Immobilization of dendrimers on Si-C linked carboxylic acid-terminated monolayers on silicon(111)

被引:25
作者
Bocking, Till
Wong, Elicia L. S.
James, Michael
Watson, Jolanta A.
Brown, Christopher L.
Chilcott, Terry C.
Barrow, Kevin D.
Coster, Hans G. L. [1 ]
机构
[1] Univ Sydney, Dept Chem & Biomol Engn, Sydney, NSW 2006, Australia
[2] Univ New S Wales, Sch Phys, Sydney, NSW 2052, Australia
[3] Australian Nucl Sci & Technol Org, Lucas Hts Res Lab, Lucas Heights, NSW 2234, Australia
[4] Griffith Univ, Nanoscale Sci & Technol Ctr, Sch Sci, Nathan, Qld 4111, Australia
[5] Univ New S Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW 2052, Australia
关键词
dendrimers; organic monolayers; silicon; structural properties; POLY(AMIDOAMINE) DENDRIMERS; SURFACE; GOLD; NANOPARTICLES; ADSORPTION; 1-ALKENES; FILMS; ALKYL;
D O I
10.1016/j.tsf.2006.07.017
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Poly(amidoamine) dendrimers were attached to activated undecanoic acid monolayers, covalently linked to smooth silicon surfaces via Si-C bonds. The resulting ultra-thin dendrimer films were characterized by X-ray photoelectron spectroscopy (XPS), X-ray reflectometry (XR) and atomic force microscopy (AFM). XPS results suggested amide bond formation between the dendrimer and the surface carboxylic acid groups. XR yielded thicknesses of 10 angstrom for the alkyl region of the undecanoic acid monolayer and 12 A for the dendrimer layer, considerably smaller than the diameter of these spherical macromolecules in solution. This was consistent with AFM images showing collapsed dendrimers on the surface. It was concluded that the deformation arose from a large number of amine groups on the surface of each dendrimer reacting efficiently with the activated surface, whereby the dendrimers can deform to fill voids while spreading over the activated surface to form a homogeneous macromolecular layer. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1857 / 1863
页数:7
相关论文
共 32 条
[1]   Particle monolayers formed under irreversible conditions: jamming coverages and structure [J].
Adamczyk, Z ;
Weronski, P ;
Siwek, B ;
Zembala, M .
TOPICS IN CATALYSIS, 2000, 11 (1-4) :435-449
[2]   Dendrimer-modified silicon oxide surfaces as platforms for the deposition of gold and silver colloid monolayers: Preparation method, characterization, and correlation between microstructure and optical properties [J].
Bar, G ;
Rubin, S ;
Cutts, RW ;
Taylor, TN ;
Zawodzinski, TA .
LANGMUIR, 1996, 12 (05) :1172-1179
[3]   Surface characterization and electrochemical properties of alkyl, fluorinated alkyl, and alkoxy monolayers on silicon [J].
Barrelet, CJ ;
Robinson, DB ;
Cheng, J ;
Hunt, TP ;
Quate, CF ;
Chidsey, CED .
LANGMUIR, 2001, 17 (11) :3460-3465
[4]   Dendrimers as potential drug carriers; encapsulation of acidic hydrophobes within water soluble PAMAM derivatives [J].
Beezer, AE ;
King, ASH ;
Martin, IK ;
Mitchell, JC ;
Twyman, LJ ;
Wain, CF .
TETRAHEDRON, 2003, 59 (22) :3873-3880
[5]   DNA microarrays with PAMAM dendritic linker systems -: art. no. e10 [J].
Benters, R ;
Niemeyer, CM ;
Drutschmann, D ;
Blohm, D ;
Wöhrle, D .
NUCLEIC ACIDS RESEARCH, 2002, 30 (02) :10
[6]  
Benters R, 2001, CHEMBIOCHEM, V2, P686, DOI 10.1002/1439-7633(20010903)2:9<686::AID-CBIC686>3.0.CO
[7]  
2-S
[8]   Tapping mode atomic force microscopy investigation of poly(amidoamine) dendrimers: Effects of substrate and pH on dendrimer deformation [J].
Betley, TA ;
Holl, MMB ;
Orr, BG ;
Swanson, DR ;
Tomalia, DA ;
Baker, JR .
LANGMUIR, 2001, 17 (09) :2768-2773
[9]   Structural characterization of organic multilayers on silicon(111) formed by immobilization of molecular films on functionalized Si-C linked monolayers [J].
Böcking, T ;
James, M ;
Coster, HGL ;
Chilcott, TC ;
Barrow, KD .
LANGMUIR, 2004, 20 (21) :9227-9235
[10]   Controlled functionalization and multistep chemical manipulation of covalently modified Si(111) surfaces [J].
Boukherroub, R ;
Wayner, DDM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (49) :11513-11515