Sonoluminescence and Sonochemistry - School of Chemical Sciences
Sonochemicaland MechanochemicalApplications in · PDF fileLow bass notes Animals Sonochemistry...
Transcript of Sonochemicaland MechanochemicalApplications in · PDF fileLow bass notes Animals Sonochemistry...
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Sonochemical and Mechanochemical Applications in Sonochemical and Mechanochemical Applications in Organic Synthesis
HovigHovig KouyoumdjianKouyoumdjian
Wednesday, March 17, 2010
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Energy sources of chemical reactionsEnergy sources of chemical reactions
PressurePressureMicrowavesMicrowaves
HeatHeat ElectricityElectricity
2https://www.kintera.com/accounttempfiles/account105257/images/heat_thermometer.jpghttp://www.mdpi.org/ecsoc/ecsoc‐6/Papers/E001/E001_files/208_files/Micro.gifhttp://wpcontent.answers.com/wikipedia/commons/thumb/3/39/ElectrochemCell.png/250px‐ElectrochemCell.pnghttp://www.americanairworks.com/images/dial_a_pressure.gif
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Ultrasound: Alternative source of energyUltrasound: Alternative source of energy
• Nanomaterials
S l t h i t• Sonoelectrochemistry
• Organic synthesisOrganic synthesis
• Glassware cleaningUltrasound bathsUltrasound baths
http://www.bransonic.com/pdf/Bransonic%20Brochure.pdf3
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OutlineOutline• Ultrasound (US)
– Definition and backgroundDefinition and background
• Cavitation phenomenon– Characteristics and influencing factors
• A sample of sonochemical reactions in organic synthesis– Kornblum‐Russell reaction
Hetero Michael reaction– Hetero‐Michael reaction– Preparation of Grignard reagent– Suzuki coupling
• Cavitation induced mechanochemistry– Cleavage of azo‐linkages– Reconfiguration of atropisomersg p– Electrocyclic opening of benzocyclobutene
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OutlineOutline• Ultrasound (US)
– Definition and backgroundDefinition and background
• Cavitation phenomenon– Characteristics and influencing factors
• A sample of sonochemical reactions in organic synthesis– Kornblum‐Russell reaction
Hetero Michael reaction– Hetero‐Michael reaction– Preparation of Grignard reagent– Suzuki coupling
• Cavitation induced mechanochemistry– Cleavage of azo‐linkages– Reconfiguration of atropisomersg p– Electrocyclic opening of benzocyclobutene
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Electromagnetic and sound spectrumElectromagnetic and sound spectrum
GammaGammaUltravioletUltravioletRadioRadio XX‐‐raysraysInfraredInfraredMicrowavesMicrowaves
30EHz300PHz3THz3GHz 750THz430THz
SONAR Medical diagnosisHuman speechEarthquake monitoring
30EHz300PHz3THz3GHz 750THz430THz
SONAR
Low bass notes Animals Sonochemistry
Medical diagnosisHuman speechEarthquake monitoring
InfrasoundInfrasound AcousticAcoustic UltrasoundUltrasound
20Hz 20KHz 2MHz 200MHz 6
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Definition of sonochemistryDefinition of sonochemistry
Sonochemistry: A branch of chemical research dealing y gwith the chemical effects and applications of ultrasonic waves, that is, sound with frequencies above 20 kHz th t li b d th li it f h h ithat lie beyond the upper limit of human hearing.
7Luche, J. L. Synthetic Organic Sonochemistry, Plenum Press, New York, 1998, pp. 1–19
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Best known uses of ultrasoundBest known uses of ultrasound• Target detection using SONAR
(SOund NAvigation and Ranging)(SOund NAvigation and Ranging)
• Medical applications:pp– Medicalsonography (ultrasonography)– Acoustic targeted drug delivery
Cleaning teeth in dental hygiene– Cleaning teeth in dental hygiene
• Industrial Applications:– Ultrasonic testing (non‐destructive)– Ultrasonic cleaning
http://www.personal.psu.edu/users/k/g/kgc5007/Project%203%20Active%20Sonar.gifhttp://www.advanceusa.org/blog/content/binary/Ultrasound%202.jpghttp://media.noria.com/sites/archive_images/Backup_200411_Tech‐Ultrasound1.jpg
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Ultrasound instruments for organic h ichemistry
Cup‐horn sonicator Probe sonicator
$2 300‐$5 000$1 200‐$1 600
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$2,300 $5,000$1,200 $1,600
http://www.nano‐lab.com/ultrasonic‐probe‐dispersion‐equipment.html
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Ultrasound reactors in process chemistryUltrasound reactors in process chemistry
UIP16000UIP16000 reactor
Ultrasonic reactor
10http://www.hielscher.com/image/7xuip1000hd_flowcell_p0500.jpghttp://www.hielscher.com/image/uip1000_uip16000_p0500.jpg
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Development of ultrasound in organic synthesisDevelopment of ultrasound in organic synthesis
19301930 Richards and Loomis applied ultrasound (100‐500KHz) in organic synthesis for the first time (1927)
19501950 Renaud reported that certain organometallics could be prepared in shorter reaction times using ultrasound bath (1950)
19801980 Luche reported metal activation reactions using ultrasound probes (1980)
19901990Mason reported switching reactions using ultrasound Cup‐horn instruments (1995)
20052005Wilson and Moore reported biasing chemical reaction pathways using ultrasound (2007)
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Richards, W. T.; Loomis, A. L. J. Am. Chem. Soc. 1927, 49, 3086‐3088Renaud, P. Bull. Soc. Chim. Fr. 1950, 1044‐1048Luche, J.‐L.; Damiano, J. C. J. Am. Chem. Soc. 1980, 102, 7926‐7927.
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OutlineOutline• Ultrasound (US)
– Definition and backgroundDefinition and background
• Cavitation phenomenon– Characteristics and influencing factors
• A sample of sonochemical reactions in organic synthesis– Kornblum‐Russell reaction
Hetero Michael reaction– Hetero‐Michael reaction– Preparation of Grignard reagent– Suzuki coupling
• Cavitation induced mechanochemistry– Cleavage of azo‐linkages– Reconfiguration of atropisomersg p– Electrocyclic opening of benzocyclobutene
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Ultrasound effectsUltrasound effects
• Direct effects:– Ultrasound waves have low Energies (20KHz – 500MHz)
(too low to alter electronic, vibrational, or rotational molecular states)
• Indirect effects:– Ultrasound waves cause cavitation phenomenon which generates higher energy
(enough energy to alter vibrational and rotational molecular states)(enough energy to alter vibrational and rotational molecular states)
Rotational and20KHz‐500KHz Ultrasound waves
Rotational and vibrational alterations
XXCavitation Phenomenon
13Luche, J. L. Synthetic Organic Sonochemistry, Plenum Press, New York, 1998, pp. 1–19
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Cavitation phenomenonCavitation phenomenon
At sufficiently high power:
‐ Pressure wave cycle exceeds thePressure wave cycle exceeds the attractive forces of the molecules
‐ Cavitation bubbles forms
‐ Bubbles grow over a few cycles
‐ Bubbles suffer sudden expansion p
‐ Bubbles collapse violently(energy generation)
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Another way of bubble collapse: i j f iMicrojet formation
S lid f
))))
• Cavitation bubble is trapped between solid surface and liquid flow
Solid surface
)))) Sound waves
Cavitation bubble
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Another way of bubble collapse: i j f i
Mi j
Microjet formation
))))
Microjet• Cavitation bubble is trapped between solid surface and liquid flow
• liquid jet forms (100 m s‐1) )))) Sound waves
liquid jet forms (100 m.s )
• Violent non‐symmetric bubble collapse
• Microjetting is the reason why ultrasound is effective in cleaning
Cavitation bubble
• Microjetting is the reason why ultrasound is effective in cleaning
• Activates surface catalysis
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• Increases mass and heat transfer
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The example of propeller bladesThe example of propeller blades
Negative pressure originate microbubblesNegative pressure originate microbubbles
When collapsing near the metal, they release enough energy to cause erosion to the blade
http://www.tecplot.com/images/showcase/contours/issue_19/01_propeller.jpghttp://www.fractureinvestigations.com/images/prop.jpg 17
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Cavitation bubbleCavitation bubble
Bulk: Intense shear forcesBulk: Intense shear forcesHOHOH ..
2
Interface:Interface:
OOHOH .2
.
22.. OOHOOHOH
Shear forcesShear forces
OHOHH 2..
22.. OHOHOH
Cavity: extreme conditionCavity: extreme condition
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Factors impacting sonochemistryFactors impacting sonochemistry
• Acidity, basicity, dipole moment, etc… do not have significant role in sonochemistry
• Volatility, viscosity, dissolved gases, and surface tension are directly involveddirectly involved
• These factors can be manipulated via two parameters:These factors can be manipulated via two parameters: – Acoustic Pressure (P)– Acoustic Intensity (I)
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Acoustic pressureAcoustic pressure
)2sin()( ftPtP )2sin()( ftPtP AP(t) = pressure at any point of an elastic medium (Pa)PA = acoustic pressure amplitude (Pa) f = frequency of the alternating pressure wave (Hz)t = time (s)
Frequency (KHz scale) amplitude of irradiation constant cavitationFrequency (KHz scale) amplitude of irradiation constant cavitation
Frequency (MHz scale) compression and rarefaction cycles’ duration
1
If compression and rarefaction cycle duration is short, cavitation might be difficult to achieve
20Luche, J. L. Synthetic Organic Sonochemistry, Plenum Press, New York, 1998, pp. 1–19
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Frequency time relationFrequency time relation
• Frequency influences the timeFrequency influences the time taken by a bubble to collapse
• High frequency (500 KHz)HOHOH ..
2 • High frequency (500 KHz)
– Collapse time is 400 ns– Less than the lifetime of most
radicals
OOHOH .2
.
.. OOHOOHOH radicals (radical reaction will be initiated)
• Low frequency (20 KHz) OHOHH ..
22 OOHOOHOH
22.. OHOHOH
• Low frequency (20 KHz) – Collapse time 10 μs– Enough time for radicals to
recombine
OHOHH 2
recombine
21Luche, J. L. Synthetic Organic Sonochemistry, Plenum Press, New York, 1998, pp. 1–19
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Acoustic pressure and frequency effectAcoustic pressure and frequency effect Sono‐oxidation of 2,2,6,6‐tetramethylpiperidin‐4‐one
N
O
O2 or Ar
1
Frequency Gas present Rate of nitroxideformation
.OH form
NO2
2 3 4
formation
520KHz O2 3.6 x 10‐6 M/min Free
520KHz Ar No nitroxide Free
20KHz O2 0.083 x 10‐6 M/min recombined
20KHz Ar 1.08 x 10‐6 M/min recombined
Petrier, C.; Jeunet, A.; Luche, J.‐L.; Reverdy, G. J. Am. Chem. Soc. 1992, 114, 3148‐315222
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Sono‐oxidation of h l i idi2,2,6,6‐tetramethylpiperidin‐4‐one
High Frequency 520KHz Low Frequency 20KHz
)))).. OOHOHOH
Presence of Ar Presence of Ar
HOHOH ..))))2
2
2
2 OOOOHOHOH
23Petrier, C.; Jeunet, A.; Luche, J.‐L.; Reverdy, G. J. Am. Chem. Soc. 1992, 114, 3148‐3152
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Acoustic intensityAcoustic intensity
PI 2/2 cPI A 2/2I = acoustic intensity (sound strength)P = acoustic pressure amplitudePA = acoustic pressure amplitudeρ = density of the fluidC = speed of transmission
• Acoustic intensity sonochemical effect
• Minimal intensity is required to reach cavitation threshold
24Luche, J. L. Synthetic Organic Sonochemistry, Plenum Press, New York, 1998, pp. 1–19
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Intensity effectIntensity effect
Ph
Chalcone Pentane‐2,4‐dione
Ph Ph
Ph
Ph
O
OOPh
OO
O OO KOH
TBAB
A B
Conditions A (%) B(%)
A B
Stirring 52 0
)))), Cup‐horn 69 0
Sound IntensityProbe >> Cup‐horn 100W 10W
)))), Probe 72 12
Mason, T. J.; Berlan, J. Current Trends in Sonochemistry, G. J. Price, Royal Society of Chemistry, Cambridge, 1992, pp. 148–157 25
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Summary (Cavitation)Summary (Cavitation)
• Ultrasound waves indirectly affect chemical reaction through cavitation phenomenon
• Cavitation generates a vacuum form bubbles which grow over a• Cavitation generates a vacuum, form bubbles which grow over a few cycles and collapse violently
• The energy generated by the collapse manipulates the reaction
• High frequency (500KHz) radical mechanism might be favored• High frequency (500KHz), radical mechanism might be favored
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OutlineOutline• Ultrasound (US)
– Definition and backgroundDefinition and background
• Cavitation phenomenon– Characteristics and influencing factors
• Sample sonochemical reactions in organic synthesis– Kornblum‐Russell reaction
Hetero Michael reaction– Hetero‐Michael reaction– Preparation of Grignard reagent– Suzuki coupling
• Cavitation induced mechanochemistry– Cleavage of azo‐linkages– Reconfiguration of atropisomersg p– Electrocyclic opening of benzocyclobutene
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Sonochemichal reactionsSonochemichal reactions
• Switching reactionsSwitching reactions– Kornblum‐Russell reaction
• Homogeneous reactions• Homogeneous reactions– Hetero Michael reaction
• Heterogeneous reactions– Metal activation reactions
• Grignard reagent preparation
– Palladium catalyzed coupling reactions• Suzuki coupling
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Ultrasound‐assisted Kornblum‐Russell ireaction
5 6 7
85 6
29Dickens, M. J.;Luche, J. L. Tetrahedron Lett. 1991, 32, 4709‐4712
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Kornblum‐Russell reaction mechanismKornblum Russell reaction mechanism
Polar pathway
O2NBr
NO
OLi
Polar pathway
SET pathway
5 6 7
8
5
30Dickens, M. J.;Luche, J. L. Tetrahedron Lett. 1991, 32, 4709‐4712
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Ultrasound‐assisted Hetero‐Michael ireaction
OH C HNR
NHRO
OEtHO
H3CH3C
OO
CH3H3C
HN
H2O, r.t., 2 h
NH2R
9
R = 90%
91%
10
11
9
12
Arcadi, A.; Alfonsi, M.; Marinelli, F. Tetrahedron Lett. 2009, 50, 2060–2064Tejedor, D.; Santos‐Expósito, A.; García‐Tellado, F. Synlett 2006, 1607‐1609 31
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Ultrasound‐assisted Grignard Reagent ipreparation
d l l• Traditional:– Oxide free Magnesium– Periodic crushing of metal
• Ultrasonication:– Any grade of Magnesium– Crushing not requiredg g q
SiMe3 SiMe3Mg, THF,
Br MgBr)))), 45oC, 1 h90%13 14
SiMe3
Br
Mg, THF,
45oC, 1 hX
13
Yamaguchi, R.; Kawasaki, H; Kawanisi, M. Synth. Commun. 1982, 12, 1027‐103732
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Ultrasound‐assisted Suzuki couplingUltrasound assisted Suzuki coupling
Ph B(OH)2 Ph Ph1 mol% Pd(OAc)2
Ar, NaOAc[bbim]+BF4
-/MeOH 92%
IPh
15 16 17, r.t., 20 min15 16 17
Ph I Ph B(OH)2 Ph Ph1 mol% Pd(OAc)2
Ar, NaOAc[bbim]+BF4
-/MeOH 25%30oC, 10 h15 16 17
Deshmukh, R. R.; Jarikote, D. V.; Srinivasan, K. V. Chem. Commun. 2002, 616–61733
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Summary (Sonochemistry)Summary (Sonochemistry)
• Sonochemistry is utilized in organic synthesis in many areas (switching homogeneous and heterogeneous reactions)(switching, homogeneous and heterogeneous reactions)
• Sonochemistry might lead to better yields faster rates andSonochemistry might lead to better yields, faster rates and milder temperatures
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OutlineOutline• Ultrasound (US)
– Definition and backgroundDefinition and background
• Cavitation phenomenon– Characteristics and influencing factors
• Sample sonochemical reactions in organic synthesis– Kornblum‐Russell reaction
Hetero Michael reaction– Hetero‐Michael reaction– Preparation of Grignard reagent– Suzuki coupling
• Cavitation induced mechanochemistry– Cleavage of azo‐linkages– Reconfiguration of atropisomersg p– Electrocyclic opening of benzocyclobutene
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Mechanochemistry definitionMechanochemistry definition
• Mechanochemistry is the molecular‐scale coupling of the ec a oc e s y s e o ecu a sca e coup g o emechanical force and the chemical reaction
– Mechanical breakage
– Chemical behavior of mechanically‐stressed solids
C it ti l t d h– Cavitation‐related phenomena
– Shockwave chemistry and physicsShockwave chemistry and physics
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Cavitation bubble revisitedCavitation bubble revisited
Bulk: shear forcesBulk: shear forces
Interface:Interface:
MechanochemistryMechanochemistry
shear forcesshear forces
Cavity: extreme conditionCavity: extreme condition
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Cavitation induces shear forcesCavitation induces shear forces
polymer
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MechanophoresMechanophores
• Possess strategically weakened bonds
• Force transfered to the mechanophore from the polymer chain segments
• Undergo bond breakage or deformation• Undergo bond breakage or deformation
• Many examples for mechanically‐induced chemical processes:Cl f li k– Cleavage of azo‐linkages
– Reconfiguration of atropisomers– Electrocyclic opening of benzocyclobutene
= Mechanophore
= Polymer
39
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Ultrasound‐induced cleavage of azo‐linkagesUltrasound induced cleavage of azo linkages
))))..
N2
Frequency = 20 kHz
|||
q yIntensity = 8.7 W/cm2
Temperature = 6‐9 °C18
40Berkowski, K. L.; Potisek, S.L.; Hickenboth,C.R.; Moore, J.S. Macromolecules 2005, 38, 8975-8978
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Specific chain scissionSpecific chain scission
40KDa
18
40KDa
20KDa18
20KDa
19
41Berkowski, K. L.; Potisek, S.L.; Hickenboth,C.R.; Moore, J.S. Macromolecules 2005, 38, 8975-8978
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Control experiment of non‐specific scissionControl experiment of non specific scission
40KDa 40KDa
20KDa
18 20
42
8 0
Berkowski, K. L.; Potisek, S.L.; Hickenboth,C.R.; Moore, J.S. Macromolecules 2005, 38, 8975-8978
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Differentiation from thermolysis productDifferentiation from thermolysis product
ThermolysisCH
3CN sis3CN, 82 oC
43Berkowski, K. L.; Potisek, S.L.; Hickenboth,C.R.; Moore, J.S. Macromolecules 2005, 38, 8975-8978
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13C NMR characterizationC NMR characterization
2219
21
18Black = after sonication for 47 minRed = after thermolysis for 24 hBlue = before thermolysis
44Berkowski, K. L.; Potisek, S.L.; Hickenboth,C.R.; Moore, J.S. Macromolecules 2005, 38, 8975-8978
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Mechanical reconfiguration of i *atropisomers*
S BINOL R BINOLIsomerization barrierS‐BINOL R‐BINOLIsomerization barrier>30kcal mol‐1
S‐BINAP R‐BINAP
*Atropisomers: chiral molecules whose asymmetric structures are derived from hindered rotations about sterically congested bonds
45Wiggins,K. M.; Hudnall,T. W.; Shen, Q.; Kryger, M. J.; Moore, J. S.; Bielawski, C. W. J. Am. Chem. Soc.2010, 132, 3256–3257
about sterically congested bonds
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Mechanochemistry is involvedMechanochemistry is involved
)))) ))))
S‐polymer R‐polymer
≡≡
23
46Wiggins,K. M.; Hudnall,T. W.; Shen, Q.; Kryger, M. J.; Moore, J. S.; Bielawski, C. W. J. Am. Chem. Soc.2010, 132, 3256–3257
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Isomerization monitoring by i l i h i ( )Circular Dichroism (CD)
Before sonication
After sonicationAfter sonication
OO O
O
CO2CH3
Br
CO CH
n
))))
CO2CH3
Brn
23
> 95% undergoes > 95% undergoes racimizationracimization
Aliquots removed at 0, 2, 4, 8, 12 and 24hAliquots removed at 0, 2, 4, 8, 12 and 24h
47Wiggins,K. M.; Hudnall,T. W.; Shen, Q.; Kryger, M. J.; Moore, J. S.; Bielawski, C. W. J. Am. Chem. Soc.2010, 132, 3256–3257
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Isomerization monitoring by i l i h i ( )Circular Dichroism (CD)
Before sonication
After sonicationAfter sonication
))))
> 95% undergoes > 95% undergoes racemizationracemization
23
Aliquots removed at 0, 2, 4, 8, 12 and 24hAliquots removed at 0, 2, 4, 8, 12 and 24h
48Wiggins,K. M.; Hudnall,T. W.; Shen, Q.; Kryger, M. J.; Moore, J. S.; Bielawski, C. W. J. Am. Chem. Soc.2010, 132, 3256–3257
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Attempts at thermal racemizationAttempts at thermal racemization
Before heating
270oC
After heating
270 C72h
Thermal Gravimetric Analysis (TGA)
49Wiggins,K. M.; Hudnall,T. W.; Shen, Q.; Kryger, M. J.; Moore, J. S.; Bielawski, C. W. J. Am. Chem. Soc.2010, 132, 3256–3257
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Importance of polymer incorporationImportance of polymer incorporation
))))26
OO O
O
Br
O
O+ ))))27
Br
O
25
OO O
O
O
O+ ))))28
25
50Wiggins,K. M.; Hudnall,T. W.; Shen, Q.; Kryger, M. J.; Moore, J. S.; Bielawski, C. W. J. Am. Chem. Soc.2010, 132, 3256–3257
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Electrocyclic opening of benzocyclobuteneElectrocyclic opening of benzocyclobutene
HN
O
O
PEG
))))
O
O
)))) ciscisLFP LFP
= MechanophoreHN
OO
PEG
29 30= Polymer
PEG = Poly ethylene glycol
29
l k f l d l
30
51Hickenboth, C. R.; Moore, J. S.; White, S. R.; Sottos, N. R.; Baudry, J; Wilson, S. R. Nature 2007, 446, 423‐427
LFPLFP = link‐functionalized polymer
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Unexpected results for ring opening?Unexpected results for ring opening?
HO
O
HN
O
PEG
O
O
O
O
O
O
O
O
mPEG-NH2
DCC, DMAP
transtransLFP LFP
Heat (E, E)
O
OH
OO
O
HN
OO
PEG
CH2Cl2 ))))(E, E)
31 32
Heat(E, Z)
ciscisLFP LFP
))))(E E)
Violation of Woodward‐Hoffmann rules
LFPLFP = link‐functionalized polymer 52
(E, E)29 30
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Woodward‐Hoffmann rulesWoodward Hoffmann rules
H CH3 H3C CH3HH
Heat
Conrotatory
ConrotatoryH3C H
HH
(E,E)trans-compound
Conrotatory
Disrotatory
Disrotatory
53Woodward, R. B.; Hoffmann, R. Angew. Chem. Int. Ed. 1969, 8, 781‐853
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Ultrasound conditionsUltrasound conditions
H CH3 H3C CH3HH
Heat
H3C HHH
(2E,4E)-hexa-2,4-diene(3R,4S)-3,4-dimethylcyclobut-1-ene
XX
54
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Ultrasound conditionsUltrasound conditions
H CH3 H3C CH3HH
Heat
H3C HHH
(2E,4E)-hexa-2,4-diene(3R,4S)-3,4-dimethylcyclobut-1-ene
55
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Mechanical effect on configurationMechanical effect on configuration
≡
( )trans (E,E)trans
Violation of Woodward‐Hoffmann rules
≡≡
(E,E)cis
56Hickenboth, C. R.; Moore, J. S.; White, S. R.; Sottos, N. R.; Baudry, J; Wilson, S. R. Nature 2007, 446, 423‐427
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Do modeling calculations agree?Do modeling calculations agree?
• Minimal energy pathwayMinimal energy pathway (MEP) calculations
• B3LYP density functional theory (DFT)
• 6‐31G** basis set
Ong, M. T.; Leiding, J.; Tao, H.; Virshup, A.M.; Martinez, T. J. J. Am. Chem. Soc. 2009, 131, 6377–637957
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Minimal energy pathwaysMinimal energy pathways
Disrotatory ConrotatoryDisrotatory Conrotatory
cis
S.M.Pdt. S.M.S.M.S.M.
Pdt.
cistrans
Pdt.Pdt.
Conrotatory and disrotatory pathways become equivalent at an applied force of 1.5nN
Ong, M. T.; Leiding, J.; Tao, H.; Virshup, A.M.; Martinez, T. J. J. Am. Chem. Soc. 2009, 131, 6377–637958
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Trapping the intermediateTrapping the intermediateHO
O
HN
O
PEG
O
O
O
O
O
O
mPEG-NH2
DCC, DMAPCH2Cl2
transtransLFP LFP
))))
OH
OO
HN
OO
PEG3133
32
HO
O
HN
O
PEGN‐(1‐pyrene)‐maleimide
(Dienophile)
34O
O
O
O
O
O
mPEG-NH2
DCC, DMAPCH2Cl2
ciscisLFP LFP
))))One product
34
OH
OO
HN
OO
PEG 59LFPLFP = link‐functionalized polymer
29 30
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Control experimentsControl experiments
LFP 3 reaction with the pyrene‐labeled dienophile, without sonicationLFP 3 reaction with the pyrene labeled dienophile, without sonication
Hickenboth, C. R.; Moore, J. S.; White, S. R.; Sottos, N. R.; Baudry, J; Wilson, S. R. Nature 2007, 446, 423‐42760
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Proof of incorporationProof of incorporation
• trans polymer product
• cis polymer product
• PEG polymer
This indicates that pyrene‐labeled dienophiles are incorporated to polymers61
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13C labeling experimentsC labeling experimentsHN
O
PEG
O
O
O
Heat or US
O*
HNPEG
O
transtransLFP LFP
HN
OO
PEG
N
O
*
*
N
OOO
*32
33
HN
O
PEG
OO
HNPEG
O
O
*
34
O
O
O
O
US
PEG
ciscisLFP LFP
HN
OO
PEG62
30
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13C NMR analysis35
C NMR analysis
Control compound
Control compound
Thermal, cis (decomposes)
Thermal, transN‐pyrene‐2,3‐naphthimide
Sonication, cis
Sonication, transSonication, trans
Arnold, B. J.; Sammes, P. G..; Wallace, T. W. J. Chem. Soc. Perkin Trans. I 1974, 41563
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Chain length factorChain length factor
4 kDa S.M.
40 kDaSonicated
4 kDaSonicated
13C NMR
cis
32 Sonicated
4 kD S M
32
4 kDa S.M.
40 kDaSonicatedtrans
4 kDaSonicated
13C NMR
30
64
Amide carbonyl (red) in the starting materialEster carbonyl (blue) in the starting materialAmide carbonyl (green) in Diels‐Alder adduct
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Summary (Mechanochemistry)Summary (Mechanochemistry)
• Ultrasound can be applied to polymer based reagents to breakUltrasound can be applied to polymer based reagents to break or reconfigure bonds in chemical reactions
• The mechanical effects can be clearly differentiated from the thermal effects in the presence of polymeric chains
• Shear forces generated by cavitation, represent the most accepted explanation for the observed mechanochemical effects
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ConclusionConclusion
• Although low in energy, ultrasound waves can indirectly effect chemical reactions ia a high energ e ent referred to as thechemical reactions, via a high energy event referred to as the cavitation phenomenon
• Recent advances in mechanochemistry show a considerable potential in the fields of polymer and organic chemistry
• Additional research needs to be conducted to better understand the physical repercussions of the cavitation phenomenon, as well as, to
l th t ti l f lt d t h lexplore the potentials of ultrasound technology
• Ultrasound technology has more potentials, other than glassware gy p , gcleaning application
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AcknowledgmentAcknowledgment
• Prof. Xuefei Huango ue e ua g• Prof. Babak Borhan• Prof James E JacksonProf. James E. Jackson• Labmates• Allison Aman D Monica Gina Luis Q Anil• Allison, Aman D., Monica, Gina, Luis Q., Anil • My family• Audience• Audience
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Now, back to…..Now, back to…..
WORK !!!
St. Patrick’s day March Madness
WORK !!!
68http://games.espn.go.com/tcmen/en/entry?entryID=2724115&print=truehttp://consequenceofsound.net/wp‐content/uploads/2008/11/st_patricks_day_graphics_04.gif
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