1981
DOI: 10.1016/0032-3861(81)90394-3
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New perfectly difunctional organolithium initiators for block copolymer synthesis: Synthesis of dilithium initiators in the absence of polar additives

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Cited by 62 publications
(14 citation statements)
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“…The elastomeric block of polybutadiene was first synthesized in pure hexane at room temperature. Initiation was made using either tert-BuLi for the synthesis of diblocks (BP) and of the graft copolymer (BGP) or a dilithium initiator (for triblocks PBP) [13].…”
Section: Methodsmentioning
confidence: 54%
“…The elastomeric block of polybutadiene was first synthesized in pure hexane at room temperature. Initiation was made using either tert-BuLi for the synthesis of diblocks (BP) and of the graft copolymer (BGP) or a dilithium initiator (for triblocks PBP) [13].…”
Section: Methodsmentioning
confidence: 54%
“…These sequences depend on the functionality of the initiator (mono-or bifunctional initiators) [172][173][174][175], on the use of coupling agents [176,177], and on the sharpness of the transition between the various blocks. Another reason for apportioning the monomer feed is the limited heat removal capacity of the reactor.…”
Section: Industrial Aspects -Production Of Living Polymersmentioning
confidence: 99%
“…BufCH21Htn-fCH2CH=CHCHz+;Li + n Styrene 2) CH 3 0H) C 6 H 5 (3) This sequential method using a monofunctional initiator cannot be used, however, to synthesize the following A-B-A type of triblock copolymer: (9) 3 to prepare dilithium initiators in hydrocarbon media have resulted in hydrocarbon-insoluble precipitates because of the strong association of organolithium chain ends in hydrocarbon media. A preliminary report has described conditions for efficient preparation and use of this initiator to generate 8 difunctional polymers.…”
Section: )mentioning
confidence: 99%
“…Other attempts to utilize both soluble and insoluble [9][10][11] dilithium initiators in hydrocarbon media have been reported recently.…”
Section: )mentioning
confidence: 99%