Ujihara Masaki, Imae Toyoko
Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan.
J Colloid Interface Sci. 2006 Jan 15;293(2):333-41. doi: 10.1016/j.jcis.2005.06.041. Epub 2005 Jul 26.
Adsorption behaviors of functional poly(amido amine) dendrimers with an azacrown core and long alkyl chain spacers were investigated on gold and self-assembled monolayer (SAM) by means of time course attenuated total reflection-surface enhanced infrared absorption and surface plasmon resonance spectroscopies. While 1.5th and 2.5th generation (G1.5 and G2.5) ester-terminated dendrimers were slightly adsorbed on all substrates examined, the adsorption of G2 amine-terminated dendrimer increased in the order dodecanethiol SAM<bare gold<3-mercaptopropionic acid (MPA) SAM. The time course results also revealed that the G2 dendrimer displayed the steep increase of adsorption on the bare gold, followed by the slight progress of adsorption. G2 dendrimers adsorbed on MPA SAM involved their subsequent conformational rearrangement, while the adsorption equilibrium was quickly attained for G3 dendrimer on the MPA SAM. It was supported that G3 dendrimer was adsorbed with the perpendicularly extended structure on the MPA SAM substrate, and G2 dendrimer varied its conformation from the globular structure to the extended one perpendicular to the substrate.
通过时间进程衰减全反射-表面增强红外吸收光谱和表面等离子体共振光谱,研究了具有氮杂冠醚核心和长烷基链间隔基的功能性聚(酰胺胺)树枝状大分子在金和自组装单分子层(SAM)上的吸附行为。虽然第1.5代和第2.5代(G1.5和G2.5)酯端基树枝状大分子在所有测试的基底上都有轻微吸附,但G2胺端基树枝状大分子的吸附量按十二烷硫醇SAM<裸金<3-巯基丙酸(MPA)SAM的顺序增加。时间进程结果还表明,G2树枝状大分子在裸金上的吸附量急剧增加,随后吸附量略有增加。吸附在MPA SAM上的G2树枝状大分子涉及随后的构象重排,而G3树枝状大分子在MPA SAM上很快达到吸附平衡。有证据表明,G3树枝状大分子以垂直伸展结构吸附在MPA SAM基底上,而G2树枝状大分子的构象从球状结构变为垂直于基底的伸展结构。