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PARTICLE-INDUCED DESORPTION OF PARTICLE-INDUCED DESORPTION OF BENZOHYDROXAMIC ACID DERIVATIVES BENZOHYDROXAMIC ACID DERIVATIVES ADSORBED ON A COPPER SURFACE ADSORBED ON A COPPER SURFACE STUDIED BY LASER IONIZATION MASS STUDIED BY LASER IONIZATION MASS SPECTROMETRY SPECTROMETRY S.Wyczawska S.Wyczawska 1 1 , E. Vandeweert , E. Vandeweert 1 , R. E. Silverans , R. E. Silverans 1 , P. Lievens , P. Lievens 1 , O.Blajiev , O.Blajiev 2 , , A. Hubin A. Hubin 2 and H. Terryn and H. Terryn 2 1 - - Laboratory of Solid State and Magnetism, Katholieke Katholieke Universiteit Leuven, Universiteit Leuven, 2 - - Department of Metallurgy, Electrochemistry and Materials Science Faculty of Applied Science, Vrije Universiteit Brussel LAP 2006, 10 – 15 SEP 200

LAP 2006, 10 – 15 SEP 2006

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PARTICLE-INDUCED DESORPTION OF BENZOHYDROXAMIC ACID DERIVATIVES ADSORBED ON A COPPER SURFACE STUDIED BY LASER IONIZATION MASS SPECTROMETRY. S.Wyczawska 1 , E. Vandeweert 1 , R. E. Silverans 1 , P. Lievens 1 , O.Blajiev 2 , A. Hubin 2 and H. Terryn 2 - PowerPoint PPT Presentation

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Page 1: LAP 2006, 10 – 15 SEP 2006

PARTICLE-INDUCED DESORPTION PARTICLE-INDUCED DESORPTION OF BENZOHYDROXAMIC ACID OF BENZOHYDROXAMIC ACID DERIVATIVES ADSORBED ON A DERIVATIVES ADSORBED ON A COPPER SURFACE STUDIED BY COPPER SURFACE STUDIED BY

LASER IONIZATION MASS LASER IONIZATION MASS SPECTROMETRYSPECTROMETRY

S.WyczawskaS.Wyczawska11, E. Vandeweert, E. Vandeweert11, R. E. Silverans, R. E. Silverans11, P. Lievens, P. Lievens11, ,

O.BlajievO.Blajiev22, A. Hubin, A. Hubin22 and H. Terrynand H. Terryn22

11 - - Laboratory of Solid State and Magnetism, Katholieke Universiteit Leuven, Katholieke Universiteit Leuven,22 - - Department of Metallurgy, Electrochemistry and Materials Science Faculty of Applied Science, Vrije Universiteit Brussel LAP 2006, 10 – 15 SEP 2006

Page 2: LAP 2006, 10 – 15 SEP 2006

BHABHA

benzohydroxamic acidsbenzohydroxamic acids Formula - Formula - CC77HH77NONO22

Page 3: LAP 2006, 10 – 15 SEP 2006

BHABHA

Hydroxamic acids and derivatives aHydroxamic acids and derivatives are re important molecules in:important molecules in:

biologybiology: antibacterial and antifungal : antibacterial and antifungal agents, enzyme inhibitors;agents, enzyme inhibitors;

medicinemedicine: anticancer agents, anemia : anticancer agents, anemia treatments, antibiotics;treatments, antibiotics;

industryindustry: pharmaceutical, corrosion : pharmaceutical, corrosion inhibitorsinhibitors..

Page 4: LAP 2006, 10 – 15 SEP 2006

BHABHA

Z- amide (water, methanol)

E –amide (acetone, methanol)

B.Garcia, et. al, Inorganic Chemistry 2005 (44) 2908

Page 5: LAP 2006, 10 – 15 SEP 2006

BHABHA

BHA p-CL-BHA

p-metoxy-BHA p-nitro-BHA

- H

- C

- O

- N

- Cl

Page 6: LAP 2006, 10 – 15 SEP 2006

OutlineOutline

BHABHA Sample preparation processSample preparation process Apparatus and measurements Apparatus and measurements

techniquestechniques MassMass spectra and flight time spectra and flight time

distributionsdistributions Summary Summary

Page 7: LAP 2006, 10 – 15 SEP 2006

Electro polishing Electro polishing processprocess

electric electric current passes current passes through through submerged submerged workpieceworkpiece

VUB - Brussels

CopperCopper

85% H3PO4

Page 8: LAP 2006, 10 – 15 SEP 2006

SpincoatingSpincoating

fluid resin fluid resin deposited in deposited in centre of centre of substratesubstrate

spun at high spun at high speed ± 3000 speed ± 3000 rpm.rpm.

VUB - Brussels

Page 9: LAP 2006, 10 – 15 SEP 2006

Measurement Measurement techniquetechnique

Ar+ ions

substrate

Page 10: LAP 2006, 10 – 15 SEP 2006

Measurement Measurement techniquetechnique

laser pulse

++

+

+

+ +

substrate

Ar+ ions

detector

Δt

K.E. selection

Mass selection

Page 11: LAP 2006, 10 – 15 SEP 2006

Measurements Measurements techniquetechnique

Neutral particles sputtered from the Neutral particles sputtered from the surface are ionized by pulsed laser surface are ionized by pulsed laser beam:beam:

resonance enhancementresonance enhancement

non-resonant ionizationnon-resonant ionization

Virtual level

Electronic ground state

Excited state (intermediate)

Ionization potential

Page 12: LAP 2006, 10 – 15 SEP 2006

ApparatusApparatus

Page 13: LAP 2006, 10 – 15 SEP 2006

ApparatusApparatus

Ion beam:Ion beam: - 15 keV Ar- 15 keV Ar++ ions bombardment ions bombardment;; - Ion current - 1 µA → ion fluence = 10- Ion current - 1 µA → ion fluence = 1011 11 ions/cmions/cm22;; Laser beam:Laser beam: - Resonant enhanced multiphoton ionization of benzene - Resonant enhanced multiphoton ionization of benzene

ring ring λ= 259 nm;λ= 259 nm; - Non-resonant ionization of Cu;- Non-resonant ionization of Cu; - Laser energy – 1 mJpp → - Laser energy – 1 mJpp → photon fluence = photon fluence = 101018 18

photons/cmphotons/cm22;; Detection: Time of Flight Mass Spectrometry; Detection: Time of Flight Mass Spectrometry; Base vacuum – around 10Base vacuum – around 10-9 -9 hPa;hPa;

Page 14: LAP 2006, 10 – 15 SEP 2006

ApparatusApparatus

Ion Gun

Manipulator with Sample Holder

Detector

Laser beam

Page 15: LAP 2006, 10 – 15 SEP 2006

Spectra Physics – MOPO-730

Page 16: LAP 2006, 10 – 15 SEP 2006

Our interestOur interest

new kind of organic layer;new kind of organic layer; orientation on the surface;orientation on the surface; BHA as non toxic corrosion BHA as non toxic corrosion

inhibitor (passivation);inhibitor (passivation); solvents and substituents solvents and substituents

dependent;dependent;

Page 17: LAP 2006, 10 – 15 SEP 2006

Mass spectraMass spectra

20 40 60 80 100 120 140

-0.042

-0.040

-0.038

-0.036

-0.034

-0.032

-0.030

-0.028

-0.026

14

24

27

2830

37

39

40

5052

56

63

6578

91 103

108

118124

133

218 241

263

average of all measurements for p-methoxy BHA/water

sign

al [

arb.

u.]

mass [amu]

Cubenzeneheavy masses

Page 18: LAP 2006, 10 – 15 SEP 2006

Mass spectraMass spectra

20 40 60 80 100 120 140

-0.011

-0.010

-0.009

-0.008

-0.007

-0.006

14

2730

37

39

5052

56

63

78

9194130

65

sign

al [

arb.

u.]

mass [amu]

BHA/waterfull average

20 40 60 80 100 120 140

-0.022

-0.021

-0.020

-0.019

-0.018

2427

2829 37

38

40

51

53

56

63

6578

92

sign

al [

arb.

u.]

mass [amu]

BHA/methanolFull average

organic molecules fragments in both cases: 78, 91; a bit less amount of organic material on MeOH dissolved samples

N

O

OH

H

Page 19: LAP 2006, 10 – 15 SEP 2006

Mass spectraMass spectra

20 40 60 80 100 120 140

-0.013

-0.012

-0.011

-0.010

-0.009

-0.008

2831

34

36

3840

51

52

56

63

65

6878

798192

98

sign

al [

arb.

u.]

mass [amu]

p-Cl-BHA/waterfull average

20 40 60 80 100 120 140-0.008

-0.007

-0.006

-0.005

-0.004

13

252627

36

38

40 50

52

56

59

63

6571

79

93104

115

sign

al [

arb.

u.]

mass [amu]

p-Cl-BHA/methanolfull average

organic molecules fragments: 78, 92; less organic signal from MeOH dissolved samples;

N

O

OH

ClH

Page 20: LAP 2006, 10 – 15 SEP 2006

Mass spectraMass spectra

20 40 60 80 100 120 140

-0.042

-0.040

-0.038

-0.036

-0.034

-0.032

-0.030

-0.028

-0.026

14

24

27

2830

37

39

40

5052

56

63

6578

91 103

108

118124

133

218 241

263

average of all measurements for p-methoxy BHA/water

sign

al [

arb.

u.]

mass [amu]

20 40 60 80 100 120 140

-0.020

-0.019

-0.018

-0.017

-0.016

15

27

29

30

37

40

42

52

56

63

6578

83 9297105 120

130133

sign

al [

arb.

u.]

mass [amu]

p-methoxy_BHA/methanolfull average

organic molecules fragments from H2O dissolved samples: 65, 78, 91, 104, 108, 118, 133 amu; a few signal from p-methoxy-BHA/MeOH samples; the best covered copper surface by molecules dissolved from water solution;

CN

O

OH

OH3C H

Page 21: LAP 2006, 10 – 15 SEP 2006

Mass spectraMass spectra

20 40 60 80 100 120 140

-0.019

-0.018

-0.017

-0.016

-0.015

13

25

27

29

38

41 51

52

56

63

6580

9194110

123

sig

na

l [a

rb.u

.]

mass [amu]

p-nitro_BHA/waterfull average

20 40 60 80 100 120 140

-0.042

-0.041

-0.040

-0.039

-0.038

-0.037

-0.036

14

26

27

37

39

4150

52

56

63

65

70

78

91108

116 128134

sign

al [

arb.

u.]

mass [amu]

p-nitro-BHA/methanolfull average

N

O

OH

NO2H

organic molecules fragments from MeOH: 78, 92, 108; a little amount of material from water dissolved surface; most probably more than one possible orientation on the surface;

Page 22: LAP 2006, 10 – 15 SEP 2006

Flight time distribution Flight time distribution

A

FT [µs]

T

W A – maximum amplitude of flight time distribution

T – flight time (FT) at maximum amplitude

W – FWHM of flight time distribution

Page 23: LAP 2006, 10 – 15 SEP 2006

CopperCopper

0 2 4 6 8 100.00

0.01

0.02

0.03

0.04

0.05

0.06

Cu/H2O

ion

sign

al [a

rb. u

.]

flight time [µs]

Cu63 Cu65

0 2 4 6 8 100.00

0.05

0.10

0.15

0.20

0.25

0.30

0.35

Cu/MeOH

flight time [µs]

Cu63 Cu65

Cu isotopes:63 amu – 69%65 amu – 31%

- copper distribution doesn’t depend on solvent;- max. of FT – 2 µs;

Page 24: LAP 2006, 10 – 15 SEP 2006

p-Cl-BHAp-Cl-BHA//CuCu

0 5 10 15 20 25 30

0.002

0.004

0.006

0.008

0.010

0.012

p-Cl-BHA/H2O

ion

sig

na

l [a

rb.

u.]

flight time [µs]

63 65

0 5 10 15 20 25 30

0.002

0.004

0.006

0.008

0.010

0.012

0.014

0.016

0.018

p-Cl-BHA/MeOH

ion

sign

al [

arb.

u.]

flight time [µs]

63 65

- H2O dissolved - distribution of copper is broader and shifted to lower kinetic energies;-MeOH dissolved – the same as for pure copper;

Page 25: LAP 2006, 10 – 15 SEP 2006

Maximum of FT Maximum of FT distributiondistribution

Cu BHA Cl-BHA methoxy-BHAnitro-BHA

2

4

6

8

10

Cu 63

time

of d

elay

[µs]

sample

water methanol

samples dissolved in methanol show small changes in distribution; copper from water dissolved samples is sputtered with lower kinetic energy; p-nitro-BHA behaves different than the others samples;

Page 26: LAP 2006, 10 – 15 SEP 2006

SummarySummary

1. Water dissolved: 1. Water dissolved:

Cu surface well covered by organic Cu surface well covered by organic molecules for BHA and p-methoxy-molecules for BHA and p-methoxy-BHA BHA

2. Methanol dissolved:2. Methanol dissolved:small density of molecules or only small density of molecules or only fragments of molecules on the fragments of molecules on the surfacesurface

Page 27: LAP 2006, 10 – 15 SEP 2006

SummarySummary

3. Samples with p-nitro-BHA in MeOH 3. Samples with p-nitro-BHA in MeOH show a distinct velocity distribution show a distinct velocity distribution

4. Organic layer formation is solvent 4. Organic layer formation is solvent dependent: dependent: water is the best solvent for sample water is the best solvent for sample preparation (except for p-nitro-BHA)preparation (except for p-nitro-BHA)

Page 28: LAP 2006, 10 – 15 SEP 2006

Thank youThank you