CHEMICAL MODIFICATION OF FLUORINATED SELF-ASSEMBLED MONOLAYER SURFACES BY LOW-ENERGY REACTIVE ION-BOMBARDMENT

被引:42
作者
PRADEEP, T
FENG, B
AST, T
PATRICK, JS
COOKS, RG
PACHUTA, SJ
机构
[1] PURDUE UNIV,DEPT CHEM,W LAFAYETTE,IN 47907
[2] THREE M CO,CORP RES LABS,ST PAUL,MN 55144
基金
美国国家科学基金会;
关键词
D O I
10.1016/1044-0305(94)00110-L
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Reactive collisions of low energy (<100-eV) mass-selected ions are used to chemically modify fluorinated self-assembled monolayer surfaces comprised of alkanethiolate chains CF3(CF2)(11)(CH2)(2)S- bound to Au. Typical experiments were done by using 1-nA/cm(2) beams and submonolayer doses of reactant ions. Characterization of the modified surface was achieved by in situ chemical sputtering (60-eV Xe-+.) and by independent high mass resolution time-of-flight-secondary ionization mass spectrometry (TOF-SIMS) (15-25-keV, Ga+) experiments. Treatment with (SiCl4+.)-Cl-35 produced a surface from which Xe-+. sputtering liberated (CF2Cl+)-Cl-35 ions, Which suggested Cl-for-F halogen exchange at the surface. Isotopic labeling studies that used (SiCl2C2+.)-Cl-35, and experiments with bromine-containing and iodine-containing projectiles, confirmed this reaction. High mass resolution TOF-SIMS spectra, as well as high spatial resolution images, provided further evidence as to the existence of halogen-exchanged species at the bombarded surface. Analogous Cl-for-F halogen substitution was observed in a model gas-phase reaction. The ion-surface reaction is suggested to proceed through an intermediate fluoronium ion in which the projectile is bonded to the target molecule. The most significant conclusion of the study is that selective chemical modification of monolayer surfaces can be achieved by using reactive ion beams, which lead to new covalent bonds at the surface and in the scattered ions.
引用
收藏
页码:187 / 194
页数:8
相关论文
共 48 条
  • [41] NEUTRALIZATION OF FAST MOLECULAR-IONS H2+ AND N2+ AT SURFACES
    WILLERDING, B
    HEILAND, W
    SNOWDON, KJ
    [J]. PHYSICAL REVIEW LETTERS, 1984, 53 (21) : 2031 - 2034
  • [42] SURFACE-INDUCED DISSOCIATION OF PEPTIDE IONS IN FOURIER-TRANSFORM MASS-SPECTROMETRY
    WILLIAMS, ER
    HENRY, KD
    MCLAFFERTY, FW
    SHABANOWITZ, J
    HUNT, DF
    [J]. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1990, 1 (05) : 413 - 416
  • [43] ION PICKUP OF LARGE, SURFACE-ADSORBED MOLECULES - A DEMONSTRATION OF THE ELEY-RIDEAL MECHANISM
    WILLIAMS, ER
    JONES, GC
    FANG, L
    ZARE, RN
    GARRISON, BJ
    BRENNER, DW
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (09) : 3207 - 3210
  • [44] WILSON RG, 1973, ION BEAMS APPLICATIO
  • [45] HYBRID BEEQ TANDEM MASS-SPECTROMETER FOR THE STUDY OF ION SURFACE COLLISION PROCESSES
    WINGER, BE
    LAUE, HJ
    HORNING, SR
    JULIAN, RK
    LAMMERT, SA
    RIEDERER, DE
    COOKS, RG
    [J]. REVIEW OF SCIENTIFIC INSTRUMENTS, 1992, 63 (12) : 5613 - 5625
  • [46] SURFACE-INDUCED DISSOCIATION MASS-SPECTRA OF PROTONATED PEPTIDES USING A 4-SECTOR MASS-SPECTROMETER
    WRIGHT, AD
    DESPEYROUX, D
    JENNINGS, KR
    EVANS, S
    RIDDOCH, A
    [J]. ORGANIC MASS SPECTROMETRY, 1992, 27 (04): : 525 - 526
  • [47] REACTIVE SCATTERING, SPUTTERING, AND DISSOCIATION OF 32-EV PYRIDINE IONS COLLIDING WITH CLEAN AND PYRIDINE-COVERED AG(111)
    WU, QY
    HANLEY, L
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (11) : 2677 - 2685
  • [48] SURFACE-INDUCED DISSOCIATION IN TANDEM QUADRUPOLE MASS SPECTROMETERS - A COMPARISON OF 3 DESIGNS
    WYSOCKI, VH
    DING, JM
    JONES, JL
    CALLAHAN, JH
    KING, FL
    [J]. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1992, 3 (01) : 27 - 32