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Synthesis of Branched, Cyclic & Functional Polymers Vijay Chavan, Dr. Roderic P. Quirk Department of Polymer Science, The University of Akron, Akron, Ohio- 44325
Department of Polymer Science at Akron Program Since  1967  First College of Polymer Science & Engineering in the world  New Building constructed in  1991
Akron & Polymer History ,[object Object],[object Object],[object Object],[object Object],[object Object]
1)   Controlled synthesis of Star Branched Polymers  Vijay Chavan, Roderic P. Quirk, Manuela Ocampo
Unique aspects of star polymers ,[object Object],[object Object],[object Object],[object Object],Grest, G. S.; Fetters, L. J.; Huang, J. S.; Richter, D.  Advances in Chemical Physics  1996 , 94 , 67-163 Foster, M. D.; Greenberg, C. C.; Teale, D. M.; Turner, C. M.; Corona-Galvan, S.; Cloutet, E.;  Butler, P. D.; Hammouda, B.; Quirk, R. P.  Macromol. Symp.  2000 , 149 , 263-268.
Applications of star / branched polymers (500 patents) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Prevents Cold Flow
Advantages of  Anionic Polymerization ,[object Object],Initiation Propagation R i >R p  most of the times No termination and no transfer Mn =  grams of monomer  Moles of initiator One initiator generates one Polymer chain
1) Star PS using DVB Degree of Branching from 5 to 39 f = Mn  branch /Mn  linear  = 5-39 [DVB]/[PSLi] = 2 to 30 Hseih, H.L.; Quirk, R.P.  Anionic Polymerization: Principles and Practical Appplications ; Marcel Dekker, Inc.: New York,  1996   Possibility of gelling
2)   Star polymers by condensing  living P - Li +  with  chlorosilanes Morton, M.; Helminiak, T. E.; Gadkary, S. D.; Bueche, F.  J. Polym. Sci.   1962 , 57 , 471-482  Mn star / Mn arm = 4.09 After fractionation PDI= 1.09
Combination of vinyl and chlorine group Nucleophilic substitution PS -  Li + VDMCS  VInyldimethylchlorosilane +
Chaumont, P.; Herz, J.; Rempp, P.  Eur. Polym. J.   1979 , 15 , 537-540.  THF, -70  0 C Excess Mn = 20k PDI = 1.1 Addition of living PSLi to VDMCS Reaction done in THF at -70  0 C
Reaction of PSLi with VDMCS Branches upon branches   Wilczek, L., US Patent 6,740,723 , Feb 11, 2003 f max = Mn  branched  / Mn  linear  = 5 THF , -78 0 C Approx 1:1 ratio Dupont
Aim of the research ,[object Object],[object Object]
Experiment Styrene Methanol VDMCS Methanol Ampoule for base sample Vacuum Methanol Solution Ampoule for base sample after 12 hrs Inlet for initiator
GPC Analysis M n base= 2,500 g/mol PDI = 1.02 M n :  23,000 g/mol PDI:  1.3
1 H NMR   No Vinyl peaks
-37.30 0 TMS PS-VDMCS-1.5-30C-3day Reported peaks for  –Si-Cl (17.65 ppm)  and  –Si-OCH 3  (6.66 ppm)  are absent  indicating complete substitution of Cl 29 Si NMR
PS-VDMCS-1.5-50C-3day PS-VDMCS-2.5-30C-3day PS-VDMCS-2.5-50C-3day PS-VDMCS-5-30C-3day PS-VDMCS-5-50C-3day
Effect of concentration of VDMCS Behavior unlike DVB
 
Viscosity of Star and Linear g η [ η ] star [ η ] linear = Contraction  parameter
Contraction factor g η   = [ η ] branched /  [ η ] linear Deffieux, A.; Schappacher, M.  Macromolecules ,  1999 , 32, 1797-1802 *Roovers, J.  Branched Polymers II , Springer,  1999 , 169 (f = Mn  star / Mn  linear  ) gη literature For f=8.9 is  0.44* Observed is 0.46
Contraction parameter observed vs theoretical 0.46 0.47 8.33 0.47 0.53 7.94 0.49 0.49 7.50 0.42 0.40 9.36 0.47 0.48 8.09 0.44 0.46 8.90 Calculated g n Observed [n]/[n]lin f
Melt Viscosity Data Linear Mn = 18k, PDI= 1.02 Star 17k, PDI = 1.21,  Star 22k , PDI = 1.30 Constant strain  Cone and plate rheometer Newtonian region
VDMCS star , Mn = 23k  , PDI = 1.47  DVB Star , Mn = 26k  , PDI =  1.58 Thermal Stability
Star Polystyrene
Conclusion ,[object Object],[object Object],[object Object],[object Object],[object Object]
Vijay Chavan*, Roderic P. Quirk, Shih Fan Wang, Mark D. Foster, Rebecca Agapov, Rahul Kulkarni, Xinfei Yu, Wumin Yu Topographical   Evidence of Cyclic Polymers
Cyclic Polymer
Two main methods of making cyclic polymers ,[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
A)Cyclization by anionic polymerization mg of product in liters of solvent Mixtures of products  Geiser, D.; Hocker, H.  Macromolecules   1980 , 13 , 653. Slow addition Tetrahydropyran Mn = 4k-24 k,  Smart way of separation Reacted the linear polymers with High MW  PSLi and fractionated
B)Cyclization by click chemistry Laurent, B.A.; Grayson, S.M. J. Am. Chem. Soc. , 2006, 128 (13), 4238 75 o  C, CuBr,PMDETA,  ATRP Mn = 2k, PDI = 1.08 200 mg product for 1 liter solvent
2)   Ring opening metathesis by Dr. Robert Grubbs Nobel Prize Winner in Chemistry 2005 http://en.wikipedia.org/wiki/File:Robert_Grubbs.jpg Can cyclic catalyst make cyclic polymer ? Fürstner, A.; Ackermann, L.; Babor, B.; Goddard, R.; Lehmann, C. W.; Mynott, R.; Stelzer, F.; Thiel, O. R.  Chem. Eur. J.   2001 , 7, 3236.
Polymer catalyst http://upload.wikimedia.org/wikipedia/commons/0/0e/Making_soapbubbles-SteveEF.jpg
Ru Complex A F ürstner, A.; Ackermann , L.; Babor, B.; Goddard, R.; Lehmann, C. W.; Mynott, R.; Stelzer, F.; Thiel, O. R.  Chem. Eur. J.   2001 , 7, 3236. Bielawski, C. W.; Benitez, D.; Grubbs, R. H.  Science  2002 , 297 , 2041-2044. Bielawski, C. W.; Benitez, D.; Grubbs, R. H.  J. Am. Chem. Soc.  2003 ,125 , 8424-8425. Complex A
Cyclic catalyst F ürstner, A.; Ackermann , L.; Babor, B.; Goddard, R.; Lehmann, C. W.; Mynott, R.; Stelzer, F.; Thiel, O. R.  Chem. Eur. J.   2001 , 7, 3236. Bielawski, C. W.; Benitez, D.; Grubbs, R. H.  Science  2002 , 297 , 2041-2044. Bielawski, C. W.; Benitez, D.; Grubbs, R. H.  J. Am. Chem. Soc.  2003 ,125 , 8424-8425. Red  Yellow
Complex 12c F ürstner, A.; Ackermann , L.; Babor, B.; Goddard, R.; Lehmann, C. W.; Mynott, R.; Stelzer, F.; Thiel, O. R.  Chem. Eur. J.   2001 , 7, 3236. Pentane/Ether : 4:1 volume ratio Argon Argon
31 P  NMR linear catalyst
31 P NMR Cyclic catalyst
Synthesis of Cyclic Polybutadiene Mn = 88 k, PDI = 2.06 CDT conc. 2.92 mol/L 5 g cyclic polymer  in 10 mL solution 80% yield
Log M n  vs elution time
Intrinsic viscosity vs Log M n  of linear   (broad polydispersity index PDI) and cyclic polybutadiene
SEC chromatogram of cyclic polybutadiene and linear polybutadiene  (narrow PDI prepared by anionic polymerization)
 
[object Object]
Synthesis of cyclic polymer brush Schappacher, M.; Deffieux, A.  Science  2008 , 319 , 1512-1515
AFM images
Example of grafting on 1,4-polybutadiene Hydrosilation on backbone Iraqi, A.; Seth, S.; Vincent, C. A.; Cole-Hamilton, D.; Watkinson, M. D.; Graham, I. M.; Jeffrey, D.  Journal of Materials Chemistry  1992 , 2 , 1057-1064.
Polybutadiene composition 1,4-polybutadiene units
Results of hydrosilation
Grafting of CyPBD with PS-SiH 0.24 mmols
SEC chromatograms of  cylic polybutadiene, starting PS-SiH and grafted polymer.
Table 1 Molecular weight data of starting and grafted polymers 6.19 12,410,000 2,004,000 Grafted Ring  3 2.06 182,600 88,400 CyPBD 2 1.01 8,300 8,300 PS-SiH 1 M w /M n M w  (g/mol) M n  (g/mol) Sample ID Sr.No
AFM imgaes Calculated: 61k Inner diameter:  70-80 nm Outer diameter:  160-190 nm Height: ~ 4 Ǻ
Conclusion ,[object Object],[object Object]
Preference for reduction over electrophilic addition by polyisobutylene cations Vijay Chavan, Prof Roderic P.Quirk, Prof. Judit E. Puskas
Cationic Stability Carey, F. A.; Tremper, H. S.  J. Org. Chem.  1971 , 36 , 758-761.
Reaction scheme Hexanes: MeCl 60 : 40 [DtBP]= 0.007 mol/L; [TMPCl] = 0.035 mol/L; [IB] = 0.577 mol/L; [VPDS]= 0.047 mol/L; [TiCl4]= 0.227 mol/L; [DMA]= 0.019 mol/L
Figure 1:  GPC trace of PIB-Cl and Part 2 a) Refractive Index (RI) detector response b) Light scattering data.
 
Table 1: Molecular weight data [DtBP]= 0.007 mol/L; [TMPCl] = 0.035 mol/L; [IB] = 0.577 mol/L; [VPDS]= 0.047 mol/L; [TiCl4]= 0.227 mol/L; [DMA]= 0.019 mol/L 1.27 2,150 1,700 1,900 1.25 1,950 1,550 PDI Part 2 M w   Part 2 (GPC) (g/mol) M n  part 2 (GPC) (g/mol) M n Base (NMR) (g/mol) PDI Base M w  base (GPC) (g/mol) M n Base (GPC) (g/mol)
Figure 2: Proton NMR of PIB-Cl  starting polymer
Figure 3: Proton NMR of part 2.
Figure 4:  13 C NMR of PIB-Cl
Figure 5:  13 C NMR of part 2
Figure 6 : Mechanism
Conclusion of cationic polymerization ,[object Object],[object Object]
Acknowledgements ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Funding Repsol YPF, Spain Dynasol Elastomers FMC, Lithium Division Chemetall Foote Corporation
[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Applications of branched polymers references
References ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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PhD Presentation

  • 1. Synthesis of Branched, Cyclic & Functional Polymers Vijay Chavan, Dr. Roderic P. Quirk Department of Polymer Science, The University of Akron, Akron, Ohio- 44325
  • 2. Department of Polymer Science at Akron Program Since 1967 First College of Polymer Science & Engineering in the world New Building constructed in 1991
  • 3.
  • 4. 1) Controlled synthesis of Star Branched Polymers Vijay Chavan, Roderic P. Quirk, Manuela Ocampo
  • 5.
  • 6.
  • 7.
  • 8. 1) Star PS using DVB Degree of Branching from 5 to 39 f = Mn branch /Mn linear = 5-39 [DVB]/[PSLi] = 2 to 30 Hseih, H.L.; Quirk, R.P. Anionic Polymerization: Principles and Practical Appplications ; Marcel Dekker, Inc.: New York, 1996 Possibility of gelling
  • 9. 2) Star polymers by condensing living P - Li + with chlorosilanes Morton, M.; Helminiak, T. E.; Gadkary, S. D.; Bueche, F. J. Polym. Sci. 1962 , 57 , 471-482 Mn star / Mn arm = 4.09 After fractionation PDI= 1.09
  • 10. Combination of vinyl and chlorine group Nucleophilic substitution PS - Li + VDMCS VInyldimethylchlorosilane +
  • 11. Chaumont, P.; Herz, J.; Rempp, P. Eur. Polym. J. 1979 , 15 , 537-540. THF, -70 0 C Excess Mn = 20k PDI = 1.1 Addition of living PSLi to VDMCS Reaction done in THF at -70 0 C
  • 12. Reaction of PSLi with VDMCS Branches upon branches Wilczek, L., US Patent 6,740,723 , Feb 11, 2003 f max = Mn branched / Mn linear = 5 THF , -78 0 C Approx 1:1 ratio Dupont
  • 13.
  • 14. Experiment Styrene Methanol VDMCS Methanol Ampoule for base sample Vacuum Methanol Solution Ampoule for base sample after 12 hrs Inlet for initiator
  • 15. GPC Analysis M n base= 2,500 g/mol PDI = 1.02 M n : 23,000 g/mol PDI: 1.3
  • 16. 1 H NMR No Vinyl peaks
  • 17. -37.30 0 TMS PS-VDMCS-1.5-30C-3day Reported peaks for –Si-Cl (17.65 ppm) and –Si-OCH 3 (6.66 ppm) are absent indicating complete substitution of Cl 29 Si NMR
  • 18. PS-VDMCS-1.5-50C-3day PS-VDMCS-2.5-30C-3day PS-VDMCS-2.5-50C-3day PS-VDMCS-5-30C-3day PS-VDMCS-5-50C-3day
  • 19. Effect of concentration of VDMCS Behavior unlike DVB
  • 20.  
  • 21. Viscosity of Star and Linear g η [ η ] star [ η ] linear = Contraction parameter
  • 22. Contraction factor g η = [ η ] branched / [ η ] linear Deffieux, A.; Schappacher, M. Macromolecules , 1999 , 32, 1797-1802 *Roovers, J. Branched Polymers II , Springer, 1999 , 169 (f = Mn star / Mn linear ) gη literature For f=8.9 is 0.44* Observed is 0.46
  • 23. Contraction parameter observed vs theoretical 0.46 0.47 8.33 0.47 0.53 7.94 0.49 0.49 7.50 0.42 0.40 9.36 0.47 0.48 8.09 0.44 0.46 8.90 Calculated g n Observed [n]/[n]lin f
  • 24. Melt Viscosity Data Linear Mn = 18k, PDI= 1.02 Star 17k, PDI = 1.21, Star 22k , PDI = 1.30 Constant strain Cone and plate rheometer Newtonian region
  • 25. VDMCS star , Mn = 23k , PDI = 1.47 DVB Star , Mn = 26k , PDI = 1.58 Thermal Stability
  • 27.
  • 28. Vijay Chavan*, Roderic P. Quirk, Shih Fan Wang, Mark D. Foster, Rebecca Agapov, Rahul Kulkarni, Xinfei Yu, Wumin Yu Topographical Evidence of Cyclic Polymers
  • 30.
  • 31.
  • 32. A)Cyclization by anionic polymerization mg of product in liters of solvent Mixtures of products Geiser, D.; Hocker, H. Macromolecules 1980 , 13 , 653. Slow addition Tetrahydropyran Mn = 4k-24 k, Smart way of separation Reacted the linear polymers with High MW PSLi and fractionated
  • 33. B)Cyclization by click chemistry Laurent, B.A.; Grayson, S.M. J. Am. Chem. Soc. , 2006, 128 (13), 4238 75 o C, CuBr,PMDETA, ATRP Mn = 2k, PDI = 1.08 200 mg product for 1 liter solvent
  • 34. 2) Ring opening metathesis by Dr. Robert Grubbs Nobel Prize Winner in Chemistry 2005 http://en.wikipedia.org/wiki/File:Robert_Grubbs.jpg Can cyclic catalyst make cyclic polymer ? Fürstner, A.; Ackermann, L.; Babor, B.; Goddard, R.; Lehmann, C. W.; Mynott, R.; Stelzer, F.; Thiel, O. R. Chem. Eur. J. 2001 , 7, 3236.
  • 36. Ru Complex A F ürstner, A.; Ackermann , L.; Babor, B.; Goddard, R.; Lehmann, C. W.; Mynott, R.; Stelzer, F.; Thiel, O. R. Chem. Eur. J. 2001 , 7, 3236. Bielawski, C. W.; Benitez, D.; Grubbs, R. H. Science 2002 , 297 , 2041-2044. Bielawski, C. W.; Benitez, D.; Grubbs, R. H. J. Am. Chem. Soc. 2003 ,125 , 8424-8425. Complex A
  • 37. Cyclic catalyst F ürstner, A.; Ackermann , L.; Babor, B.; Goddard, R.; Lehmann, C. W.; Mynott, R.; Stelzer, F.; Thiel, O. R. Chem. Eur. J. 2001 , 7, 3236. Bielawski, C. W.; Benitez, D.; Grubbs, R. H. Science 2002 , 297 , 2041-2044. Bielawski, C. W.; Benitez, D.; Grubbs, R. H. J. Am. Chem. Soc. 2003 ,125 , 8424-8425. Red Yellow
  • 38. Complex 12c F ürstner, A.; Ackermann , L.; Babor, B.; Goddard, R.; Lehmann, C. W.; Mynott, R.; Stelzer, F.; Thiel, O. R. Chem. Eur. J. 2001 , 7, 3236. Pentane/Ether : 4:1 volume ratio Argon Argon
  • 39. 31 P NMR linear catalyst
  • 40. 31 P NMR Cyclic catalyst
  • 41. Synthesis of Cyclic Polybutadiene Mn = 88 k, PDI = 2.06 CDT conc. 2.92 mol/L 5 g cyclic polymer in 10 mL solution 80% yield
  • 42. Log M n vs elution time
  • 43. Intrinsic viscosity vs Log M n of linear (broad polydispersity index PDI) and cyclic polybutadiene
  • 44. SEC chromatogram of cyclic polybutadiene and linear polybutadiene (narrow PDI prepared by anionic polymerization)
  • 45.  
  • 46.
  • 47. Synthesis of cyclic polymer brush Schappacher, M.; Deffieux, A. Science 2008 , 319 , 1512-1515
  • 49. Example of grafting on 1,4-polybutadiene Hydrosilation on backbone Iraqi, A.; Seth, S.; Vincent, C. A.; Cole-Hamilton, D.; Watkinson, M. D.; Graham, I. M.; Jeffrey, D. Journal of Materials Chemistry 1992 , 2 , 1057-1064.
  • 52. Grafting of CyPBD with PS-SiH 0.24 mmols
  • 53. SEC chromatograms of cylic polybutadiene, starting PS-SiH and grafted polymer.
  • 54. Table 1 Molecular weight data of starting and grafted polymers 6.19 12,410,000 2,004,000 Grafted Ring 3 2.06 182,600 88,400 CyPBD 2 1.01 8,300 8,300 PS-SiH 1 M w /M n M w (g/mol) M n (g/mol) Sample ID Sr.No
  • 55. AFM imgaes Calculated: 61k Inner diameter: 70-80 nm Outer diameter: 160-190 nm Height: ~ 4 Ǻ
  • 56.
  • 57. Preference for reduction over electrophilic addition by polyisobutylene cations Vijay Chavan, Prof Roderic P.Quirk, Prof. Judit E. Puskas
  • 58. Cationic Stability Carey, F. A.; Tremper, H. S.  J. Org. Chem.  1971 , 36 , 758-761.
  • 59. Reaction scheme Hexanes: MeCl 60 : 40 [DtBP]= 0.007 mol/L; [TMPCl] = 0.035 mol/L; [IB] = 0.577 mol/L; [VPDS]= 0.047 mol/L; [TiCl4]= 0.227 mol/L; [DMA]= 0.019 mol/L
  • 60. Figure 1: GPC trace of PIB-Cl and Part 2 a) Refractive Index (RI) detector response b) Light scattering data.
  • 61.  
  • 62. Table 1: Molecular weight data [DtBP]= 0.007 mol/L; [TMPCl] = 0.035 mol/L; [IB] = 0.577 mol/L; [VPDS]= 0.047 mol/L; [TiCl4]= 0.227 mol/L; [DMA]= 0.019 mol/L 1.27 2,150 1,700 1,900 1.25 1,950 1,550 PDI Part 2 M w Part 2 (GPC) (g/mol) M n part 2 (GPC) (g/mol) M n Base (NMR) (g/mol) PDI Base M w base (GPC) (g/mol) M n Base (GPC) (g/mol)
  • 63. Figure 2: Proton NMR of PIB-Cl starting polymer
  • 64. Figure 3: Proton NMR of part 2.
  • 65. Figure 4: 13 C NMR of PIB-Cl
  • 66. Figure 5: 13 C NMR of part 2
  • 67. Figure 6 : Mechanism
  • 68.
  • 69.
  • 70.
  • 71.
  • 72.