发光学报
髮光學報
발광학보
CHINESE JOURNAL OF LUMINESCENCE
2014年
7期
777-784
,共8页
罗春华%董秋静%王丹%张宏%陶栋梁%崔玉民
囉春華%董鞦靜%王丹%張宏%陶棟樑%崔玉民
라춘화%동추정%왕단%장굉%도동량%최옥민
聚(甲基)丙烯酸酯%光交联%查尔酮%荧光
聚(甲基)丙烯痠酯%光交聯%查爾酮%熒光
취(갑기)병희산지%광교련%사이동%형광
poly( meth) acrylates%photocrosslink%chalcone%fluorescence
采用红外光谱、热重分析、紫外光谱和荧光光谱对侧链含查尔酮基团的聚(4-甲基丙烯酰氧基-4忆-二甲氨基查尔酮)(PMADMAC)和聚(4-丙烯酰氧基查尔酮)(PAC)的光交联特性进行了研究。随着光照时间的增加,PMADMAC和PAC聚合物光致环加成反应迅速进行,波长短的紫外线更易使得聚合物发生[2+2]环加成反应。与溶液状态相比,固体薄膜状态下的光交联反应速率较慢。 PMADMAC聚合物更容易发生光致环加成反应,其光交联速率要比PAC聚合物快,环加成反应也更彻底。采用荧光光谱研究了聚合物的发光特性,发现PAC聚合物无荧光,而PMADMAC聚合物具有溶剂极性敏感的荧光特性。在PMADMAC聚合物的稀溶液中,随着365 nm 紫外光照时间的增加,荧光强度迅速降低,其荧光特征波长在紫外光照射后发生蓝移。PMADMAC和PAC聚合物的热稳定性较好,光交联后形成热不稳定的环丁烷结构,其热稳定性有所降低。
採用紅外光譜、熱重分析、紫外光譜和熒光光譜對側鏈含查爾酮基糰的聚(4-甲基丙烯酰氧基-4憶-二甲氨基查爾酮)(PMADMAC)和聚(4-丙烯酰氧基查爾酮)(PAC)的光交聯特性進行瞭研究。隨著光照時間的增加,PMADMAC和PAC聚閤物光緻環加成反應迅速進行,波長短的紫外線更易使得聚閤物髮生[2+2]環加成反應。與溶液狀態相比,固體薄膜狀態下的光交聯反應速率較慢。 PMADMAC聚閤物更容易髮生光緻環加成反應,其光交聯速率要比PAC聚閤物快,環加成反應也更徹底。採用熒光光譜研究瞭聚閤物的髮光特性,髮現PAC聚閤物無熒光,而PMADMAC聚閤物具有溶劑極性敏感的熒光特性。在PMADMAC聚閤物的稀溶液中,隨著365 nm 紫外光照時間的增加,熒光彊度迅速降低,其熒光特徵波長在紫外光照射後髮生藍移。PMADMAC和PAC聚閤物的熱穩定性較好,光交聯後形成熱不穩定的環丁烷結構,其熱穩定性有所降低。
채용홍외광보、열중분석、자외광보화형광광보대측련함사이동기단적취(4-갑기병희선양기-4억-이갑안기사이동)(PMADMAC)화취(4-병희선양기사이동)(PAC)적광교련특성진행료연구。수착광조시간적증가,PMADMAC화PAC취합물광치배가성반응신속진행,파장단적자외선경역사득취합물발생[2+2]배가성반응。여용액상태상비,고체박막상태하적광교련반응속솔교만。 PMADMAC취합물경용역발생광치배가성반응,기광교련속솔요비PAC취합물쾌,배가성반응야경철저。채용형광광보연구료취합물적발광특성,발현PAC취합물무형광,이PMADMAC취합물구유용제겁성민감적형광특성。재PMADMAC취합물적희용액중,수착365 nm 자외광조시간적증가,형광강도신속강저,기형광특정파장재자외광조사후발생람이。PMADMAC화PAC취합물적열은정성교호,광교련후형성열불은정적배정완결구,기열은정성유소강저。
The photocrosslinking properties of poly ( 4-methacryloyloxy-4’-dimethyl aminochalcone ) ( PMADMAC) and poly(4-acryloyloxychalcone) ( PAC) homopolymers were investigated by Fourier transform infrared spectoscopy ( FT-IR) , thermogravimetric analysis, UV-visible spectroscopy ( UV-Vis) , and fluorescence spectroscopy. Photocrosslinking results of PMADMAC and PAC indicate the photo-induced [2+2] cycloaddition reaction takes place rapidly with the increase of light irradiation time and is carried out easily at presence of shortwave UV light. The photocrosslinking rate of poly-mers in the state of thin film is slower than that of solution due to the limited molecular motion in sol-id. Compared to PAC, the cycloaddition reaction of PMADMAC with intramolecular charge transfer properties takes place more easily and completely, and the photocrosslinking rate more rapidly. The photoluminescent properties were investigated by fluorescence spectroscopic techniques and the re-sults show PMADMAC with solvent polarity sensitive fluorescence and PAC without fluorescence. With the increase of 365 nm UV light irradiation time, the fluorescent intensity of PMADMAC dilute solution decreases drastically and the fluorescent wavelength blueshifts in the late of UV irradiation. Thermogravimetric analysis results show a good thermalstability of PMADMAC and PAC, and a de-crease in thermalstability after the formation of cyclobutane ring by photocrosslinking.