/DRS films and doesnt show the first order reaction for both films.
文摘A novel multiplayer film was assembled from poly[(4 carboxyphenyl)acetylene](PCPA) and diazoresin(DR) in aqueous solution via electrostatic attraction. Under UV irradiation, following the decomposition of diazonium group between the adjacent interfaces of the multiplayers, the ionic bonds of the self assembly film convert to covalent bonds and the film becomes very stable toward electrolyte solutions. Thus the photoelectric conversion property of poly[(4 carboxyphenyl)acetylene] containing film can be measured in conventional three electrode photoelectrochemical cell, and 0.5 mol/L KCl solution can be used as the supporting electrolyte. The photocurrent spectroscopy responses coincide with the absorption spectrum of the irradiated self assembly film, which indicates that the irradiated DR/PCPA film is responsible for the photocurrent generation.
文摘The self assembly between diazoresin(DR) and the homopolymer or copolymers of 4 N hydroxyphenyl acrylamide(NHPA) has been investigated.It was confirmed that the driven force of the assembly is H bonding attraction, in which the DR plays a role of H acceptor, while the NHPA polymers act as a H donor, Under UV, the multiayer films become very stable towards polar solvents. For example, no any change was observed when the irradiated film was immersed in DMF at 20 ℃ for 12 h, but the unirradiated film was destroyled completely when it was immersed in DMF at the same temperature for 20 min. The dramatically improvement for the stability of the film towards polar solvents should be attributed to the bond conversion of the layers from H bond to covalent bond under UV irradiation.
