Chen Chunyan, Wang Jie, Loch Cheryl L, Ahn Dongchan, Chen Zhan
Department of Macromolecular Science and Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
J Am Chem Soc. 2004 Feb 4;126(4):1174-9. doi: 10.1021/ja0390911.
In this paper, the feasibility of monitoring molecular structures at a moving polymer/liquid interface by sum frequency generation (SFG) vibrational spectroscopy has been demonstrated. N-(2-Aminoethyl)-3-aminopropyltrimethoxysilane (AATM, NH2(CH2)2NH(CH2)3Si(OCH3)3) has been brought into contact with a deuterated poly(methyl methacrylate) (d-PMMA) film, and the interfacial silane structure has been monitored using SFG. Upon initial contact, the SFG spectra can be detected, but as time progresses, the spectral intensity changes and finally disappears. Additional experiments indicate that these silane molecules can diffuse into the polymer film and the detected SFG signals are actually from the moving polymer/silane interface. Our results show that the molecular order of the polymer/silane interface exists during the entire diffusion process and is lost when the silane molecules traverse through the thickness of the d-PMMA film. The loss of the SFG signal is due to the formation of a new disordered substrate/silane interface, which contributes no detectable SFG signal. The kinetics of the diffusion of the silane into the polymer have been deduced from the time-dependent SFG signals detected from the AATM molecules as they diffuse through polymer films of different thickness.
本文证明了通过和频产生(SFG)振动光谱监测移动的聚合物/液体界面处分子结构的可行性。已使N-(2-氨乙基)-3-氨丙基三甲氧基硅烷(AATM,NH2(CH2)2NH(CH2)3Si(OCH3)3)与氘代聚甲基丙烯酸甲酯(d-PMMA)薄膜接触,并使用SFG监测界面硅烷结构。初始接触时,可以检测到SFG光谱,但随着时间的推移,光谱强度发生变化并最终消失。额外的实验表明,这些硅烷分子可以扩散到聚合物薄膜中,检测到的SFG信号实际上来自移动的聚合物/硅烷界面。我们的结果表明,聚合物/硅烷界面的分子有序性在整个扩散过程中都存在,而当硅烷分子穿过d-PMMA薄膜的厚度时会消失。SFG信号的消失是由于形成了新的无序基底/硅烷界面,该界面不产生可检测的SFG信号。从AATM分子扩散穿过不同厚度聚合物薄膜时检测到的随时间变化的SFG信号推导出了硅烷扩散到聚合物中的动力学。