An acrylic monomer having phenoxazine moiety, i.e., N-acryloylphenoxazine (APO), has been synthesized by dehydrochlorination of N-(3-chloropropionyl)phenoxazine with 1,5-diazabicyclo[5.4.0]undec-5-ene in dimethyl sulfoxide. The monomer can be polymerized with AIBN as an initiator. The photochemical
Vinyl monomers bearing chromophore moieties and their polymers. VII. Synthesis, photochemical, and initiation behavior of acrylic monomers bearing phenothiazine oxide moieties and their polymers
β Scribed by Xiang-Qian Liu; Fu-Sheng Du; Zi-Chen Li; Fu-Mian Li; Qing-Yu Gao; Geng-Xu Yang; Ju-Xian Zhang
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 203 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
β¦ Synopsis
Four acrylic monomers bearing phenothiazine oxide moieties, that is, N-acryloyl-phenothiazine-5-oxide (APTO), N-acryloyl-2-chlorophenothiazine-5-oxide (ACPTO), N-acryloyl-phenothiazine-5,5-dioxide (APTDO), and N-acryloyl-2-chlorophenothiazine-5,5-dioxide (ACPTDO) were synthesized by oxidation of corresponding Nacryloyl-phenothiazine (APT) and N-acryloyl-2-chlorophenothiazine (ACPT) using sodium perborate as an oxidant. These monomers could easily be polymerized by initiation of AIBN. The emission fluorescence spectra of the monomers and their polymers were recorded, and the results indicated that these 4 new monomers possess a fluorescence structural self-quenching effect (SSQE), as we have reported previously. Moreover, with the change of the electronic structure of sulfur atom in the phenothiazine chromophore, that is, from sulfide to sulfoxide and sulfone groups, the tendency of SSQE of these monomers is in the order of APT ΟΎ APTO ΟΎ APTDO. This would be ascribed mainly to the decrease of electron-donating abilities of monomers in a sequence of sulfide, sulfoxide, and sulfone groups; that is, at the sulfur atom of these monomers, APT has 2 lone-pair electrons, APTO has 1 lone-pair electrons, and APTDO completely loses its lone-pair electrons. Based on the exciplex formation, the monomers APTO, APTDO, ACPO, and ACPTDO could act as sensitizers for the photopolymerization of acrylonitrile (AN). The combination of APTO or ACPTO with organic peroxides such as BPO could also initiate the polymerization of vinyl monomers, such as AN, by redox nature.
π SIMILAR VOLUMES
Two acrylic monomers bearing a pyrimidinyl moiety, N-acryloyl-NΠ-2-pyrimidinylpiperazine (APMP) and N-methacryloyl-NΠ-2-pyrimidinylpiperazine (MPMP), are prepared by reactions of N-2-pyrimidinylpiperazine with corresponding acryloyl chlorides in the presence of triethylamine. APMP and MPMP can be po
Three carbazole-containing methacrylic monomers, 2-(N-carbazolyl)ethyl methacrylate(CzEMA), 6-(N-carbazolyl)hexyl methacrylate(CzHMA), and 11-(N-carbazolyl)undecyl methacrylate (CzUMA), and their saturated model compounds, 2-(Ncarbazolyl)ethyl isobutyrate, 6-(N-carbazolyl)hexyl isobutyrate, and 11-(
Two novel acrylic monomers bearing aromatic tertiary amino groups, i.e., N-acryloyl-Nphenylpiperazine (APP) and N-methacryloyl-N'-phenylpiperazine (MPP) are synthesized by the reaction of N-phenylpiperazine and the corresponding acryloyl chlorides in the presence of triethylamine. They can be polyme
Acrylic monomers bearing electron-donating quinolyl moiety, i.e., 8-acryloyloxyquinoline (AQ) was prepared and polymerized. It was found that the fluorescence intensity of AQ was much lower than that of P(AQ) at the same chromophore concentration. The fluorescence of P(AQ) could be quenched by elect