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  • Electronic Resource  (3)
  • polymerization  (2)
  • trityl tetrakis(pentafluorophenyl)borate  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1899-1909 
    ISSN: 0887-624X
    Keywords: spiro(benzoxasilole) ; oxetane ; catalysis ; polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A spiro(benzoxasilole) catalyst, 3,3,3′,3′-tetrakis(trifluoromethyl)-1,1′-(3H,3H′)-spirobis(1,2-benzoxasilole) was used to polymerize 3,3-R,R′-oxetanes: BEMO (R, R′ = ethoxymethyl), AMMO (R = azidomethyl, R′ = methyl), NMMO (R = nitratomethyl, R′ = methyl), BAMO (R, R′ = azidomethyl), and BCMO (R, R′ = chloromethyl) with descending rates in this order. 31P-NMR of polymerization mixtures quenched using Bu3P are consistent with an oxonium ion propagating species. Water is not a cocatalyst because it increases the induction period which is not eliminated by the proton trap 2,6-di-t-bu-tylpyridine. The propagating chains were terminated by transfer with the ether oxygen of the polymer either intermolecularly or intramolecularly. The index of propagation to chain transfer, Kkikp/ktr, varies over more than three orders of magnitude for BEMO 〉 AMMO 〉 NMMO 〉 BAMO. However, kp/ktr for the four monomers differ by less than a factor of five indicating the same factors are affecting propagation and chain transfer. Addition of benzyl alcohol and propandiol produced poly(BEMO) having one and two hydroxyl termini, respectively. These telechelic polymers can be used to synthesize linear triblock or multiblock copolymers of oxetane derivatives. © 1992 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 8 (1994), S. 393-396 
    ISSN: 0268-2605
    Keywords: Polystyrene ; syndiotactic ; syndioselective ; MAO ; cationic catalysts ; trityl tetrakis(pentafluorophenyl)borate ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An equimolar mixture of Cp*Ti(CH3)3 (2) and Ph3C+[B(C6F5)4]- (1) forms a highly active and syndioselective catalyst for the polymerization of styrene, producing 96% syndiotactic polystyrene (PS) at an activity of 0.91 × 107 g PS (mol Ti)-1 (mol styrene)-1 h-1. Both activity and syndioselectivity can be increased using tri-isobutylaluminum (TIBA) to scavenge the system. ESR measurements indicate that the polymerization proceeds via titanium(IV) intermediates. Catalysts derived from 2/methylaluminoxane (MAO) as well as Cp*TiCl3/MAO also function as syndioselective styrene polymerization catalysts, but are less active than the ‘cationic’; system derived from 1 and 2.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 7 (1993), S. 71-74 
    ISSN: 0268-2605
    Keywords: Polypropylene ; polymerization ; isospecificity ; alkylzirconocene-type cations ; stereoselectivity ; MAO ; cationic catalysts ; trityl tetrakis(pentafluorophenyl)borate ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rac-ethylenebis(indenyl)methylzirconium ‘cation’ (1), generated from rac-Et(Ind)2ZrMe2 and Ph3CB(C6F5)4, has recently been shown to be exceedingly active and stereoselective in propylene polymerization. The ethyl analog (2) can be produced by an alternate, efficient route involving a reaction between rac-Et(Ind)2ZrCl2 and AlEt3 (TEA), followed by addition of Ph3CB(C6F5)4. The use of excess AlEt3 serves both to alkylate the zirconium complex as well as to scavenge the system. The propylene polymerization activity of the ‘cation’ 2 is about 7000 times greater than the activity of rac-Et(Ind)2ZrCl2/methylaluminoxane (MAO) at Tp=-20°C. The related catalyst system rac-Me2Si(Ind)2ZrCl2/TEA/Ph3CB(C6F5)4 (3) was found to produce 98.3% i-PP with Tm 156.3°C and an activity of 1.8 × 109 g PP {(mol Zr) [C3H6]h}-1.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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