翁志焕

个人信息Personal Information

教授

博士生导师

硕士生导师

任职 : 高分子材料教研室副主任,高分子材料系教工党支部副书记

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:高分子材料. 高分子化学与物理

办公地点:化工实验楼A402-2

联系方式:zweng@dlut.edu.cn

电子邮箱:zweng@dlut.edu.cn

扫描关注

论文成果

当前位置: 绿色高性能高分子材料 >> 科学研究 >> 论文成果

Construction of flexible and stable near-infrared absorbing polymer films containing nickel-bis(dithiolene) moieties via ligand-exchange post-polymerization modification

点击次数:

论文类型:期刊论文

发表时间:2017-07-21

发表刊物:POLYMER CHEMISTRY

卷号:8

期号:27

页面范围:3977-3991

ISSN号:1759-9954

摘要:Flexible and stable near-infrared (NIR) absorbing polymer films were prepared from the corresponding poly(aryl ether) precursors through subsequent ligand-exchange post-polymerization modification. The additional ligand triggers the ligand-exchange reaction during the post-polymerization modification process, which can significantly enhance the polymer yield, as well as the coordination ratio of the nickel-bis(dithiolene) segment in the polymer backbone by suppressing cross-linking side reactions. The presented ligand-exchange post-polymerization modification overcomes the limitations of the post-polymerization modification reaction, i.e. a high degree of cross-linking between the same reactive groups, and enhances the modification methods of analogous polymers. Upon incorporating the nickel-bis(dithiolene) moiety into the polymer backbone, the resulting polymers exhibit both strong near-infrared absorption at approximately 1200 nm with epsilon > 10(4) mol(-1) L cm(-1) in an NMP solution and excellent freestanding film formation properties. The long-term aging-resistance test indicates that the incorporation of the nickel-bis(dithiolene) moiety into the polymer chain via chemical bonding is superior to physical blending for stabilizing the nickel-bis(dithiolene) moiety. Although the absorbance of the micromolecular NIR dyes Ni-O and Ni-N at the maximum wavelength gradually decreased up to 34% during the aging test (70 degrees C for 144 h), it should be noted that the NiO-P6 (10 mol% nickel-bis(dithiolene) segments) and NiN-P8 (34 mol% nickel-bis(dithiolene) segments) polymer films exhibited no decrease in the NIR absorption range. Finally, this work shows that the post-polymerization modification between the same reactive groups could also be an effective approach to install functional groups in a polymer backbone while avoiding a high degree of cross-linking side reactions, as well as offers an approach to design near-infrared absorbing polymeric materials with balanced near-infrared absorption and solution-processing properties.